TY  - JOUR
  - Murphy, K,O'Sullivan, O,Rea, MC,Cotter, PD,Ross, RP,Hill, C
  - 2011
  - January
  - Plos One
  - Genome Mining for Radical SAM Protein Determinants Reveals Multiple Sactibiotic-Like Gene Clusters
  - Validated
  - ()
  - LACTIC-ACID BACTERIA CLOSTRIDIUM-DIFFICILE BACILLUS-SUBTILIS ANAEROBIC BACTERIUM NARROW-SPECTRUM SP-NOV IDENTIFICATION SEQUENCE METHYLTRANSFERASE BIOSYNTHESIS
  - 6
  - 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, Trn beta and Trn alpha, which both possess 3 intrapeptide sulphur to alpha-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.
  - ARTN e20852
DA  - 2011/01
ER  - 

@article{V160748541,
   = {Murphy,  K and O'Sullivan,  O and Rea,  MC and Cotter,  PD and Ross,  RP and Hill,  C },
   = {2011},
   = {January},
   = {Plos One},
   = {Genome Mining for Radical SAM Protein Determinants Reveals Multiple Sactibiotic-Like Gene Clusters},
   = {Validated},
   = {()},
   = {LACTIC-ACID BACTERIA CLOSTRIDIUM-DIFFICILE BACILLUS-SUBTILIS ANAEROBIC BACTERIUM NARROW-SPECTRUM SP-NOV IDENTIFICATION SEQUENCE METHYLTRANSFERASE BIOSYNTHESIS},
   = {6},
   = {{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, Trn beta and Trn alpha, which both possess 3 intrapeptide sulphur to alpha-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.}},
   = {ARTN e20852},
  source = {IRIS}
}