<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sugrue I</submitter><funding>Science Foundation Ireland</funding><pagination>e00529-19</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6989792</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>202(4)</volume><pubmed_abstract>We identified a strain of Actinomyces ruminicola which produces a potent bacteriocin with activity against a broad range of Gram-positive bacteria, many of which are pathogenic to animals and humans. The bacteriocin was purified and found to have a mass of 4,091 ± 1 Da with a sequence of GFGCNLITSNPYQCSNHCKSVGYRGGYCKLRTVCTCY containing three disulfide bridges. Surprisingly, near relatives of actifensin were found to be a series of related eukaryotic defensins displaying greater than 50% identity to the bacteriocin. A pangenomic screen further revealed that production of actifensin-related bacteriocins is a common trait within the genus, with 47 being encoded in 161 genomes. Furthermore, these bacteriocins displayed a remarkable level of diversity with a mean amino acid identity of only 52%</pubmed_abstract><journal>Journal of bacteriology</journal><pubmed_title>Actinomyces Produces Defensin-Like Bacteriocins (Actifensins) with a Highly Degenerate Structure and Broad Antimicrobial Activity.</pubmed_title><pmcid>PMC6989792</pmcid><funding_grant_id>SFI/12/RC/2273</funding_grant_id><pubmed_authors>Hill C</pubmed_authors><pubmed_authors>Ross RP</pubmed_authors><pubmed_authors>O'Connor PM</pubmed_authors><pubmed_authors>Stanton C</pubmed_authors><pubmed_authors>Sugrue I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Actinomyces Produces Defensin-Like Bacteriocins (Actifensins) with a Highly Degenerate Structure and Broad Antimicrobial Activity.</name><description>We identified a strain of Actinomyces ruminicola which produces a potent bacteriocin with activity against a broad range of Gram-positive bacteria, many of which are pathogenic to animals and humans. The bacteriocin was purified and found to have a mass of 4,091 ± 1 Da with a sequence of GFGCNLITSNPYQCSNHCKSVGYRGGYCKLRTVCTCY containing three disulfide bridges. Surprisingly, near relatives of actifensin were found to be a series of related eukaryotic defensins displaying greater than 50% identity to the bacteriocin. A pangenomic screen further revealed that production of actifensin-related bacteriocins is a common trait within the genus, with 47 being encoded in 161 genomes. Furthermore, these bacteriocins displayed a remarkable level of diversity with a mean amino acid identity of only 52%</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2025-05-18T11:47:29.175Z</modification><creation>2025-05-18T11:47:29.175Z</creation></dates><accession>S-EPMC6989792</accession><cross_references><pubmed>31767775</pubmed><doi>10.1128/JB.00529-19</doi></cross_references></HashMap>