Improved Lanthipeptide Detection and Prediction for antiSMASH

Lanthipeptides are a class of ribosomally synthesised and post-translationally modified peptide (RiPP) natural products from the bacterial secondary metabolism. Their name is derived from the characteristic lanthionine or methyl-lanthionine residues contained in the processed peptide. Lanthipeptides that possess an antibacterial activity are called lantibiotics. Whereas multiple tools exist to identify lanthipeptide gene clusters from genomic data, no programs are available to predict the post-translational modifications of lanthipeptides, such as the proteolytic cleavage of the leader peptide part or tailoring modifications based on the analysis of the gene cluster sequence. antiSMASH is a software pipeline for the identification of secondary metabolite biosynthetic clusters from genomic input and the prediction of products produced by the identified clusters. Here we present a novel antiSMASH module using a rule-based approach to combine signature motifs for biosynthetic enzymes and lanthipeptide-specific cleavage site motifs to identify lanthipeptide clusters in genomic data, assign the specific lanthipeptide class, predict prepeptide cleavage, tailoring reactions, and the processed molecular weight of the mature peptide products.

[1]  M. Bibb,et al.  The antibiotic planosporicin coordinates its own production in the actinomycete Planomonospora alba , 2013, Proceedings of the National Academy of Sciences.

[2]  Kai Blin,et al.  antiSMASH 2.0—a versatile platform for genome mining of secondary metabolite producers , 2013, Nucleic Acids Res..

[3]  Oscar P. Kuipers,et al.  BAGEL3: automated identification of genes encoding bacteriocins and (non-)bactericidal posttranslationally modified peptides , 2013, Nucleic Acids Res..

[4]  M. Wilcox,et al.  Evaluation of NVB302 versus vancomycin activity in an in vitro human gut model of Clostridium difficile infection. , 2013, The Journal of antimicrobial chemotherapy.

[5]  P. G. Arnison,et al.  Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature. , 2013, Natural product reports.

[6]  W. Neupert A mitochondrial odyssey. , 2012, Annual review of biochemistry.

[7]  W. A. van der Donk,et al.  Discovery, biosynthesis, and engineering of lantipeptides. , 2012, Annual review of biochemistry.

[8]  Neha Garg,et al.  Lantibiotics from Geobacillus thermodenitrificans , 2012, Proceedings of the National Academy of Sciences.

[9]  D. Brede,et al.  Salivaricin D, a Novel Intrinsically Trypsin-Resistant Lantibiotic from Streptococcus salivarius 5M6c Isolated from a Healthy Infant , 2011, Applied and Environmental Microbiology.

[10]  W. A. van der Donk,et al.  Biosynthesis of the antimicrobial peptide epilancin 15X and its N-terminal lactate. , 2011, Chemistry & biology.

[11]  H. Sahl,et al.  Expression of the Lantibiotic Mersacidin in Bacillus amyloliquefaciens FZB42 , 2011, PloS one.

[12]  Kai Blin,et al.  antiSMASH: rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences , 2011, Nucleic Acids Res..

[13]  J. Vederas,et al.  Biosynthesis of aminovinyl-cysteine-containing peptides and its application in the production of potential drug candidates. , 2011, Accounts of chemical research.

[14]  K. Entian,et al.  Entianin, a Novel Subtilin-Like Lantibiotic from Bacillus subtilis subsp. spizizenii DSM 15029T with High Antimicrobial Activity , 2011, Applied and Environmental Microbiology.

[15]  R. Rink,et al.  Requirements of the Engineered Leader Peptide of Nisin for Inducing Modification, Export, and Cleavage , 2010, Applied and Environmental Microbiology.

[16]  M. Bibb,et al.  Microbisporicin gene cluster reveals unusual features of lantibiotic biosynthesis in actinomycetes , 2010, Proceedings of the National Academy of Sciences.

[17]  H. Sahl,et al.  Production of the Novel Two-Peptide Lantibiotic Lichenicidin by Bacillus licheniformis DSM 13 , 2009, PloS one.

[18]  B. Rudd,et al.  Organization of the genes encoding the biosynthesis of actagardine and engineering of a variant generation system , 2009, Molecular microbiology.

[19]  Y. Seto,et al.  A unique lantibiotic, thermophilin 1277, containing a disulfide bridge and two thioether bridges , 2009, Journal of applied microbiology.

[20]  E. Birney,et al.  Pfam: the protein families database , 2013, Nucleic Acids Res..

[21]  F. Castiglione,et al.  Determining the structure and mode of action of microbisporicin, a potent lantibiotic active against multiresistant pathogens. , 2008, Chemistry & biology.

[22]  J. Tagg,et al.  Salivaricin A2 and the Novel Lantibiotic Salivaricin B Are Encoded at Adjacent Loci on a 190-Kilobase Transmissible Megaplasmid in the Oral Probiotic Strain Streptococcus salivarius K12 , 2006, Applied and Environmental Microbiology.

[23]  V. Eijsink,et al.  Purification, Characterization, and Gene Sequence of Michiganin A, an Actagardine-Like Lantibiotic Produced by the Tomato Pathogen Clavibacter michiganensis subsp. michiganensis , 2006, Applied and Environmental Microbiology.

[24]  C. J. Moore,et al.  Production of the Lantibiotic Salivaricin A and Its Variants by Oral Streptococci and Use of a Specific Induction Assay To Detect Their Presence in Human Saliva , 2006, Applied and Environmental Microbiology.

[25]  UbnIdownRev,et al.  Molecular and Genetic Characterization of a Novel Nisin Variant Produced by Streptococcus uberis , 2006 .

[26]  J. Tagg,et al.  Purification and Characterization of Streptin, a Type A1 Lantibiotic Produced by Streptococcus pyogenes , 2003, Applied and Environmental Microbiology.

[27]  M. Gasson,et al.  Cloning and engineering of the cinnamycin biosynthetic gene cluster from Streptomyces cinnamoneus cinnamoneus DSM 40005 , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[28]  J. Nakayama,et al.  Identification of the Lantibiotic Nisin Q, a New Natural Nisin Variant Produced by Lactococcus lactis 61-14 Isolated from a River in Japan , 2003, Bioscience, biotechnology, and biochemistry.

[29]  G. Bierbaum,et al.  Biosynthesis of the Lantibiotic Mersacidin: Organization of a Type B Lantibiotic Gene Cluster , 2000, Applied and Environmental Microbiology.

[30]  H. Sahl,et al.  Extensive Post-translational Modification, Including Serine to d-Alanine Conversion, in the Two-component Lantibiotic, Lacticin 3147* , 1999, The Journal of Biological Chemistry.

[31]  J. Ferretti,et al.  Nucleotide sequence of the streptococcin A-FF22 lantibiotic regulon: model for production of the lantibiotic SA-FF22 by strains of Streptococcus pyogenes. , 1999, FEMS microbiology letters.

[32]  H. Sahl,et al.  Isolation, Characterization, and Heterologous Expression of the Novel Lantibiotic Epicidin 280 and Analysis of Its Biosynthetic Gene Cluster , 1998, Applied and Environmental Microbiology.

[33]  Sean R. Eddy,et al.  Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids , 1998 .

[34]  E. J. Miller,et al.  Isolation and biochemical characterization of a novel lantibiotic mutacin from Streptococcus mutans , 1994, Journal of bacteriology.

[35]  J. Tagg,et al.  Cloning of the gene encoding Streptococcin A-FF22, a novel lantibiotic produced by Streptococcus pyogenes, and determination of its nucleotide sequence , 1993, Applied and environmental microbiology.

[36]  K. Entian,et al.  Gallidermin: a new lanthionine-containing polypeptide antibiotic. , 1988, European journal of biochemistry.