Characterization of the ‘pristinamycin supercluster’ of Streptomyces pristinaespiralis

Pristinamycin, produced by Streptomyces pristinaespiralis Pr11, is a streptogramin antibiotic consisting of two chemically unrelated compounds, pristinamycin I and pristinamycin II. The semi‐synthetic derivatives of these compounds are used in human medicine as therapeutic agents against methicillin‐resistant Staphylococcus aureus strains. Only the partial sequence of the pristinamycin biosynthetic gene cluster has been previously reported. To complete the sequence, overlapping cosmids were isolated from a S. pristinaespiralis Pr11 gene library and sequenced. The boundaries of the cluster were deduced, limiting the cluster size to approximately 210 kb. In the central region of the cluster, previously unknown pristinamycin biosynthetic genes were identified. Combining the current and previously identified sequence information, we propose that all essential pristinamycin biosynthetic genes are included in the 210 kb region. A pristinamycin biosynthetic pathway was established. Furthermore, the pristinamycin gene cluster was found to be interspersed by a cryptic secondary metabolite cluster, which probably codes for a glycosylated aromatic polyketide. Gene inactivation experiments revealed that this cluster has no influence on pristinamycin production. Overall, this work provides new insights into pristinamycin biosynthesis and the unique genetic organization of the pristinamycin gene region, which is the largest antibiotic ‘supercluster’ known so far.

[1]  C. Thompson,et al.  Pleiotropic Functions of a Streptomyces pristinaespiralis Autoregulator Receptor in Development, Antibiotic Biosynthesis, and Expression of a Superoxide Dismutase* , 2001, The Journal of Biological Chemistry.

[2]  J R Roth,et al.  Selfish operons: horizontal transfer may drive the evolution of gene clusters. , 1996, Genetics.

[3]  Daniel H. Huson,et al.  Dendroscope: An interactive viewer for large phylogenetic trees , 2007, BMC Bioinformatics.

[4]  F. Lombó,et al.  The Mithramycin Gene Cluster of Streptomyces argillaceus Contains a Positive Regulatory Gene and Two Repeated DNA Sequences That Are Located at Both Ends of the Cluster , 1999, Journal of bacteriology.

[5]  T. Nihira,et al.  Identification of the varR Gene as a Transcriptional Regulator of Virginiamycin S Resistance inStreptomyces virginiae , 2001, Journal of bacteriology.

[6]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[7]  K. Ishida,et al.  Orchestration of discoid polyketide cyclization in the resistomycin pathway. , 2008, Journal of the American Chemical Society.

[8]  B. Shen,et al.  Type I polyketide synthase requiring a discrete acyltransferase for polyketide biosynthesis , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[9]  W. Bullock XL1-Blue: a high efficiency plasmid transforming recA Escherichia coli strain with beta-galactosidase selection. , 1987 .

[10]  G. Talbot,et al.  Successful administration of quinupristin/dalfopristin in the outpatient setting. , 2001, The Journal of antimicrobial chemotherapy.

[11]  Christopher T. Walsh,et al.  The evolution of gene collectives: How natural selection drives chemical innovation , 2008, Proceedings of the National Academy of Sciences.

[12]  T. Weber,et al.  Molecular analysis of the kirromycin biosynthetic gene cluster revealed beta-alanine as precursor of the pyridone moiety. , 2008, Chemistry & biology.

[13]  P. Leadlay,et al.  Role of type II thioesterases: evidence for removal of short acyl chains produced by aberrant decarboxylation of chain extender units. , 2001, Chemistry & biology.

[14]  W. Wohlleben,et al.  Cloning and analysis of a peptide synthetase gene of the balhimycin producer Amycolatopsis mediterranei DSM5908 and development of a gene disruption/replacement system. , 1997, Journal of biotechnology.

[15]  S. Kitani,et al.  Characterization of biosynthetic gene cluster for the production of virginiamycin M, a streptogramin type A antibiotic, in Streptomyces virginiae. , 2007, Gene.

[16]  Hans-Peter Fiedler,et al.  Biosynthetic Capacities of Actinomycetes. 1 Screening for Secondary Metabolites by HPLC and UV-Visible Absorbance Spectral Libraries , 1993 .

[17]  Robert C. Edgar,et al.  MUSCLE: a multiple sequence alignment method with reduced time and space complexity , 2004, BMC Bioinformatics.

[18]  J. Martín,et al.  CcaR Is an Autoregulatory Protein That Binds to the ccaR and cefD-cmcI Promoters of the Cephamycin C-Clavulanic Acid Cluster in Streptomyces clavuligerus , 2002, Journal of bacteriology.

[19]  L. Debussche,et al.  Purification of peptide synthetases involved in pristinamycin I biosynthesis , 1997, Journal of bacteriology.

[20]  K. Hiratsu,et al.  The large linear plasmid pSLA2‐L of Streptomyces rochei has an unusually condensed gene organization for secondary metabolism , 2003, Molecular microbiology.

[21]  J. Crouzet,et al.  Cluster organization of the genes of Streptomyces pristinaespiralis involved in pristinamycin biosynthesis and resistance elucidated by pulsed‐field gel electrophoresis , 1999, Journal of applied microbiology.

[22]  T. Kieser Practical streptomyces genetics , 2000 .

[23]  J. Walton,et al.  Horizontal gene transfer and the evolution of secondary metabolite gene clusters in fungi: an hypothesis. , 2000, Fungal genetics and biology : FG & B.

[24]  E. Myers,et al.  Basic local alignment search tool. , 1990, Journal of molecular biology.

[25]  K. O'Brien,et al.  Plasmid cloning vectors for the conjugal transfer of DNA from Escherichia coli to Streptomyces spp. , 1992, Gene.

[26]  P. Wipf,et al.  Metamorphic enzyme assembly in polyketide diversification , 2009, Nature.

[27]  Daniel H. Huson,et al.  SplitsTree: analyzing and visualizing evolutionary data , 1998, Bioinform..

[28]  J. Crouzet,et al.  Cloning and analysis of structural genes from Streptomyces pristinaespiralis encoding enzymes involved in the conversion of pristinamycin IIB to pristinamycin IIA (PIIA): PIIA synthase and NADH:riboflavin 5'-phosphate oxidoreductase , 1995, Journal of bacteriology.

[29]  L. Debussche,et al.  Purification of the two-enzyme system catalyzing the oxidation of the D-proline residue of pristinamycin IIB during the last step of pristinamycin IIA biosynthesis , 1995, Journal of bacteriology.

[30]  J. Suh,et al.  Widespread activation of antibiotic biosynthesis by S-adenosylmethionine in streptomycetes. , 2004, FEMS microbiology letters.

[31]  W. Saurin,et al.  Streptogramin B biosynthesis in Streptomyces pristinaespiralis and Streptomyces virginiae: molecular characterization of the last structural peptide synthetase gene , 1997, Antimicrobial agents and chemotherapy.

[32]  Kim Rutherford,et al.  Artemis: sequence visualization and annotation , 2000, Bioinform..

[33]  S. Kitani,et al.  Identification of the bkdAB gene cluster, a plausible source of the starter-unit for virginiamycin M production in Streptomyces virginiae , 2007, Archives of Microbiology.

[34]  C. Khosla,et al.  Engineered biosynthesis of novel polyketides: influence of a downstream enzyme on the catalytic specificity of a minimal aromatic polyketide synthase. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[35]  I. Hoof,et al.  CLUSEAN: a computer-based framework for the automated analysis of bacterial secondary metabolite biosynthetic gene clusters. , 2009, Journal of biotechnology.

[36]  C. Cocito Antibiotics of the virginiamycin family, inhibitors which contain synergistic components , 1979, Microbiological reviews.

[37]  L. Debussche,et al.  Identification and analysis of genes from Streptomyces pristinaespiralis encoding enzymes involved in the biosynthesis of the 4‐dimethylamino‐l‐phenylalanine precursor of pristinamycin I , 1997, Molecular microbiology.

[38]  James Staunton,et al.  Engineering specificity of starter unit selection by the erythromycin‐producing polyketide synthase , 2002, Molecular microbiology.

[39]  M. Marahiel,et al.  Regeneration of misprimed nonribosomal peptide synthetases by type II thioesterases , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[40]  David Posada,et al.  ProtTest: selection of best-fit models of protein evolution , 2005, Bioinform..