<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Taylor ZA</submitter><funding>NIDCR NIH HHS</funding><funding>HHS | NIH | National Institute of Dental and Craniofacial Research (NIDCR)</funding><funding>HHS | NIH | National Institute of Dental and Craniofacial Research</funding><pagination>e0193524</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11784104</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>91(1)</volume><pubmed_abstract>Previous work reported that deletion of the Enzyme IIAB subunits (EIIAB&lt;sup>Man&lt;/sup> and &lt;i>manL&lt;/i>) of the glucose phosphotransferase system (PTS) (glucose-PTS, &lt;i>manLMNO&lt;/i>) in &lt;i>Streptococcus sanguinis&lt;/i> impacted carbon catabolite repression and bacterial fitness. Here, a single-nucleotide polymorphism in ManN, ManNA91E, produced the unusual phenotype of increased excretion of organic acids and H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> yet elevated PTS activities. To characterize the contributions of each component of the glucose-PTS to bacterial fitness, we performed genetic analyses by deleting from &lt;i>S. sanguinis&lt;/i> SK36 the entire operon and each EII&lt;sup>Man&lt;/sup> subunit individually; and genes encoding the catabolite control protein A (Δ&lt;i>ccpA&lt;/i>) and the redox regulator Rex (Δ&lt;i>rex&lt;</pubmed_abstract><journal>Applied and environmental microbiology</journal><pubmed_title>Systematic analysis of the glucose-PTS in &amp;lt;i&amp;gt;Streptococcus sanguinis&amp;lt;/i&amp;gt; highlighted its importance in central metabolism and bacterial fitness.</pubmed_title><pmcid>PMC11784104</pmcid><funding_grant_id>T90 DE021990</funding_grant_id><funding_grant_id>DE12236</funding_grant_id><funding_grant_id>R01 DE012236</funding_grant_id><pubmed_authors>Taylor ZA</pubmed_authors><pubmed_authors>Pham DN</pubmed_authors><pubmed_authors>Zeng L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Systematic analysis of the glucose-PTS in &amp;lt;i&amp;gt;Streptococcus sanguinis&amp;lt;/i&amp;gt; highlighted its importance in central metabolism and bacterial fitness.</name><description>Previous work reported that deletion of the Enzyme IIAB subunits (EIIAB&lt;sup>Man&lt;/sup> and &lt;i>manL&lt;/i>) of the glucose phosphotransferase system (PTS) (glucose-PTS, &lt;i>manLMNO&lt;/i>) in &lt;i>Streptococcus sanguinis&lt;/i> impacted carbon catabolite repression and bacterial fitness. Here, a single-nucleotide polymorphism in ManN, ManNA91E, produced the unusual phenotype of increased excretion of organic acids and H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> yet elevated PTS activities. To characterize the contributions of each component of the glucose-PTS to bacterial fitness, we performed genetic analyses by deleting from &lt;i>S. sanguinis&lt;/i> SK36 the entire operon and each EII&lt;sup>Man&lt;/sup> subunit individually; and genes encoding the catabolite control protein A (Δ&lt;i>ccpA&lt;/i>) and the redox regulator Rex (Δ&lt;i>rex&lt;</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2025-04-18T16:49:52.893Z</modification><creation>2025-04-07T04:15:44.295Z</creation></dates><accession>S-EPMC11784104</accession><cross_references><pubmed>39584828</pubmed><doi>10.1128/aem.01935-24</doi></cross_references></HashMap>