<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Joshi GS</submitter><funding>NIAID NIH HHS</funding><pagination>9-20</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3183340</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>82(1)</volume><pubmed_abstract>Polyamines, including spermine (Spm) and spermidine (Spd), are aliphatic cations that are reportedly synthesized by all living organisms. They exert pleiotropic effects on cells and are required for efficient nucleic acid and protein synthesis. Here, we report that the human pathogen Staphylococcus aureus lacks identifiable polyamine biosynthetic genes, and consequently produces no Spm/Spd or their precursor compounds putrescine and agmatine. Moreover, while supplementing defined medium with polyamines generally enhances bacterial growth, Spm and Spd exert bactericidal effects on S. aureus at physiological concentrations. Small colony variants specifically lacking menaquinone biosynthesis arose after prolonged Spm exposure and exhibited reduced polyamine sensitivity. However, other respira</pubmed_abstract><journal>Molecular microbiology</journal><pubmed_title>Arginine catabolic mobile element encoded speG abrogates the unique hypersensitivity of Staphylococcus aureus to exogenous polyamines.</pubmed_title><pmcid>PMC3183340</pmcid><funding_grant_id>R21 AI088158</funding_grant_id><funding_grant_id>AI088158</funding_grant_id><funding_grant_id>R21 AI088158-01</funding_grant_id><funding_grant_id>R21 AI088158-02</funding_grant_id><pubmed_authors>Klapper DG</pubmed_authors><pubmed_authors>Joshi GS</pubmed_authors><pubmed_authors>Spontak JS</pubmed_authors><pubmed_authors>Richardson AR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Arginine catabolic mobile element encoded speG abrogates the unique hypersensitivity of Staphylococcus aureus to exogenous polyamines.</name><description>Polyamines, including spermine (Spm) and spermidine (Spd), are aliphatic cations that are reportedly synthesized by all living organisms. They exert pleiotropic effects on cells and are required for efficient nucleic acid and protein synthesis. Here, we report that the human pathogen Staphylococcus aureus lacks identifiable polyamine biosynthetic genes, and consequently produces no Spm/Spd or their precursor compounds putrescine and agmatine. Moreover, while supplementing defined medium with polyamines generally enhances bacterial growth, Spm and Spd exert bactericidal effects on S. aureus at physiological concentrations. Small colony variants specifically lacking menaquinone biosynthesis arose after prolonged Spm exposure and exhibited reduced polyamine sensitivity. However, other respira</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Oct</publication><modification>2025-04-04T20:45:30.451Z</modification><creation>2019-03-27T00:44:28Z</creation></dates><accession>S-EPMC3183340</accession><cross_references><pubmed>21902734</pubmed><doi>10.1111/j.1365-2958.2011.07809.x</doi></cross_references></HashMap>