<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Franklin DS</submitter><funding>NIDCR NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>HHS | NIH | National Institute of Dental and Craniofacial Research (NIDCR)</funding><funding>HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID)</funding><pagination>e0340524</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11796344</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(2)</volume><pubmed_abstract>Many bacteria metabolize ethanolamine as a nutrient source through cytoplasmic organelles named bacterial microcompartments (BMCs). Here we investigated the molecular assembly, regulation, and function of BMCs in &lt;i>Fusobacterium nucleatum-&lt;/i>a Gram-negative oral pathobiont that is associated with adverse pregnancy outcomes. The &lt;i>F. nucleatum&lt;/i> genome harbors a conserved ethanolamine utilization (&lt;i>eut&lt;/i>) locus with 21 genes that encode several putative BMC shell proteins and a two-component signal transduction system (TCS), in addition to the enzymes for ethanolamine transport and catabolism. We show that the expression of most of these genes and BMC formation are highly increased in wild-type fusobacteria when cultured in the presence of ethanolamine as a nutrient source. Deletio</pubmed_abstract><journal>mBio</journal><pubmed_title>Ethanolamine-induced assembly of microcompartments is required for &amp;lt;i&amp;gt;Fusobacterium nucleatum&amp;lt;/i&amp;gt; virulence.</pubmed_title><pmcid>PMC11796344</pmcid><funding_grant_id>R01 DE026758</funding_grant_id><funding_grant_id>T90DE030860</funding_grant_id><funding_grant_id>R21 DE032906</funding_grant_id><funding_grant_id>T32AI007323</funding_grant_id><funding_grant_id>T32 AI007323</funding_grant_id><funding_grant_id>DE032906, DE026758</funding_grant_id><funding_grant_id>T90 DE030860</funding_grant_id><pubmed_authors>Zhou ZH</pubmed_authors><pubmed_authors>Ton-That H</pubmed_authors><pubmed_authors>Wittchen M</pubmed_authors><pubmed_authors>Luu A</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Whitelegge JP</pubmed_authors><pubmed_authors>Das A</pubmed_authors><pubmed_authors>Franklin DS</pubmed_authors><pubmed_authors>Agnew A</pubmed_authors><pubmed_authors>Tauch A</pubmed_authors><pubmed_authors>Chen Y-W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ethanolamine-induced assembly of microcompartments is required for &amp;lt;i&amp;gt;Fusobacterium nucleatum&amp;lt;/i&amp;gt; virulence.</name><description>Many bacteria metabolize ethanolamine as a nutrient source through cytoplasmic organelles named bacterial microcompartments (BMCs). Here we investigated the molecular assembly, regulation, and function of BMCs in &lt;i>Fusobacterium nucleatum-&lt;/i>a Gram-negative oral pathobiont that is associated with adverse pregnancy outcomes. The &lt;i>F. nucleatum&lt;/i> genome harbors a conserved ethanolamine utilization (&lt;i>eut&lt;/i>) locus with 21 genes that encode several putative BMC shell proteins and a two-component signal transduction system (TCS), in addition to the enzymes for ethanolamine transport and catabolism. We show that the expression of most of these genes and BMC formation are highly increased in wild-type fusobacteria when cultured in the presence of ethanolamine as a nutrient source. Deletio</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-26T01:36:44.682Z</modification><creation>2025-04-06T10:15:11.133Z</creation></dates><accession>S-EPMC11796344</accession><cross_references><pubmed>39714188</pubmed><doi>10.1128/mbio.03405-24</doi></cross_references></HashMap>