Genome mining for radical SAM protein determinants reveals multiple sactibiotic-like gene clusters.

Thuricin CD is a two-component bacteriocin produced by Bacillus thuringiensis that kills a wide range of clinically significant Clostridium difficile. This bacteriocin has recently been characterized and consists of two distinct peptides, Trnβ and Trnα, which both possess 3 intrapeptide sulphur to α...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Kiera Murphy, Orla O'Sullivan, Mary C Rea, Paul D Cotter, R Paul Ross, Colin Hill
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2011
Materias:
R
Q
Acceso en línea:https://doaj.org/article/e17376b224fe43bd89bf9b6b355bb21b
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:e17376b224fe43bd89bf9b6b355bb21b
record_format dspace
spelling oai:doaj.org-article:e17376b224fe43bd89bf9b6b355bb21b2021-11-18T06:50:34ZGenome mining for radical SAM protein determinants reveals multiple sactibiotic-like gene clusters.1932-620310.1371/journal.pone.0020852https://doaj.org/article/e17376b224fe43bd89bf9b6b355bb21b2011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21760885/?tool=EBIhttps://doaj.org/toc/1932-6203Thuricin CD is a two-component bacteriocin produced by Bacillus thuringiensis that kills a wide range of clinically significant Clostridium difficile. This bacteriocin has recently been characterized and consists of two distinct peptides, Trnβ and Trnα, which both possess 3 intrapeptide sulphur to α-carbon bridges and act synergistically. Indeed, thuricin CD and subtilosin A are the only antimicrobials known to possess these unusual structures and are known as the sactibiotics (sulplur to alpha carbon-containing antibiotics). Analysis of the thuricin CD-associated gene cluster revealed the presence of genes encoding two highly unusual SAM proteins (TrnC and TrnD) which are proposed to be responsible for these unusual post-translational modifications. On the basis of the frequently high conservation among enzymes responsible for the post-translational modification of specific antimicrobials, we performed an in silico screen for novel thuricin CD-like gene clusters using the TrnC and TrnD radical SAM proteins as driver sequences to perform an initial homology search against the complete non-redundant database. Fifteen novel thuricin CD-like gene clusters were identified, based on the presence of TrnC and TrnD homologues in the context of neighbouring genes encoding potential bacteriocin structural peptides. Moreover, metagenomic analysis revealed that TrnC or TrnD homologs are present in a variety of metagenomic environments, suggesting a widespread distribution of thuricin-like operons in a variety of environments. In-silico analysis of radical SAM proteins is sufficient to identify novel putative sactibiotic clusters.Kiera MurphyOrla O'SullivanMary C ReaPaul D CotterR Paul RossColin HillPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 7, p e20852 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Kiera Murphy
Orla O'Sullivan
Mary C Rea
Paul D Cotter
R Paul Ross
Colin Hill
Genome mining for radical SAM protein determinants reveals multiple sactibiotic-like gene clusters.
description Thuricin CD is a two-component bacteriocin produced by Bacillus thuringiensis that kills a wide range of clinically significant Clostridium difficile. This bacteriocin has recently been characterized and consists of two distinct peptides, Trnβ and Trnα, which both possess 3 intrapeptide sulphur to α-carbon bridges and act synergistically. Indeed, thuricin CD and subtilosin A are the only antimicrobials known to possess these unusual structures and are known as the sactibiotics (sulplur to alpha carbon-containing antibiotics). Analysis of the thuricin CD-associated gene cluster revealed the presence of genes encoding two highly unusual SAM proteins (TrnC and TrnD) which are proposed to be responsible for these unusual post-translational modifications. On the basis of the frequently high conservation among enzymes responsible for the post-translational modification of specific antimicrobials, we performed an in silico screen for novel thuricin CD-like gene clusters using the TrnC and TrnD radical SAM proteins as driver sequences to perform an initial homology search against the complete non-redundant database. Fifteen novel thuricin CD-like gene clusters were identified, based on the presence of TrnC and TrnD homologues in the context of neighbouring genes encoding potential bacteriocin structural peptides. Moreover, metagenomic analysis revealed that TrnC or TrnD homologs are present in a variety of metagenomic environments, suggesting a widespread distribution of thuricin-like operons in a variety of environments. In-silico analysis of radical SAM proteins is sufficient to identify novel putative sactibiotic clusters.
format article
author Kiera Murphy
Orla O'Sullivan
Mary C Rea
Paul D Cotter
R Paul Ross
Colin Hill
author_facet Kiera Murphy
Orla O'Sullivan
Mary C Rea
Paul D Cotter
R Paul Ross
Colin Hill
author_sort Kiera Murphy
title Genome mining for radical SAM protein determinants reveals multiple sactibiotic-like gene clusters.
title_short Genome mining for radical SAM protein determinants reveals multiple sactibiotic-like gene clusters.
title_full Genome mining for radical SAM protein determinants reveals multiple sactibiotic-like gene clusters.
title_fullStr Genome mining for radical SAM protein determinants reveals multiple sactibiotic-like gene clusters.
title_full_unstemmed Genome mining for radical SAM protein determinants reveals multiple sactibiotic-like gene clusters.
title_sort genome mining for radical sam protein determinants reveals multiple sactibiotic-like gene clusters.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/e17376b224fe43bd89bf9b6b355bb21b
work_keys_str_mv AT kieramurphy genomeminingforradicalsamproteindeterminantsrevealsmultiplesactibioticlikegeneclusters
AT orlaosullivan genomeminingforradicalsamproteindeterminantsrevealsmultiplesactibioticlikegeneclusters
AT marycrea genomeminingforradicalsamproteindeterminantsrevealsmultiplesactibioticlikegeneclusters
AT pauldcotter genomeminingforradicalsamproteindeterminantsrevealsmultiplesactibioticlikegeneclusters
AT rpaulross genomeminingforradicalsamproteindeterminantsrevealsmultiplesactibioticlikegeneclusters
AT colinhill genomeminingforradicalsamproteindeterminantsrevealsmultiplesactibioticlikegeneclusters
_version_ 1718424325447483392