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    <title>Recent lbnl_bs_egsb items</title>
    <link>https://escholarship.org/uc/lbnl_bs_egsb/rss</link>
    <description>Recent eScholarship items from Environ Genomics &amp; Systems Bio</description>
    <pubDate>Fri, 15 May 2026 10:09:39 +0000</pubDate>
    <item>
      <title>Many paths, similar destinations: viruses and bacterial microcompartments form polyhedra inside cells.</title>
      <link>https://escholarship.org/uc/item/4fd96726</link>
      <description>A large number of biological entities assemble into icosahedral structures, and these are ubiquitous throughout nature. Examples include eukaryotic and prokaryotic viral capsids and more recently discovered bacterial microcompartments. Viral capsids and bacterial microcompartments are both composed of pentameric and hexameric subunits; however, they differ in the type of cargo they encapsulate: nucleic acid or protein. Also, both depart from strict icosahedral symmetry: while this is less common in viruses, among bacterial microcompartments, diverse and heterogeneous polyhedra are common. We review shared principles and key distinctions between the self-directed assembly of various icosahedral architectures and their polyhedral variants in nature and explore the concept that there are multiple paths, influenced by their cargo, to arriving at similar protein cage morphologies.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4fd96726</guid>
      <pubDate>Wed, 13 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Parent, Kristin N</name>
      </author>
      <author>
        <name>Kerfeld, Cheryl A</name>
        <uri>https://orcid.org/0000-0002-9977-8482</uri>
      </author>
    </item>
    <item>
      <title>Phenylpropanoid methyl esterase unlocks catabolism of aromatic biological nitrification inhibitors</title>
      <link>https://escholarship.org/uc/item/5kf76306</link>
      <description>Microbial nitrification of fertilizers represents is a significant global source of greenhouse gas emissions. This process increases emissions, fosters toxic algal blooms, and raises crop production costs. Some plants naturally release biological nitrification inhibitors to suppress ammonium-oxidizing microbes and reduce nitrification. Engineering nitrification inhibitor production into food and bioenergy crops via synthetic biology offers a promising mitigation strategy, but its success depends on addressing gaps in our understanding of inhibitor degradation in soil. This study begins to fill this gap by identifying a previously unknown microbial pathway for degrading phenylpropanoid methyl esters, a key class of aromatic nitrification inhibitors. Using transcriptomics and high-throughput functional genomics, we discovered genes essential for phenylpropanoid methyl ester degradation. Genetic and biochemical analyses revealed two novel enzymes, including a newly identified phenylpropanoid...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5kf76306</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wilson, Andrew</name>
      </author>
      <author>
        <name>Van Fossen, Elise</name>
      </author>
      <author>
        <name>Shrestha, Ritu</name>
      </author>
      <author>
        <name>Frank, Andrew</name>
      </author>
      <author>
        <name>Trotter, Valentine</name>
        <uri>https://orcid.org/0000-0002-1784-9487</uri>
      </author>
      <author>
        <name>Baldino, Henri</name>
      </author>
      <author>
        <name>Poirier, Brenton</name>
      </author>
      <author>
        <name>Kim, Young-Mo</name>
      </author>
      <author>
        <name>Nelson, William</name>
      </author>
      <author>
        <name>Simmons, Tuesday</name>
      </author>
      <author>
        <name>Coleman-Derr, Devin</name>
      </author>
      <author>
        <name>Deutschbauer, Adam</name>
      </author>
      <author>
        <name>Egbert, Robert</name>
      </author>
      <author>
        <name>Elmore, Joshua</name>
      </author>
    </item>
    <item>
      <title>Contrasting effects of glutamate and branched-chain amino acid metabolism on acid tolerance in a Castellaniella isolate from acidic groundwater</title>
      <link>https://escholarship.org/uc/item/2sp79776</link>
      <description>ABSTRACT    Groundwater acidification co-occurring with nitrate pollution is a common, global environmental health hazard. Denitrifying bacteria have been leveraged for the in situ removal of nitrate in groundwater. However, co-existing stressors—such as low pH—reduce the efficacy of biological removal processes. Castellaniella sp. str. MT123 is a complete denitrifier that was isolated from acidic, nitrate-contaminated groundwater. The strain grows robustly by nitrate respiration at pH &amp;lt; 6.0, completely reducing nitrate to dinitrogen gas. Genomic analyses of MT123 revealed few previously characterized acid tolerance genes. Thus, we utilized a combination of proteomics, metabolomics, and competitive mutant fitness to characterize the genetic mechanisms of MT123 acclimation to growth under mildly acidic conditions. We found that glutamate accumulation is critical in the acid acclimation of MT123, possibly through consumption of intracellular protons via glutamate decarboxylation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2sp79776</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Goff, Jennifer L</name>
      </author>
      <author>
        <name>Durrence, Konnor L</name>
      </author>
      <author>
        <name>Thorgersen, Michael P</name>
      </author>
      <author>
        <name>Trotter, Valentine V</name>
        <uri>https://orcid.org/0000-0002-1784-9487</uri>
      </author>
      <author>
        <name>Chen, Yan</name>
      </author>
      <author>
        <name>Kosina, Suzanne M</name>
        <uri>https://orcid.org/0000-0003-2885-1248</uri>
      </author>
      <author>
        <name>Wang, Audrey LW</name>
      </author>
      <author>
        <name>Poole, Farris L</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
      </author>
      <author>
        <name>Petzold, Christopher J</name>
        <uri>https://orcid.org/0000-0002-8270-5228</uri>
      </author>
      <author>
        <name>Deutschbauer, Adam M</name>
      </author>
      <author>
        <name>Adams, Michael WW</name>
      </author>
    </item>
    <item>
      <title>STREAMS guidelines: standards for technical reporting in environmental and host-associated microbiome studies</title>
      <link>https://escholarship.org/uc/item/0nt0t4k2</link>
      <description>The interdisciplinary nature of microbiome research, coupled with the generation of complex multi-omics data, makes knowledge sharing challenging. The Strengthening the Organization and Reporting of Microbiome Studies (STORMS) guidelines provide a checklist for the reporting of study information, experimental design and analytical methods within a scientific manuscript on human microbiome research. Here, in this Consensus Statement, we present the standards for technical reporting in environmental and host-associated microbiome studies (STREAMS) guidelines. The guidelines expand on STORMS and include 67 items to support the reporting and review of environmental (for example, terrestrial, aquatic, atmospheric and engineered), synthetic and non-human host-associated microbiome studies in a standardized and machine-actionable manner. Based on input from 248 researchers spanning 28 countries, we provide detailed guidance, including comparisons with STORMS, and case studies that demonstrate...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0nt0t4k2</guid>
      <pubDate>Wed, 6 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kelliher, Julia M</name>
      </author>
      <author>
        <name>Mirzayi, Chloe</name>
      </author>
      <author>
        <name>Bordenstein, Sarah R</name>
      </author>
      <author>
        <name>Oliver, Aaron</name>
        <uri>https://orcid.org/0000-0002-0410-8284</uri>
      </author>
      <author>
        <name>Kellogg, Christina A</name>
      </author>
      <author>
        <name>Hatcher, Eneida L</name>
      </author>
      <author>
        <name>Berg, Maureen</name>
      </author>
      <author>
        <name>Baldrian, Petr</name>
      </author>
      <author>
        <name>Aljumaah, Mashael</name>
      </author>
      <author>
        <name>Miller, Cassandra Maria Luz</name>
      </author>
      <author>
        <name>Mungall, Christopher</name>
      </author>
      <author>
        <name>Novak, Vlastimil</name>
        <uri>https://orcid.org/0000-0001-7890-4593</uri>
      </author>
      <author>
        <name>Palucki, Alexis</name>
      </author>
      <author>
        <name>Smith, Ethan</name>
      </author>
      <author>
        <name>Tabassum, Nazifa</name>
      </author>
      <author>
        <name>Bonito, Gregory</name>
      </author>
      <author>
        <name>Brister, J Rodney</name>
      </author>
      <author>
        <name>Chain, Patrick SG</name>
      </author>
      <author>
        <name>Chen, Mingfei</name>
      </author>
      <author>
        <name>Degregori, Samuel</name>
      </author>
      <author>
        <name>Dundore-Arias, Jose Pablo</name>
      </author>
      <author>
        <name>Emerson, Joanne B</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
      <author>
        <name>Moreira C. Fernandes, Vanessa</name>
      </author>
      <author>
        <name>Flores, Roberto</name>
      </author>
      <author>
        <name>Gonzalez, Antonio</name>
      </author>
      <author>
        <name>Hansen, Zoe A</name>
      </author>
      <author>
        <name>Jackson, Scott A</name>
      </author>
      <author>
        <name>Moustafa, Ahmed M</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Pariente, Nonia</name>
      </author>
      <author>
        <name>Pett-Ridge, Jennifer</name>
      </author>
      <author>
        <name>Record, Sydne</name>
      </author>
      <author>
        <name>Reji, Linta</name>
      </author>
      <author>
        <name>Reysenbach, Anna-Louise</name>
      </author>
      <author>
        <name>Rich, Virginia I</name>
      </author>
      <author>
        <name>Richardson, Lorna</name>
      </author>
      <author>
        <name>Roux, Simon</name>
        <uri>https://orcid.org/0000-0002-5831-5895</uri>
      </author>
      <author>
        <name>Schriml, Lynn M</name>
      </author>
      <author>
        <name>Shabman, Reed S</name>
      </author>
      <author>
        <name>Sierra, Maria A</name>
      </author>
      <author>
        <name>Sullivan, Matthew B</name>
      </author>
      <author>
        <name>Sundaramurthy, Punithavathi</name>
      </author>
      <author>
        <name>Thibault, Katherine M</name>
      </author>
      <author>
        <name>Thompson, Luke R</name>
      </author>
      <author>
        <name>Tighe, Scott</name>
      </author>
      <author>
        <name>Vereen, Ethell</name>
      </author>
      <author>
        <name>Eloe-Fadrosh, Emiley A</name>
        <uri>https://orcid.org/0000-0002-8162-1276</uri>
      </author>
    </item>
    <item>
      <title>OpenScientist: evaluating an open agentic AI co-scientist to accelerate biomedical discovery</title>
      <link>https://escholarship.org/uc/item/8s85j1vr</link>
      <description>Background: Advances in medicine depend on analyzing large and complex data sources, but discovery is partly constrained by the limited time and domain expertise of human researchers. Agentic artificial intelligence (agentic AI) can accelerate discovery by automating components of the scientific workflow, including information retrieval, data analysis, and knowledge synthesis.
Aim: OpenScientist, an open-source agentic AI co-scientist, aims to accelerate biomedical discovery by semi-autonomously investigating scientist-defined queries and generating clinically relevant, verifiable scientific insights.
Methods: Domain experts evaluated OpenScientist for novel discoveries in four clinical case studies: (1) a prespecified analysis in a community-based Alzheimer's disease biomarker cohort, (2) unsupervised modeling for plasma proteomic survival prediction, (3) hypothesis investigation in single-cell transcriptomic data from neurons with neurofibrillary tangles, and (4) hypothesis...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8s85j1vr</guid>
      <pubDate>Tue, 5 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Roberts, Kaleigh F</name>
      </author>
      <author>
        <name>Abrams, Zachary B</name>
      </author>
      <author>
        <name>Cappelletti, Luca</name>
      </author>
      <author>
        <name>Moqri, Mahdi</name>
      </author>
      <author>
        <name>Heugel, Nicholas</name>
      </author>
      <author>
        <name>Caufield, J Harry</name>
      </author>
      <author>
        <name>Bourdenx, Mathieu</name>
      </author>
      <author>
        <name>Li, Yan</name>
      </author>
      <author>
        <name>Banerjee, Jineta</name>
      </author>
      <author>
        <name>Foschini, Luca</name>
      </author>
      <author>
        <name>Galeano, Diego</name>
      </author>
      <author>
        <name>Harris, Nomi L</name>
      </author>
      <author>
        <name>Li, Melody</name>
      </author>
      <author>
        <name>Ying, Kejun</name>
      </author>
      <author>
        <name>Melendez, Justin A</name>
      </author>
      <author>
        <name>Barthélemy, Nicolas R</name>
      </author>
      <author>
        <name>Bollinger, James G</name>
      </author>
      <author>
        <name>He, Yingxin</name>
      </author>
      <author>
        <name>Ovod, Vitaliy</name>
      </author>
      <author>
        <name>Benzinger, Tammie LS</name>
      </author>
      <author>
        <name>Flores, Shaney</name>
      </author>
      <author>
        <name>Gordon, Brian A</name>
      </author>
      <author>
        <name>Ojewole, Adegoke A</name>
      </author>
      <author>
        <name>Phatak, Mukta</name>
      </author>
      <author>
        <name>Elbert, Donald L</name>
      </author>
      <author>
        <name>Biber, Sarah</name>
      </author>
      <author>
        <name>Landsness, Eric C</name>
      </author>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
      <author>
        <name>Bateman, Randall J</name>
      </author>
      <author>
        <name>Reese, Justin T</name>
      </author>
    </item>
    <item>
      <title>Quantitative Dissection of Agrobacterium Virulence to Generate a Synthetic Ti Plasmid</title>
      <link>https://escholarship.org/uc/item/7931m174</link>
      <description>&lt;i&gt;Agrobacterium&lt;/i&gt; is not only a costly plant pathogen but is also an essential tool for plant transformation. Though &lt;i&gt;Agrobacterium&lt;/i&gt;-mediated transformation (AMT) has been heavily studied, its polygenic nature and complex transcriptional regulation make identification of the genetic basis of transformational efficiency difficult through traditional genetic and bioinformatic approaches. Here, we use a bottom-up synthetic approach to systematically engineer the tumor-inducing plasmid (pTi), wherein the majority of virulence machinery is encoded. Using a validated toolkit to control &lt;i&gt;Agrobacterium&lt;/i&gt; gene expression &lt;i&gt;in planta&lt;/i&gt;, we perform a quantitative dissection of AMT to investigate the contributions of critical &lt;i&gt;vir&lt;/i&gt;-genes at different expression levels. We construct a synthetic pTi capable of transient plant and stable fungal transformation and characterize bottlenecks and solutions for complex polygenic synthetic pTi designs. Our reductionist approach...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7931m174</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Thompson, Mitchell G</name>
      </author>
      <author>
        <name>Kirkpatrick, Liam D</name>
      </author>
      <author>
        <name>Szarzanowicz, Matthew J</name>
      </author>
      <author>
        <name>Geiselman, Gina M</name>
      </author>
      <author>
        <name>Waldburger, Lucas M</name>
      </author>
      <author>
        <name>Pearson, Allison N</name>
      </author>
      <author>
        <name>Vuu, Khanh M</name>
      </author>
      <author>
        <name>Markel, Kasey</name>
      </author>
      <author>
        <name>Hummel, Niklas FC</name>
      </author>
      <author>
        <name>Incha, Matthew R</name>
      </author>
      <author>
        <name>Suazo, Dennis D</name>
      </author>
      <author>
        <name>Tahmin, Claudine</name>
      </author>
      <author>
        <name>Cui, Ruoming</name>
      </author>
      <author>
        <name>Liu, Shuying</name>
      </author>
      <author>
        <name>Cevallos, Jasmine</name>
      </author>
      <author>
        <name>Pannu, Hamreet</name>
      </author>
      <author>
        <name>Lapp, Nathan</name>
      </author>
      <author>
        <name>Liu, Di</name>
      </author>
      <author>
        <name>Gin, Jennifer W</name>
      </author>
      <author>
        <name>Chen, Yan</name>
      </author>
      <author>
        <name>Petzold, Christopher J</name>
        <uri>https://orcid.org/0000-0002-8270-5228</uri>
      </author>
      <author>
        <name>Gladden, John M</name>
        <uri>https://orcid.org/0000-0002-6985-2485</uri>
      </author>
      <author>
        <name>Keasling, Jay D</name>
        <uri>https://orcid.org/0000-0003-4170-6088</uri>
      </author>
      <author>
        <name>Chang, Jeff H</name>
      </author>
      <author>
        <name>Weisberg, Alexandra J</name>
      </author>
      <author>
        <name>Shih, Patrick M</name>
      </author>
    </item>
    <item>
      <title>The WalRK two-component system in Streptococcus pneumoniae ensures robustness of secondary wall polymer attachment</title>
      <link>https://escholarship.org/uc/item/7007x17t</link>
      <description>Capsular polysaccharide (CPS) is essential for &lt;i&gt;Streptococcus pneumoniae&lt;/i&gt; virulence. Yet, the mechanism linking CPS to peptidoglycan (PG) remains unclear. Here, we identified a strong negative genetic interaction between the genes encoding the putative capsule ligase CpsA and the WalK histidine kinase, a component of the WalRK two-component system regulating cell wall homeostasis. In the absence of &lt;i&gt;cpsA&lt;/i&gt; , capsule polymers compete with wall teichoic acids for ligase activity to PG. This induces cell wall stress and is sensed by the WalRK system. Overexpression of the PG hydrolase &lt;i&gt;pcsB&lt;/i&gt; or disruption of the PG-modifying enzymes &lt;i&gt;pgdA&lt;/i&gt; and &lt;i&gt;oatA&lt;/i&gt; restored growth of strains lacking &lt;i&gt;cpsA&lt;/i&gt; and &lt;i&gt;walK&lt;/i&gt; . Furthermore, CpsA overproduction compensates for the loss of other LytR-Cps2A-Psr (LCP) ligases, suggesting it can support capsule and wall teichoic acid syntheses. These findings support the model that LCP ligases are semi-redundant, although they...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7007x17t</guid>
      <pubDate>Tue, 21 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Zik, Justin J</name>
      </author>
      <author>
        <name>Fu, Zeyu</name>
      </author>
      <author>
        <name>Price, Morgan N</name>
      </author>
      <author>
        <name>Li, Yujie</name>
      </author>
      <author>
        <name>Qiao, Yuan</name>
      </author>
      <author>
        <name>Arkin, Adam P</name>
        <uri>https://orcid.org/0000-0002-4999-2931</uri>
      </author>
      <author>
        <name>Deutschbauer, Adam M</name>
      </author>
      <author>
        <name>Flores-Kim, Josue</name>
      </author>
      <author>
        <name>Sham, Lok-To</name>
      </author>
    </item>
    <item>
      <title>Genomic and metagenomic survey of microbial carbonic anhydrase genes reveals novel clades, high diversity, and biome-specificity</title>
      <link>https://escholarship.org/uc/item/1wr5z22w</link>
      <description>Abstract Carbonic anhydrase (CA) enzymes catalyze the interconversion of carbon dioxide and bicarbonate with an efficiency exceeded only by superoxide dismutase. CA enzymes have convergently evolved multiple times from phylogenetically distant organisms into eight classes that are structurally unrelated, but share physiological functions involved in photosynthesis, respiration, pH homeostasis, CO2 transport, and carbonyl sulfide hydrolysis that play central roles in medicine and the environment. Here, we leverage the recent surge in publicly available genomes and metagenomes to re-examine our understanding of the abundance, diversity, and phylogenetic relationships of the three major CA classes in Bacteria/Archaea and microbial Eukaryotes (Fungi, algae). We recovered a total of 57,218 α-, β-, and γ-CA sequences from 24,184 metagenomes and genomes, including the first detection of α-CA from an archaeal species. CA sequences formed 3,859 protein clusters (1,188 with ≥ 3 sequences)...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1wr5z22w</guid>
      <pubDate>Tue, 21 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Franco, Mario EE</name>
      </author>
      <author>
        <name>Singer, Esther</name>
        <uri>https://orcid.org/0000-0002-3126-2199</uri>
      </author>
      <author>
        <name>Roux, Simon</name>
        <uri>https://orcid.org/0000-0002-5831-5895</uri>
      </author>
      <author>
        <name>Meredith, Laura K</name>
      </author>
      <author>
        <name>U’Ren, Jana M</name>
      </author>
    </item>
    <item>
      <title>Reduced methane emissions in transgenic rice genotypes are associated with altered rhizosphere microbial hydrogen cycling</title>
      <link>https://escholarship.org/uc/item/7rr0p6zq</link>
      <description>Rice paddies significantly contribute to atmospheric methane (CH4). Here, we show that two independent rice genotypes overexpressing genes for PLANT PEPTIDES CONTAINING SULFATED TYROSINE (PSY) reduce cumulative CH4 emissions by 38% (PSY1) and 58% (PSY2) over 70 days of growth compared with controls. Genome-resolved metatranscriptomic data from PSY rhizosphere soils reveal lower ratios of gene activities for (mostly hydrogenotrophic) CH4 production versus consumption, decreased activity of H2-producing genes, and increased activity of bacterial H2 oxidation pathways. Metabolic modeling using metagenomic and metabolomic data predicts elevated H2 oxidation and suppressed H2 production in the PSY rhizosphere. Assembled genomes of rhizosphere H2-oxidizing bacteria are enriched in genes utilizing gluconeogenic acids compared with H2-producing counterparts, and their activities are likely stimulated by elevated levels of gluconeogenic acids, primarily amino acids, in PSY root exudates....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7rr0p6zq</guid>
      <pubDate>Fri, 17 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Shi, Ling-Dong</name>
      </author>
      <author>
        <name>Ercoli, Maria Florencia</name>
        <uri>https://orcid.org/0000-0001-5587-6227</uri>
      </author>
      <author>
        <name>Kim, Junhyeong</name>
      </author>
      <author>
        <name>de Araujo Junior, Artur Teixeira</name>
      </author>
      <author>
        <name>Estera-Molina, Katerina</name>
      </author>
      <author>
        <name>Soni, Subah</name>
      </author>
      <author>
        <name>Weitz, Tracy Satomi</name>
      </author>
      <author>
        <name>Shigenaga, Alexandra M</name>
      </author>
      <author>
        <name>Dukovski, Ilija</name>
      </author>
      <author>
        <name>Sachdeva, Rohan</name>
      </author>
      <author>
        <name>Turumtay, Halbay</name>
        <uri>https://orcid.org/0000-0003-4224-8103</uri>
      </author>
      <author>
        <name>Louie, Katherine B</name>
      </author>
      <author>
        <name>Bowen, Benjamin P</name>
        <uri>https://orcid.org/0000-0003-1368-3958</uri>
      </author>
      <author>
        <name>Kosina, Suzanne M</name>
        <uri>https://orcid.org/0000-0003-2885-1248</uri>
      </author>
      <author>
        <name>Scheller, Henrik V</name>
        <uri>https://orcid.org/0000-0002-6702-3560</uri>
      </author>
      <author>
        <name>Pett-Ridge, Jennifer</name>
      </author>
      <author>
        <name>Segrè, Daniel</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
      </author>
      <author>
        <name>Ronald, Pamela C</name>
        <uri>https://orcid.org/0000-0002-4107-1345</uri>
      </author>
      <author>
        <name>Banfield, Jillian F</name>
      </author>
    </item>
    <item>
      <title>Causes and consequences of experimental variation in Nicotiana benthamiana transient expression</title>
      <link>https://escholarship.org/uc/item/8zn495ch</link>
      <description>Infiltration of Agrobacterium tumefaciens into Nicotiana benthamiana has become a foundational technique in plant biology, enabling efficient delivery of transgenes in planta with technical ease, robust signal, and relatively high throughput. Despite transient expression’s prevalence in disciplines such as synthetic biology, little work has been done to describe and address the variability inherent in this system, a concern for experiments that rely on highly quantitative readouts. In a comprehensive analysis of N. benthamiana agroinfiltration experiments, we model sources of variability that affect transient expression. Our findings emphasize the need to validate normalization methods under the specific conditions of each study, as distinct normalization schemes do not always reduce variation either within or between experiments. Using a dataset of 1915 plants collected over three years, we develop a model of variation in N. benthamiana transient expression, using power analysis...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8zn495ch</guid>
      <pubDate>Tue, 14 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Tang, Sophia N</name>
      </author>
      <author>
        <name>Szarzanowicz, Matthew J</name>
      </author>
      <author>
        <name>Lanctot, Amy</name>
      </author>
      <author>
        <name>Sirirungruang, Sasilada</name>
      </author>
      <author>
        <name>Kirkpatrick, Liam D</name>
      </author>
      <author>
        <name>Drako, Krista</name>
      </author>
      <author>
        <name>Alamos, Simon</name>
      </author>
      <author>
        <name>Cheng, Lyurui</name>
      </author>
      <author>
        <name>Waldburger, Lucas M</name>
      </author>
      <author>
        <name>Liu, Shuying</name>
      </author>
      <author>
        <name>Huang, Lena</name>
      </author>
      <author>
        <name>Kazaz, Sami</name>
      </author>
      <author>
        <name>Akyuz Turumtay, Emine</name>
      </author>
      <author>
        <name>Baidoo, Edward</name>
        <uri>https://orcid.org/0000-0001-5787-1219</uri>
      </author>
      <author>
        <name>Eudes, Aymerick</name>
        <uri>https://orcid.org/0000-0002-1387-6111</uri>
      </author>
      <author>
        <name>Thompson, Mitchell G</name>
      </author>
      <author>
        <name>Shih, Patrick M</name>
      </author>
    </item>
    <item>
      <title>Systematic benchmarking demonstrates large language models have not reached the diagnostic accuracy of traditional rare-disease decision support tools</title>
      <link>https://escholarship.org/uc/item/64v8j4b5</link>
      <description>Large language models (LLMs) show promise in supporting differential diagnosis, but their performance is challenging to evaluate due to the unstructured nature of their responses, and their accuracy compared to existing diagnostic tools is not well characterized. To assess the current capabilities of LLMs to diagnose genetic diseases, we benchmarked these models on 5213 previously published case reports using the Phenopacket Schema, the Human Phenotype Ontology and Mondo disease ontology. Prompts generated from each phenopacket were sent to seven LLMs, including four generalist models and three LLMs specialized for medical applications. The same phenopackets were used as input to a widely used diagnostic tool, Exomiser, in phenotype-only mode. The best LLM ranked the correct diagnosis first in 23.6% of cases, whereas Exomiser did so in 35.5% of cases. While the performance of LLMs for supporting differential diagnosis has been improving, it has not reached the level of commonly...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/64v8j4b5</guid>
      <pubDate>Tue, 14 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Reese, Justin T</name>
      </author>
      <author>
        <name>Chimirri, Leonardo</name>
      </author>
      <author>
        <name>Bridges, Yasemin</name>
      </author>
      <author>
        <name>Danis, Daniel</name>
      </author>
      <author>
        <name>Caufield, J Harry</name>
      </author>
      <author>
        <name>Gargano, Michael A</name>
      </author>
      <author>
        <name>Kroll, Carlo</name>
      </author>
      <author>
        <name>Schmeder, Andrew</name>
      </author>
      <author>
        <name>Liu, Fengchen</name>
      </author>
      <author>
        <name>Wissink, Kyran</name>
      </author>
      <author>
        <name>McMurry, Julie A</name>
      </author>
      <author>
        <name>Graefe, Adam SL</name>
      </author>
      <author>
        <name>Niyonkuru, Enock</name>
      </author>
      <author>
        <name>Korn, Daniel R</name>
      </author>
      <author>
        <name>Casiraghi, Elena</name>
      </author>
      <author>
        <name>Valentini, Giorgio</name>
      </author>
      <author>
        <name>Jacobsen, Julius OB</name>
      </author>
      <author>
        <name>Haendel, Melissa</name>
      </author>
      <author>
        <name>Smedley, Damian</name>
      </author>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
      <author>
        <name>Robinson, Peter N</name>
      </author>
    </item>
    <item>
      <title>LinkML: An Open Data Modeling Framework</title>
      <link>https://escholarship.org/uc/item/895730mq</link>
      <description>BACKGROUND: Scientific research relies on well-structured, standardized data; however, much of it is stored in formats such as free-text lab notebooks, non-standardized spreadsheets, or data repositories. This lack of structure challenges interoperability, making data integration, validation, and reuse difficult.
FINDINGS: LinkML (Linked Data Modeling Language) is an open framework that simplifies the process of authoring, validating, and sharing data. LinkML can describe a range of data structures, from flat, list-based models to complex, interrelated, and normalized models that utilize polymorphism and compound inheritance. It offers an approachable syntax that is not tied to any one technical architecture and can be integrated seamlessly with many existing frameworks. The LinkML syntax provides a standard way to describe schemas, classes, and relationships, allowing modelers to build well-defined, stable, and optionally ontology-aligned data structures. Once defined, LinkML...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/895730mq</guid>
      <pubDate>Mon, 6 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Moxon, Sierra AT</name>
      </author>
      <author>
        <name>Solbrig, Harold</name>
      </author>
      <author>
        <name>Harris, Nomi L</name>
        <uri>https://orcid.org/0000-0001-6315-3707</uri>
      </author>
      <author>
        <name>Kalita, Patrick</name>
      </author>
      <author>
        <name>Miller, Mark A</name>
      </author>
      <author>
        <name>Patil, Sujay</name>
      </author>
      <author>
        <name>Schaper, Kevin</name>
      </author>
      <author>
        <name>Bizon, Chris</name>
      </author>
      <author>
        <name>Caufield, J Harry</name>
      </author>
      <author>
        <name>Cuesta, Silvano Cirujano</name>
      </author>
      <author>
        <name>Cox, Corey</name>
      </author>
      <author>
        <name>Dekervel, Frank</name>
      </author>
      <author>
        <name>Dooley, Damion M</name>
      </author>
      <author>
        <name>Duncan, William D</name>
      </author>
      <author>
        <name>Fliss, Tim</name>
      </author>
      <author>
        <name>Gehrke, Sarah</name>
      </author>
      <author>
        <name>Graefe, Adam SL</name>
      </author>
      <author>
        <name>Hegde, Harshad</name>
      </author>
      <author>
        <name>Ireland, AJ</name>
      </author>
      <author>
        <name>Jacobsen, Julius OB</name>
      </author>
      <author>
        <name>Krishnamurthy, Madan</name>
      </author>
      <author>
        <name>Kroll, Carlo</name>
      </author>
      <author>
        <name>Linke, David</name>
      </author>
      <author>
        <name>Ly, Ryan</name>
        <uri>https://orcid.org/0000-0001-9238-0642</uri>
      </author>
      <author>
        <name>Matentzoglu, Nicolas</name>
      </author>
      <author>
        <name>Overton, James A</name>
      </author>
      <author>
        <name>Saunders, Jonny L</name>
      </author>
      <author>
        <name>Unni, Deepak R</name>
      </author>
      <author>
        <name>Vaidya, Gaurav</name>
      </author>
      <author>
        <name>Vierdag, Wouter-Michiel AM</name>
      </author>
      <author>
        <name>Ruebel, Oliver</name>
      </author>
      <author>
        <name>Chute, Christopher G</name>
      </author>
      <author>
        <name>Brush, Matthew H</name>
      </author>
      <author>
        <name>Haendel, Melissa A</name>
      </author>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
    </item>
    <item>
      <title>Mondo: integrating disease terminology across communities</title>
      <link>https://escholarship.org/uc/item/7d51t1mb</link>
      <description>Precision medicine aims to enhance diagnosis, treatment, and prognosis by integrating multimodal data at the point of care. However, challenges arise due to the vast number of diseases, differing methods of classification, and conflicting terminological coding systems and practices used to represent molecular definitions of disease. This lack of interoperability artificially constrains the potential for diagnosis, clinical decision support, care outcome analysis, as well as data linkage across research domains to support the development or repurposing of therapeutics. There is a clear and pressing need for a unified system for managing disease entities ⁠- including identifiers, synonyms, and definitions. To address these issues, we created the Mondo disease ontology-a community-driven, open-source, unified disease classification system that harmonizes diverse terminologies into a consistent, computable framework. Mondo integrates key medical and biomedical terminologies, including...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7d51t1mb</guid>
      <pubDate>Tue, 31 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Vasilevsky, Nicole A</name>
      </author>
      <author>
        <name>Toro, Sabrina</name>
      </author>
      <author>
        <name>Matentzoglu, Nicolas</name>
      </author>
      <author>
        <name>Flack, Joseph E</name>
      </author>
      <author>
        <name>Mullen, Kathleen R</name>
      </author>
      <author>
        <name>Hegde, Harshad</name>
      </author>
      <author>
        <name>Gehrke, Sarah</name>
      </author>
      <author>
        <name>Whetzel, Patricia L</name>
      </author>
      <author>
        <name>Shwetar, Yousif</name>
      </author>
      <author>
        <name>Harris, Nomi L</name>
        <uri>https://orcid.org/0000-0001-6315-3707</uri>
      </author>
      <author>
        <name>Ngu, Mee S</name>
      </author>
      <author>
        <name>Alyea, Gioconda L</name>
      </author>
      <author>
        <name>Kane, Megan S</name>
      </author>
      <author>
        <name>Roncaglia, Paola</name>
      </author>
      <author>
        <name>Sid, Eric</name>
      </author>
      <author>
        <name>Thaxton, Courtney L</name>
      </author>
      <author>
        <name>Wood, Valerie</name>
      </author>
      <author>
        <name>Abraham, Roshini S</name>
      </author>
      <author>
        <name>Achatz, Maria Isabel</name>
      </author>
      <author>
        <name>Ajuyah, Pamela</name>
      </author>
      <author>
        <name>Amberger, Joanna S</name>
      </author>
      <author>
        <name>Babb, Lawrence</name>
      </author>
      <author>
        <name>Baker, Jasmine</name>
      </author>
      <author>
        <name>Balhoff, James P</name>
      </author>
      <author>
        <name>Berg, Jonathan S</name>
      </author>
      <author>
        <name>Bhalla, Amol</name>
      </author>
      <author>
        <name>Ros, Xavier Bofill-De</name>
      </author>
      <author>
        <name>Braun, Ian R</name>
      </author>
      <author>
        <name>Broeren, Eleanor C</name>
      </author>
      <author>
        <name>Byer, Blake K</name>
      </author>
      <author>
        <name>Byrne, Alicia B</name>
      </author>
      <author>
        <name>Callahan, Tiffany J</name>
      </author>
      <author>
        <name>Carmody, Leigh C</name>
      </author>
      <author>
        <name>Chan, Lauren E</name>
      </author>
      <author>
        <name>Clause, Amanda R</name>
      </author>
      <author>
        <name>Cohen, Julie S</name>
      </author>
      <author>
        <name>DeLuca, Marcello</name>
      </author>
      <author>
        <name>Deuitch, Natalie T</name>
      </author>
      <author>
        <name>Flowers, May</name>
      </author>
      <author>
        <name>Fraser, Jamie</name>
      </author>
      <author>
        <name>Fujiwara, Toyofumi</name>
      </author>
      <author>
        <name>Gitau, Vanessa</name>
      </author>
      <author>
        <name>Goldstein, Jennifer L</name>
      </author>
      <author>
        <name>Gration, Dylan</name>
      </author>
      <author>
        <name>Groza, Tudor</name>
      </author>
      <author>
        <name>Gyori, Benjamin M</name>
      </author>
      <author>
        <name>Hankey, William</name>
      </author>
      <author>
        <name>Hilton, Jason A</name>
      </author>
      <author>
        <name>Himmelstein, Daniel S</name>
      </author>
      <author>
        <name>Hong, Stephanie S</name>
      </author>
      <author>
        <name>Hoyt, Charles T</name>
      </author>
      <author>
        <name>Huether, Robert</name>
      </author>
      <author>
        <name>Hurwitz, Eric</name>
      </author>
      <author>
        <name>Jacobsen, Julius OB</name>
      </author>
      <author>
        <name>Kikuchi, Atsuo</name>
      </author>
      <author>
        <name>Köhler, Sebastian</name>
      </author>
      <author>
        <name>Korn, Daniel R</name>
      </author>
      <author>
        <name>Lagorce, David</name>
      </author>
      <author>
        <name>Laraway, Bryan J</name>
      </author>
      <author>
        <name>Li, Jane Y</name>
      </author>
      <author>
        <name>Malheiro, Adriana J</name>
      </author>
      <author>
        <name>McLaughlin, James</name>
      </author>
      <author>
        <name>Meldal, Birgit HM</name>
      </author>
      <author>
        <name>Mohan, Shruthi</name>
      </author>
      <author>
        <name>Moxon, Sierra AT</name>
      </author>
      <author>
        <name>Munoz-Torres, Monica C</name>
        <uri>https://orcid.org/0000-0001-8430-6039</uri>
      </author>
      <author>
        <name>Nelson, Tristan H</name>
      </author>
      <author>
        <name>Nicholas, Frank W</name>
      </author>
      <author>
        <name>Ochoa, David</name>
      </author>
      <author>
        <name>Olson, Daniel</name>
      </author>
      <author>
        <name>Oprea, Tudor I</name>
      </author>
      <author>
        <name>Oskotsky, Tomiko T</name>
        <uri>https://orcid.org/0000-0001-7393-5120</uri>
      </author>
      <author>
        <name>Osumi-Sutherland, David</name>
      </author>
      <author>
        <name>Paris, Kelley</name>
      </author>
      <author>
        <name>Parkinson, Helen E</name>
      </author>
      <author>
        <name>Pendlington, Zoë M</name>
      </author>
      <author>
        <name>Peng, Xiao P</name>
      </author>
      <author>
        <name>Pizzino, Amy</name>
      </author>
      <author>
        <name>Plon, Sharon E</name>
      </author>
      <author>
        <name>Powell, Bradford C</name>
      </author>
      <author>
        <name>Ratliff, Julie C</name>
      </author>
      <author>
        <name>Rehm, Heidi L</name>
      </author>
      <author>
        <name>Remennik, Lyubov</name>
      </author>
      <author>
        <name>Riggs, Erin R</name>
      </author>
      <author>
        <name>Roberts, Sean</name>
      </author>
      <author>
        <name>Robinson, Peter N</name>
      </author>
      <author>
        <name>Ross, Justyne E</name>
      </author>
      <author>
        <name>Schaper, Kevin</name>
      </author>
      <author>
        <name>Schilder, Brian M</name>
      </author>
      <author>
        <name>Schmidt, Johanna L</name>
      </author>
      <author>
        <name>Sharp, Elliott W</name>
      </author>
      <author>
        <name>Similuk, Morgan N</name>
      </author>
      <author>
        <name>Smedley, Damian</name>
      </author>
      <author>
        <name>Sneddon, Tam P</name>
      </author>
      <author>
        <name>Sparks, Rachel</name>
      </author>
      <author>
        <name>Stefancsik, Ray</name>
      </author>
      <author>
        <name>Stupp, Gregory S</name>
      </author>
      <author>
        <name>Sundar, Shilpa</name>
      </author>
      <author>
        <name>Takatsuki, Terue</name>
      </author>
      <author>
        <name>Tammen, Imke</name>
      </author>
    </item>
    <item>
      <title>Assessing the effectiveness of ontology-grounded AI term extraction using OntoGPT for environmental evidence synthesis</title>
      <link>https://escholarship.org/uc/item/2xh2p0x0</link>
      <description>Evidence syntheses are valuable sources of robust and transparent knowledge that can identify gaps in research and inform evidence-based decision making. However, the process of synthesis is time consuming and costly. We investigate a new AI-based method that uses a large-language model (LLM) grounded in ontologies (i.e. structured machine-interpretable glossaries of domain terminology) to extract information from a set of 80 articles on coastal wetland restoration outcomes. We evaluated this method by comparing human-extracted data with data extracted by OntoGPT — a Python package that combines an LLM with ontologies to extract structured information. We found that OntoGPT achieved 65% average agreement with human reviewers but varied based on information type requested for extraction. The highest agreement scores were found when extracting standardized information, and lower agreement scores were found for study-specific and interpretation-heavy information. Precision and recall...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2xh2p0x0</guid>
      <pubDate>Tue, 24 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Hodgson, Ryan Y</name>
      </author>
      <author>
        <name>Robinson, Steven A</name>
      </author>
      <author>
        <name>Boutin, Amélie C</name>
      </author>
      <author>
        <name>Chan, Felix K</name>
      </author>
      <author>
        <name>Bennett, Joseph R</name>
      </author>
      <author>
        <name>Buxton, Rachel T</name>
      </author>
      <author>
        <name>Caufield, J Harry</name>
      </author>
      <author>
        <name>Hanna, Dalal EL</name>
      </author>
      <author>
        <name>Alamenciak, Tim</name>
      </author>
    </item>
    <item>
      <title>Increasing the Scale of the Mass Spectrometry Query Language Compendium with Explainable AI</title>
      <link>https://escholarship.org/uc/item/9766056n</link>
      <description>A significant bottleneck in metabolomics data interpretation is the effective use of domain knowledge to assign structural information based on fragmentation patterns. The mass spectrometry query language (MassQL) aims to make this process accessible and applicable across multiple analysis platforms. While advanced computational methods are capable of predicting compound structures from fragmentation data, AI/ML approaches often rely on complex, opaque criteria that are difficult to interpret or modify. As a result, their predictive patterns cannot be readily translated into human-readable rules, such as those used in MassQL. In this study, we introduce ChemEcho, a machine learning embedding method that converts tandem mass spectrometry data into sparse feature vectors containing peak and neutral mass subformulae to enhance explainable AI/ML-based methods. An advantage of this approach is that decision trees trained using these feature vectors can be directly translated to MassQL....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9766056n</guid>
      <pubDate>Thu, 19 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Harwood, Thomas V</name>
      </author>
      <author>
        <name>Wang, Mingxun</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Bowen, Benjamin P</name>
        <uri>https://orcid.org/0000-0003-1368-3958</uri>
      </author>
    </item>
    <item>
      <title>GenomeDepot: data management system for microbial comparative genomics</title>
      <link>https://escholarship.org/uc/item/65h8d8fk</link>
      <description>Summary: GenomeDepot is an open-source web-based platform for annotation, management, and comparative analysis of microbial genomic sequences and associated data including ortholog families, protein domains, operons, regulatory interactions, strain taxonomy, and sample metadata. GenomeDepot supports rapid creation of websites for user-defined genome collections that include bioinformatic tools for interactive genome browsing, Basic Local Alignment Search Tool (BLAST)&amp;nbsp;search, annotation search, comparative genomic neighborhood visualization, and sequence download. Gene function annotations are generated by a customizable annotation pipeline. The pipeline runs annotation tools in Conda environments and can be easily extended with additional user-specified tools.
Availability and implementation: GenomeDepot is open source and distributed under the GNU General Public License via GitHub (https://github.com/aekazakov/genome-depot). GenomeDepot is implemented in Python and was tested...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/65h8d8fk</guid>
      <pubDate>Tue, 10 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kazakov, Alexey</name>
      </author>
      <author>
        <name>Deutschbauer, Adam M</name>
      </author>
    </item>
    <item>
      <title>KBase: Open-source platform for collaborative biological data analysis and publication</title>
      <link>https://escholarship.org/uc/item/1pz5386s</link>
      <description>The U.S. Department of Energy’s Systems Biology Knowledgebase (KBase; www.kbase.us ) is an open, collaborative platform that integrates data, models, and analysis tools to accelerate discovery in microbiology, plant biology, and environmental systems. Recently, KBase expanded as a comprehensive, multi-omics ecosystem. KBase enables representation of scientific samples, long-read sequence analysis, protein structure integration, and scalable modeling of microbial communities across diverse environments. KBase also generates digital notebooks as citable, executable research objects that link data, methods, and interpretation. KBase also supports a global education community focused on training the next generation of scientists to use high-performance computational tools. Together, these advances position KBase as a central hub for open, reproducible systems biology. In turn, this enables us to integrate many of the emerging advances in data federation, semantic interoperability,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1pz5386s</guid>
      <pubDate>Tue, 10 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wood-Charlson, Elisha M</name>
        <uri>https://orcid.org/0000-0001-9557-7715</uri>
      </author>
      <author>
        <name>Henry, Christopher</name>
      </author>
      <author>
        <name>Dehal, Paramvir</name>
        <uri>https://orcid.org/0000-0001-5810-2497</uri>
      </author>
      <author>
        <name>Mahmud, Gazi</name>
      </author>
      <author>
        <name>Allen, Ben</name>
      </author>
      <author>
        <name>Bielsmith, Kathleen</name>
      </author>
      <author>
        <name>Blair, D Dakota</name>
      </author>
      <author>
        <name>Canon, Shane</name>
      </author>
      <author>
        <name>Cashman, Mikaela</name>
      </author>
      <author>
        <name>Chivian, Dylan</name>
      </author>
      <author>
        <name>Cottingham, Robert</name>
      </author>
      <author>
        <name>Crocket, Zach</name>
      </author>
      <author>
        <name>Dow, Ellen</name>
        <uri>https://orcid.org/0000-0002-2079-0260</uri>
      </author>
      <author>
        <name>Drake, Meghan</name>
      </author>
      <author>
        <name>Edirisinghe, Janaka N</name>
      </author>
      <author>
        <name>Faria, José P</name>
      </author>
      <author>
        <name>Freiburger, Andrew</name>
      </author>
      <author>
        <name>Gu, Tianhao</name>
      </author>
      <author>
        <name>Gupta, Prachi</name>
        <uri>https://orcid.org/0000-0002-1255-2684</uri>
      </author>
      <author>
        <name>Ireland, AJ</name>
      </author>
      <author>
        <name>Jungbluth, Sean</name>
      </author>
      <author>
        <name>Kamimura, Roy</name>
      </author>
      <author>
        <name>Keller, Keith</name>
      </author>
      <author>
        <name>Khan, Ahmed</name>
      </author>
      <author>
        <name>Kishore, Dileep</name>
      </author>
      <author>
        <name>Klos, Dan</name>
      </author>
      <author>
        <name>Liu, Filipe</name>
      </author>
      <author>
        <name>Lyon, David</name>
      </author>
      <author>
        <name>Neely, Christopher</name>
      </author>
      <author>
        <name>O’Grady, Katherine</name>
      </author>
      <author>
        <name>Price, Gavin</name>
      </author>
      <author>
        <name>Ranjan, Priya</name>
      </author>
      <author>
        <name>Riehl, William J</name>
      </author>
      <author>
        <name>Sadkhin, Boris</name>
      </author>
      <author>
        <name>Seaver, Sam</name>
      </author>
      <author>
        <name>Terry, Gwyneth A</name>
      </author>
      <author>
        <name>Wang, Yue</name>
      </author>
      <author>
        <name>Weisenhorn, Pamela</name>
      </author>
      <author>
        <name>Yang, Ziming</name>
      </author>
      <author>
        <name>Yoo, Shinjae</name>
      </author>
      <author>
        <name>Arkin, Adam P</name>
      </author>
    </item>
    <item>
      <title>Molecular Modeling and Molecular Dynamics Simulation of a Packed and Intact Bacterial Microcompartment</title>
      <link>https://escholarship.org/uc/item/2tn8j8fc</link>
      <description>Bacterial microcompartments (BMCs) are protein-bound organelles found in some bacteria which encapsulate enzymes for enhanced catalytic activity. These compartments spatially sequester enzymes within semipermeable shell proteins and are packed full of enzyme cargoes and metabolites as they fulfill their function. Coupling together recent SAXS and proteomics work, it is possible to develop molecular models for these microcompartments and interrogate enzyme and metabolite dynamics within. Our primary goal of this study is to quantify the permeability of metabolite glyceraldehyde-3-phosphate (G3P) and dihydroxyacetone phosphate (DHAP) across the BMC shell through classical molecular dynamics simulation. The &lt;i&gt;Haliangium ochraceum&lt;/i&gt; model of BMC shell (PDB: 6MZX) was used to model an intact BMC of approximately 10 million atoms. Working at this scale presented its own challenges in managing large data sets, with multiple challenges and hardware advances discussed that facilitated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2tn8j8fc</guid>
      <pubDate>Thu, 5 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Raza, Saad</name>
      </author>
      <author>
        <name>Yadav, Neetu Singh</name>
      </author>
      <author>
        <name>Jussupow, Alexander</name>
      </author>
      <author>
        <name>Kerfeld, Cheryl A</name>
        <uri>https://orcid.org/0000-0002-9977-8482</uri>
      </author>
      <author>
        <name>Feig, Michael</name>
      </author>
      <author>
        <name>Vermaas, Josh V</name>
      </author>
    </item>
    <item>
      <title>Photoactivation Transition State and Dynamical Response of the Orange Carotenoid Protein</title>
      <link>https://escholarship.org/uc/item/2cw5c11x</link>
      <description>The orange carotenoid protein (OCP) regulates light harvesting in cyanobacteria by acting as a photoreceptor in its resting form, OCP&lt;sup&gt;O&lt;/sup&gt;, and by effecting the quenching of bilin excitons upon binding to the core of the phycobilisome in its photoactivated red form, OCP&lt;sup&gt;R&lt;/sup&gt;. We show herein using fluorescence anisotropy measurements and the action spectra for the rate constants of the two light-driven steps in the mechanism that the photoactivation of the OCP from &lt;i&gt;Synechocystis&lt;/i&gt; sp. PCC 6803 is triggered by excited-state motions of the canthaxanthin chromophore that yield a twisted and bent conformation. Well-tempered metadynamics simulations reveal that a bicycle-pedal configuration, due to twisting of the two adjacent C═C bonds at the C13-C14 and C15-C15&lt;i&gt;'&lt;/i&gt; positions in the center of canthaxanthin's π-conjugated isoprenoid backbone, can be accommodated by the binding site in the OCP, with the energy of a captured photon required to cross the local activation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2cw5c11x</guid>
      <pubDate>Thu, 5 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Rose, JustinB</name>
      </author>
      <author>
        <name>Gascón, José A</name>
      </author>
      <author>
        <name>Sheppard, Damien I</name>
      </author>
      <author>
        <name>Kerfeld, Cheryl A</name>
        <uri>https://orcid.org/0000-0002-9977-8482</uri>
      </author>
      <author>
        <name>Beck, Warren F</name>
      </author>
    </item>
    <item>
      <title>Engineering 2‐Pyrone‐4,6‐Dicarboxylic Acid Production Reveals Metabolic Plasticity of Poplar</title>
      <link>https://escholarship.org/uc/item/0fq375xg</link>
      <description>Woody biomass is a promising source of fermentable sugars for biofuels and bio-based chemicals, but its industrial use is limited by the costly biorefinery process. A viable strategy to reduce costs involves enhancing both biomass processability and the generation of high-value co-products. Here, we report the implementation of a synthetic metabolic pathway in Populus tremula × P. alba to produce 2-pyrone-4,6-dicarboxylic acid (PDC), a key building block for biodegradable plastics and high-performance materials. This artificial pathway-comprising microbial genes AroG, QsuB, PmdA, PmdB, and PmdC-enabled de novo PDC production in the stems of transgenic poplar. Pathway expression also induced substantial metabolic reprogramming and altered cell wall composition. These include the hyperaccumulation of simple phenolics like protocatechuic acid (PCA) and vanillic acid (VA), alongside reduced levels of p-hydroxybenzoic acid. A large portion of VA was ester-linked to cell wall lignin,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0fq375xg</guid>
      <pubDate>Tue, 3 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Dwivedi, Nidhi</name>
      </author>
      <author>
        <name>Ji, Pingping</name>
      </author>
      <author>
        <name>Tian, Yang</name>
      </author>
      <author>
        <name>Kaur, Dasmeet</name>
      </author>
      <author>
        <name>Vulavala, Vijaya Kumar Reddy</name>
      </author>
      <author>
        <name>Tobimatsu, Yuki</name>
      </author>
      <author>
        <name>Eudes, Aymerick</name>
        <uri>https://orcid.org/0000-0002-1387-6111</uri>
      </author>
      <author>
        <name>Liu, Chang‐Jun</name>
      </author>
    </item>
    <item>
      <title>Aligning Standards Communities for Omics Biodiversity Data: Sustainable Darwin Core-MIxS Interoperability</title>
      <link>https://escholarship.org/uc/item/71w2w2rv</link>
      <description>The standardization of data, encompassing both primary and contextual information (metadata), plays a pivotal role in facilitating data (re-)use, integration, and knowledge generation. However, the biodiversity and omics communities, converging on omics biodiversity data, have historically developed and adopted their own distinct standards, hindering effective (meta)data integration and collaboration. In response to this challenge, the Task Group (TG) for Sustainable DwC-MIxS Interoperability was established. Convening experts from the Biodiversity Information Standards (TDWG) and the Genomic Standards Consortium (GSC) alongside external stakeholders, the TG aimed to promote sustainable interoperability between the Minimum Information about any (x) Sequence (MIxS) and Darwin Core (DwC) specifications. To achieve this goal, the TG utilized the Simple Standard for Sharing Ontology Mappings (SSSOM) to create a comprehensive mapping of DwC keys to MIxS keys. This mapping, combined...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/71w2w2rv</guid>
      <pubDate>Tue, 24 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Meyer, Raïssa</name>
      </author>
      <author>
        <name>Appeltans, Ward</name>
      </author>
      <author>
        <name>Duncan, William D</name>
      </author>
      <author>
        <name>Dimitrova, Mariya</name>
      </author>
      <author>
        <name>Gan, Yi-Ming</name>
      </author>
      <author>
        <name>Jeppesen, Thomas Stjernegaard</name>
      </author>
      <author>
        <name>Mungall, Christopher</name>
      </author>
      <author>
        <name>Paul, Deborah L</name>
      </author>
      <author>
        <name>Provoost, Pieter</name>
      </author>
      <author>
        <name>Robertson, Tim</name>
      </author>
      <author>
        <name>Schriml, Lynn</name>
      </author>
      <author>
        <name>Suominen, Saara</name>
      </author>
      <author>
        <name>Walls, Ramona</name>
      </author>
      <author>
        <name>Sweetlove, Maxime</name>
      </author>
      <author>
        <name>Ung, Visotheary</name>
      </author>
      <author>
        <name>Van de Putte, Anton</name>
      </author>
      <author>
        <name>Wallis, Elycia</name>
      </author>
      <author>
        <name>Wieczorek, John</name>
      </author>
      <author>
        <name>Buttigieg, Pier Luigi</name>
      </author>
    </item>
    <item>
      <title>Ecolink: Towards a Knowledge Graph Schema for Complex Environmental Systems</title>
      <link>https://escholarship.org/uc/item/7gr7x0gx</link>
      <description>Research findings in ecology have the potential to drive evidence-based actions that could reverse biodiversity decline, inspire nature-based solutions to climate change and enhance restoration of severely degraded waters and lands. However, publishing findings in peer-reviewed papers alone is not sufficient to turn ecological research into action, as evidenced by the burgeoning field of translational ecology. Scholarly literature remains inaccessible to many conservation and restoration practitioners. While the open access publishing movement has increased the availability of research, the knowledge is still poorly indexed and unstructured, leading to inadequate findability.We present a solution to these challenges in the form of the Ecolink Model (ELM) – an open-source schema for creating knowledge graphs that describe environmental variables, ecological processes and the relationships between them. Drawing on core concepts from ecological modeling and advances in biomedical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7gr7x0gx</guid>
      <pubDate>Wed, 11 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Alamenciak, Tim</name>
      </author>
      <author>
        <name>Arnillas, Carlos Alberto</name>
      </author>
      <author>
        <name>Caufield, Harry</name>
        <uri>https://orcid.org/0000-0001-5705-7831</uri>
      </author>
      <author>
        <name>Compton, Katherine</name>
      </author>
      <author>
        <name>Drew, Kian</name>
      </author>
      <author>
        <name>Frühstückl, Robert</name>
      </author>
      <author>
        <name>Heger, Tina</name>
      </author>
      <author>
        <name>König-Ries, Birgitta</name>
      </author>
      <author>
        <name>Mungall, Chris</name>
      </author>
      <author>
        <name>Moxon, Sierra</name>
      </author>
      <author>
        <name>Reese, Justin</name>
      </author>
      <author>
        <name>Tardif, Jordan</name>
      </author>
      <author>
        <name>Vogt, Lars</name>
      </author>
    </item>
    <item>
      <title>A Simple and Versatile Cell-Free Expression Method for Producing Secondary Metabolites.</title>
      <link>https://escholarship.org/uc/item/6w29p465</link>
      <description>Secondary metabolites are a major source of natural products with industrially relevant bioactivities. Lysate-based cell-free expression (CFE) is an emerging platform for accelerating the discovery and engineering of these natural products. While &lt;i&gt;Escherichia coli&lt;/i&gt; cell extracts are widely used for CFE, &lt;i&gt;Streptomyces&lt;/i&gt; extracts are likely to offer a more biochemically compatible environment for their expression. However, current &lt;i&gt;Streptomyces&lt;/i&gt;-based CFE systems remain underdeveloped, with protocols that are either strain-specific or not readily scalable. To address these limitations and enable broader access to cell-free natural product biosynthesis, we present a generalizable and simple set of reaction conditions that support high-yield protein expression (180-230 μg/mL) in lysates derived from &lt;i&gt;Streptomyces venezuelae&lt;/i&gt; NRRL B-65422 and &lt;i&gt;Streptomyces lividans&lt;/i&gt; TK24. Like &lt;i&gt;E. coli&lt;/i&gt;-based systems, these extracts enable iterative and pathway-level biosynthesis,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6w29p465</guid>
      <pubDate>Thu, 29 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Dinglasan, Jaime Lorenzo N</name>
      </author>
      <author>
        <name>Lee, Namil</name>
      </author>
      <author>
        <name>Pham, Nam Ngoc</name>
        <uri>https://orcid.org/0000-0001-7640-1001</uri>
      </author>
      <author>
        <name>Faltane, Meghana</name>
      </author>
      <author>
        <name>Lynde, Marie</name>
      </author>
      <author>
        <name>Louie, Katherine B</name>
      </author>
      <author>
        <name>Nath, Sangeeta</name>
      </author>
      <author>
        <name>Keasling, Jay D</name>
        <uri>https://orcid.org/0000-0003-4170-6088</uri>
      </author>
      <author>
        <name>Otani, Hiroshi</name>
      </author>
      <author>
        <name>Mouncey, Nigel J</name>
        <uri>https://orcid.org/0000-0001-5380-1256</uri>
      </author>
    </item>
    <item>
      <title>The Linked Data Modeling Language (LinkML): A General-Purpose Data Modeling Framework Grounded in Machine-Readable Semantics</title>
      <link>https://escholarship.org/uc/item/2dt9329r</link>
      <description>Data integration is a major challenge in the life sciences, due to heterogeneity, complexity, the proliferation of ad-hoc formats and data structures, and poor compliance with FAIR guidelines. The Linked data Modeling Language (LinkML, https://linkml.github.io) is an object-oriented data modeling framework that aims to bring semantic web standards to the masses, simplifying the production of FAIR ontology-ready data. It can be used for schematizing a variety of kinds of data, ranging from simple flat checklist-style standards to complex interrelated normalized data utilizing polymorphism/inheritance. Although it is still a young and evolving standard, LinkML is already in use across a wide variety of projects with different applications including cancer data harmonization, environmental genomics, and knowledge graph integration.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2dt9329r</guid>
      <pubDate>Thu, 29 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Moxon, S</name>
        <uri>https://orcid.org/0000-0002-8719-7760</uri>
      </author>
      <author>
        <name>Solbrig, H</name>
        <uri>https://orcid.org/0000-0002-5928-3071</uri>
      </author>
      <author>
        <name>Unni, D</name>
        <uri>https://orcid.org/0000-0002-3583-7340</uri>
      </author>
      <author>
        <name>Jiao, D</name>
        <uri>https://orcid.org/0000-0001-5052-3836</uri>
      </author>
      <author>
        <name>Bruskiewich, R</name>
        <uri>https://orcid.org/0000-0002-4447-5978</uri>
      </author>
      <author>
        <name>Balhoff, J</name>
        <uri>https://orcid.org/0000-0002-8688-6599</uri>
      </author>
      <author>
        <name>Vaidya, G</name>
        <uri>https://orcid.org/0000-0003-0587-0454</uri>
      </author>
      <author>
        <name>Duncan, W</name>
        <uri>https://orcid.org/0000-0001-9625-1899</uri>
      </author>
      <author>
        <name>Hegde, H</name>
        <uri>https://orcid.org/0000-0002-2411-565X</uri>
      </author>
      <author>
        <name>Miller, M</name>
        <uri>https://orcid.org/0000-0001-9076-6066</uri>
      </author>
      <author>
        <name>Brush, M</name>
        <uri>https://orcid.org/0000-0002-1048-5019</uri>
      </author>
      <author>
        <name>Harris, N</name>
        <uri>https://orcid.org/0000-0001-6315-3707</uri>
      </author>
      <author>
        <name>Haendel, M</name>
        <uri>https://orcid.org/0000-0001-9114-8737</uri>
      </author>
      <author>
        <name>Mungall, C</name>
        <uri>https://orcid.org/0000-0002-6601-2165</uri>
      </author>
    </item>
    <item>
      <title>The Gene Ontology knowledgebase in 2026</title>
      <link>https://escholarship.org/uc/item/20v234dt</link>
      <description>The Gene Ontology (GO) knowledgebase (https://geneontology.org) is a comprehensive resource describing the functions of genes. The GO knowledgebase is regularly updated and improved. We describe here the major updates that have been made in the past 3 years. The ontology and annotations have been expanded and revised, particularly in several areas of biology: cellular metabolism, multi-organism interactions (e.g. host-pathogen), extracellular matrix proteins, chromatin remodeling (e.g. the "histone code"), and noncoding RNA functions. We have released version 2 of a comprehensive set of integrated, reviewed annotations for human genes, which we call the "functionome." We have also dramatically increased the number of GO-CAM models, with over 1500 models of metabolic and signaling pathways, primarily in human, mouse, budding and fission yeast, and fruit fly. Finally, we discuss our current recommendations and future prospects of AI in the use and development of GO.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/20v234dt</guid>
      <pubDate>Thu, 29 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Aleksander, Suzi A</name>
      </author>
      <author>
        <name>Balhoff, James P</name>
      </author>
      <author>
        <name>Carbon, Seth</name>
        <uri>https://orcid.org/0000-0001-8244-1536</uri>
      </author>
      <author>
        <name>Cherry, J Michael</name>
      </author>
      <author>
        <name>Ebert, Dustin</name>
      </author>
      <author>
        <name>Feuermann, Marc</name>
      </author>
      <author>
        <name>Gaudet, Pascale</name>
      </author>
      <author>
        <name>Harris, Nomi L</name>
        <uri>https://orcid.org/0000-0001-6315-3707</uri>
      </author>
      <author>
        <name>Hill, David P</name>
      </author>
      <author>
        <name>Kalita, Patrick</name>
      </author>
      <author>
        <name>Lee, Raymond</name>
      </author>
      <author>
        <name>Mi, Huaiyu</name>
      </author>
      <author>
        <name>Moxon, Sierra</name>
      </author>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
      <author>
        <name>Muruganujan, Anushya</name>
      </author>
      <author>
        <name>Mushayahama, Tremayne</name>
      </author>
      <author>
        <name>Sternberg, Paul W</name>
      </author>
      <author>
        <name>Thomas, Paul D</name>
      </author>
      <author>
        <name>Van Auken, Kimberly</name>
      </author>
      <author>
        <name>Wong, Edith D</name>
      </author>
      <author>
        <name>Wood, Valerie</name>
      </author>
      <author>
        <name>Ramsey, Jolene</name>
      </author>
      <author>
        <name>Siegele, Deborah A</name>
      </author>
      <author>
        <name>Chisholm, Rex L</name>
      </author>
      <author>
        <name>Dodson, Robert</name>
      </author>
      <author>
        <name>Fey, Petra</name>
      </author>
      <author>
        <name>Aspromonte, Maria Cristina</name>
      </author>
      <author>
        <name>Nugnes, Maria Victoria</name>
      </author>
      <author>
        <name>Naser, Ximena Aixa Castro</name>
      </author>
      <author>
        <name>Tosatto, Silvio CE</name>
      </author>
      <author>
        <name>Giglio, Michelle</name>
      </author>
      <author>
        <name>Nadendla, Suvarna</name>
      </author>
      <author>
        <name>Antonazzo, Giulia</name>
      </author>
      <author>
        <name>Attrill, Helen</name>
      </author>
      <author>
        <name>Brown, Nicholas H</name>
      </author>
      <author>
        <name>dos Santos, Gil</name>
      </author>
      <author>
        <name>Marygold, Steven</name>
      </author>
      <author>
        <name>Röper, Katja</name>
      </author>
      <author>
        <name>Strelets, Victor</name>
      </author>
      <author>
        <name>Tabone, Christopher J</name>
      </author>
      <author>
        <name>Thurmond, Jim</name>
      </author>
      <author>
        <name>Zhou, Pinglei</name>
      </author>
      <author>
        <name>Zaru, Rossana</name>
      </author>
      <author>
        <name>Lovering, Ruth C</name>
      </author>
      <author>
        <name>Logie, Colin</name>
      </author>
      <author>
        <name>Chen, Daqing</name>
      </author>
      <author>
        <name>Naba, Alexandra</name>
      </author>
      <author>
        <name>Christie, Karen</name>
      </author>
      <author>
        <name>Corbani, Lori</name>
      </author>
      <author>
        <name>Ni, Li</name>
      </author>
      <author>
        <name>Sitnikov, Dmitry</name>
      </author>
      <author>
        <name>Smith, Cynthia</name>
      </author>
      <author>
        <name>Seager, James</name>
      </author>
      <author>
        <name>Cooper, Laurel</name>
      </author>
      <author>
        <name>Elser, Justin</name>
      </author>
      <author>
        <name>Jaiswal, Pankaj</name>
      </author>
      <author>
        <name>Gupta, Parul</name>
      </author>
      <author>
        <name>Naithani, Sushma</name>
      </author>
      <author>
        <name>Carme, Pascal</name>
      </author>
      <author>
        <name>Rutherford, Kim</name>
      </author>
      <author>
        <name>De Pons, Jeffrey L</name>
      </author>
      <author>
        <name>Dwinell, Melinda R</name>
      </author>
      <author>
        <name>Hayman, G Thomas</name>
      </author>
      <author>
        <name>Kaldunski, Mary L</name>
      </author>
      <author>
        <name>Kwitek, Anne E</name>
      </author>
      <author>
        <name>Laulederkind, Stanley JF</name>
      </author>
      <author>
        <name>Tutaj, Marek A</name>
      </author>
      <author>
        <name>Vedi, Mahima</name>
      </author>
      <author>
        <name>Wang, Shur-Jen</name>
      </author>
      <author>
        <name>D’Eustachio, Peter</name>
      </author>
      <author>
        <name>Aimo, Lucila</name>
      </author>
      <author>
        <name>Axelsen, Kristian</name>
      </author>
      <author>
        <name>Bridge, Alan</name>
      </author>
      <author>
        <name>Hyka-Nouspikel, Nevila</name>
      </author>
      <author>
        <name>Morgat, Anne</name>
      </author>
      <author>
        <name>Goldbold, Gene</name>
      </author>
      <author>
        <name>Engel, Stacia R</name>
      </author>
      <author>
        <name>Miyasato, Stuart R</name>
      </author>
      <author>
        <name>Nash, Robert S</name>
      </author>
      <author>
        <name>Sherlock, Gavin</name>
      </author>
      <author>
        <name>Weng, Shuai</name>
      </author>
      <author>
        <name>Bakker, Erika</name>
      </author>
      <author>
        <name>Berardini, Tanya Z</name>
      </author>
      <author>
        <name>Reiser, Leonore</name>
      </author>
      <author>
        <name>Auchincloss, Andrea</name>
      </author>
      <author>
        <name>Argoud-Puy, Ghislaine</name>
      </author>
      <author>
        <name>Blatter, Marie-Claude</name>
      </author>
      <author>
        <name>Boutet, Emmanuel</name>
      </author>
      <author>
        <name>Breuza, Lionel</name>
      </author>
      <author>
        <name>Casals-Casas, Cristina</name>
      </author>
      <author>
        <name>Coudert, Elisabeth</name>
      </author>
      <author>
        <name>Estreicher, Anne</name>
      </author>
      <author>
        <name>Famiglietti, Maria Livia</name>
      </author>
      <author>
        <name>Gos, Arnaud</name>
      </author>
      <author>
        <name>Gruaz-Gumowski, Nadine</name>
      </author>
      <author>
        <name>Hulo, Chantal</name>
      </author>
      <author>
        <name>Jungo, Florence</name>
      </author>
      <author>
        <name>Le Mercier, Philippe</name>
      </author>
      <author>
        <name>Lieberherr, Damien</name>
      </author>
      <author>
        <name>Masson, Patrick</name>
      </author>
    </item>
    <item>
      <title>25 Years of BOSC, the Bioinformatics Open Source Conference</title>
      <link>https://escholarship.org/uc/item/0650t5d9</link>
      <description>The 25th annual Bioinformatics Open Source Conference (BOSC 2024, open-bio.org/events/bosc-2024) was part of the 2024 conference on Intelligent Systems for Molecular Biology (ISMB 2024). Launched in 2000 and held yearly since, BOSC is the premier meeting covering open-source bioinformatics and open science. ISMB 2024 was held in Montréal, Canada, with an online participation option. A total of nearly 2000 people attended; about 200 people participated in BOSC sessions. Over the course of two days, BOSC covered a wide range of topics in open science and open source bioinformatics, including Data Analysis, Open Data, Visualization, Developer Tools and Libraries, Standards and Frameworks for Open Science, and Open AI/ML. Mélanie Courtot delivered an impactful first keynote with a perspective on how “The Data Shows We Need Better Data”. The second keynote speaker, Andrew Su, discussed “Open Data, Knowledge Graphs, and Large Language Models.” BOSC ended with a panel, “Open Source AI/ML:...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0650t5d9</guid>
      <pubDate>Thu, 29 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Harris, Nomi L</name>
        <uri>https://orcid.org/0000-0001-6315-3707</uri>
      </author>
      <author>
        <name>Hokamp, Karsten</name>
      </author>
      <author>
        <name>Maia, Jessica</name>
      </author>
      <author>
        <name>Ménager, Hervé</name>
      </author>
      <author>
        <name>Munoz-Torres, Monica C</name>
      </author>
      <author>
        <name>Sawant, Swapnil</name>
      </author>
      <author>
        <name>Unni, Deepak</name>
      </author>
      <author>
        <name>Williams, Jason</name>
      </author>
    </item>
    <item>
      <title>Engineered Production of Hydroxycinnamoyl Tyramine Conjugates Limits the Growth of the Pathogen Pseudomonas syringae in Arabidopsis</title>
      <link>https://escholarship.org/uc/item/7mn976np</link>
      <description>Hydroxycinnamoyl tyramine conjugates are phenolamides produced by plants in response to pathogen attack and biotic stresses. Their proposed mechanisms of action include cytotoxicity towards pathogens, cell wall reinforcement to restrict pathogen proliferation, and signaling activity to trigger general stress responses. Here, we engineered the production of the tyramine conjugates p-coumaroyltyramine (CT) and feruloyltyramine (FT) in Arabidopsis to gain insight into their mode of action. Co-expression of feedback-insensitive 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase and tyrosine decarboxylase increased tyramine content. Additional expression of tyramine hydroxycinnamoyltransferase led to de-novo production of CT and FT, which were found as soluble and cell-wall-bound forms. FT was associated with lignin in stems. The growth of pathogenic Pseudomonas syringae was reduced in rosettes of the Arabidopsis CT- and FT-producing lines compared to wild type. These lines also...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7mn976np</guid>
      <pubDate>Tue, 27 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Turumtay, Halbay</name>
        <uri>https://orcid.org/0000-0003-4224-8103</uri>
      </author>
      <author>
        <name>Hassan, Jana A</name>
      </author>
      <author>
        <name>Kazaz, Sami</name>
      </author>
      <author>
        <name>Gao, Yu</name>
      </author>
      <author>
        <name>Tian, Yang</name>
      </author>
      <author>
        <name>Chen, Yi‐Chun</name>
      </author>
      <author>
        <name>Kakumanu, Ramu</name>
      </author>
      <author>
        <name>Turumtay, Emine Akyuz</name>
      </author>
      <author>
        <name>Cetiz, Mehmet Veysi</name>
      </author>
      <author>
        <name>Choudhary, Hemant</name>
      </author>
      <author>
        <name>Baidoo, Edward EK</name>
        <uri>https://orcid.org/0000-0001-5787-1219</uri>
      </author>
      <author>
        <name>Simmons, Blake A</name>
        <uri>https://orcid.org/0000-0002-1918-3463</uri>
      </author>
      <author>
        <name>Scheller, Henrik V</name>
        <uri>https://orcid.org/0000-0002-6702-3560</uri>
      </author>
      <author>
        <name>Lewis, Jennifer D</name>
        <uri>https://orcid.org/0000-0003-4337-8292</uri>
      </author>
      <author>
        <name>Eudes, Aymerick</name>
        <uri>https://orcid.org/0000-0002-1387-6111</uri>
      </author>
    </item>
    <item>
      <title>Phycobilisome core architecture influences photoprotective quenching by the Orange Carotenoid Protein</title>
      <link>https://escholarship.org/uc/item/5gt7621g</link>
      <description>Photosynthetic organisms rely on sophisticated photoprotective mechanisms to prevent oxidative damage under high or fluctuating solar illumination. Cyanobacteria, which have evolved a unique, water-soluble light-harvesting complex-the phycobilisome-achieve photoprotection through a photoactivatable quencher called the Orange Carotenoid Protein (OCP). Phycobilisomes are highly symmetric and modular, formed by hierarchical assembly of conserved subunits into diverse geometries ranging from simple bundles to elaborate fan- or bouquet-like macromolecular architectures. Although OCP is known to provide photoprotection across species of cyanobacteria with different phycobilisome structures, it is not known whether or how these structural variations relate to changes in the photoprotective function of OCP. For example, OCP was recently discovered to bind as a dimer at two specific instances of an abundant structural motif on the tricylindrical phycobilisome of &lt;i&gt;Synechocystis&lt;/i&gt; sp....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5gt7621g</guid>
      <pubDate>Mon, 26 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ejaz, Ayesha</name>
      </author>
      <author>
        <name>Sutter, Markus</name>
        <uri>https://orcid.org/0000-0001-6290-4820</uri>
      </author>
      <author>
        <name>Lechno-Yossef, Sigal</name>
      </author>
      <author>
        <name>Kerfeld, Cheryl A</name>
        <uri>https://orcid.org/0000-0002-9977-8482</uri>
      </author>
      <author>
        <name>Squires, Allison H</name>
      </author>
    </item>
    <item>
      <title>Enrichment of root-associated Streptomyces strains in response to drought is driven by diverse functional traits and does not predict beneficial effects on plant growth</title>
      <link>https://escholarship.org/uc/item/7520f3k0</link>
      <description>The genus Streptomyces has consistently been found enriched in drought-stressed plant root microbiomes, yet the ecological basis and functional variation underlying this enrichment at the strain and isolate level remain unclear. Using two 16S rRNA sequencing methods with different levels of taxonomic resolution, we confirmed drought-associated enrichment (DE) of Streptomyces in field-grown sorghum roots and identified five closely related but distinct amplicon sequence variants (ASVs) belonging to the genus with variable drought enrichment patterns. From a culture collection of sorghum root endophytes, we selected 12 Streptomyces isolates representing these ASVs for phenotypic and genomic characterization. Whole-genome sequencing revealed substantial variation in gene content, even among closely related isolates, and exometabolomic profiling showed distinct metabolic responses to media supplemented with drought- versus well-watered root tissue. Traits linked to drought survival,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7520f3k0</guid>
      <pubDate>Thu, 15 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Fonseca-Garcia, Citlali</name>
      </author>
      <author>
        <name>Pettinga, Dean</name>
      </author>
      <author>
        <name>Caddell, Daniel</name>
      </author>
      <author>
        <name>Ploemacher, Hannah</name>
      </author>
      <author>
        <name>Louie, Katherine</name>
      </author>
      <author>
        <name>Bowen, Benjamin P</name>
      </author>
      <author>
        <name>Park, Joelle</name>
      </author>
      <author>
        <name>Sanchez, Jesus</name>
      </author>
      <author>
        <name>Zimic-Sheen, Alen</name>
      </author>
      <author>
        <name>Traxler, Matthew F</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Coleman-Derr, Devin</name>
      </author>
    </item>
    <item>
      <title>Acclimation to high and low diurnal light is flexible in Chlamydomonas reinhardtii.</title>
      <link>https://escholarship.org/uc/item/684534gk</link>
      <description>Chlamydomonas acclimates to repeated low (LL) or high light (HL) days by changing the abundance of photosynthetic complexes and the ultrastructure of its thylakoid membranes. These phenotypes persist through the night phases, suggesting a readiness for the daylight environment that is routinely experienced despite the intervening dark periods [S. Dupuis &lt;i&gt;et al.&lt;/i&gt;, &lt;i&gt;Plant Cell&lt;/i&gt; &lt;b&gt;37&lt;/b&gt;, koaf086 (2025), 10.1093/plcell/koaf086]. Here, we investigate how prior acclimation impacts algal fitness upon a change in daylight intensity and how quickly Chlamydomonas can reprogram its photoprotective strategy in a diurnal context. We performed a systems analysis of synchronized populations acclimated to diurnal LL when subjected to HL days and of populations acclimated to diurnal HL when subjected to LL days. In the latter case, diurnal photoacclimation decreased fitness during the first day at a new light intensity: HL-acclimated cells barely increased in size over the first LL...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/684534gk</guid>
      <pubDate>Wed, 14 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Dupuis, Sunnyjoy</name>
      </author>
      <author>
        <name>Chastain, Jordan L</name>
      </author>
      <author>
        <name>Han, Genevieve</name>
      </author>
      <author>
        <name>Zhong, Victor</name>
      </author>
      <author>
        <name>Gallaher, Sean D</name>
        <uri>https://orcid.org/0000-0002-9773-6051</uri>
      </author>
      <author>
        <name>Nicora, Carrie D</name>
      </author>
      <author>
        <name>Purvine, Samuel O</name>
      </author>
      <author>
        <name>Lipton, Mary S</name>
      </author>
      <author>
        <name>Niyogi, Krishna K</name>
      </author>
      <author>
        <name>Iwai, Masakazu</name>
        <uri>https://orcid.org/0000-0002-0986-9015</uri>
      </author>
      <author>
        <name>Merchant, Sabeeha S</name>
      </author>
    </item>
    <item>
      <title>Genetically pliable green algae for bioproduction of modified fatty acids, nutritional therapeutic oils, and biopharmaceuticals</title>
      <link>https://escholarship.org/uc/item/1bs824ng</link>
      <description>Homologous recombination (HR) is an essential tool for complex metabolic engineering in yeast, but transgene integration into plant and green algal nuclear genomes predominantly occurs by non-homologous end-joining. Species of the closely related, oleaginous trebouxiophytes Auxenochlorella and Prototheca, are unusual among the green algae in that HR is the favored mechanism for DNA integration into the nuclear genome. This property enables locus-specific targeting of gene cassettes encoding multiple enzymes for manipulating existing biochemical pathways or introducing new functions. Genetic malleability, and regulatory approval for human consumption, coupled with robust fermentation performance at industrial scale, establishes Auxenochlorella and Prototheca as prime candidates for algal production of biochemicals and biomaterials. The examples presented here highlight strain improvement and engineering for synthesis of hydroxylated fatty acids for biomaterials, structured triglycerides...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1bs824ng</guid>
      <pubDate>Fri, 9 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Moseley, Jeffrey L</name>
        <uri>https://orcid.org/0000-0001-8603-8488</uri>
      </author>
      <author>
        <name>Merchant, Sabeeha S</name>
      </author>
    </item>
    <item>
      <title>Identification of proteins influencing CRISPR-associated transposases for enhanced genome editing</title>
      <link>https://escholarship.org/uc/item/3nm6z453</link>
      <description>CRISPR-associated transposases (CASTs) hold tremendous potential for microbial genome editing because of their ability to integrate large DNA cargos in a programmable, site-specific manner. However, their widespread application has been hindered by poorly understood host factor requirements for transposition. To address this gap, we conducted the first genome-wide screen for host factors affecting &lt;i&gt;Vibrio cholerae&lt;/i&gt; CAST (&lt;i&gt;Vch&lt;/i&gt;CAST) activity using an &lt;i&gt;Escherichia coli&lt;/i&gt; RB-TnSeq library and identified 15 genes affecting &lt;i&gt;Vch&lt;/i&gt;CAST transposition. Of these, seven factors were validated to improve &lt;i&gt;Vch&lt;/i&gt;CAST activity, and two were inhibitory. Guided by the identification of homologous recombination effectors, RecD and RecA, we tested the λ-Red recombineering system in our &lt;i&gt;Vch&lt;/i&gt;CAST editing vectors and increased editing efficiency by 55.2-fold in &lt;i&gt;E. coli&lt;/i&gt;, 5.6-fold in &lt;i&gt;Pseudomonas putida&lt;/i&gt;, and 10.8-fold in &lt;i&gt;Klebsiella michiganensis&lt;/i&gt; while...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3nm6z453</guid>
      <pubDate>Tue, 6 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Song, Leo CT</name>
      </author>
      <author>
        <name>Alker, Amanda TP</name>
      </author>
      <author>
        <name>Oromí-Bosch, Agnès</name>
      </author>
      <author>
        <name>Swartz, Sophia E</name>
      </author>
      <author>
        <name>Martinson, Jonathan NV</name>
      </author>
      <author>
        <name>Arora, Jigyasa</name>
      </author>
      <author>
        <name>Wang, Abby M</name>
      </author>
      <author>
        <name>Rovinsky, Rachel</name>
      </author>
      <author>
        <name>Smith, Sara J</name>
        <uri>https://orcid.org/0009-0005-7076-1475</uri>
      </author>
      <author>
        <name>Pierce, Emily C</name>
      </author>
      <author>
        <name>Deutschbauer, Adam M</name>
      </author>
      <author>
        <name>Doudna, Jennifer A</name>
      </author>
      <author>
        <name>Cress, Brady F</name>
        <uri>https://orcid.org/0000-0002-2948-2846</uri>
      </author>
      <author>
        <name>Rubin, Benjamin E</name>
      </author>
    </item>
    <item>
      <title>The linker protein ApcI regulates light harvesting under red light in Synechocystis sp. PCC 6803</title>
      <link>https://escholarship.org/uc/item/7sf8n6zc</link>
      <description>Phycobilisomes (PBSs) are versatile cyanobacterial antenna complexes that harvest light energy to drive photosynthesis. They can adapt to various light conditions; for example, dismantling under high light to prevent photo-oxidation and arranging in rows under low light to increase light harvesting efficiency. Light quality also influences PBS structure and function, as observed under far-red light exposure. Here, we describe a PBS linker protein, ApcI (previously hypothetical protein Sll1911), expressed specifically under red light (620 nm) or upon chemically induced reduction of the plastoquinone pool. We characterized ApcI in Synechocystis sp. PCC 6803 using mutant analyses, PBS binding experiments, and protein interaction studies. Deletion of apcI conferred high light tolerance on Synechocystis sp. PCC 6803 compared to the wild-type strain, leading to reduced energy transfer from PBSs to the photosystems under high light. Binding experiments revealed that ApcI replaces the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7sf8n6zc</guid>
      <pubDate>Tue, 16 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Espinoza-Corral, Roberto</name>
      </author>
      <author>
        <name>Zavřel, Tomáš</name>
      </author>
      <author>
        <name>Sutter, Markus</name>
        <uri>https://orcid.org/0000-0001-6290-4820</uri>
      </author>
      <author>
        <name>Leslie, Chase H</name>
      </author>
      <author>
        <name>Yang, Kunwei</name>
      </author>
      <author>
        <name>Beck, Warren F</name>
      </author>
      <author>
        <name>Červený, Jan</name>
      </author>
      <author>
        <name>Kerfeld, Cheryl A</name>
        <uri>https://orcid.org/0000-0002-9977-8482</uri>
      </author>
    </item>
    <item>
      <title>A multi-omic characterization of the physiological responses to salt stress in Scenedesmus obliquus UTEX393</title>
      <link>https://escholarship.org/uc/item/4t54b3f6</link>
      <description>Scenedesmus obliquus UTEX393 is a promising microalgal candidate for sustainable biomanufacturing but its limited halotolerance hinders large-scale cultivation in saline environments. To investigate the molecular basis of salt stress responses, we conducted a comprehensive multi-omic analysis integrating genomics, transcriptomics, proteomics, lipidomics, metabolomics, and DNA affinity purification sequencing (DAP-seq). An improved nuclear genome assembly and annotation yielded 19,017 gene models and a 97% BUSCO completeness score, enabling construction of a genome-scale metabolic model. Comparing 15 ppt salinity stress to 5 ppt control, growth and productivity were significantly reduced, accompanied by widespread transcriptomic and proteomic changes. Transcriptomic analysis revealed downregulation of photosynthetic machinery and energy conservation genes, and upregulation of stress-responsive elements such as expansins, flavodoxins, and osmoprotectants. Lipidomic profiling showed...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4t54b3f6</guid>
      <pubDate>Tue, 16 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kruse, Colin PS</name>
      </author>
      <author>
        <name>Calhoun, Sara</name>
        <uri>https://orcid.org/0000-0003-2942-1338</uri>
      </author>
      <author>
        <name>Kamel, Bishoy</name>
      </author>
      <author>
        <name>Edmundson, Scott J</name>
      </author>
      <author>
        <name>Holguin, Omar</name>
      </author>
      <author>
        <name>Mach, Phillip M</name>
      </author>
      <author>
        <name>McKie-Krisberg, Zaid</name>
      </author>
      <author>
        <name>Baumgart, Leo</name>
        <uri>https://orcid.org/0000-0002-2773-5897</uri>
      </author>
      <author>
        <name>Blaby, Ian K</name>
        <uri>https://orcid.org/0000-0002-1631-3154</uri>
      </author>
      <author>
        <name>Bowen, Benjamin</name>
        <uri>https://orcid.org/0000-0003-1368-3958</uri>
      </author>
      <author>
        <name>Chen, Cindy</name>
      </author>
      <author>
        <name>Kunde, Yuliya</name>
      </author>
      <author>
        <name>Grimwood, Jane</name>
      </author>
      <author>
        <name>Lipzen, Anna</name>
        <uri>https://orcid.org/0000-0003-2293-9329</uri>
      </author>
      <author>
        <name>Louie, Katherine</name>
      </author>
      <author>
        <name>Mewalal, Ritesh</name>
      </author>
      <author>
        <name>Gleasner, Cheryl D</name>
      </author>
      <author>
        <name>Northen, Trent</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Talag, Jayson</name>
      </author>
      <author>
        <name>Treen, Daniel</name>
      </author>
      <author>
        <name>Zhang, Yu</name>
      </author>
      <author>
        <name>Gutknecht, Andrew</name>
      </author>
      <author>
        <name>O’Malley, Ronan C</name>
      </author>
      <author>
        <name>Glaros, Trevor G</name>
      </author>
      <author>
        <name>Polle, Juergen</name>
      </author>
      <author>
        <name>Umen, James</name>
      </author>
      <author>
        <name>Huesemann, Michael</name>
      </author>
      <author>
        <name>Grigoriev, Igor V</name>
        <uri>https://orcid.org/0000-0002-3136-8903</uri>
      </author>
      <author>
        <name>Starkenburg, Shawn R</name>
      </author>
    </item>
    <item>
      <title>Engineered Accumulation of Protocatechuate in Corn Biomass to Enhance Biomanufacturing</title>
      <link>https://escholarship.org/uc/item/3107w8sr</link>
      <description>The in-planta accumulation of coproducts in crops can enhance the value of lignocellulosic biomass and facilitate a sustainable bioeconomy. Corn stover represents a major renewable source of lignocellulose for the production of advanced biofuels and bioproducts. In this study, we engineered corn with a bacterial gene encoding a dehydroshikimate dehydratase (QsuB) to overproduce protocatechuate (DHBA). Transgenic corn lines accumulate up to 2.9% DHBA on a dry weight basis in leaf and stem biomass. DHBA occurs in the form of glucosides that are extractable from biomass using aqueous methanol as the solvent. The analysis of lignin did not show any evidence for the incorporation of DHBA; however, an increase in the lignin syringyl to guaiacyl ratio and a higher relative abundance of &lt;i&gt;p&lt;/i&gt;-coumarate groups compared with total lignin units were observed in QsuB-modified corn. Alkaline hydrolysates prepared from QsuB corn were enriched in DHBA compared to the hydrolysates obtained...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3107w8sr</guid>
      <pubDate>Tue, 16 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Tian, Yang</name>
      </author>
      <author>
        <name>Kim, Bumkyu</name>
      </author>
      <author>
        <name>Pamukçu, Irem</name>
      </author>
      <author>
        <name>Turumtay, Emine Akyuz</name>
      </author>
      <author>
        <name>Tan, Alexis H</name>
      </author>
      <author>
        <name>Saini, Victoria</name>
      </author>
      <author>
        <name>Chavez, Ariana Irma</name>
      </author>
      <author>
        <name>Tang, Anna</name>
      </author>
      <author>
        <name>Su, Anna Z</name>
      </author>
      <author>
        <name>Baidoo, Edward EK</name>
        <uri>https://orcid.org/0000-0001-5787-1219</uri>
      </author>
      <author>
        <name>Rencoret, Jorge</name>
      </author>
      <author>
        <name>del Río, José C</name>
      </author>
      <author>
        <name>Donohue, Timothy J</name>
      </author>
      <author>
        <name>Noguera, Daniel R</name>
      </author>
      <author>
        <name>Eudes, Aymerick</name>
        <uri>https://orcid.org/0000-0002-1387-6111</uri>
      </author>
    </item>
    <item>
      <title>Synchronizing Germination Rates Across Plant Species for Fabricated Ecosystems EcoFAB 2.0</title>
      <link>https://escholarship.org/uc/item/8k1750k1</link>
      <description>Roots are essential organs for plants, facilitating water and nutrient uptake from the soil to support growth. Traditional methods for studying root systems, such as rhizoboxes and rhizotrons, have provided valuable insights. However, advanced methods such as fabricated ecosystems (EcoFAB) combined with new generation microscopes now enable a more detailed investigation of the rhizosphere, the microenvironment surrounding roots, allowing a deeper understanding of root tissue, exudates, and plant-soil interactions. This microenvironment can be used to investigate the adaptation of plants to environmental stress (salinity, drought, higher temperatures). Our procedure focuses on establishing standardized protocols for plant growth tailored to the EcoFAB system, which offers a controlled environment to study root dynamics. This work also contributes new insights into the early stages of plant germination, an area currently underexplored in the literature. While numerous studies focus...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8k1750k1</guid>
      <pubDate>Wed, 10 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Charbeaux, Romane SF</name>
      </author>
      <author>
        <name>Waymouth, Vicky J</name>
      </author>
      <author>
        <name>Calabria, Jacob</name>
      </author>
      <author>
        <name>Miller, Troy</name>
      </author>
      <author>
        <name>Andeer, Peter</name>
      </author>
      <author>
        <name>Watt, Michelle</name>
      </author>
    </item>
    <item>
      <title>EcoBOT: an AI/ML enabled automated phenotyping capability for model plants</title>
      <link>https://escholarship.org/uc/item/73z863ks</link>
      <description>Introduction: Advances in automation and AI/ML offer new opportunities for plant science, including design, modeling, and analysis. This study aimed to develop an automated platform for researching small model plants under axenic conditions and integrate it with AI/ML tools.
Methods: The EcoBOT platform was developed, which consists of sterile containers (EcoFABs) for growing plants and imaging for monitoring plant growth and health. &lt;i&gt;Brachypodium distachyon&lt;/i&gt; was grown on the EcoBOT, and its response to nutrient limitation and copper stress was evaluated.
Results: The results showed that Brachypodium distachyon grown in the EcoBOT maintained sterility and responded to nutrient limitation and copper stress. Analysis of over 6,500 root and shoot images revealed varying sensitivity and response rates to copper. Bayesian Optimization was used to improve model accuracies relating copper concentrations to plant biomass via sequential experiments, resulting in a &amp;gt;30% improvement.
Discussion:...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/73z863ks</guid>
      <pubDate>Wed, 10 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Andeer, Peter F</name>
      </author>
      <author>
        <name>Zwart, Petrus H</name>
      </author>
      <author>
        <name>Ushizima, Daniela</name>
        <uri>https://orcid.org/0000-0002-7363-9468</uri>
      </author>
      <author>
        <name>Noack, Marcus M</name>
        <uri>https://orcid.org/0000-0003-2750-6565</uri>
      </author>
      <author>
        <name>Cornmesser, Lloyd T</name>
      </author>
      <author>
        <name>Vess, Thomas M</name>
      </author>
      <author>
        <name>Sordo, Zineb</name>
      </author>
      <author>
        <name>Tan, Stephen</name>
      </author>
      <author>
        <name>Zorzi, Joseph</name>
      </author>
      <author>
        <name>Hernandez, Chelsea</name>
      </author>
      <author>
        <name>Novak, Vlastimil</name>
        <uri>https://orcid.org/0000-0001-7890-4593</uri>
      </author>
      <author>
        <name>Ding, Yezhang</name>
      </author>
      <author>
        <name>Vogel, John P</name>
      </author>
      <author>
        <name>Bowen, Benjamin P</name>
      </author>
      <author>
        <name>Sethian, James A</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
      </author>
    </item>
    <item>
      <title>Engineering Polyketide Stereocenters with Ketoreductase Domain Exchanges</title>
      <link>https://escholarship.org/uc/item/3427k60n</link>
      <description>Polyketide synthases (PKSs) are versatile biosynthetic megasynthases capable of producing a diverse range of natural products with many applications, including in pharmaceuticals. The stereochemical precision of PKSs makes them a powerful tool for engineering tailored, unnatural polyketides; however, modifying the stereocenters of a PKS product while maintaining production levels remains a significant challenge. In this study, we systematically tested and evaluated strategies for ketoreductase (KR) domain exchanges, the domain responsible for setting stereocenters of polyketide products. After first optimizing the method for KR exchanges, we then performed 44 KR domain exchanges on three different PKSs to obtain high production of all four stereoisomers in vivo. By testing both one- and two-module PKS systems, we investigated how downstream modules process intermediates with altered stereochemistry and found that the configuration of the α-substituents was critical for gatekeeping...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3427k60n</guid>
      <pubDate>Mon, 8 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Keiser, Leah S</name>
      </author>
      <author>
        <name>Gatenil, Panarai Primrose</name>
      </author>
      <author>
        <name>Zhu, Yolanda</name>
      </author>
      <author>
        <name>Deng, Kai</name>
      </author>
      <author>
        <name>Waldburger, Lucas</name>
      </author>
      <author>
        <name>Gin, Jennifer W</name>
      </author>
      <author>
        <name>Chen, Yan</name>
      </author>
      <author>
        <name>Baidoo, Edward EK</name>
        <uri>https://orcid.org/0000-0001-5787-1219</uri>
      </author>
      <author>
        <name>Petzold, Christopher J</name>
        <uri>https://orcid.org/0000-0002-8270-5228</uri>
      </author>
      <author>
        <name>Lanclos, Nathan</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Englund, Elias</name>
      </author>
      <author>
        <name>Keasling, Jay D</name>
        <uri>https://orcid.org/0000-0003-4170-6088</uri>
      </author>
    </item>
    <item>
      <title>Engineered plants for the production of the antioxidants arbutin and gallate</title>
      <link>https://escholarship.org/uc/item/0s34d2jd</link>
      <description>The shikimate pathway is a crucial metabolic route for the biosynthesis of numerous valuable chemicals. In this study, we engineered the shikimate pathway in plants via expression of microbial enzymes to produce the two important antioxidants gallate and arbutin. The engineered pathways utilize the aromatics protocatechuate and 4-hydroxybenzoate as metabolic intermediates. Through transient expression in Nicotiana benthamiana leaves, we first identified biosynthetic routes for the production of gallate from either chorismate or 3-dehydroshikimate. Gallate production was then achieved in Arabidopsis using a genetic background that overproduces protocatechuate and via expression of a mutated version of the 4-hydroxybenzoate hydroxylase PobA from Pseudomonas sp. Arbutin production was obtained in Arabidopsis using a genetic background that overproduces 4-hydroxybenzoate and via expression of the monooxygenase MNX1 from Candida parapsilosis. The best Arabidopsis transgenic lines accumulated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0s34d2jd</guid>
      <pubDate>Mon, 8 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kazaz, Sami</name>
      </author>
      <author>
        <name>Chen, Yu-Ton</name>
      </author>
      <author>
        <name>Yamamoto, Senri</name>
      </author>
      <author>
        <name>Tian, Yang</name>
      </author>
      <author>
        <name>Lin, Chien-Yuan</name>
      </author>
      <author>
        <name>Chin, Dylan</name>
      </author>
      <author>
        <name>Pamukçu, İrem</name>
      </author>
      <author>
        <name>Al Shammaa, Ibraheem Mohammed</name>
      </author>
      <author>
        <name>Akbas, Yusuf Selman</name>
      </author>
      <author>
        <name>Nimavat, Monikaben</name>
      </author>
      <author>
        <name>Akyuz Turumtay, Emine</name>
      </author>
      <author>
        <name>Baidoo, Edward EK</name>
        <uri>https://orcid.org/0000-0001-5787-1219</uri>
      </author>
      <author>
        <name>Kausch, Albert P</name>
      </author>
      <author>
        <name>Tobimatsu, Yuki</name>
      </author>
      <author>
        <name>Eudes, Aymerick</name>
        <uri>https://orcid.org/0000-0002-1387-6111</uri>
      </author>
    </item>
    <item>
      <title>Optimal production of Phanerochaete chrysosporium manganese peroxidases and Trametes sp. C30 laccase hybrid Lac131 in Aspergillus niger for lignin bioconversion</title>
      <link>https://escholarship.org/uc/item/3552n2dg</link>
      <description>BackgroundIncorporating the production of related ligninolytic enzymes into industrial filamentous fungus Aspergillus niger will enhance the bioconversion of lignocelluloses to various chemical products.ResultsIn this study, transgenic expression of Phanerochaete chrysosporium manganese peroxidases (mnps) and Trametes sp. C30 laccase hybrid Lac131 (lac131) were examined and optimized in A. niger 11414 prtT∆ strain. Five mnps (mnp1, mnp2, mnp3, mnp4, and mnp5) and lac131 genes were expressed separately or in combination. The transgenic strain containing the entire mnp2 genomic coding sequence (gmnp2) exhibited the highest mnP activity among the five mnp over-expression strains in the modified minimal medium (mMM) with addition of 5&amp;nbsp;g/L bovine hemoglobin (bHg). We examined the effects of hemin and bHg on mnP production in the gmnp2 strain cultures and found that at least 1&amp;nbsp;g/L bHg was required, while hemin was not. Culture conditions for mnP production were further optimized...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3552n2dg</guid>
      <pubDate>Tue, 2 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Dai, Ziyu</name>
      </author>
      <author>
        <name>Robles, Ana L</name>
      </author>
      <author>
        <name>Lemmon, Sarah L</name>
      </author>
      <author>
        <name>Yuan, Guoliang</name>
      </author>
      <author>
        <name>Hu, Dehong</name>
      </author>
      <author>
        <name>Onley, Jenny</name>
        <uri>https://orcid.org/0000-0003-0842-7378</uri>
      </author>
      <author>
        <name>Jia, Jiayuan</name>
      </author>
      <author>
        <name>Deng, Kai</name>
      </author>
      <author>
        <name>Gupta, Kshitiz</name>
        <uri>https://orcid.org/0000-0002-1732-6176</uri>
      </author>
      <author>
        <name>Northen, Trent R</name>
      </author>
      <author>
        <name>Simmons, Blake A</name>
        <uri>https://orcid.org/0000-0002-1918-3463</uri>
      </author>
      <author>
        <name>Baker, Scott E</name>
      </author>
      <author>
        <name>Magnuson, Jon K</name>
      </author>
      <author>
        <name>Kim, Joonhoon</name>
      </author>
    </item>
    <item>
      <title>Perspectives for artificial intelligence in bioprocess automation</title>
      <link>https://escholarship.org/uc/item/2ws980bb</link>
      <description>Recent advances in artificial intelligence (AI)&amp;nbsp;have rapidly changed the lab automation landscape, promoting self-driving laboratories (SDLs) that enable autonomous scientific discovery. These trends are increasingly applied in bioprocess development, yet bioprocessing faces unique challenges&amp;nbsp;-&amp;nbsp;biological complexity, regulatory and safety requirements, and multiscale experimentation&amp;nbsp;-&amp;nbsp;that distinguish it from other automation domains. Rather than pursuing full autonomy, we foresee that hybrid SDLs, combining AI-driven decision-making with sustained human oversight, represent the most practical near-term trajectory. This review examines three interconnected perspectives: (i) hybrid human-machine decision-making for bioprocessing; (ii) laboratory design considerations in the era of AI; and (iii) scale-up challenges when transitioning from screening to manufacturing. We highlight critical gaps in data standardization and the required community efforts necessary...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2ws980bb</guid>
      <pubDate>Tue, 2 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Helleckes, Laura Marie</name>
      </author>
      <author>
        <name>Putz, Sebastian</name>
      </author>
      <author>
        <name>Gupta, Kshitiz</name>
        <uri>https://orcid.org/0000-0002-1732-6176</uri>
      </author>
      <author>
        <name>Franzreb, Matthias</name>
      </author>
      <author>
        <name>Garcia Martin, Hector</name>
        <uri>https://orcid.org/0000-0002-4556-9685</uri>
      </author>
    </item>
    <item>
      <title>Correction: Myco-Ed: Mycological curriculum for education and discovery</title>
      <link>https://escholarship.org/uc/item/9t1012f8</link>
      <description>[This corrects the article DOI: 10.1371/journal.ppat.1013303.].</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9t1012f8</guid>
      <pubDate>Mon, 1 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Branco, Sara</name>
      </author>
      <author>
        <name>Avis, Peter G</name>
      </author>
      <author>
        <name>Barry, Kerrie</name>
        <uri>https://orcid.org/0000-0002-8999-6785</uri>
      </author>
      <author>
        <name>Bates, Scott</name>
      </author>
      <author>
        <name>Cobián, Gerald M</name>
      </author>
      <author>
        <name>Dow, Ellen G</name>
        <uri>https://orcid.org/0000-0002-2079-0260</uri>
      </author>
      <author>
        <name>Gremillion, Sara</name>
      </author>
      <author>
        <name>Honan, Amy</name>
      </author>
      <author>
        <name>Knight, Chinyere A</name>
      </author>
      <author>
        <name>LaButti, Kurt</name>
        <uri>https://orcid.org/0000-0002-5838-1972</uri>
      </author>
      <author>
        <name>Quandt, C Alisha</name>
      </author>
      <author>
        <name>Stewart, Jane E</name>
      </author>
      <author>
        <name>Talag, Jayson</name>
      </author>
      <author>
        <name>Wilson, Andrew W</name>
      </author>
      <author>
        <name>Lofgren, Lotus</name>
      </author>
      <author>
        <name>Mondo, Stephen James</name>
        <uri>https://orcid.org/0000-0001-5797-0647</uri>
      </author>
    </item>
    <item>
      <title>Chemical classification program synthesis using generative artificial intelligence</title>
      <link>https://escholarship.org/uc/item/8s29j3r4</link>
      <description>Accurately classifying chemical structures is essential for cheminformatics and bioinformatics, including tasks such as identifying bioactive compounds of interest, screening molecules for toxicity to humans, finding non-organic compounds with desirable material properties, or organizing large chemical libraries for drug discovery or environmental monitoring. However, manual classification is labor-intensive and difficult to scale to large chemical databases. Existing automated approaches either rely on manually constructed classification rules, or are deep learning methods that lack explainability. This work presents an approach that uses generative artificial intelligence to automatically write chemical classifier programs for classes in the Chemical Entities of Biological Interest (ChEBI) database. These programs can be used for efficient deterministic run-time classification of SMILES structures, with natural language explanations. The programs themselves constitute an explainable...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8s29j3r4</guid>
      <pubDate>Mon, 1 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
      <author>
        <name>Malik, Adnan</name>
      </author>
      <author>
        <name>Korn, Daniel R</name>
      </author>
      <author>
        <name>Reese, Justin T</name>
      </author>
      <author>
        <name>O’Boyle, Noel M</name>
      </author>
      <author>
        <name>Hastings, Janna</name>
      </author>
    </item>
    <item>
      <title>BOSC 2025, the 26th Bioinformatics Open Source Conference</title>
      <link>https://escholarship.org/uc/item/1ks8k286</link>
      <description>The 26th annual Bioinformatics Open Source Conference (BOSC 2025, open-bio.org/events/bosc-2025) brought its community-driven focus on open-source bioinformatics and open science to the 2025 conference on Intelligent Systems for Molecular Biology and the European Conference on Computational Biology (ISMB/ECCB 2025). Since its launch in 2000, BOSC has been the premier annual meeting covering open-source bioinformatics and open science. Framed by two keynote addresses and a thought-provoking panel discussion, the two-day conference included sessions dedicated to open data, analytic tools and pipelines, workflow platforms, knowledge representation, and the application of AI/ML. The first keynote talk was delivered by Christine Orengo: “Working together to develop, promote and protect our data resources: Lessons learnt developing CATH and TED.” A joint session with the Bio-Ontologies and Knowledge Representation (BOKR) track the second day of BOSC started with a keynote talk by Chris...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1ks8k286</guid>
      <pubDate>Mon, 1 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Harris, Nomi L</name>
        <uri>https://orcid.org/0000-0001-6315-3707</uri>
      </author>
      <author>
        <name>Hokamp, Karsten</name>
      </author>
      <author>
        <name>Maia, Jessica</name>
      </author>
      <author>
        <name>Ménager, Hervé</name>
      </author>
      <author>
        <name>Munoz-Torres, Monia C</name>
      </author>
      <author>
        <name>Ohta, Tazro</name>
      </author>
      <author>
        <name>Unni, Deepak</name>
      </author>
      <author>
        <name>Williams, Jason</name>
      </author>
    </item>
    <item>
      <title>Author Correction: A universal language for finding mass spectrometry data patterns</title>
      <link>https://escholarship.org/uc/item/4dv456qx</link>
      <description>Correction to: Nature Methodshttps://doi.org/10.1038/s41592-025-02660-z, published online 12 May 2025. This article was originally published under standard Springer Nature license (© The Author(s), under exclusive licence to Springer Nature America, Inc.). It is now available as an open-access paper under a Creative Commons Attribution 4.0 International license, © The Author(s). The error has been corrected in the HTML and PDF versions of the article.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4dv456qx</guid>
      <pubDate>Fri, 21 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Damiani, Tito</name>
      </author>
      <author>
        <name>Jarmusch, Alan K</name>
      </author>
      <author>
        <name>Aron, Allegra T</name>
      </author>
      <author>
        <name>Petras, Daniel</name>
      </author>
      <author>
        <name>Phelan, Vanessa V</name>
      </author>
      <author>
        <name>Zhao, Haoqi Nina</name>
      </author>
      <author>
        <name>Bittremieux, Wout</name>
      </author>
      <author>
        <name>Acharya, Deepa D</name>
      </author>
      <author>
        <name>Ahmed, Mohammed MA</name>
      </author>
      <author>
        <name>Bauermeister, Anelize</name>
      </author>
      <author>
        <name>Bertin, Matthew J</name>
      </author>
      <author>
        <name>Boudreau, Paul D</name>
      </author>
      <author>
        <name>Borges, Ricardo M</name>
      </author>
      <author>
        <name>Bowen, Benjamin P</name>
        <uri>https://orcid.org/0000-0003-1368-3958</uri>
      </author>
      <author>
        <name>Brown, Christopher J</name>
      </author>
      <author>
        <name>Chagas, Fernanda O</name>
      </author>
      <author>
        <name>Clevenger, Kenneth D</name>
      </author>
      <author>
        <name>Correia, Mario SP</name>
      </author>
      <author>
        <name>Crandall, William J</name>
      </author>
      <author>
        <name>Crüsemann, Max</name>
      </author>
      <author>
        <name>Fahy, Eoin</name>
      </author>
      <author>
        <name>Fiehn, Oliver</name>
        <uri>https://orcid.org/0000-0002-6261-8928</uri>
      </author>
      <author>
        <name>Garg, Neha</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
      </author>
      <author>
        <name>Gilbert, Jeffrey R</name>
      </author>
      <author>
        <name>Globisch, Daniel</name>
      </author>
      <author>
        <name>Gomes, Paulo Wender P</name>
      </author>
      <author>
        <name>Heuckeroth, Steffen</name>
      </author>
      <author>
        <name>James, C Andrew</name>
      </author>
      <author>
        <name>Jarmusch, Scott A</name>
      </author>
      <author>
        <name>Kakhkhorov, Sarvar A</name>
      </author>
      <author>
        <name>Kang, Kyo Bin</name>
      </author>
      <author>
        <name>Kessler, Nikolas</name>
      </author>
      <author>
        <name>Kersten, Roland D</name>
      </author>
      <author>
        <name>Kim, Hyunwoo</name>
      </author>
      <author>
        <name>Kirk, Riley D</name>
      </author>
      <author>
        <name>Kohlbacher, Oliver</name>
      </author>
      <author>
        <name>Kontou, Eftychia E</name>
      </author>
      <author>
        <name>Liu, Ken</name>
      </author>
      <author>
        <name>Lizama-Chamu, Itzel</name>
      </author>
      <author>
        <name>Luu, Gordon T</name>
      </author>
      <author>
        <name>Luzzatto Knaan, Tal</name>
      </author>
      <author>
        <name>Mannochio-Russo, Helena</name>
      </author>
      <author>
        <name>Marty, Michael T</name>
      </author>
      <author>
        <name>Matsuzawa, Yuki</name>
      </author>
      <author>
        <name>McAvoy, Andrew C</name>
      </author>
      <author>
        <name>McCall, Laura-Isobel</name>
      </author>
      <author>
        <name>Mohamed, Osama G</name>
      </author>
      <author>
        <name>Nahor, Omri</name>
      </author>
      <author>
        <name>Neuweger, Heiko</name>
      </author>
      <author>
        <name>Niedermeyer, Timo HJ</name>
      </author>
      <author>
        <name>Nishida, Kozo</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Overdahl, Kirsten E</name>
      </author>
      <author>
        <name>Rainer, Johannes</name>
      </author>
      <author>
        <name>Reher, Raphael</name>
      </author>
      <author>
        <name>Rodriguez, Elys</name>
      </author>
      <author>
        <name>Sachsenberg, Timo T</name>
      </author>
      <author>
        <name>Sanchez, Laura M</name>
        <uri>https://orcid.org/0000-0001-9223-7977</uri>
      </author>
      <author>
        <name>Schmid, Robin</name>
      </author>
      <author>
        <name>Stevens, Cole</name>
      </author>
      <author>
        <name>Subramaniam, Shankar</name>
      </author>
      <author>
        <name>Tian, Zhenyu</name>
      </author>
      <author>
        <name>Tripathi, Ashootosh</name>
      </author>
      <author>
        <name>Tsugawa, Hiroshi</name>
      </author>
      <author>
        <name>van der Hooft, Justin JJ</name>
      </author>
      <author>
        <name>Vicini, Andrea</name>
      </author>
      <author>
        <name>Walter, Axel</name>
      </author>
      <author>
        <name>Weber, Tilmann</name>
      </author>
      <author>
        <name>Xiong, Quanbo</name>
      </author>
      <author>
        <name>Xu, Tao</name>
      </author>
      <author>
        <name>Pluskal, Tomáš</name>
      </author>
      <author>
        <name>Dorrestein, Pieter C</name>
      </author>
      <author>
        <name>Wang, Mingxun</name>
        <uri>https://orcid.org/0000-0001-7647-6097</uri>
      </author>
    </item>
    <item>
      <title>Belowground cross-trophic networks impact CH4 and CO2 emissions in degraded alpine peatlands</title>
      <link>https://escholarship.org/uc/item/33m3c36s</link>
      <description>Belowground organisms forming complex cross-trophic ecological networks are essential for maintaining peatland carbon stability and energy flow. However, how peatland degradation affects the biodiversity and cross-trophic ecological networks of soil communities remains poorly understood. Here, we examined the degradation effects on soil prokaryotes (i.e., bacteria, archaea), fungi and nematodes in alpine peatlands on the eastern Tibetan Plateau, characterized by varying water table depths (indicating degradation levels). We found that peatland degradation, accompanied by significant shifts in soil moisture and pH (P&amp;nbsp;&amp;lt;&amp;nbsp;0.05), reduced the taxonomic richness and phylogenetic diversity of prokaryotes, fungi, and nematodes, particularly in deeper soil layers (20–50&amp;nbsp;cm). Crucially, peatland degradation weakened potential cross-trophic interactions within bipartite networks of prokaryotes-nematodes and fungi-nematodes, resulting in less than 6.5&amp;nbsp;%–28.8&amp;nbsp;% of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/33m3c36s</guid>
      <pubDate>Fri, 21 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Dengbo</name>
      </author>
      <author>
        <name>Sun, Feng</name>
      </author>
      <author>
        <name>Qiu, Qiongyi</name>
      </author>
      <author>
        <name>Huang, Xueli</name>
      </author>
      <author>
        <name>Xu, Weitong</name>
      </author>
      <author>
        <name>Liu, Suo</name>
      </author>
      <author>
        <name>He, Songbing</name>
      </author>
      <author>
        <name>Zhao, Mengying</name>
      </author>
      <author>
        <name>Fu, Shuai</name>
      </author>
      <author>
        <name>Zeng, Yufei</name>
      </author>
      <author>
        <name>Yang, Yunfeng</name>
      </author>
      <author>
        <name>Ning, Daliang</name>
        <uri>https://orcid.org/0000-0002-3368-5988</uri>
      </author>
      <author>
        <name>Zhou, Jizhong</name>
        <uri>https://orcid.org/0000-0003-2014-0564</uri>
      </author>
      <author>
        <name>Wang, Mei</name>
      </author>
      <author>
        <name>Guo, Xue</name>
      </author>
    </item>
    <item>
      <title>Bacterial fitness for plant colonization is influenced by plant growth substrate</title>
      <link>https://escholarship.org/uc/item/0jn6c7h8</link>
      <description>Despite advances in our understanding of bacterial plant colonization, the extent to which growth substrate influences the molecular mechanisms enabling bacteria to efficiently colonize plants remains poorly understood. To address this, we used randomly barcoded transposon mutagenesis sequencing (RB-TnSeq) in Paraburkholderia graminis OAS925, an efficient rhizosphere colonizer, and Brachypodium distachyon grown in six different substrates. Of the 382 rhizosphere colonization genes that we identified in OAS925, 348 genes (91.1%) are dependent on the growth substrate evaluated, and 34 genes (8.9%) are shared across all the substrates. Both the core and substrate-dependent colonization genes are from multiple functional categories, demonstrating the multifaceted and major impact that plant growth substrate has on bacterial colonization. The identified colonization genes and their varied importance across plant growth substrates could not be readily explained by differences in root...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0jn6c7h8</guid>
      <pubDate>Fri, 21 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Torres, Marta</name>
      </author>
      <author>
        <name>Price, Morgan N</name>
        <uri>https://orcid.org/0000-0002-4251-0362</uri>
      </author>
      <author>
        <name>Khasanova, Albina</name>
      </author>
      <author>
        <name>Kosina, Suzanne M</name>
        <uri>https://orcid.org/0000-0003-2885-1248</uri>
      </author>
      <author>
        <name>Zhalnina, Kateryna</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Deutschbauer, Adam M</name>
      </author>
    </item>
    <item>
      <title>Statistical learning for predicting density–matrix‐based electron dynamics</title>
      <link>https://escholarship.org/uc/item/2424v0wj</link>
      <description>We consider the problem of learning density‐dependent molecular Hamiltonian matrices from time series of electron density matrices, all in the context of Hartree–Fock theory. Prior work developed a solution to this problem for small molecular systems with density and Hamiltonian matrices of size at most 6 × 6. Here, using a battery of techniques, we scale prior methods to larger molecular systems with, for example, 29 × 29 matrices. This includes systems that either have more electrons or are expressed in large basis sets such as 6‐311++G**. Scaling the method to larger systems enhances its relevance for realistic applications in chemistry and physics. To achieve this scaling, we apply dimensionality reduction, ridge regression and analytic computation of Hessians. Through the combination of these techniques, we are able to learn Hamiltonians by minimizing an objective function that encodes local propagation error. Importantly, these learned Hamiltonians can then be used to predict...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2424v0wj</guid>
      <pubDate>Tue, 11 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gupta, Prachi</name>
        <uri>https://orcid.org/0000-0002-1255-2684</uri>
      </author>
      <author>
        <name>Bhat, Harish S</name>
        <uri>https://orcid.org/0000-0001-7631-1831</uri>
      </author>
      <author>
        <name>Ranka, Karnamohit</name>
      </author>
      <author>
        <name>Isborn, Christine M</name>
      </author>
    </item>
    <item>
      <title>Targeted genetic manipulation and yeast-like evolutionary genomics in the green alga Auxenochlorella</title>
      <link>https://escholarship.org/uc/item/1pq468t5</link>
      <description>Auxenochlorella spp. are diploid oleaginous green algae whose streamlined genomes can be readily manipulated by homologous recombination, making them highly amenable to discovery research and bioengineering. Vegetatively diploid organisms experience specific evolutionary phenomena, including allodiploid hybridization, mitotic recombination, loss-of-heterozygosity, and aneuploidy; however, studies of these forces have largely focused on yeasts. Here, we present a telomere-to-telomere phased diploid genome assembly of Auxenochlorella UTEX 250-A (haploid length 22 Mb) and introduce a genetic toolkit for site-specific manipulation of the nuclear genome in multiple strains, featuring several selectable markers, inducible promoters, and fluorescent reporters for protein localization. UTEX 250-A is an allodiploid hybrid of Auxenochlorella protothecoides and Auxenochlorella symbiontica, two species differentiated by extensive chromosomal rearrangements. UTEX 250-A haplotypes are a mosaic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1pq468t5</guid>
      <pubDate>Mon, 10 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Craig, Rory J</name>
      </author>
      <author>
        <name>Dueñas, Marco A</name>
      </author>
      <author>
        <name>Camacho, Dimitrios J</name>
      </author>
      <author>
        <name>Gallaher, Sean D</name>
        <uri>https://orcid.org/0000-0002-9773-6051</uri>
      </author>
      <author>
        <name>Avendaño-Monsalve, Maria Clara</name>
      </author>
      <author>
        <name>Lin, Yang-Tsung</name>
      </author>
      <author>
        <name>Blaby-Haas, Crysten E</name>
        <uri>https://orcid.org/0000-0002-1583-1291</uri>
      </author>
      <author>
        <name>Moseley, Jeffrey L</name>
        <uri>https://orcid.org/0000-0001-8603-8488</uri>
      </author>
      <author>
        <name>Merchant, Sabeeha S</name>
      </author>
    </item>
    <item>
      <title>Improving Biomedical Knowledge Graph Quality: A Community Approach.</title>
      <link>https://escholarship.org/uc/item/5930j61p</link>
      <description>Biomedical knowledge graphs (KGs) are widely used across research and translational settings, yet their design decisions and implementation are often opaque. Unlike ontologies that more frequently adhere to established creation principles, biomedical KGs lack consistent practices for construction, documentation, and dissemination. To address this gap, we introduce a set of evaluation criteria grounded in widely accepted data standards and principles from related fields. We apply these criteria to 16 biomedical KGs, revealing that even those that appear to align with best practices often obscure essential information required for external reuse. Moreover, biomedical KGs, despite pursuing similar goals and ingesting the same sources in some cases, display substantial variation in models, source integration, and terminology for node types. Reaping the potential benefits of knowledge graphs for biomedical research while reducing duplicated effort requires community-wide adoption of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5930j61p</guid>
      <pubDate>Tue, 4 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Cortes, Katherina G</name>
      </author>
      <author>
        <name>Sundar, Shilpa</name>
      </author>
      <author>
        <name>Gehrke, Sarah</name>
      </author>
      <author>
        <name>Manpearl, Keenan</name>
      </author>
      <author>
        <name>Lin, Junxia</name>
      </author>
      <author>
        <name>Korn, Daniel Robert</name>
      </author>
      <author>
        <name>Caufield, Harry</name>
        <uri>https://orcid.org/0000-0001-5705-7831</uri>
      </author>
      <author>
        <name>Schaper, Kevin</name>
      </author>
      <author>
        <name>Reese, Justin</name>
      </author>
      <author>
        <name>Koirala, Kushal</name>
      </author>
      <author>
        <name>Hunter, Lawrence E</name>
      </author>
      <author>
        <name>Carter, E Kathleen</name>
      </author>
      <author>
        <name>DeLuca, Marcello</name>
      </author>
      <author>
        <name>Krishnan, Arjun</name>
      </author>
      <author>
        <name>Mungall, Chris</name>
      </author>
      <author>
        <name>Haendel, Melissa</name>
      </author>
    </item>
    <item>
      <title>Consistent performance of large language models in rare disease diagnosis across ten languages and 4917 cases</title>
      <link>https://escholarship.org/uc/item/1f868195</link>
      <description>BACKGROUND: Large language models (LLMs) are increasingly used medicine for diverse applications including differential diagnostic support. The training data used to create LLMs such as the Generative Pretrained Transformer (GPT) predominantly consist of English-language texts, but LLMs could be used across the globe to support diagnostics if language barriers could be overcome. Initial pilot studies on the utility of LLMs for differential diagnosis in languages other than English have shown promise, but a large-scale assessment on the relative performance of these models in a variety of European and non-European languages on a comprehensive corpus of challenging rare-disease cases is lacking.
METHODS: We created 4917 clinical vignettes using structured data captured with Human Phenotype Ontology (HPO) terms with the Global Alliance for Genomics and Health (GA4GH) Phenopacket Schema. These clinical vignettes span a total of 360 distinct genetic diseases with 2525 associated phenotypic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1f868195</guid>
      <pubDate>Tue, 4 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Chimirri, Leonardo</name>
      </author>
      <author>
        <name>Caufield, J Harry</name>
      </author>
      <author>
        <name>Bridges, Yasemin</name>
      </author>
      <author>
        <name>Matentzoglu, Nicolas</name>
      </author>
      <author>
        <name>Gargano, Michael</name>
      </author>
      <author>
        <name>Cazalla, Mario</name>
      </author>
      <author>
        <name>Chen, Shihan</name>
      </author>
      <author>
        <name>Danis, Daniel</name>
      </author>
      <author>
        <name>Dingemans, Alexander JM</name>
      </author>
      <author>
        <name>Gehle, Klara</name>
      </author>
      <author>
        <name>Gehle, Petra</name>
      </author>
      <author>
        <name>Graefe, Adam SL</name>
      </author>
      <author>
        <name>Gu, Weihong</name>
      </author>
      <author>
        <name>Ladewig, Markus S</name>
      </author>
      <author>
        <name>Lapunzina, Pablo</name>
      </author>
      <author>
        <name>Nevado, Julián</name>
      </author>
      <author>
        <name>Niyonkuru, Enock</name>
      </author>
      <author>
        <name>Ogishima, Soichi</name>
      </author>
      <author>
        <name>Seelow, Dominik</name>
      </author>
      <author>
        <name>Castaño, Jair A Tenorio</name>
      </author>
      <author>
        <name>Turnovec, Marek</name>
      </author>
      <author>
        <name>de Vries, Bert BA</name>
      </author>
      <author>
        <name>Wang, Kai</name>
      </author>
      <author>
        <name>Wissink, Kyran</name>
      </author>
      <author>
        <name>Yüksel, Zafer</name>
      </author>
      <author>
        <name>Zucca, Gabriele</name>
      </author>
      <author>
        <name>Haendel, Melissa A</name>
      </author>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
      <author>
        <name>Reese, Justin</name>
      </author>
      <author>
        <name>Robinson, Peter N</name>
      </author>
    </item>
    <item>
      <title>Quorum-driven microbial consortium for Bioplastic production from agro-waste</title>
      <link>https://escholarship.org/uc/item/4rf200hv</link>
      <description>Microbial consortia have high relevance in natural environments. Here we present the production of polyhydroxyalkanoates (PHA) from agro-industrial residues by a synthetic interkingdom consortium formed by the saprotrophic fungus &lt;i&gt;Ophiostoma piceae&lt;/i&gt; CECT 20146, which encodes a wide range of lignocellulolytic enzymes, and a natural PHA producer, &lt;i&gt;Pseudomonas putida&lt;/i&gt; KT2440. Two agro-industrial residues were utilized: Brewer's Spent Grain (BSG) as a carbon/nitrogen source and biofilm scaffold and waste cooking oil (WCO) as a carbon source for PHA synthesis. Through biochemistry, microscopy, and omics analyses, it is shown that &lt;i&gt;P. putida&lt;/i&gt; accumulates up to 40.2% of intracellular PHA when the quorum sensing molecule, farnesol (naturally produced by &lt;i&gt;O. piceae&lt;/i&gt;) is added, thanks to the increased proliferation of &lt;i&gt;P. putida&lt;/i&gt; cells. An interactive Shiny application has also been developed for an easy visualization and comprehension of all the transcriptomics...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4rf200hv</guid>
      <pubDate>Mon, 13 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Crespo-Roche, Diego</name>
      </author>
      <author>
        <name>Herráez, Marta</name>
      </author>
      <author>
        <name>Guerrero-Flores, Javier</name>
      </author>
      <author>
        <name>Martínez, M Jesús</name>
      </author>
      <author>
        <name>Louie, Katherine</name>
      </author>
      <author>
        <name>Northen, Trent</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Prieto, Alicia</name>
      </author>
      <author>
        <name>Barriuso, Jorge</name>
      </author>
    </item>
    <item>
      <title>RB-TnSeq elucidates dicarboxylic-acid-specific catabolism in β-proteobacteria for improved plastic monomer upcycling</title>
      <link>https://escholarship.org/uc/item/2k13p644</link>
      <description>Dicarboxylic acids are key components of many polymers and plastics, making them a target for both engineered microbial degradation and sustainable bioproduction. In this study, we generated a comprehensive data set of functional evidence for the genetic basis of dicarboxylic and fatty acid metabolism using randomly barcoded transposon sequencing (RB-TnSeq). We identified four β-proteobacteria that displayed robust growth with dicarboxylic acid sole carbon source and cultured their mutant libraries with dicarboxylic and fatty acids with carbon chain lengths from C3 to C12. The resulting fitness data suggested that dicarboxylic and fatty acid metabolisms are largely distinct, and different sets of β-oxidation genes are required for catabolizing dicarboxylic versus fatty acids of the same carbon chain lengths. In addition, we identified transcriptional regulators and transporters with strong fitness phenotypes related to dicarboxylic acid utilization. In &lt;i&gt;Ralstonia sp&lt;/i&gt;. UNC404CL21Col...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2k13p644</guid>
      <pubDate>Tue, 7 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Pearson, Allison N</name>
      </author>
      <author>
        <name>Lynch, Julie M</name>
      </author>
      <author>
        <name>Ho, Cindy N</name>
      </author>
      <author>
        <name>Hudson, Graham A</name>
      </author>
      <author>
        <name>Roberts, Jacob B</name>
      </author>
      <author>
        <name>Menasalvas, Javier</name>
        <uri>https://orcid.org/0000-0002-4003-4999</uri>
      </author>
      <author>
        <name>Vilchez, Aaron A</name>
      </author>
      <author>
        <name>Incha, Matthew R</name>
      </author>
      <author>
        <name>Schmidt, Matthias</name>
      </author>
      <author>
        <name>Mukhopadhyay, Aindrila</name>
        <uri>https://orcid.org/0000-0002-6513-7425</uri>
      </author>
      <author>
        <name>Deutschbauer, Adam M</name>
      </author>
      <author>
        <name>Thompson, Mitchell G</name>
      </author>
      <author>
        <name>Shih, Patrick M</name>
      </author>
      <author>
        <name>Keasling, Jay D</name>
        <uri>https://orcid.org/0000-0003-4170-6088</uri>
      </author>
    </item>
    <item>
      <title>Untargeted metabolomics reveals anion and organ‐specific metabolic responses of salinity tolerance in willow</title>
      <link>https://escholarship.org/uc/item/0j51b62j</link>
      <description>Willows can alleviate soil salinisation while generating sustainable feedstock for biorefinery, yet the metabolomic adaptations underlying their tolerance remain poorly understood. Salix miyabeana was treated with two environmentally abundant salts, NaCl and Na&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt;, in a 12-week pot trial. Willows tolerated salts across all treatments (up to 9.1 dS m&lt;sup&gt;-1&lt;/sup&gt; soil EC&lt;sub&gt;e&lt;/sub&gt;), maintaining biomass while selectively partitioning ions, confining Na&lt;sup&gt;+&lt;/sup&gt; to roots and accumulating Cl&lt;sup&gt;-&lt;/sup&gt; and SO42-$$ {\mathrm{SO}}_4^{2-} $$ in the canopy and adapting to osmotic stress via reduced stomatal conductance. Untargeted metabolomics captured &amp;gt;5000 putative compounds, including 278 core willow metabolome compounds constitutively produced across organs. Across all treatments, salinity drove widespread metabolic reprogramming, altering 28% of the overall metabolome, with organ-tailored strategies. Comparing salt forms at equimolar sodium, shared...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0j51b62j</guid>
      <pubDate>Wed, 24 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sas, Eszter</name>
      </author>
      <author>
        <name>Frémont, Adrien</name>
      </author>
      <author>
        <name>Gonzalez, Emmanuel</name>
      </author>
      <author>
        <name>Sarrazin, Mathieu</name>
      </author>
      <author>
        <name>Barnabé, Simon</name>
      </author>
      <author>
        <name>Labrecque, Michel</name>
      </author>
      <author>
        <name>Brereton, Nicholas James Beresford</name>
      </author>
      <author>
        <name>Pitre, Frédéric Emmanuel</name>
      </author>
    </item>
    <item>
      <title>Synthetic Scientific Image Generation with VAE, GAN, and Diffusion Model Architectures</title>
      <link>https://escholarship.org/uc/item/8sr171mx</link>
      <description>Generative AI (genAI) has emerged as a powerful tool for synthesizing diverse and complex image data, offering new possibilities for scientific imaging applications. This review presents a comprehensive comparative analysis of leading generative architectures, ranging from Variational Autoencoders (VAEs) to Generative Adversarial Networks (GANs) on through to Diffusion Models, in the context of scientific image synthesis. We examine each model's foundational principles, recent architectural advancements, and practical trade-offs. Our evaluation, conducted on domain-specific datasets including microCT scans of rocks and composite fibers, as well as high-resolution images of plant roots, integrates both quantitative metrics (SSIM, LPIPS, FID, CLIPScore) and expert-driven qualitative assessments. Results show that GANs, particularly StyleGAN, produce images with high perceptual quality and structural coherence. Diffusion-based models for inpainting and image variation, such as DALL-E...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8sr171mx</guid>
      <pubDate>Tue, 23 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sordo, Zineb</name>
      </author>
      <author>
        <name>Chagnon, Eric</name>
      </author>
      <author>
        <name>Hu, Zixi</name>
        <uri>https://orcid.org/0000-0002-5365-7351</uri>
      </author>
      <author>
        <name>Donatelli, Jeffrey J</name>
        <uri>https://orcid.org/0009-0003-7173-0174</uri>
      </author>
      <author>
        <name>Andeer, Peter</name>
      </author>
      <author>
        <name>Nico, Peter S</name>
      </author>
      <author>
        <name>Northen, Trent</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Ushizima, Daniela</name>
        <uri>https://orcid.org/0000-0002-7363-9468</uri>
      </author>
    </item>
    <item>
      <title>Breaking the reproducibility barrier with standardized protocols for plant–microbiome research</title>
      <link>https://escholarship.org/uc/item/3f14n3jm</link>
      <description>Inter-laboratory replicability is crucial yet challenging in microbiome research. Leveraging microbiomes to promote soil health and plant growth requires understanding underlying molecular mechanisms using reproducible experimental systems. In a global collaborative effort involving five laboratories, we aimed to help advance reproducibility in microbiome studies by testing our ability to replicate synthetic community assembly experiments. Our study compared fabricated ecosystems constructed using two different synthetic bacterial communities, the model grass Brachypodium distachyon, and sterile EcoFAB 2.0 devices. All participating laboratories observed consistent inoculum-dependent changes in plant phenotype, root exudate composition, and final bacterial community structure, where Paraburkholderia sp. OAS925 could dramatically shift microbiome composition. Comparative genomics and exudate utilization linked the pH-dependent colonization ability of Paraburkholderia, which was...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3f14n3jm</guid>
      <pubDate>Tue, 23 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Novak, Vlastimil</name>
        <uri>https://orcid.org/0000-0001-7890-4593</uri>
      </author>
      <author>
        <name>Andeer, Peter F</name>
      </author>
      <author>
        <name>King, Eoghan</name>
      </author>
      <author>
        <name>Calabria, Jacob</name>
      </author>
      <author>
        <name>Fitzpatrick, Connor</name>
      </author>
      <author>
        <name>Kelm, Jana M</name>
      </author>
      <author>
        <name>Wippel, Kathrin</name>
      </author>
      <author>
        <name>Kosina, Suzanne M</name>
      </author>
      <author>
        <name>Bowen, Benjamin P</name>
      </author>
      <author>
        <name>Daum, Chris</name>
      </author>
      <author>
        <name>Zane, Matthew</name>
      </author>
      <author>
        <name>Yadav, Archana</name>
      </author>
      <author>
        <name>Chen, Mingfei</name>
        <uri>https://orcid.org/0000-0002-6281-2480</uri>
      </author>
      <author>
        <name>Russ, Dor</name>
      </author>
      <author>
        <name>Adams, Catharine A</name>
      </author>
      <author>
        <name>Owens, Trenton K</name>
      </author>
      <author>
        <name>Lee, Bradie</name>
      </author>
      <author>
        <name>Ding, Yezhang</name>
      </author>
      <author>
        <name>Sordo, Zineb</name>
      </author>
      <author>
        <name>Chakraborty, Romy</name>
      </author>
      <author>
        <name>Roux, Simon</name>
      </author>
      <author>
        <name>Deutschbauer, Adam M</name>
      </author>
      <author>
        <name>Ushizima, Daniela</name>
        <uri>https://orcid.org/0000-0002-7363-9468</uri>
      </author>
      <author>
        <name>Zengler, Karsten</name>
      </author>
      <author>
        <name>Arsova, Borjana</name>
      </author>
      <author>
        <name>Dangl, Jeffery L</name>
      </author>
      <author>
        <name>Schulze-Lefert, Paul</name>
      </author>
      <author>
        <name>Watt, Michelle</name>
      </author>
      <author>
        <name>Vogel, John P</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
      </author>
    </item>
    <item>
      <title>Breaking the reproducibility barrier with standardized protocols for plant–microbiome research</title>
      <link>https://escholarship.org/uc/item/7n07963x</link>
      <description>Inter-laboratory replicability is crucial yet challenging in microbiome research. Leveraging microbiomes to promote soil health and plant growth requires understanding underlying molecular mechanisms using reproducible experimental systems. In a global collaborative effort involving five laboratories, we aimed to help advance reproducibility in microbiome studies by testing our ability to replicate synthetic community assembly experiments. Our study compared fabricated ecosystems constructed using two different synthetic bacterial communities, the model grass Brachypodium distachyon, and sterile EcoFAB 2.0 devices. All participating laboratories observed consistent inoculum-dependent changes in plant phenotype, root exudate composition, and final bacterial community structure, where Paraburkholderia sp. OAS925 could dramatically shift microbiome composition. Comparative genomics and exudate utilization linked the pH-dependent colonization ability of Paraburkholderia, which was...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7n07963x</guid>
      <pubDate>Thu, 11 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Novak, Vlastimil</name>
        <uri>https://orcid.org/0000-0001-7890-4593</uri>
      </author>
      <author>
        <name>Andeer, Peter F</name>
      </author>
      <author>
        <name>King, Eoghan</name>
      </author>
      <author>
        <name>Calabria, Jacob</name>
      </author>
      <author>
        <name>Fitzpatrick, Connor</name>
      </author>
      <author>
        <name>Kelm, Jana M</name>
      </author>
      <author>
        <name>Wippel, Kathrin</name>
      </author>
      <author>
        <name>Kosina, Suzanne M</name>
      </author>
      <author>
        <name>Bowen, Benjamin P</name>
      </author>
      <author>
        <name>Daum, Chris</name>
      </author>
      <author>
        <name>Zane, Matthew</name>
      </author>
      <author>
        <name>Yadav, Archana</name>
      </author>
      <author>
        <name>Chen, Mingfei</name>
        <uri>https://orcid.org/0000-0002-6281-2480</uri>
      </author>
      <author>
        <name>Russ, Dor</name>
      </author>
      <author>
        <name>Adams, Catharine A</name>
      </author>
      <author>
        <name>Owens, Trenton K</name>
      </author>
      <author>
        <name>Lee, Bradie</name>
      </author>
      <author>
        <name>Ding, Yezhang</name>
      </author>
      <author>
        <name>Sordo, Zineb</name>
      </author>
      <author>
        <name>Chakraborty, Romy</name>
      </author>
      <author>
        <name>Roux, Simon</name>
        <uri>https://orcid.org/0000-0002-5831-5895</uri>
      </author>
      <author>
        <name>Deutschbauer, Adam M</name>
      </author>
      <author>
        <name>Ushizima, Daniela</name>
        <uri>https://orcid.org/0000-0002-7363-9468</uri>
      </author>
      <author>
        <name>Zengler, Karsten</name>
      </author>
      <author>
        <name>Arsova, Borjana</name>
      </author>
      <author>
        <name>Dangl, Jeffery L</name>
      </author>
      <author>
        <name>Schulze-Lefert, Paul</name>
      </author>
      <author>
        <name>Watt, Michelle</name>
      </author>
      <author>
        <name>Vogel, John P</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
      </author>
    </item>
    <item>
      <title>Rational Modulation of Plant Root Development Using Engineered Cytokinin Regulators</title>
      <link>https://escholarship.org/uc/item/12z5j1x4</link>
      <description>Achieving precise control over quantitative developmental phenotypes is a key objective in plant biology. Recent advances in synthetic biology have enabled tools to reprogram entire developmental pathways; however, the complexity of designing synthetic genetic programs and the inherent interactions between various signaling processes remains a critical challenge. Here, we leverage Type-B response regulators to modulate the expression of genes involved in cytokinin-dependent growth and development processes. We rationally engineered these regulators to modulate their transcriptional activity (i.e., repression or activation) and potency while reducing their sensitivity to cytokinin. By localizing the expression of these engineered transcription factors using tissue-specific promoters, we can predictably tune cytokinin-regulated traits. As a proof of principle, we deployed this synthetic system in &lt;i&gt;Arabidopsis thaliana&lt;/i&gt; to either decrease or increase the number of lateral roots....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/12z5j1x4</guid>
      <pubDate>Tue, 9 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Rattan, Rohan</name>
      </author>
      <author>
        <name>Alamos, Simon</name>
      </author>
      <author>
        <name>Szarzanowicz, Matthew</name>
      </author>
      <author>
        <name>Markel, Kasey</name>
      </author>
      <author>
        <name>Shih, Patrick M</name>
      </author>
    </item>
    <item>
      <title>Identifying microbial functional guilds performing cryptic organotrophic and lithotrophic redox cycles in anaerobic granular biofilms</title>
      <link>https://escholarship.org/uc/item/2f5873jd</link>
      <description>Granular biofilms used in anaerobic digester systems contain diverse microbial populations that interact to hydrolyze organic matter and produce methane within controlled environments. Prior research investigated the feasibility of utilizing granular biofilms obtained from an anaerobic digester to remove nitrate without the addition of exogenous electron donors. These granules possessed a unique structure of alternating light and dark iron sulfide and pyrite rich layers that potentially served as both an electron source and sink, linking carbon, nitrogen, sulfur, and iron cycles. To characterize the functional roles of diverse microbial populations enriched within these layered biofilms, we analyzed metagenomes obtained from three different granules. Comparisons between the functional gene content of forty metagenome assembled genomes (MAGs) identified phylogenetically cohesive functional guilds. Each of these functional MAG clusters was assigned to specific steps in anaerobic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2f5873jd</guid>
      <pubDate>Mon, 8 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Flinkstrom, Zachary</name>
      </author>
      <author>
        <name>Bryson, Samuel J</name>
      </author>
      <author>
        <name>Pelivano, Bojan</name>
      </author>
      <author>
        <name>Candry, Pieter</name>
      </author>
      <author>
        <name>Hunt, Kristopher A</name>
      </author>
      <author>
        <name>Winkler, Mari-Karoliina H</name>
      </author>
    </item>
    <item>
      <title>Microbial maintenance energy quantified and modeled with microcalorimetry</title>
      <link>https://escholarship.org/uc/item/16z729cf</link>
      <description>Refining the energetic costs of cellular maintenance is essential for predicting microbial growth and survival in the environment. Here, we evaluate a simple batch culture method to quantify energy partitioning between growth and maintenance using microcalorimetry and thermodynamic modeling. The constants derived from the batch culture system were comparable to those that have been reported from meta-analyses of data derived from chemostat studies. The model accurately predicted temperature-dependent biomass yield and the upper temperature limit of growth for Desulfovibrio alaskensis G20, suggesting the method may have broad application. An Arrhenius temperature dependence for the specific energy consumption rate, inferred from substrate consumption and heat evolution, was observed over the entire viable temperature range. By combining this relationship for specific energy consumption rates and observed specific growth rates, the model describes an increase in nongrowth associated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/16z729cf</guid>
      <pubDate>Mon, 8 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hunt, Kristopher A</name>
      </author>
      <author>
        <name>von Netzer, Frederick</name>
      </author>
      <author>
        <name>Gorman‐Lewis, Drew</name>
      </author>
      <author>
        <name>Stahl, David A</name>
      </author>
    </item>
    <item>
      <title>Leveraging generative AI to assist biocuration of medical actions for rare disease</title>
      <link>https://escholarship.org/uc/item/800270t9</link>
      <description>Motivation: Structured representations of clinical data can support computational analysis of individuals and cohorts, and ontologies representing disease entities and phenotypic abnormalities are now commonly used for translational research. The Medical Action Ontology (MAxO) provides a computational representation of treatments and other actions taken for clinical management. Currently, manual biocuration is used to annotate MAxO terms to rare diseases. However, it is challenging to scale manual curation to comprehensively capture information about medical actions for the more than 10&amp;nbsp;000 rare diseases.
Results: We present AutoMAxO, a semi-automated workflow that leverages Large Language Models (LLMs) to streamline MAxO biocuration. AutoMAxO first uses LLMs to retrieve candidate curations from abstracts of relevant publications. Next, the candidate curations are matched to ontology terms from MAxO, Human Phenotype Ontology (HPO), and MONDO disease ontology via a combination...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/800270t9</guid>
      <pubDate>Tue, 26 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Niyonkuru, Enock</name>
      </author>
      <author>
        <name>Caufield, J Harry</name>
      </author>
      <author>
        <name>Carmody, Leigh C</name>
      </author>
      <author>
        <name>Gargano, Michael A</name>
      </author>
      <author>
        <name>Toro, Sabrina</name>
      </author>
      <author>
        <name>Whetzel, Patricia L</name>
      </author>
      <author>
        <name>Blau, Hannah</name>
      </author>
      <author>
        <name>Gomez, Mauricio Soto</name>
      </author>
      <author>
        <name>Casiraghi, Elena</name>
      </author>
      <author>
        <name>Chimirri, Leonardo</name>
      </author>
      <author>
        <name>Reese, Justin T</name>
      </author>
      <author>
        <name>Valentini, Giorgio</name>
      </author>
      <author>
        <name>Haendel, Melissa A</name>
      </author>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
      <author>
        <name>Robinson, Peter N</name>
      </author>
    </item>
    <item>
      <title>Uncovering hidden enhancers through unbiased in vivo testing</title>
      <link>https://escholarship.org/uc/item/5545578s</link>
      <description>Chromatin signatures are widely used to identify tissue-specific in vivo enhancers, but their sensitivity and specificity remains unclear. Here we show that many developmental enhancers remain undetectable using currently available chromatin data. In an initial comparison of over 1200 developmental enhancers with tissue-matched chromatin data, 14% (n = 285) lacked canonical enhancer-associated chromatin signatures. To further assess the prevalence of enhancers missed by chromatin profiling approaches, we used a high-throughput transgenic enhancer assay to screen the regulatory landscapes of two key developmental genes at 5 kb resolution, spanning 1.3 Mb of mouse sequence in total. We observed that 23 of 88 (26%) in vivo enhancers discovered by this approach lacked enhancer-associated chromatin signatures in the respective tissue. Our findings suggest the existence of tens of thousands of enhancers that remain undiscovered by currently available chromatin data, underscoring the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5545578s</guid>
      <pubDate>Tue, 26 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Mannion, Brandon J</name>
      </author>
      <author>
        <name>Tran, Stella</name>
      </author>
      <author>
        <name>Plajzer-Frick, Ingrid</name>
      </author>
      <author>
        <name>Novak, Catherine S</name>
      </author>
      <author>
        <name>Afzal, Veena</name>
      </author>
      <author>
        <name>Akiyama, Jennifer A</name>
        <uri>https://orcid.org/0000-0002-4130-7784</uri>
      </author>
      <author>
        <name>Sospedra-Arrufat, Ismael</name>
      </author>
      <author>
        <name>Barton, Sarah</name>
      </author>
      <author>
        <name>Beckman, Erik</name>
      </author>
      <author>
        <name>Garvin, Tyler H</name>
      </author>
      <author>
        <name>Godfrey, Patrick</name>
      </author>
      <author>
        <name>Godoy, Janeth</name>
      </author>
      <author>
        <name>Hunter, Riana D</name>
        <uri>https://orcid.org/0000-0002-2888-1079</uri>
      </author>
      <author>
        <name>Kato, Momoe</name>
      </author>
      <author>
        <name>Kosicki, Michael</name>
      </author>
      <author>
        <name>Kronshage, Anne N</name>
      </author>
      <author>
        <name>Lee, Elizabeth A</name>
      </author>
      <author>
        <name>Meky, Eman M</name>
      </author>
      <author>
        <name>Pham, Quan T</name>
      </author>
      <author>
        <name>von Maydell, Kianna</name>
      </author>
      <author>
        <name>Zhu, Yiwen</name>
        <uri>https://orcid.org/0000-0002-2282-1913</uri>
      </author>
      <author>
        <name>Lopez-Rios, Javier</name>
      </author>
      <author>
        <name>Dickel, Diane E</name>
      </author>
      <author>
        <name>Osterwalder, Marco</name>
      </author>
      <author>
        <name>Visel, Axel</name>
        <uri>https://orcid.org/0000-0002-4130-7784</uri>
      </author>
      <author>
        <name>Pennacchio, Len A</name>
        <uri>https://orcid.org/0000-0002-8748-3732</uri>
      </author>
    </item>
    <item>
      <title>Spectral broadening and vibronic dynamics of the S2 state of canthaxanthin in the orange carotenoid protein</title>
      <link>https://escholarship.org/uc/item/2qd2c9bq</link>
      <description>We have performed a series of broadband multidimensional electronic spectroscopy experiments to probe the electronic and vibrational dynamics of the canthaxanthin chromophore of the Orange Carotenoid Protein (OCP) from Synechocystis sp. PCC 6803 in its photoactivated red state, OCPR. Cross-peaks observed below the diagonal of the two-dimensional electronic spectrum indicate that absorption transitions prepare the bright S2 state of the ketocarotenoid canthaxanthin near to a sequence of conical intersections, allowing passage to the dark S1 state via the Sx intermediate in &amp;lt;50&amp;nbsp;fs. Rapid damping of excited-state coherent wavepacket motions suggests that the branching coordinates of the conical intersections include out-of-plane deformation and C=C stretching coordinates of the π-conjugated isoprenoid backbone. The unusual proximity of the Franck–Condon S2 state structure to the conical intersections with Sx and S1 suggests that the protein surroundings of canthaxanthin prepare...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2qd2c9bq</guid>
      <pubDate>Wed, 20 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Yang, Kunwei</name>
      </author>
      <author>
        <name>M., Nila Mohan T</name>
      </author>
      <author>
        <name>Rose, Justin B</name>
      </author>
      <author>
        <name>Leslie, Chase H</name>
      </author>
      <author>
        <name>Sutter, Markus</name>
        <uri>https://orcid.org/0000-0001-6290-4820</uri>
      </author>
      <author>
        <name>Kerfeld, Cheryl A</name>
        <uri>https://orcid.org/0000-0002-9977-8482</uri>
      </author>
      <author>
        <name>Beck, Warren F</name>
      </author>
    </item>
    <item>
      <title>SetBERT: the deep learning platform for contextualized embeddings and explainable predictions from high-throughput sequencing</title>
      <link>https://escholarship.org/uc/item/7b07t0b7</link>
      <description>MOTIVATION: High-throughput sequencing (HTS) is a modern sequencing technology used to profile microbiomes by sequencing thousands of short genomic fragments from the microorganisms within a given sample. This technology presents a unique opportunity for artificial intelligence to comprehend the underlying functional relationships of microbial communities. However, due to the unstructured nature of HTS data, nearly all computational models are limited to processing DNA sequences individually. This limitation causes them to miss out on key interactions between microorganisms, significantly hindering our understanding of how these interactions influence the microbial communities as a whole. Furthermore, most computational methods rely on post-processing of samples which could inadvertently introduce unintentional protocol-specific bias.
RESULTS: Addressing these concerns, we present SetBERT, a robust pre-training methodology for creating generalized deep learning models for processing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7b07t0b7</guid>
      <pubDate>Thu, 14 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ludwig, David W</name>
      </author>
      <author>
        <name>Guptil, Christopher</name>
      </author>
      <author>
        <name>Alexander, Nicholas R</name>
      </author>
      <author>
        <name>Zhalnina, Kateryna</name>
      </author>
      <author>
        <name>Wipf, Edi M-L</name>
      </author>
      <author>
        <name>Khasanova, Albina</name>
      </author>
      <author>
        <name>Barber, Nicholas A</name>
      </author>
      <author>
        <name>Swingley, Wesley</name>
      </author>
      <author>
        <name>Walker, Donald M</name>
      </author>
      <author>
        <name>Phillips, Joshua L</name>
      </author>
    </item>
    <item>
      <title>Range extender mediates long-distance enhancer activity</title>
      <link>https://escholarship.org/uc/item/71g6991g</link>
      <description>Although most mammalian transcriptional enhancers regulate their cognate promoters over distances of tens of kilobases, some enhancers act over distances in the megabase range1. The sequence features that enable such long-distance enhancer–promoter interactions remain unclear. Here we used in vivo enhancer-replacement experiments at the mouse Shh locus to show that short- and medium-range limb enhancers cannot initiate gene expression at long-distance range. We identify a cis-acting element, range extender (REX), that confers long-distance regulatory activity and is located next to a long-range limb enhancer of Sall1. The REX element has no endogenous enhancer activity. However, addition of the REX to other short- and mid-range limb enhancers substantially increases their genomic interaction range. In the most extreme example observed, addition of REX increased the range of an enhancer by an order of magnitude from its native 73 kb to 848 kb. The REX element contains highly conserved...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/71g6991g</guid>
      <pubDate>Thu, 14 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Bower, Grace</name>
      </author>
      <author>
        <name>Hollingsworth, Ethan W</name>
      </author>
      <author>
        <name>Jacinto, Sandra H</name>
      </author>
      <author>
        <name>Alcantara, Joshua A</name>
      </author>
      <author>
        <name>Clock, Benjamin</name>
      </author>
      <author>
        <name>Cao, Kaitlyn</name>
      </author>
      <author>
        <name>Liu, Mandy</name>
      </author>
      <author>
        <name>Dziulko, Adam</name>
      </author>
      <author>
        <name>Alcaina-Caro, Ana</name>
      </author>
      <author>
        <name>Xu, Qianlan</name>
      </author>
      <author>
        <name>Skowronska-Krawczyk, Dorota</name>
        <uri>https://orcid.org/0000-0002-5758-4225</uri>
      </author>
      <author>
        <name>Lopez-Rios, Javier</name>
      </author>
      <author>
        <name>Dickel, Diane E</name>
      </author>
      <author>
        <name>Bardet, Anaïs F</name>
      </author>
      <author>
        <name>Pennacchio, Len A</name>
        <uri>https://orcid.org/0000-0002-8748-3732</uri>
      </author>
      <author>
        <name>Visel, Axel</name>
        <uri>https://orcid.org/0000-0002-4130-7784</uri>
      </author>
      <author>
        <name>Kvon, Evgeny Z</name>
        <uri>https://orcid.org/0000-0002-1562-0945</uri>
      </author>
    </item>
    <item>
      <title>Myco-Ed: Mycological curriculum for education and discovery</title>
      <link>https://escholarship.org/uc/item/3k27n13z</link>
      <description>Fungi are important and hyperdiverse organisms, yet chronically understudied. Most fungal clades have no reference genomes, impeding our understanding of their ecosystem functions and use as solutions in health and biotechnology. Also, opportunities for training in fungal biology and genomics are lacking, creating a bottleneck that hinders the recruitment and cultivation of a talented future mycological workforce. To address these issues, we developed Myco-Ed, an educational program offering training and scientific contributions through genome sequencing and analysis. Myco-Ed empowers students to pursue careers in fungal biology while improving fungal resources. Myco-Ed has been piloted at 12 institutions (15 classrooms) ranging from online e-Campuses to R1 universities, resulting in hundreds of fungal observations and many new high-quality reference genomes.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3k27n13z</guid>
      <pubDate>Thu, 14 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Branco, Sara</name>
      </author>
      <author>
        <name>Avis, Peter G</name>
      </author>
      <author>
        <name>Barry, Kerrie</name>
        <uri>https://orcid.org/0000-0002-8999-6785</uri>
      </author>
      <author>
        <name>Bates, Scott</name>
      </author>
      <author>
        <name>Cobián, Gerald M</name>
      </author>
      <author>
        <name>Dow, Ellen G</name>
        <uri>https://orcid.org/0000-0002-2079-0260</uri>
      </author>
      <author>
        <name>Gremillion, Sara</name>
      </author>
      <author>
        <name>Honan, Amy</name>
      </author>
      <author>
        <name>Knight, Chinyere A</name>
      </author>
      <author>
        <name>LaButti, Kurt</name>
        <uri>https://orcid.org/0000-0002-5838-1972</uri>
      </author>
      <author>
        <name>Quandt, C Alisha</name>
      </author>
      <author>
        <name>Stewart, Jane E</name>
      </author>
      <author>
        <name>Talag, Jayson</name>
      </author>
      <author>
        <name>Wilson, Andrew W</name>
      </author>
      <author>
        <name>Lofgren, Lotus</name>
      </author>
      <author>
        <name>Mondo, Stephen James</name>
        <uri>https://orcid.org/0000-0001-5797-0647</uri>
      </author>
    </item>
    <item>
      <title>Tetranucleotide frequencies differentiate genomic boundaries and metabolic strategies across environmental microbiomes</title>
      <link>https://escholarship.org/uc/item/7159081k</link>
      <description>Microbiomes are constrained by physicochemical conditions, nutrient regimes, and community interactions across diverse environments, yet genomic signatures of this adaptation remain unclear. Metagenome sequencing is a powerful technique to analyze genomic content in the context of natural environments, establishing concepts of microbial ecological trends. Here, we developed a data discovery tool-a tetranucleotide-informed metagenome stability diagram-that is publicly available in the integrated microbial genomes and microbiomes (IMG/M) platform for metagenome ecosystem analyses. We analyzed the tetranucleotide frequencies from quality-filtered and unassembled sequence data of over 12,000 metagenomes to assess ecosystem-specific microbial community composition and function. We found that tetranucleotide frequencies can differentiate communities across various natural environments and that specific functional and metabolic trends can be observed in this structuring. Our tool places...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7159081k</guid>
      <pubDate>Wed, 30 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kellom, Matthew</name>
        <uri>https://orcid.org/0000-0002-8310-7078</uri>
      </author>
      <author>
        <name>Berg, Maureen</name>
      </author>
      <author>
        <name>Chen, I-Min A</name>
      </author>
      <author>
        <name>Chu, Ken</name>
        <uri>https://orcid.org/0000-0002-9602-1433</uri>
      </author>
      <author>
        <name>Clum, Alicia</name>
        <uri>https://orcid.org/0000-0002-5004-3362</uri>
      </author>
      <author>
        <name>Huntemann, Marcel</name>
        <uri>https://orcid.org/0000-0002-1284-3748</uri>
      </author>
      <author>
        <name>Ivanova, Natalia N</name>
      </author>
      <author>
        <name>Kyrpides, Nikos C</name>
        <uri>https://orcid.org/0000-0002-6131-0462</uri>
      </author>
      <author>
        <name>Mukherjee, Supratim</name>
        <uri>https://orcid.org/0000-0002-6322-2271</uri>
      </author>
      <author>
        <name>Reddy, TBK</name>
        <uri>https://orcid.org/0000-0002-0871-5567</uri>
      </author>
      <author>
        <name>Roux, Simon</name>
        <uri>https://orcid.org/0000-0002-5831-5895</uri>
      </author>
      <author>
        <name>Seshadri, Rekha</name>
        <uri>https://orcid.org/0000-0003-3219-2900</uri>
      </author>
      <author>
        <name>Szabo, Gitta</name>
      </author>
      <author>
        <name>Varghese, Neha J</name>
      </author>
      <author>
        <name>Woyke, Tanja</name>
        <uri>https://orcid.org/0000-0002-9485-5637</uri>
      </author>
      <author>
        <name>Eloe-Fadrosh, Emiley A</name>
        <uri>https://orcid.org/0000-0002-8162-1276</uri>
      </author>
    </item>
    <item>
      <title>High-Throughput Microfluidic Electroporation (HTME): A Scalable, 384-Well Platform for Multiplexed Cell Engineering</title>
      <link>https://escholarship.org/uc/item/5xf4s2kv</link>
      <description>Electroporation-mediated gene delivery is a cornerstone of synthetic biology, offering several advantages over other methods: higher efficiencies, broader applicability, and simpler sample preparation. Yet, electroporation protocols are often challenging to integrate into highly multiplexed workflows, owing to limitations in their scalability and tunability. These challenges ultimately increase the time and cost per transformation. As a result, rapidly screening genetic libraries, exploring combinatorial designs, or optimizing electroporation parameters requires extensive iterations, consuming large quantities of expensive custom-made DNA and cell lines or primary cells. To address these limitations, we have developed a High-Throughput Microfluidic Electroporation (HTME) platform that includes a 384-well electroporation plate (E-Plate) and control electronics capable of rapidly electroporating all wells in under a minute with individual control of each well. Fabricated using scalable...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5xf4s2kv</guid>
      <pubDate>Tue, 29 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gaillard, William R</name>
      </author>
      <author>
        <name>Sustarich, Jess</name>
      </author>
      <author>
        <name>Li, Yuerong</name>
      </author>
      <author>
        <name>Carruthers, David N</name>
        <uri>https://orcid.org/0000-0002-8275-2278</uri>
      </author>
      <author>
        <name>Gupta, Kshitiz</name>
        <uri>https://orcid.org/0000-0002-1732-6176</uri>
      </author>
      <author>
        <name>Liang, Yan</name>
      </author>
      <author>
        <name>Kuo, Rita</name>
      </author>
      <author>
        <name>Tan, Stephen</name>
      </author>
      <author>
        <name>Yoder, Sam</name>
      </author>
      <author>
        <name>Adams, Paul D</name>
        <uri>https://orcid.org/0000-0001-9333-8219</uri>
      </author>
      <author>
        <name>Martin, Hector Garcia</name>
      </author>
      <author>
        <name>Hillson, Nathan J</name>
        <uri>https://orcid.org/0000-0002-9169-3978</uri>
      </author>
      <author>
        <name>Singh, Anup K</name>
      </author>
    </item>
    <item>
      <title>In vivo mapping of mutagenesis sensitivity of human enhancers</title>
      <link>https://escholarship.org/uc/item/9xj5835q</link>
      <description>Distant-acting enhancers are central to human development1. However, our limited understanding of their functional sequence features prevents the interpretation of enhancer mutations in disease2. Here we determined the functional sensitivity to mutagenesis of human developmental enhancers in vivo. Focusing on seven enhancers that are active in the developing brain, heart, limb and face, we created over 1,700 transgenic mice for over 260 mutagenized enhancer alleles. Systematic mutation of 12-base-pair blocks collectively altered each sequence feature in each enhancer at least once. We show that 69% of all blocks are required for normal in vivo activity, with mutations more commonly resulting in loss (60%) than in gain (9%) of function. Using predictive modelling, we annotated critical nucleotides at the base-pair resolution. The vast majority of motifs predicted by these machine learning models (88%) coincided with changes in in vivo function, and the models showed considerable...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9xj5835q</guid>
      <pubDate>Fri, 25 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kosicki, Michael</name>
        <uri>https://orcid.org/0000-0001-7173-8852</uri>
      </author>
      <author>
        <name>Zhang, Boyang</name>
      </author>
      <author>
        <name>Hecht, Vivian</name>
      </author>
      <author>
        <name>Pampari, Anusri</name>
      </author>
      <author>
        <name>Cook, Laura E</name>
        <uri>https://orcid.org/0000-0002-4459-2592</uri>
      </author>
      <author>
        <name>Slaven, Neil</name>
      </author>
      <author>
        <name>Akiyama, Jennifer A</name>
        <uri>https://orcid.org/0000-0002-4130-7784</uri>
      </author>
      <author>
        <name>Plajzer-Frick, Ingrid</name>
      </author>
      <author>
        <name>Novak, Catherine S</name>
      </author>
      <author>
        <name>Kato, Momoe</name>
      </author>
      <author>
        <name>Tran, Stella</name>
      </author>
      <author>
        <name>Hunter, Riana D</name>
        <uri>https://orcid.org/0000-0002-2888-1079</uri>
      </author>
      <author>
        <name>von Maydell, Kianna</name>
      </author>
      <author>
        <name>Barton, Sarah</name>
      </author>
      <author>
        <name>Beckman, Erik</name>
      </author>
      <author>
        <name>Zhu, Yiwen</name>
        <uri>https://orcid.org/0000-0002-2282-1913</uri>
      </author>
      <author>
        <name>Dickel, Diane E</name>
      </author>
      <author>
        <name>Kundaje, Anshul</name>
      </author>
      <author>
        <name>Visel, Axel</name>
        <uri>https://orcid.org/0000-0002-4130-7784</uri>
      </author>
      <author>
        <name>Pennacchio, Len A</name>
        <uri>https://orcid.org/0000-0002-8748-3732</uri>
      </author>
    </item>
    <item>
      <title>A universal language for finding mass spectrometry data patterns</title>
      <link>https://escholarship.org/uc/item/28x5h3tn</link>
      <description>Despite being information rich, the vast majority of untargeted mass spectrometry data are underutilized; most analytes are not used for downstream interpretation or reanalysis after publication. The inability to dive into these rich raw mass spectrometry datasets is due to the limited flexibility and scalability of existing software tools. Here we introduce a new language, the Mass Spectrometry Query Language (MassQL), and an accompanying software ecosystem that addresses these issues by enabling the community to directly query mass spectrometry data with an expressive set of user-defined mass spectrometry patterns. Illustrated by real-world examples, MassQL provides a data-driven definition of chemical diversity by enabling the reanalysis of all public untargeted metabolomics data, empowering scientists across many disciplines to make new discoveries. MassQL has been widely implemented in multiple open-source and commercial mass spectrometry analysis tools, which enhances the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/28x5h3tn</guid>
      <pubDate>Fri, 25 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Damiani, Tito</name>
      </author>
      <author>
        <name>Jarmusch, Alan K</name>
      </author>
      <author>
        <name>Aron, Allegra T</name>
      </author>
      <author>
        <name>Petras, Daniel</name>
      </author>
      <author>
        <name>Phelan, Vanessa V</name>
      </author>
      <author>
        <name>Zhao, Haoqi Nina</name>
      </author>
      <author>
        <name>Bittremieux, Wout</name>
      </author>
      <author>
        <name>Acharya, Deepa D</name>
      </author>
      <author>
        <name>Ahmed, Mohammed MA</name>
      </author>
      <author>
        <name>Bauermeister, Anelize</name>
      </author>
      <author>
        <name>Bertin, Matthew J</name>
      </author>
      <author>
        <name>Boudreau, Paul D</name>
      </author>
      <author>
        <name>Borges, Ricardo M</name>
      </author>
      <author>
        <name>Bowen, Benjamin P</name>
        <uri>https://orcid.org/0000-0003-1368-3958</uri>
      </author>
      <author>
        <name>Brown, Christopher J</name>
      </author>
      <author>
        <name>Chagas, Fernanda O</name>
      </author>
      <author>
        <name>Clevenger, Kenneth D</name>
      </author>
      <author>
        <name>Correia, Mario SP</name>
      </author>
      <author>
        <name>Crandall, William J</name>
      </author>
      <author>
        <name>Crüsemann, Max</name>
      </author>
      <author>
        <name>Fahy, Eoin</name>
      </author>
      <author>
        <name>Fiehn, Oliver</name>
        <uri>https://orcid.org/0000-0002-6261-8928</uri>
      </author>
      <author>
        <name>Garg, Neha</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
      </author>
      <author>
        <name>Gilbert, Jeffrey R</name>
      </author>
      <author>
        <name>Globisch, Daniel</name>
      </author>
      <author>
        <name>Gomes, Paulo Wender P</name>
      </author>
      <author>
        <name>Heuckeroth, Steffen</name>
      </author>
      <author>
        <name>James, C Andrew</name>
      </author>
      <author>
        <name>Jarmusch, Scott A</name>
      </author>
      <author>
        <name>Kakhkhorov, Sarvar A</name>
      </author>
      <author>
        <name>Kang, Kyo Bin</name>
      </author>
      <author>
        <name>Kessler, Nikolas</name>
      </author>
      <author>
        <name>Kersten, Roland D</name>
      </author>
      <author>
        <name>Kim, Hyunwoo</name>
      </author>
      <author>
        <name>Kirk, Riley D</name>
      </author>
      <author>
        <name>Kohlbacher, Oliver</name>
      </author>
      <author>
        <name>Kontou, Eftychia E</name>
      </author>
      <author>
        <name>Liu, Ken</name>
      </author>
      <author>
        <name>Lizama-Chamu, Itzel</name>
      </author>
      <author>
        <name>Luu, Gordon T</name>
      </author>
      <author>
        <name>Luzzatto Knaan, Tal</name>
      </author>
      <author>
        <name>Mannochio-Russo, Helena</name>
      </author>
      <author>
        <name>Marty, Michael T</name>
      </author>
      <author>
        <name>Matsuzawa, Yuki</name>
      </author>
      <author>
        <name>McAvoy, Andrew C</name>
      </author>
      <author>
        <name>McCall, Laura-Isobel</name>
      </author>
      <author>
        <name>Mohamed, Osama G</name>
      </author>
      <author>
        <name>Nahor, Omri</name>
      </author>
      <author>
        <name>Neuweger, Heiko</name>
      </author>
      <author>
        <name>Niedermeyer, Timo HJ</name>
      </author>
      <author>
        <name>Nishida, Kozo</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Overdahl, Kirsten E</name>
      </author>
      <author>
        <name>Rainer, Johannes</name>
      </author>
      <author>
        <name>Reher, Raphael</name>
      </author>
      <author>
        <name>Rodriguez, Elys</name>
      </author>
      <author>
        <name>Sachsenberg, Timo T</name>
      </author>
      <author>
        <name>Sanchez, Laura M</name>
        <uri>https://orcid.org/0000-0001-9223-7977</uri>
      </author>
      <author>
        <name>Schmid, Robin</name>
      </author>
      <author>
        <name>Stevens, Cole</name>
      </author>
      <author>
        <name>Subramaniam, Shankar</name>
      </author>
      <author>
        <name>Tian, Zhenyu</name>
      </author>
      <author>
        <name>Tripathi, Ashootosh</name>
      </author>
      <author>
        <name>Tsugawa, Hiroshi</name>
      </author>
      <author>
        <name>van der Hooft, Justin JJ</name>
      </author>
      <author>
        <name>Vicini, Andrea</name>
      </author>
      <author>
        <name>Walter, Axel</name>
      </author>
      <author>
        <name>Weber, Tilmann</name>
      </author>
      <author>
        <name>Xiong, Quanbo</name>
      </author>
      <author>
        <name>Xu, Tao</name>
      </author>
      <author>
        <name>Pluskal, Tomáš</name>
      </author>
      <author>
        <name>Dorrestein, Pieter C</name>
      </author>
      <author>
        <name>Wang, Mingxun</name>
        <uri>https://orcid.org/0000-0001-7647-6097</uri>
      </author>
    </item>
    <item>
      <title>N-Terminal domain homologs of the orange carotenoid protein increase quenching of cyanobacterial phycobilisomes</title>
      <link>https://escholarship.org/uc/item/9br7d72k</link>
      <description>Stress exerted by excess captured light energy in cyanobacteria is prevented by the photoprotective activity of the orange carotenoid protein (OCP). Under high light, the OCP converts from an orange, inactive form (OCPO) into the red form (OCPR) that binds to and quenches the phycobilisome (PBS). Structurally, the OCP consists of 2 domains: the N-terminal effector domain and a C-terminal regulatory domain. Structural analysis of the OCP-PBS complex showed that the N-terminal domains of an OCP dimer interact with the PBS core. These N-terminal OCP domains have single-domain protein paralogs known as helical carotenoid proteins (HCPs). Using PBS quenching assays, we show that the HCP4 and HCP5 homologs efficiently quench PBS fluorescence in vitro, surpassing the quenching ability of the OCP. This is consistent with computational quantum mechanics/molecular mechanics results. Interestingly, when using a maximum quenching concentration of OCP with PBSs, HCP5 addition further increases...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9br7d72k</guid>
      <pubDate>Thu, 24 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sheppard, Damien I</name>
      </author>
      <author>
        <name>Espinoza-Corral, Roberto</name>
      </author>
      <author>
        <name>Lechno-Yossef, Sigal</name>
      </author>
      <author>
        <name>Sutter, Markus</name>
        <uri>https://orcid.org/0000-0001-6290-4820</uri>
      </author>
      <author>
        <name>Arcidiacono, Amanda</name>
      </author>
      <author>
        <name>Cignoni, Edoardo</name>
      </author>
      <author>
        <name>Cupellini, Lorenzo</name>
      </author>
      <author>
        <name>Mennucci, Benedetta</name>
      </author>
      <author>
        <name>Kerfeld, Cheryl A</name>
        <uri>https://orcid.org/0000-0002-9977-8482</uri>
      </author>
    </item>
    <item>
      <title>Creb5 controls its own expression and directly induces the joint interzone regulatory program</title>
      <link>https://escholarship.org/uc/item/97k945bz</link>
      <description>Prior studies have indicated that the transcription factor &lt;i&gt;Creb5&lt;/i&gt; is expressed in the joint interzone, which contains the progenitors for all synovial joint tissues in both mouse and human embryos. In the absence of Creb5 function, most synovial joint interzones fail to form and the cartilage templates in the long bones remain fused. This earlier work did not clarify whether Creb5 initiates a cascade of signaling molecules, such as growth and differentiation factor 5 (Gdf5) and Wnt-family members, that in turn induce the formation of the joint interzone, or instead directly activates the expression of joint interzone markers. In the present study, an integrative analysis of the transcriptome, chromatin accessibility, and Creb5-occupancy in joint progenitors revealed that Creb5 directly binds to both its own two promoters and to the regulatory regions of &lt;i&gt;Gdf5&lt;/i&gt; and &lt;i&gt;Sfrp2&lt;/i&gt;, each of whose expression in the joint interzone is Creb5-dependent. Functional enhancer analysis...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/97k945bz</guid>
      <pubDate>Thu, 24 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Cheng-Hai</name>
      </author>
      <author>
        <name>Shahini, Aref</name>
      </author>
      <author>
        <name>Cook, Laura E</name>
        <uri>https://orcid.org/0000-0002-4459-2592</uri>
      </author>
      <author>
        <name>Mistry, Meeta</name>
      </author>
      <author>
        <name>Kim, Jongkil</name>
      </author>
      <author>
        <name>Wick, Heather</name>
      </author>
      <author>
        <name>Pennacchio, Len A</name>
        <uri>https://orcid.org/0000-0002-8748-3732</uri>
      </author>
      <author>
        <name>Lassar, Andrew B</name>
      </author>
    </item>
    <item>
      <title>Bacterial microcompartment architectures as biomaterials for conversion of gaseous substrates</title>
      <link>https://escholarship.org/uc/item/5483p3sd</link>
      <description>Bacterial microcompartments (BMCs) are protein shells encapsulating multiple enzymes of a metabolic pathway. Interpretations of early experiments on carboxysomes led to the narrative that transport of small gases (CO&lt;sub&gt;2&lt;/sub&gt;, O&lt;sub&gt;2&lt;/sub&gt;) across the shell membrane is restricted. Since then, this notion has been largely contradicted by studies of engineered shells, although these shell constructs lack important proteins present in the native BMCs, altering the synthetic shells' topology, surface and mechanical properties. We discuss here an updated model of gas permeability that informs the design of engineered shells for catalysis on gas substrates and outline how nonshell suprastructures of BMC shell proteins could be used in formulating sustainable biomaterials for hydrogen generation via methane pyrolysis and for other greenhouse gas mitigations.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5483p3sd</guid>
      <pubDate>Tue, 22 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Snyder, Samuel N</name>
      </author>
      <author>
        <name>Wang, Yali</name>
      </author>
      <author>
        <name>Dwyer, Matthew E</name>
      </author>
      <author>
        <name>Sarkar, Daipayan</name>
      </author>
      <author>
        <name>Kerfeld, Cheryl A</name>
        <uri>https://orcid.org/0000-0002-9977-8482</uri>
      </author>
    </item>
    <item>
      <title>Announcing the Biomedical Data Translator: Initial Public Release</title>
      <link>https://escholarship.org/uc/item/9c43g8c7</link>
      <description>The growing availability of biomedical data offers vast potential to improve human health, but the complexity and lack of integration of these datasets often limit their utility. To address this, the Biomedical Data Translator Consortium has developed an open-source knowledge graph-based system-Translator-designed to integrate, harmonize, and make inferences over diverse biomedical data sources. We announce here Translator's initial public release and provide an overview of its architecture, standards, user interface, and core features. Translator employs a scalable, federated, knowledge graph framework for the integration of clinical, genomic, pharmacological, and other biomedical knowledge sources, enabling query retrieval, inference, and hypothesis generation. Translator's user interface is designed to support the exploration of knowledge relationships and the generation of insights, without requiring deep technical expertise and gradually revealing more detailed evidence,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9c43g8c7</guid>
      <pubDate>Fri, 18 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Fecho, Karamarie</name>
      </author>
      <author>
        <name>Glusman, Gwênlyn</name>
      </author>
      <author>
        <name>Baranzini, Sergio E</name>
      </author>
      <author>
        <name>Bizon, Chris</name>
      </author>
      <author>
        <name>Brush, Matthew</name>
      </author>
      <author>
        <name>Byrd, William</name>
      </author>
      <author>
        <name>Chung, Lawrence</name>
      </author>
      <author>
        <name>Crouse, Andrew</name>
      </author>
      <author>
        <name>Deutsch, Eric</name>
      </author>
      <author>
        <name>Dumontier, Michel</name>
      </author>
      <author>
        <name>Foksinska, Aleksandra</name>
      </author>
      <author>
        <name>Hadlock, Jennifer</name>
      </author>
      <author>
        <name>He, Kaiwen</name>
      </author>
      <author>
        <name>Huang, Sui</name>
      </author>
      <author>
        <name>Hubal, Robert</name>
      </author>
      <author>
        <name>Hyde, Gregory M</name>
      </author>
      <author>
        <name>Israni, Sharat</name>
      </author>
      <author>
        <name>Kenmogne, Kelyne</name>
      </author>
      <author>
        <name>Koslicki, David</name>
      </author>
      <author>
        <name>Marcette, Jana Dorfman</name>
      </author>
      <author>
        <name>Mathe, Ewy A</name>
      </author>
      <author>
        <name>Mesbah, Abrar</name>
      </author>
      <author>
        <name>Moxon, Sierra AT</name>
      </author>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
      <author>
        <name>Osborne, John</name>
      </author>
      <author>
        <name>Pasfield, Carrie</name>
      </author>
      <author>
        <name>Qin, Guangrong</name>
      </author>
      <author>
        <name>Ramsey, Stephen A</name>
      </author>
      <author>
        <name>Reese, Justin</name>
      </author>
      <author>
        <name>Roach, Jared C</name>
      </author>
      <author>
        <name>Rose, Reese</name>
      </author>
      <author>
        <name>Soman, Karthik</name>
      </author>
      <author>
        <name>Su, Andrew I</name>
      </author>
      <author>
        <name>Ta, Casey</name>
      </author>
      <author>
        <name>Vaidya, Gaurav</name>
      </author>
      <author>
        <name>Weber, Rosina</name>
      </author>
      <author>
        <name>Wei, Qi</name>
      </author>
      <author>
        <name>Williams, Mark</name>
      </author>
      <author>
        <name>Wu, Chunlei</name>
      </author>
      <author>
        <name>Xu, Colleen</name>
      </author>
      <author>
        <name>Yakaboski, Chase</name>
      </author>
      <author>
        <name>Arab, Michel</name>
      </author>
      <author>
        <name>Abdollahi, Shervin</name>
      </author>
      <author>
        <name>Acosta, Nichollette</name>
      </author>
      <author>
        <name>Agrawal, Ayushi</name>
      </author>
      <author>
        <name>Ahalt, Stanley</name>
      </author>
      <author>
        <name>Amin, Nada</name>
      </author>
      <author>
        <name>Bada, Michael</name>
      </author>
      <author>
        <name>Balar, Krish</name>
      </author>
      <author>
        <name>Balhoff, Jim</name>
      </author>
      <author>
        <name>Baumgartner, William</name>
      </author>
      <author>
        <name>Beasley, Jon‐Michael</name>
      </author>
      <author>
        <name>Blake, Emily</name>
      </author>
      <author>
        <name>Brandon, Namdi</name>
      </author>
      <author>
        <name>Bruskiewich, Richard</name>
      </author>
      <author>
        <name>Burtt, Noel</name>
      </author>
      <author>
        <name>Callaghan, Jackson</name>
      </author>
      <author>
        <name>Camp, Terese</name>
      </author>
      <author>
        <name>Cano, Marco Alvarado</name>
      </author>
      <author>
        <name>Carter, Kathleen</name>
      </author>
      <author>
        <name>Celebi, Remzi</name>
      </author>
      <author>
        <name>Chung, Cheng‐Han</name>
      </author>
      <author>
        <name>Chung, Larry</name>
      </author>
      <author>
        <name>Costanzo, Maria</name>
      </author>
      <author>
        <name>Cousin, Margot</name>
      </author>
      <author>
        <name>Curry, Tim</name>
      </author>
      <author>
        <name>Dancik, Vlado</name>
      </author>
      <author>
        <name>Dougherty, Jennifer</name>
      </author>
      <author>
        <name>Duby, Marc</name>
      </author>
      <author>
        <name>Edwards, Stephen</name>
      </author>
      <author>
        <name>Farris, Joe</name>
      </author>
      <author>
        <name>Fehrmann, Nate</name>
      </author>
      <author>
        <name>Figueiral, Marta</name>
      </author>
      <author>
        <name>Flannick, Jason</name>
      </author>
      <author>
        <name>Fox, Charlie</name>
      </author>
      <author>
        <name>Glen, Amy</name>
      </author>
      <author>
        <name>Goel, Prateek</name>
      </author>
      <author>
        <name>Goetz, Skye</name>
      </author>
      <author>
        <name>Gormley, Joseph</name>
      </author>
      <author>
        <name>Haaland, Perry</name>
      </author>
      <author>
        <name>Hanspers, Kristina</name>
      </author>
      <author>
        <name>Harris, Nomi</name>
      </author>
      <author>
        <name>Henrickson, Jeff</name>
      </author>
      <author>
        <name>Hickey, Anthony</name>
      </author>
      <author>
        <name>Hinderer, Eugene</name>
      </author>
      <author>
        <name>Hoatlin, Maureen</name>
      </author>
      <author>
        <name>Issabekova, Tursynay</name>
      </author>
      <author>
        <name>Karty, Rhea</name>
      </author>
      <author>
        <name>Kebede, Yaphet</name>
      </author>
      <author>
        <name>Kim, Keum Joo</name>
      </author>
      <author>
        <name>King, Simon</name>
      </author>
      <author>
        <name>Klee, Eric</name>
      </author>
      <author>
        <name>Knowles, Michael R</name>
      </author>
      <author>
        <name>Koesterer, Ryan</name>
      </author>
      <author>
        <name>Korn, Daniel</name>
      </author>
      <author>
        <name>Krishnamurthy, Ashok</name>
      </author>
      <author>
        <name>Lambert, Laura</name>
      </author>
      <author>
        <name>Leigh, Margaret W</name>
      </author>
      <author>
        <name>Lin, Jason</name>
      </author>
      <author>
        <name>Lupey, Max</name>
      </author>
    </item>
    <item>
      <title>The Artificial Intelligence Ontology: LLM-Assisted Construction of AI Concept Hierarchies</title>
      <link>https://escholarship.org/uc/item/9315g04c</link>
      <description>The Artificial Intelligence Ontology (AIO) is a systematization of artificial intelligence (AI) concepts, methodologies, and their interrelations. Developed via manual curation, with the additional assistance of large language models (LLMs), AIO aims to address the rapidly evolving landscape of AI by providing a comprehensive framework that encompasses both technical and ethical aspects of AI technologies. The primary audience for AIO includes AI researchers, developers, and educators seeking standardized terminology and concepts within the AI domain. We use the term “branches” for classes, and their subclasses, in our ontology that are subclasses of owl:Thing. AIO contains eight branches: Bias, Layer, Machine Learning Task, Mathematical Function, Model, Network, Preprocessing, and Training Strategy, each designed to support the modular composition of AI methods and facilitate a deeper understanding of deep learning architectures and ethical considerations in AI. AIO uses the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9315g04c</guid>
      <pubDate>Wed, 16 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Joachimiak, Marcin P</name>
      </author>
      <author>
        <name>Miller, Mark A</name>
      </author>
      <author>
        <name>Caufield, J Harry</name>
      </author>
      <author>
        <name>Ly, Ryan</name>
        <uri>https://orcid.org/0000-0001-9238-0642</uri>
      </author>
      <author>
        <name>Harris, Nomi L</name>
        <uri>https://orcid.org/0000-0001-6315-3707</uri>
      </author>
      <author>
        <name>Tritt, Andrew</name>
      </author>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
      <author>
        <name>Bouchard, Kristofer E</name>
        <uri>https://orcid.org/0000-0002-1974-4603</uri>
      </author>
    </item>
    <item>
      <title>Massively parallel reporter assays and mouse transgenic assays provide correlated and complementary information about neuronal enhancer activity</title>
      <link>https://escholarship.org/uc/item/7r18r5f0</link>
      <description>High-throughput massively parallel reporter assays (MPRAs) and phenotype-rich in vivo transgenic mouse assays are two potentially complementary ways to study the impact of noncoding variants associated with psychiatric diseases. Here, we investigate the utility of combining these assays. Specifically, we carry out an MPRA in induced human neurons on over 50,000 sequences derived from fetal neuronal ATAC-seq datasets and enhancers validated in mouse assays. We also test the impact of over 20,000 variants, including synthetic mutations and 167 common variants associated with psychiatric disorders. We find a strong and specific correlation between MPRA and mouse neuronal enhancer activity. Four out of five tested variants with significant MPRA effects affected neuronal enhancer activity in mouse embryos. Mouse assays also reveal pleiotropic variant effects that could not be observed in MPRA. Our work provides a catalog of functional neuronal enhancers and variant effects and highlights...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7r18r5f0</guid>
      <pubDate>Tue, 15 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kosicki, Michael</name>
        <uri>https://orcid.org/0000-0001-7173-8852</uri>
      </author>
      <author>
        <name>Laboy Cintrón, Dianne</name>
      </author>
      <author>
        <name>Keukeleire, Pia</name>
      </author>
      <author>
        <name>Schubach, Max</name>
      </author>
      <author>
        <name>Page, Nicholas F</name>
      </author>
      <author>
        <name>Georgakopoulos-Soares, Ilias</name>
      </author>
      <author>
        <name>Akiyama, Jennifer A</name>
        <uri>https://orcid.org/0000-0002-4130-7784</uri>
      </author>
      <author>
        <name>Plajzer-Frick, Ingrid</name>
      </author>
      <author>
        <name>Novak, Catherine S</name>
      </author>
      <author>
        <name>Kato, Momoe</name>
      </author>
      <author>
        <name>Hunter, Riana D</name>
        <uri>https://orcid.org/0000-0002-2888-1079</uri>
      </author>
      <author>
        <name>von Maydell, Kianna</name>
      </author>
      <author>
        <name>Barton, Sarah</name>
      </author>
      <author>
        <name>Godfrey, Patrick</name>
      </author>
      <author>
        <name>Beckman, Erik</name>
      </author>
      <author>
        <name>Sanders, Stephan J</name>
        <uri>https://orcid.org/0000-0001-9112-5148</uri>
      </author>
      <author>
        <name>Kircher, Martin</name>
      </author>
      <author>
        <name>Pennacchio, Len A</name>
        <uri>https://orcid.org/0000-0002-8748-3732</uri>
      </author>
      <author>
        <name>Ahituv, Nadav</name>
      </author>
    </item>
    <item>
      <title>Enabling pan-repository reanalysis for big data science of public metabolomics data</title>
      <link>https://escholarship.org/uc/item/4xx8p7nh</link>
      <description>Public untargeted metabolomics data is a growing resource for metabolite and phenotype discovery; however, accessing and utilizing these data across repositories pose significant challenges. Therefore, here we develop pan-repository universal identifiers and harmonized cross-repository metadata. This ecosystem facilitates discovery by integrating diverse data sources from public repositories including MetaboLights, Metabolomics Workbench, and GNPS/MassIVE. Our approach simplified data handling and unlocks previously inaccessible reanalysis workflows, fostering unmatched research opportunities.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4xx8p7nh</guid>
      <pubDate>Tue, 15 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>El Abiead, Yasin</name>
      </author>
      <author>
        <name>Strobel, Michael</name>
      </author>
      <author>
        <name>Payne, Thomas</name>
      </author>
      <author>
        <name>Fahy, Eoin</name>
      </author>
      <author>
        <name>O’Donovan, Claire</name>
      </author>
      <author>
        <name>Subramamiam, Shankar</name>
      </author>
      <author>
        <name>Vizcaíno, Juan Antonio</name>
      </author>
      <author>
        <name>Yurekten, Ozgur</name>
      </author>
      <author>
        <name>Deleray, Victoria</name>
      </author>
      <author>
        <name>Zuffa, Simone</name>
        <uri>https://orcid.org/0000-0001-7237-3402</uri>
      </author>
      <author>
        <name>Xing, Shipei</name>
      </author>
      <author>
        <name>Mannochio-Russo, Helena</name>
      </author>
      <author>
        <name>Mohanty, Ipsita</name>
      </author>
      <author>
        <name>Zhao, Haoqi Nina</name>
      </author>
      <author>
        <name>Caraballo-Rodriguez, Andres M</name>
      </author>
      <author>
        <name>P. Gomes, Paulo Wender</name>
      </author>
      <author>
        <name>Avalon, Nicole E</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Bowen, Benjamin P</name>
        <uri>https://orcid.org/0000-0003-1368-3958</uri>
      </author>
      <author>
        <name>Louie, Katherine B</name>
      </author>
      <author>
        <name>Dorrestein, Pieter C</name>
      </author>
      <author>
        <name>Wang, Mingxun</name>
        <uri>https://orcid.org/0000-0001-7647-6097</uri>
      </author>
    </item>
    <item>
      <title>Author Correction: Machine learning-led semi-automated medium optimization reveals salt as key for flaviolin production in Pseudomonas putida</title>
      <link>https://escholarship.org/uc/item/3805r1sb</link>
      <description>Author Correction: Machine learning-led semi-automated medium optimization reveals salt as key for flaviolin production in Pseudomonas putida</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3805r1sb</guid>
      <pubDate>Tue, 15 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zournas, Apostolos</name>
      </author>
      <author>
        <name>Incha, Matthew R</name>
      </author>
      <author>
        <name>Radivojevic, Tijana</name>
      </author>
      <author>
        <name>Blay, Vincent</name>
      </author>
      <author>
        <name>Martí, Jose Manuel</name>
      </author>
      <author>
        <name>Costello, Zak</name>
      </author>
      <author>
        <name>Schmidt, Matthias</name>
      </author>
      <author>
        <name>Chung, Tan</name>
      </author>
      <author>
        <name>Thompson, Mitchell G</name>
      </author>
      <author>
        <name>Pearson, Allison</name>
      </author>
      <author>
        <name>Kinnunen, Patrick C</name>
      </author>
      <author>
        <name>Eng, Thomas</name>
        <uri>https://orcid.org/0000-0002-4974-3863</uri>
      </author>
      <author>
        <name>Lawson, Christopher E</name>
      </author>
      <author>
        <name>Tan, Stephen</name>
      </author>
      <author>
        <name>Ogorzalek, Tadeusz</name>
      </author>
      <author>
        <name>Kaplan, Nurgul</name>
      </author>
      <author>
        <name>Forrer, Mark</name>
      </author>
      <author>
        <name>Backman, Tyler</name>
      </author>
      <author>
        <name>Mukhopadhyay, Aindrila</name>
      </author>
      <author>
        <name>Hillson, Nathan J</name>
        <uri>https://orcid.org/0000-0002-9169-3978</uri>
      </author>
      <author>
        <name>Keasling, Jay D</name>
        <uri>https://orcid.org/0000-0003-4170-6088</uri>
      </author>
      <author>
        <name>Garcia Martin, Hector</name>
        <uri>https://orcid.org/0000-0002-4556-9685</uri>
      </author>
    </item>
    <item>
      <title>Engineering Pseudomonas putida for production of 3-hydroxyacids using hybrid type I polyketide synthases</title>
      <link>https://escholarship.org/uc/item/0tf6j10d</link>
      <description>Engineered type I polyketide synthases (T1PKSs) are a potentially transformative platform for the biosynthesis of small molecules. Due to their modular nature, T1PKSs can be rationally designed to produce a wide range of bulk or specialty chemicals. While heterologous PKS expression is best studied in microbes of the genus &lt;i&gt;Streptomyces&lt;/i&gt;, recent studies have focused on the exploration of non-native PKS hosts. The biotechnological production of chemicals in fast growing and industrial relevant hosts has numerous economic and logistic advantages. With its native ability to utilize alternative feedstocks, &lt;i&gt;Pseudomonas putida&lt;/i&gt; has emerged as a promising workhorse for the sustainable production of small molecules. Here, we outline the assessment of &lt;i&gt;P. putida&lt;/i&gt; as a host for the expression of engineered T1PKSs and production of 3-hydroxyacids. After establishing the functional expression of an engineered T1PKS, we successfully expanded and increased the pool of available...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0tf6j10d</guid>
      <pubDate>Tue, 15 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Schmidt, Matthias</name>
      </author>
      <author>
        <name>Vilchez, Aaron A</name>
      </author>
      <author>
        <name>Lee, Namil</name>
      </author>
      <author>
        <name>Keiser, Leah S</name>
      </author>
      <author>
        <name>Pearson, Allison N</name>
      </author>
      <author>
        <name>Thompson, Mitchell G</name>
      </author>
      <author>
        <name>Zhu, Yolanda</name>
      </author>
      <author>
        <name>Haushalter, Robert W</name>
      </author>
      <author>
        <name>Deutschbauer, Adam M</name>
      </author>
      <author>
        <name>Yuzawa, Satoshi</name>
      </author>
      <author>
        <name>Blank, Lars M</name>
      </author>
      <author>
        <name>Keasling, Jay D</name>
        <uri>https://orcid.org/0000-0003-4170-6088</uri>
      </author>
    </item>
    <item>
      <title>Comparison of stress tolerance mechanisms between Saccharomyces cerevisiae and the multistress-tolerant Pichia kudriavzevii</title>
      <link>https://escholarship.org/uc/item/5jj7c9ds</link>
      <description>Yeasts play a vital role in both research and industrial biomanufacturing. Saccharomyces cerevisiae has been extensively utilized as a model system. However, its application is often constrained by limited tolerance to the diverse stress conditions encountered in bioprocesses. These challenges have driven increasing interest in nonconventional, multistress-tolerant yeasts as alternative biomanufacturing hosts. This review highlights Pichia kudriavzevii as a promising nonconventional yeast for industrial applications. Unlike S. cerevisiae, P. kudriavzevii exhibits exceptional tolerance to high temperatures, elevated concentrations of furanic and phenolic inhibitors, osmotic stress, salinity, and extreme pH. These traits make it an attractive candidate for industrial processes without requiring extensive genetic modifications to enhance stress resistance. As a result, P. kudriavzevii has emerged as a flagship species for advancing bioeconomy. Despite its industrial potential, the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5jj7c9ds</guid>
      <pubDate>Mon, 14 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Frousnoon, Thasneem Banu</name>
      </author>
      <author>
        <name>Pham, Nam Ngoc</name>
        <uri>https://orcid.org/0000-0001-7640-1001</uri>
      </author>
      <author>
        <name>Wu, Zong-Yen</name>
      </author>
      <author>
        <name>Hsieh, Ping-Hung</name>
      </author>
      <author>
        <name>Yoshikuni, Yasuo</name>
      </author>
    </item>
    <item>
      <title>Spatially structured bacterial interactions alter algal carbon flow to bacteria</title>
      <link>https://escholarship.org/uc/item/4nn4b2fd</link>
      <description>Phytoplankton account for nearly half of global photosynthetic carbon fixation, and the fate of that carbon is regulated in large part by microbial food web processing. We currently lack a mechanistic understanding of how interactions among heterotrophic bacteria impact the fate of photosynthetically fixed carbon. Here, we used a set of bacterial isolates capable of growing on exudates from the diatom Phaeodactylum tricornutum to investigate how bacteria-bacteria interactions affect the balance between exudate remineralization and incorporation into biomass. With exometabolomics and genome-scale metabolic modeling, we estimated the degree of resource competition between bacterial pairs. In a sequential spent media experiment, we found that pairwise interactions were more beneficial than predicted based on resource competition alone, and 30% exhibited facilitative interactions. To link this to carbon fate, we used single-cell isotope tracing in a custom cultivation system to compare...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4nn4b2fd</guid>
      <pubDate>Mon, 14 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kim, Hyungseok</name>
      </author>
      <author>
        <name>Brisson, Vanessa L</name>
      </author>
      <author>
        <name>Casey, John R</name>
      </author>
      <author>
        <name>Swink, Courtney</name>
      </author>
      <author>
        <name>Rolison, Kristina A</name>
      </author>
      <author>
        <name>McCall, Nathan</name>
      </author>
      <author>
        <name>Golini, Amber N</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Veličković, Dušan</name>
      </author>
      <author>
        <name>Weber, Peter K</name>
      </author>
      <author>
        <name>Buie, Cullen R</name>
      </author>
      <author>
        <name>Mayali, Xavier</name>
      </author>
      <author>
        <name>Stuart, Rhona K</name>
      </author>
    </item>
    <item>
      <title>Opening doors to physical sample tracking and attribution in Earth and environmental sciences</title>
      <link>https://escholarship.org/uc/item/2qq792g7</link>
      <description>Physical samples and their associated data and metadata underpin scientific discoveries across disciplines and can enable new science when appropriately archived. However, there are significant gaps in current practices and infrastructure that prevent accurate provenance tracking, reproducibility, and attribution. For most samples, descriptive metadata are often sparse, inaccessible, or absent. Samples and associated data and metadata may also be scattered across numerous physical collections, data repositories, laboratories, data files, and papers with no clear linkage or provenance tracking as new information is generated over time. The Earth Science Information Partners (ESIP) Physical Samples Curation Cluster has therefore developed guidance for scientific authors on ‘Publishing Open Research Using Physical Samples.’ This involved synthesizing existing practices, gathering&amp;nbsp;community feedback, and assessing real-world examples. We identified improvements needed to enable...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2qq792g7</guid>
      <pubDate>Mon, 7 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Damerow, Joan E</name>
        <uri>https://orcid.org/0000-0003-2601-5043</uri>
      </author>
      <author>
        <name>Raia, Natalie H</name>
      </author>
      <author>
        <name>Stanley, Val</name>
      </author>
      <author>
        <name>Choe, Saebyul</name>
      </author>
      <author>
        <name>Borton, Mikayla A</name>
      </author>
      <author>
        <name>Byers, Neil</name>
        <uri>https://orcid.org/0000-0001-5332-2255</uri>
      </author>
      <author>
        <name>Cassidy, Ellen R</name>
      </author>
      <author>
        <name>Cholia, Shreyas</name>
        <uri>https://orcid.org/0000-0002-4775-8201</uri>
      </author>
      <author>
        <name>Edmunds, Rorie</name>
      </author>
      <author>
        <name>Forbes, Brieanne</name>
      </author>
      <author>
        <name>Forrest, Kathleen</name>
      </author>
      <author>
        <name>Goldman, Amy E</name>
      </author>
      <author>
        <name>Kunze, John</name>
      </author>
      <author>
        <name>Lafia, Sara</name>
      </author>
      <author>
        <name>Lehnert, Kerstin</name>
      </author>
      <author>
        <name>McIntyre-Redden, Marcella</name>
      </author>
      <author>
        <name>Naples, Richard</name>
      </author>
      <author>
        <name>O’Ryan, Dylan</name>
      </author>
      <author>
        <name>Parker, Charles</name>
        <uri>https://orcid.org/0000-0002-7436-3176</uri>
      </author>
      <author>
        <name>Plomp, Esther</name>
      </author>
      <author>
        <name>Powers-McCormack, Beck</name>
      </author>
      <author>
        <name>Ramdeen, Sarah</name>
      </author>
      <author>
        <name>Richard, Stephen</name>
      </author>
      <author>
        <name>Thessen, Anne</name>
      </author>
      <author>
        <name>Thompson, Cody W</name>
      </author>
      <author>
        <name>Vieglais, Dave</name>
      </author>
      <author>
        <name>Vrouwenvelder, Kristina</name>
      </author>
      <author>
        <name>Wood-Charlson, Elisha M</name>
        <uri>https://orcid.org/0000-0001-9557-7715</uri>
      </author>
      <author>
        <name>Wyborn, Lesley</name>
      </author>
      <author>
        <name>Reddy, TBK</name>
        <uri>https://orcid.org/0000-0002-0871-5567</uri>
      </author>
      <author>
        <name>Thomer, Andrea K</name>
      </author>
    </item>
    <item>
      <title>A distinct LHCI arrangement is recruited to photosystem I in Fe-starved green algae</title>
      <link>https://escholarship.org/uc/item/74j24106</link>
      <description>Iron (Fe) availability limits photosynthesis at a global scale where Fe-rich photosystem (PS) I abundance is drastically reduced in Fe-poor environments. We used single-particle cryoelectron microscopy to reveal a unique Fe starvation-dependent arrangement of light-harvesting chlorophyll (LHC) proteins where Fe starvation-induced TIDI1 is found in an additional tetramer of LHC proteins associated with PSI in &lt;i&gt;Dunaliella tertiolecta&lt;/i&gt; and &lt;i&gt;Dunaliella salina&lt;/i&gt;. These cosmopolitan green algae are resilient to poor Fe nutrition. TIDI1 is a distinct LHC protein that co-occurs in diverse algae with flavodoxin (an Fe-independent replacement for the Fe-containing ferredoxin). The antenna expansion in eukaryotic algae we describe here is reminiscent of the iron-starvation induced (&lt;i&gt;isiA-&lt;/i&gt;encoding) antenna ring in cyanobacteria, which typically co-occurs with &lt;i&gt;isiB&lt;/i&gt;, encoding flavodoxin. Our work showcases the convergent strategies that evolved after the Great Oxidation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/74j24106</guid>
      <pubDate>Tue, 1 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Liu, Helen W</name>
      </author>
      <author>
        <name>Khera, Radhika</name>
      </author>
      <author>
        <name>Grob, Patricia</name>
      </author>
      <author>
        <name>Gallaher, Sean D</name>
        <uri>https://orcid.org/0000-0002-9773-6051</uri>
      </author>
      <author>
        <name>Purvine, Samuel O</name>
      </author>
      <author>
        <name>Nicora, Carrie D</name>
      </author>
      <author>
        <name>Lipton, Mary S</name>
      </author>
      <author>
        <name>Niyogi, Krishna K</name>
      </author>
      <author>
        <name>Nogales, Eva</name>
        <uri>https://orcid.org/0000-0001-9816-3681</uri>
      </author>
      <author>
        <name>Iwai, Masakazu</name>
        <uri>https://orcid.org/0000-0002-0986-9015</uri>
      </author>
      <author>
        <name>Merchant, Sabeeha S</name>
      </author>
    </item>
    <item>
      <title>Sediment and groundwater metagenomes from subsurface microbial communities from the Oak Ridge National Laboratory Oak Ridge Reservation, Oak Ridge, Tennessee, USA</title>
      <link>https://escholarship.org/uc/item/7wt272gh</link>
      <description>We report 26 subsurface sediment and 9 groundwater metagenomes from the Oak Ridge Reservation at Oak Ridge, TN, USA. Samples were collected from various depths and phases (attached vs planktonic) to study subsurface microbial metabolism, the effect of contamination on microbial communities, and differences across groundwater and sediment microbial communities.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7wt272gh</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lui, Lauren M</name>
        <uri>https://orcid.org/0000-0001-8720-5268</uri>
      </author>
      <author>
        <name>Nielsen, Torben N</name>
      </author>
      <author>
        <name>Smith, Heidi J</name>
      </author>
      <author>
        <name>Chandonia, John-Marc</name>
        <uri>https://orcid.org/0000-0002-5153-9079</uri>
      </author>
      <author>
        <name>Kuehl, Jennifer V</name>
      </author>
      <author>
        <name>Song, Fangchao</name>
        <uri>https://orcid.org/0000-0002-9427-9879</uri>
      </author>
      <author>
        <name>Sczesnak, Andrew</name>
      </author>
      <author>
        <name>Hendrickson, Andrew</name>
      </author>
      <author>
        <name>Hazen, Terry C</name>
        <uri>https://orcid.org/0000-0002-2536-9993</uri>
      </author>
      <author>
        <name>Fields, Matthew W</name>
      </author>
      <author>
        <name>Arkin, Adam P</name>
        <uri>https://orcid.org/0000-0002-4999-2931</uri>
      </author>
    </item>
    <item>
      <title>RWRtoolkit: multi-omic network analysis using random walks on multiplex networks in any species</title>
      <link>https://escholarship.org/uc/item/8xf6s5bk</link>
      <description>We introduce RWRtoolkit, a multiplex generation, exploration, and statistical package built for R and command-line users. RWRtoolkit enables the efficient exploration of large and highly complex biological networks generated from custom experimental data and/or from publicly available datasets, and is species agnostic. A range of functions can be used to find topological distances between biological entities, determine relationships within sets of interest, search for topological context around sets of interest, and statistically evaluate the strength of relationships within and between sets. The command-line interface is designed for parallelization on high-performance cluster systems, which enables high-throughput analysis such as permutation testing. Several tools in the package have also been made available for use in reproducible workflows via the KBase web application.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8xf6s5bk</guid>
      <pubDate>Tue, 24 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kainer, David</name>
      </author>
      <author>
        <name>Lane, Matthew</name>
      </author>
      <author>
        <name>Sullivan, Kyle A</name>
      </author>
      <author>
        <name>Miller, J Izaak</name>
      </author>
      <author>
        <name>Cashman, Mikaela</name>
      </author>
      <author>
        <name>Morgan, Mallory</name>
      </author>
      <author>
        <name>Cliff, Ashley</name>
      </author>
      <author>
        <name>Romero, Jonathon</name>
      </author>
      <author>
        <name>Walker, Angelica</name>
      </author>
      <author>
        <name>Blair, D Dakota</name>
      </author>
      <author>
        <name>Chhetri, Hari</name>
      </author>
      <author>
        <name>Wang, Yongqin</name>
      </author>
      <author>
        <name>Pavicic, Mirko</name>
      </author>
      <author>
        <name>Furches, Anna</name>
      </author>
      <author>
        <name>Noshay, Jaclyn</name>
      </author>
      <author>
        <name>Drake, Meghan</name>
      </author>
      <author>
        <name>Ireland, AJ</name>
      </author>
      <author>
        <name>Missaoui, Ali</name>
      </author>
      <author>
        <name>Kang, Yun</name>
      </author>
      <author>
        <name>Sedbrook, John C</name>
      </author>
      <author>
        <name>Dehal, Paramvir</name>
        <uri>https://orcid.org/0000-0001-5810-2497</uri>
      </author>
      <author>
        <name>Canon, Shane</name>
      </author>
      <author>
        <name>Jacobson, Daniel</name>
      </author>
    </item>
    <item>
      <title>Replacing non-biomedical concepts improves embedding of biomedical concepts</title>
      <link>https://escholarship.org/uc/item/43k9s6k4</link>
      <description>Embeddings are semantically meaningful representations of words in a vector space, commonly used to enhance downstream machine learning applications. Traditional biomedical embedding techniques often replace all synonymous words representing biological or medical concepts with a unique token, ensuring consistent representation and improving embedding quality. However, the potential impact of replacing non-biomedical concept synonyms has received less attention. Embedding approaches often employ concept replacement to replace concepts that span multiple words, such as non-small-cell lung carcinoma, with a single concept identifier (e.g., D002289). Also, all synonyms of each concept are merged into the same identifier. Here, we additionally leveraged WordNet to identify and replace sets of non-biomedical synonyms with their most common representatives. This combined approach aimed to reduce embedding noise from non-biomedical terms while preserving the integrity of biomedical concept...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/43k9s6k4</guid>
      <pubDate>Tue, 24 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Niyonkuru, Enock</name>
      </author>
      <author>
        <name>Gomez, Mauricio Soto</name>
      </author>
      <author>
        <name>Casarighi, Elena</name>
      </author>
      <author>
        <name>Antogiovanni, Stephan</name>
      </author>
      <author>
        <name>Blau, Hannah</name>
      </author>
      <author>
        <name>Reese, Justin T</name>
      </author>
      <author>
        <name>Valentini, Giorgio</name>
      </author>
      <author>
        <name>Robinson, Peter N</name>
      </author>
    </item>
    <item>
      <title>Quantitative dissection of Agrobacterium T-DNA expression in single plant cells reveals density-dependent synergy and antagonism</title>
      <link>https://escholarship.org/uc/item/6b05z73s</link>
      <description>Agrobacterium pathogenesis, which involves transferring T-DNA into plant cells, is the cornerstone of plant genetic engineering. As the applications that rely on Agrobacterium increase in sophistication, it becomes critical to achieve a quantitative and predictive understanding of T-DNA expression at the level of single plant cells. Here we examine if a classic Poisson model of interactions between pathogens and host cells holds true for Agrobacterium infecting Nicotiana benthamiana. Systematically challenging this model revealed antagonistic and synergistic density-dependent interactions between bacteria that do not require quorum sensing. Using various approaches, we studied the molecular basis of these interactions. To overcome the engineering constraints imposed by antagonism, we created a dual binary vector system termed ‘BiBi’, which can improve the efficiency of a reconstituted complex metabolic pathway in a predictive fashion. Our findings illustrate how combining theoretical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6b05z73s</guid>
      <pubDate>Mon, 23 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Alamos, Simon</name>
      </author>
      <author>
        <name>Szarzanowicz, Matthew J</name>
      </author>
      <author>
        <name>Thompson, Mitchell G</name>
      </author>
      <author>
        <name>Stevens, Danielle M</name>
      </author>
      <author>
        <name>Kirkpatrick, Liam D</name>
      </author>
      <author>
        <name>Dee, Amanda</name>
      </author>
      <author>
        <name>Pannu, Hamreet</name>
      </author>
      <author>
        <name>Cui, Ruoming</name>
      </author>
      <author>
        <name>Liu, Shuying</name>
      </author>
      <author>
        <name>Nimavat, Monikaben</name>
      </author>
      <author>
        <name>Krasileva, Ksenia</name>
        <uri>https://orcid.org/0000-0002-1679-0700</uri>
      </author>
      <author>
        <name>Baidoo, Edward EK</name>
        <uri>https://orcid.org/0000-0001-5787-1219</uri>
      </author>
      <author>
        <name>Shih, Patrick M</name>
      </author>
    </item>
    <item>
      <title>Microbiome data management in action workshop: Atlanta, GA, USA, June 12–13, 2024</title>
      <link>https://escholarship.org/uc/item/5tz1m4qf</link>
      <description>Microbiome research is revolutionizing human and environmental health, but the value and reuse of microbiome data are significantly hampered by the limited development and adoption of data standards. While several ongoing efforts are aimed at improving microbiome data management, significant gaps still remain in terms of defining and promoting adoption of consensus standards for these datasets. The Strengthening the Organization and Reporting of Microbiome Studies (STORMS) guidelines for human microbiome research have been endorsed and successfully utilized by many research organizations, publishers, and funding agencies, and have been recognized as a consensus community standard. No equivalent effort has occurred for environmental, synthetic, and non-human host-associated microbiomes. To address this growing need within the microbiome research community, we convened the Microbiome Data Management in Action Workshop (June 12–13, 2024, in Atlanta, GA, USA), to bring together key...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5tz1m4qf</guid>
      <pubDate>Mon, 23 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kelliher, Julia M</name>
      </author>
      <author>
        <name>Aljumaah, Mashael</name>
      </author>
      <author>
        <name>Bordenstein, Sarah R</name>
      </author>
      <author>
        <name>Brister, J Rodney</name>
      </author>
      <author>
        <name>Chain, Patrick SG</name>
      </author>
      <author>
        <name>Dundore-Arias, Jose Pablo</name>
      </author>
      <author>
        <name>Emerson, Joanne B</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
      <author>
        <name>Fernandes, Vanessa Moreira C</name>
      </author>
      <author>
        <name>Flores, Roberto</name>
      </author>
      <author>
        <name>Gonzalez, Antonio</name>
      </author>
      <author>
        <name>Hansen, Zoe A</name>
      </author>
      <author>
        <name>Hatcher, Eneida L</name>
      </author>
      <author>
        <name>Jackson, Scott A</name>
      </author>
      <author>
        <name>Kellogg, Christina A</name>
      </author>
      <author>
        <name>Madupu, Ramana</name>
      </author>
      <author>
        <name>Miller, Cassandra Maria Luz</name>
      </author>
      <author>
        <name>Mirzayi, Chloe</name>
      </author>
      <author>
        <name>Moustafa, Ahmed M</name>
      </author>
      <author>
        <name>Mungall, Christopher</name>
      </author>
      <author>
        <name>Oliver, Aaron</name>
        <uri>https://orcid.org/0000-0002-0410-8284</uri>
      </author>
      <author>
        <name>Pariente, Nonia</name>
      </author>
      <author>
        <name>Pett-Ridge, Jennifer</name>
      </author>
      <author>
        <name>Record, Sydne</name>
      </author>
      <author>
        <name>Reji, Linta</name>
      </author>
      <author>
        <name>Reysenbach, Anna-Louise</name>
      </author>
      <author>
        <name>Rich, Virginia I</name>
      </author>
      <author>
        <name>Richardson, Lorna</name>
      </author>
      <author>
        <name>Schriml, Lynn M</name>
      </author>
      <author>
        <name>Shabman, Reed S</name>
      </author>
      <author>
        <name>Sierra, Maria A</name>
      </author>
      <author>
        <name>Sullivan, Matthew B</name>
      </author>
      <author>
        <name>Sundaramurthy, Punithavathi</name>
      </author>
      <author>
        <name>Thibault, Katherine M</name>
      </author>
      <author>
        <name>Thompson, Luke R</name>
      </author>
      <author>
        <name>Tighe, Scott</name>
      </author>
      <author>
        <name>Vereen, Ethell</name>
      </author>
      <author>
        <name>Eloe-Fadrosh, Emiley A</name>
        <uri>https://orcid.org/0000-0002-8162-1276</uri>
      </author>
    </item>
    <item>
      <title>The Bee Microbiome: Impact on Bee Health and Model for Evolution and Ecology of Host-Microbe Interactions</title>
      <link>https://escholarship.org/uc/item/6x21s3x4</link>
      <description>The Bee Microbiome: Impact on Bee Health and Model for Evolution and Ecology of Host-Microbe Interactions</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6x21s3x4</guid>
      <pubDate>Fri, 20 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Engel, Philipp</name>
      </author>
      <author>
        <name>Kwong, Waldan K</name>
      </author>
      <author>
        <name>McFrederick, Quinn</name>
        <uri>https://orcid.org/0000-0003-0740-6954</uri>
      </author>
      <author>
        <name>Anderson, Kirk E</name>
      </author>
      <author>
        <name>Barribeau, Seth Michael</name>
      </author>
      <author>
        <name>Chandler, James Angus</name>
      </author>
      <author>
        <name>Cornman, R Scott</name>
      </author>
      <author>
        <name>Dainat, Jacques</name>
      </author>
      <author>
        <name>de Miranda, Joachim R</name>
      </author>
      <author>
        <name>Doublet, Vincent</name>
      </author>
      <author>
        <name>Emery, Olivier</name>
      </author>
      <author>
        <name>Evans, Jay D</name>
      </author>
      <author>
        <name>Farinelli, Laurent</name>
      </author>
      <author>
        <name>Flenniken, Michelle L</name>
      </author>
      <author>
        <name>Granberg, Fredrik</name>
      </author>
      <author>
        <name>Grasis, Juris A</name>
        <uri>https://orcid.org/0000-0002-3945-0135</uri>
      </author>
      <author>
        <name>Gauthier, Laurent</name>
      </author>
      <author>
        <name>Hayer, Juliette</name>
      </author>
      <author>
        <name>Koch, Hauke</name>
      </author>
      <author>
        <name>Kocher, Sarah</name>
      </author>
      <author>
        <name>Martinson, Vincent G</name>
      </author>
      <author>
        <name>Moran, Nancy</name>
      </author>
      <author>
        <name>Munoz-Torres, Monica</name>
        <uri>https://orcid.org/0000-0001-8430-6039</uri>
      </author>
      <author>
        <name>Newton, Irene</name>
      </author>
      <author>
        <name>Paxton, Robert J</name>
      </author>
      <author>
        <name>Powell, Eli</name>
      </author>
      <author>
        <name>Sadd, Ben M</name>
      </author>
      <author>
        <name>Schmid-Hempel, Paul</name>
      </author>
      <author>
        <name>Schmid-Hempel, Regula</name>
      </author>
      <author>
        <name>Song, Se Jin</name>
      </author>
      <author>
        <name>Schwarz, Ryan S</name>
      </author>
      <author>
        <name>vanengelsdorp, Dennis</name>
      </author>
      <author>
        <name>Dainat, Benjamin</name>
      </author>
    </item>
    <item>
      <title>Too dim, too bright, and just right: Systems analysis of the Chlamydomonas diurnal program under limiting and excess light</title>
      <link>https://escholarship.org/uc/item/7mj5f629</link>
      <description>Photosynthetic organisms coordinate their metabolism and growth with diurnal light, which can range in intensity from limiting to excessive. Little is known about how light intensity impacts the diurnal program in Chlamydomonas reinhardtii, or how diurnal rhythms in gene expression and metabolism shape photoprotective responses at different times of day. To address these questions, we performed a systems analysis of synchronized Chlamydomonas populations acclimated to low, moderate, and high diurnal light. Transcriptomic and proteomic data revealed that the Chlamydomonas rhythmic gene expression program is resilient to limiting and excess light: genome-wide, waves of transcripts, and proteins peak at the same times in populations acclimated to stressful light intensities as in populations acclimated to moderate light. Yet, diurnal photoacclimation gives rise to hundreds of gene expression changes, even at night. Time course measurements of photosynthetic efficiency and pigments...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7mj5f629</guid>
      <pubDate>Thu, 19 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Dupuis, Sunnyjoy</name>
      </author>
      <author>
        <name>Ojeda, Valle</name>
      </author>
      <author>
        <name>Gallaher, Sean D</name>
        <uri>https://orcid.org/0000-0002-9773-6051</uri>
      </author>
      <author>
        <name>Purvine, Samuel O</name>
      </author>
      <author>
        <name>Glaesener, Anne G</name>
      </author>
      <author>
        <name>Ponce, Raquel</name>
      </author>
      <author>
        <name>Nicora, Carrie D</name>
      </author>
      <author>
        <name>Bloodsworth, Kent</name>
      </author>
      <author>
        <name>Lipton, Mary S</name>
      </author>
      <author>
        <name>Niyogi, Krishna K</name>
      </author>
      <author>
        <name>Iwai, Masakazu</name>
        <uri>https://orcid.org/0000-0002-0986-9015</uri>
      </author>
      <author>
        <name>Merchant, Sabeeha S</name>
      </author>
    </item>
    <item>
      <title>Emergence and disruption of cooperativity in a denitrifying microbial community</title>
      <link>https://escholarship.org/uc/item/8c594549</link>
      <description>Anthropogenic perturbations to the nitrogen cycle, primarily through use of synthetic fertilizers, is driving an unprecedented increase in the emission of nitrous oxide (N2O), a potent greenhouse gas and an ozone depleting substance, causing urgency in identifying the sources and sinks of N2O. Microbial denitrification is a primary contributor to biotic production of N2O in anoxic regions of soil, marine systems, and wastewater treatment facilities. Here, through comprehensive genome analysis, we show that pathway partitioning is a ubiquitous mechanism of complete denitrification within microbial communities. We have investigated mechanisms and consequences of process partitioning of denitrification through detailed physiological characterization and kinetic modeling of a synthetic community of Rhodanobacter thiooxydans FW510-R12 and Acidovorax sp. GW101-3H11. We have discovered that these two bacterial isolates, from a heavily nitrate (NO3-) contaminated superfund site, complete...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8c594549</guid>
      <pubDate>Wed, 4 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Carr, Alex V</name>
      </author>
      <author>
        <name>Otwell, Anne E</name>
      </author>
      <author>
        <name>Hunt, Kristopher A</name>
      </author>
      <author>
        <name>Chen, Yan</name>
      </author>
      <author>
        <name>Wilson, James</name>
      </author>
      <author>
        <name>Faria, José P</name>
      </author>
      <author>
        <name>Liu, Filipe</name>
      </author>
      <author>
        <name>Edirisinghe, Janaka N</name>
      </author>
      <author>
        <name>Valenzuela, Jacob J</name>
      </author>
      <author>
        <name>Turkarslan, Serdar</name>
      </author>
      <author>
        <name>Lui, Lauren M</name>
        <uri>https://orcid.org/0000-0001-8720-5268</uri>
      </author>
      <author>
        <name>Nielsen, Torben N</name>
      </author>
      <author>
        <name>Arkin, Adam P</name>
        <uri>https://orcid.org/0000-0002-4999-2931</uri>
      </author>
      <author>
        <name>Henry, Christopher S</name>
      </author>
      <author>
        <name>Petzold, Christopher J</name>
        <uri>https://orcid.org/0000-0002-8270-5228</uri>
      </author>
      <author>
        <name>Stahl, David A</name>
      </author>
      <author>
        <name>Baliga, Nitin S</name>
      </author>
    </item>
    <item>
      <title>BioPortal: an open community resource for sharing, searching, and utilizing biomedical ontologies</title>
      <link>https://escholarship.org/uc/item/86s6g6wf</link>
      <description>BioPortal (https://bioportal.bioontology.org) is the world's most comprehensive repository of biomedical ontologies. It provides infrastructure for finding, sharing, searching, and utilizing biomedical ontologies. Launched in 2005, BioPortal now includes 1549 ontologies (1182 of them public). Its open, freely accessible website enables anyone (i) to browse the ontology library, (ii) to search for terms across ontologies, (iii) to browse mappings between terms, (iv) to see popularity ratings and recommendations on which ontologies are most relevant to their use cases, (v) to annotate text with ontology terms, (vi) to submit an ontology, and (vii) to request ontology changes. The library of ontologies can be accessed programmatically via a REST application programming interface (API). Recent enhancements include a BioPortal knowledge graph that integrates knowledge from multiple ontologies; a unified data model for interoperability with other knowledge sources; ontology popularity...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/86s6g6wf</guid>
      <pubDate>Tue, 3 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Vendetti, Jennifer</name>
      </author>
      <author>
        <name>Harris, Nomi L</name>
        <uri>https://orcid.org/0000-0001-6315-3707</uri>
      </author>
      <author>
        <name>Dorf, Michael V</name>
      </author>
      <author>
        <name>Skrenchuk, Alex</name>
      </author>
      <author>
        <name>Caufield, J Harry</name>
      </author>
      <author>
        <name>Gonçalves, Rafael S</name>
      </author>
      <author>
        <name>Graybeal, John B</name>
      </author>
      <author>
        <name>Hegde, Harshad</name>
      </author>
      <author>
        <name>Redmond, Timothy</name>
      </author>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
      <author>
        <name>Musen, Mark A</name>
      </author>
    </item>
    <item>
      <title>A change language for ontologies and knowledge graphs</title>
      <link>https://escholarship.org/uc/item/4mt2h97r</link>
      <description>Ontologies and knowledge graphs (KGs) are general-purpose computable representations of some domain, such as human anatomy, and are frequently a crucial part of modern information systems. Most of these structures change over time, incorporating new knowledge or information that was previously missing. Managing these changes is a challenge, both in terms of communicating changes to users and providing mechanisms to make it easier for multiple stakeholders to contribute. To fill that need, we have created KGCL, the Knowledge Graph Change Language (https://github.com/INCATools/kgcl), a standard data model for describing changes to KGs and ontologies at a high level, and an accompanying human-readable Controlled Natural Language (CNL). This language serves two purposes: a curator can use it to request desired changes, and it can also be used to describe changes that have already happened, corresponding to the concepts of "apply patch" and "diff" commonly used for managing changes...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4mt2h97r</guid>
      <pubDate>Tue, 3 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hegde, Harshad</name>
      </author>
      <author>
        <name>Vendetti, Jennifer</name>
      </author>
      <author>
        <name>Goutte-Gattat, Damien</name>
      </author>
      <author>
        <name>Caufield, J Harry</name>
      </author>
      <author>
        <name>Graybeal, John B</name>
      </author>
      <author>
        <name>Harris, Nomi L</name>
        <uri>https://orcid.org/0000-0001-6315-3707</uri>
      </author>
      <author>
        <name>Karam, Naouel</name>
      </author>
      <author>
        <name>Kindermann, Christian</name>
      </author>
      <author>
        <name>Matentzoglu, Nicolas</name>
      </author>
      <author>
        <name>Overton, James A</name>
      </author>
      <author>
        <name>Musen, Mark A</name>
      </author>
      <author>
        <name>Mungall, Christopher J</name>
      </author>
    </item>
    <item>
      <title>Atomic view of photosynthetic metabolite permeability pathways and confinement in synthetic carboxysome shells</title>
      <link>https://escholarship.org/uc/item/2mb5p1sq</link>
      <description>Carboxysomes are protein microcompartments found in cyanobacteria, whose shell encapsulates rubisco at the heart of carbon fixation in the Calvin cycle. Carboxysomes are thought to locally concentrate CO&lt;sub&gt;2&lt;/sub&gt; in the shell interior to improve rubisco efficiency through selective metabolite permeability, creating a concentrated catalytic center. However, permeability coefficients have not previously been determined for these gases, or for Calvin-cycle intermediates such as bicarbonate ([Formula: see text]), 3-phosphoglycerate, or ribulose-1,5-bisphosphate. Starting from a high-resolution cryogenic electron microscopy structure of a synthetic [Formula: see text]-carboxysome shell, we perform unbiased all-atom molecular dynamics to track metabolite permeability across the shell. The synthetic carboxysome shell structure, lacking the bacterial microcompartment trimer proteins and encapsulation peptides, is found to have similar permeability coefficients for multiple metabolites,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2mb5p1sq</guid>
      <pubDate>Thu, 15 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sarkar, Daipayan</name>
      </author>
      <author>
        <name>Maffeo, Christopher</name>
      </author>
      <author>
        <name>Sutter, Markus</name>
        <uri>https://orcid.org/0000-0001-6290-4820</uri>
      </author>
      <author>
        <name>Aksimentiev, Aleksei</name>
      </author>
      <author>
        <name>Kerfeld, Cheryl A</name>
        <uri>https://orcid.org/0000-0002-9977-8482</uri>
      </author>
      <author>
        <name>Vermaas, Josh V</name>
      </author>
    </item>
    <item>
      <title>Quantitative Measurement of Molecular Permeability to a Synthetic Bacterial Microcompartment Shell System</title>
      <link>https://escholarship.org/uc/item/5wr436pr</link>
      <description>Naturally evolved and synthetically designed forms of compartmentalization benefit encapsulated function by increasing local concentrations of substrates and protecting cargo from destabilizing environments and inhibitors. Crucial to understanding the fundamental principles of compartmentalization are experimental systems enabling the measurement of the permeability rates of small molecules. Here, we report the experimental measurement of the small-molecule permeability of a 40 nm icosahedral bacterial microcompartment shell. This was accomplished by heterologous loading of light-producing luciferase enzymes and kinetic measurement of luminescence using stopped-flow spectrophotometry. Compared to free enzyme, the luminescence signal kinetics was slower when the luciferase was encapsulated in bacterial microcompartment shells. The results indicate that substrates and products can still exchange across the shell, and modeling of the experimental data suggest that a 50× permeability...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5wr436pr</guid>
      <pubDate>Wed, 14 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Young, Eric J</name>
      </author>
      <author>
        <name>Kirst, Henning</name>
      </author>
      <author>
        <name>Dwyer, Matthew E</name>
      </author>
      <author>
        <name>Vermaas, Josh V</name>
      </author>
      <author>
        <name>Kerfeld, Cheryl A</name>
        <uri>https://orcid.org/0000-0002-9977-8482</uri>
      </author>
    </item>
    <item>
      <title>A polyketide-based biosynthetic platform for diols, amino alcohols and hydroxy acids</title>
      <link>https://escholarship.org/uc/item/6vt2q37t</link>
      <description>Medium- and branched-chain diols and amino alcohols are important industrial solvents, polymer building blocks, cosmetics and pharmaceutical ingredients, yet biosynthetically challenging to produce. Here we present an approach that uses a modular polyketide synthase (PKS) platform for the efficient production of these compounds. This platform takes advantage of a versatile loading module from the rimocidin PKS and nicotinamide adenine dinucleotide phosphate-dependent terminal thioester reductases. Reduction of the terminal aldehyde with alcohol dehydrogenases enables the production of diols, oxidation enables the production of hydroxy acids and specific transaminases allow the production of various amino alcohols. Furthermore, replacement of the malonyl-coenzyme A-specific acyltransferase in the extension module with methyl- or ethylmalonyl-coenzyme A-specific acyltransferase enables the production of branched-chain diols, amino alcohols and carboxylic acids in high titres. Use...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6vt2q37t</guid>
      <pubDate>Tue, 13 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Dan, Qingyun</name>
        <uri>https://orcid.org/0000-0002-3110-9450</uri>
      </author>
      <author>
        <name>Chiu, Yan</name>
      </author>
      <author>
        <name>Lee, Namil</name>
      </author>
      <author>
        <name>Pereira, Jose Henrique</name>
      </author>
      <author>
        <name>Rad, Behzad</name>
      </author>
      <author>
        <name>Zhao, Xixi</name>
      </author>
      <author>
        <name>Deng, Kai</name>
      </author>
      <author>
        <name>Rong, Yiou</name>
      </author>
      <author>
        <name>Zhan, Chunjun</name>
      </author>
      <author>
        <name>Chen, Yan</name>
      </author>
      <author>
        <name>Cheong, Seokjung</name>
      </author>
      <author>
        <name>Li, Chenyi</name>
        <uri>https://orcid.org/0000-0001-8294-1880</uri>
      </author>
      <author>
        <name>Gin, Jennifer W</name>
      </author>
      <author>
        <name>Rodrigues, Andria</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Backman, Tyler WH</name>
      </author>
      <author>
        <name>Baidoo, Edward EK</name>
        <uri>https://orcid.org/0000-0001-5787-1219</uri>
      </author>
      <author>
        <name>Petzold, Christopher J</name>
        <uri>https://orcid.org/0000-0002-8270-5228</uri>
      </author>
      <author>
        <name>Adams, Paul D</name>
        <uri>https://orcid.org/0000-0001-9333-8219</uri>
      </author>
      <author>
        <name>Keasling, Jay D</name>
        <uri>https://orcid.org/0000-0003-4170-6088</uri>
      </author>
    </item>
    <item>
      <title>Sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection</title>
      <link>https://escholarship.org/uc/item/10h0243m</link>
      <description>Many eukaryotic viruses require membrane-bound compartments for replication, but no such organelles are known to be formed by prokaryotic viruses. Bacteriophages of the Chimalliviridae family sequester their genomes within a phage-generated organelle, the phage nucleus, which is enclosed by a lattice of the viral protein ChmA. We show that inhibiting phage nucleus formation arrests infections at an early stage in which the injected phage genome is enclosed within a membrane-bound early phage infection (EPI) vesicle. Early phage genes are expressed from the EPI vesicle, demonstrating its functionality as a prokaryotic, transcriptionally active, membrane-bound organelle. We also show that the phage nucleus is essential, with genome replication beginning after the injected DNA is transferred from the EPI vesicle to the phage nucleus. Our results show that Chimalliviridae require two sophisticated subcellular compartments of distinct compositions and functions that facilitate successive...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/10h0243m</guid>
      <pubDate>Mon, 12 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Armbruster, Emily G</name>
      </author>
      <author>
        <name>Rani, Phoolwanti</name>
      </author>
      <author>
        <name>Lee, Jina</name>
      </author>
      <author>
        <name>Klusch, Niklas</name>
      </author>
      <author>
        <name>Hutchings, Joshua</name>
      </author>
      <author>
        <name>Hoffman, Lizbeth Y</name>
      </author>
      <author>
        <name>Buschkaemper, Hannah</name>
      </author>
      <author>
        <name>Enustun, Eray</name>
      </author>
      <author>
        <name>Adler, Benjamin A</name>
      </author>
      <author>
        <name>Inlow, Koe</name>
        <uri>https://orcid.org/0000-0002-2535-9613</uri>
      </author>
      <author>
        <name>VanderWal, Arica R</name>
      </author>
      <author>
        <name>Hoffman, Madelynn Y</name>
      </author>
      <author>
        <name>Daksh, Daksh</name>
      </author>
      <author>
        <name>Aindow, Ann</name>
      </author>
      <author>
        <name>Deep, Amar</name>
      </author>
      <author>
        <name>Rodriguez, Zaida K</name>
      </author>
      <author>
        <name>Morgan, Chase J</name>
      </author>
      <author>
        <name>Ghassemian, Majid</name>
        <uri>https://orcid.org/0000-0003-1026-5152</uri>
      </author>
      <author>
        <name>Laughlin, Thomas G</name>
      </author>
      <author>
        <name>Charles, Emeric</name>
      </author>
      <author>
        <name>Cress, Brady F</name>
        <uri>https://orcid.org/0000-0002-2948-2846</uri>
      </author>
      <author>
        <name>Savage, David F</name>
      </author>
      <author>
        <name>Doudna, Jennifer A</name>
      </author>
      <author>
        <name>Pogliano, Kit</name>
      </author>
      <author>
        <name>Corbett, Kevin D</name>
      </author>
      <author>
        <name>Villa, Elizabeth</name>
        <uri>https://orcid.org/0000-0003-4677-9809</uri>
      </author>
      <author>
        <name>Pogliano, Joe</name>
      </author>
    </item>
    <item>
      <title>Modest functional diversity decline and pronounced composition shifts of microbial communities in a mixed waste-contaminated aquifer</title>
      <link>https://escholarship.org/uc/item/99q6p52g</link>
      <description>BackgroundMicrobial taxonomic diversity declines with increased environmental stress. Yet, few studies have explored whether phylogenetic and functional diversities track taxonomic diversity along the stress gradient. Here, we investigated microbial communities within an aquifer in Oak Ridge, Tennessee, USA, which is characterized by a broad spectrum of stressors, including extremely high levels of nitrate, heavy metals like cadmium and chromium, radionuclides such as uranium, and extremely low pH (&amp;lt; 3).ResultsBoth taxonomic and phylogenetic α-diversities were reduced in the most impacted wells, while the decline in functional α-diversity was modest and statistically insignificant, indicating a more robust buffering capacity to environmental stress. Differences in functional gene composition (i.e., functional β-diversity) were pronounced in highly contaminated wells, while convergent functional gene composition was observed in uncontaminated wells. The relative abundances of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/99q6p52g</guid>
      <pubDate>Fri, 9 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Fan, Yupeng</name>
      </author>
      <author>
        <name>Wang, Dongyu</name>
      </author>
      <author>
        <name>Yang, Joy X</name>
      </author>
      <author>
        <name>Ning, Daliang</name>
      </author>
      <author>
        <name>He, Zhili</name>
      </author>
      <author>
        <name>Zhang, Ping</name>
      </author>
      <author>
        <name>Rocha, Andrea M</name>
      </author>
      <author>
        <name>Xiao, Naijia</name>
      </author>
      <author>
        <name>Michael, Jonathan P</name>
      </author>
      <author>
        <name>Walker, Katie F</name>
      </author>
      <author>
        <name>Joyner, Dominique C</name>
      </author>
      <author>
        <name>Pan, Chongle</name>
      </author>
      <author>
        <name>Adams, Michael WW</name>
      </author>
      <author>
        <name>Fields, Matthew W</name>
      </author>
      <author>
        <name>Alm, Eric J</name>
      </author>
      <author>
        <name>Stahl, David A</name>
      </author>
      <author>
        <name>Hazen, Terry C</name>
        <uri>https://orcid.org/0000-0002-2536-9993</uri>
      </author>
      <author>
        <name>Adams, Paul D</name>
        <uri>https://orcid.org/0000-0001-9333-8219</uri>
      </author>
      <author>
        <name>Arkin, Adam P</name>
        <uri>https://orcid.org/0000-0002-4999-2931</uri>
      </author>
      <author>
        <name>Zhou, Jizhong</name>
        <uri>https://orcid.org/0000-0003-2014-0564</uri>
      </author>
    </item>
    <item>
      <title>Global diversity and distribution of antibiotic resistance genes in human wastewater treatment systems</title>
      <link>https://escholarship.org/uc/item/3dr4w8r4</link>
      <description>Antibiotic resistance poses a significant threat to human health, and wastewater treatment plants (WWTPs) are important reservoirs of antibiotic resistance genes (ARGs). Here, we analyze the antibiotic resistomes of 226 activated sludge samples from 142 WWTPs across six continents, using a consistent pipeline for sample collection, DNA sequencing and analysis. We find that ARGs are diverse and similarly abundant, with a core set of 20 ARGs present in all WWTPs. ARG composition differs across continents and is distinct from that of the human gut and the oceans. ARG composition strongly correlates with bacterial taxonomic composition, with Chloroflexi, Acidobacteria and Deltaproteobacteria being the major carriers. ARG abundance positively correlates with the&amp;nbsp;presence of mobile genetic elements, and 57% of the 1112 recovered high-quality genomes possess putatively mobile ARGs. Resistome variations appear to be driven by a complex combination of stochastic processes and deterministic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3dr4w8r4</guid>
      <pubDate>Thu, 8 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhu, Congmin</name>
      </author>
      <author>
        <name>Wu, Linwei</name>
      </author>
      <author>
        <name>Ning, Daliang</name>
        <uri>https://orcid.org/0000-0002-3368-5988</uri>
      </author>
      <author>
        <name>Tian, Renmao</name>
      </author>
      <author>
        <name>Gao, Shuhong</name>
      </author>
      <author>
        <name>Zhang, Bing</name>
      </author>
      <author>
        <name>Zhao, Jianshu</name>
        <uri>https://orcid.org/0000-0002-2586-3852</uri>
      </author>
      <author>
        <name>Zhang, Ya</name>
      </author>
      <author>
        <name>Xiao, Naijia</name>
      </author>
      <author>
        <name>Wang, Yajiao</name>
      </author>
      <author>
        <name>Brown, Mathew R</name>
      </author>
      <author>
        <name>Tu, Qichao</name>
      </author>
      <author>
        <name>Ju, Feng</name>
      </author>
      <author>
        <name>Wells, George F</name>
      </author>
      <author>
        <name>Guo, Jianhua</name>
      </author>
      <author>
        <name>He, Zhili</name>
      </author>
      <author>
        <name>Nielsen, Per H</name>
      </author>
      <author>
        <name>Wang, Aijie</name>
      </author>
      <author>
        <name>Zhang, Yu</name>
      </author>
      <author>
        <name>Chen, Ting</name>
      </author>
      <author>
        <name>He, Qiang</name>
      </author>
      <author>
        <name>Criddle, Craig S</name>
      </author>
      <author>
        <name>Wagner, Michael</name>
      </author>
      <author>
        <name>Tiedje, James M</name>
      </author>
      <author>
        <name>Curtis, Thomas P</name>
      </author>
      <author>
        <name>Wen, Xianghua</name>
      </author>
      <author>
        <name>Yang, Yunfeng</name>
      </author>
      <author>
        <name>Alvarez-Cohen, Lisa</name>
      </author>
      <author>
        <name>Stahl, David A</name>
      </author>
      <author>
        <name>Alvarez, Pedro JJ</name>
      </author>
      <author>
        <name>Rittmann, Bruce E</name>
      </author>
      <author>
        <name>Zhou, Jizhong</name>
        <uri>https://orcid.org/0000-0003-2014-0564</uri>
      </author>
    </item>
    <item>
      <title>Editorial: Transcriptional and epigenetic landscapes of abiotic stress response in plants</title>
      <link>https://escholarship.org/uc/item/7541f075</link>
      <description>Editorial: Transcriptional and epigenetic landscapes of abiotic stress response in plants</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7541f075</guid>
      <pubDate>Thu, 1 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Khan, Aamir W</name>
      </author>
      <author>
        <name>Ding, Yezhang</name>
        <uri>https://orcid.org/0000-0001-5903-1870</uri>
      </author>
      <author>
        <name>Muthamilarasan, Mehanathan</name>
      </author>
    </item>
  </channel>
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