A glutamic acid 3‐methyltransferase encoded by an accessory gene locus important for daptomycin biosynthesis in Streptomyces roseosporus

• Published in: Molecular microbiology 2006-09, Vol.61 (5), p.1294-1307
• Main Authors: Nguyen, Kien T., Kau, David, Gu, Jian‐Qiao, Brian, Paul, Wrigley, Stephen K., Baltz, Richard H., Miao, Vivian
• Format: Article
• Language: English
• Subjects: Amino Acid Motifs - genetics; Amino Acid Sequence; Amino acids; Anti-Bacterial Agents - metabolism; Antibiotics; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Bacteriology; Biological and medical sciences; Chromatography, High Pressure Liquid - methods; Chromatography, Liquid - methods; Daptomycin - biosynthesis; Fundamental and applied biological sciences. Psychology; Gene loci; Glutamic Acid - analogs & derivatives; Glutamic Acid - metabolism; Mass Spectrometry - methods; Methyltransferases - genetics; Methyltransferases - metabolism; Microbiology; Miscellaneous; Molecular Sequence Data; Molecular Structure; Mutation - genetics; Peptides; Protein synthesis; Sequence Homology, Amino Acid; Staphylococcus aureus; Streptomyces - chemistry; Streptomyces - genetics; Streptomyces - metabolism; Streptomyces coelicolor; Streptomyces fradiae
• ISSN: 0950-382X; 1365-2958
• DOI: 10.1111/j.1365-2958.2006.05305.x

Summary In many peptide antibiotics, modified amino acids are important for biological activity. The amino acid 3‐methyl‐glutamic acid (3mGlu) has been found only in three cyclic lipopeptide antibiotics: daptomycin and the A21978C family produced by Streptomyces roseosporus, calcium‐dependent antibiotic produced by Streptomyces coelicolor and A54145 produced by Streptomyces fradiae. We studied the non‐ribosomal peptide synthetase genes involved in A21978C biosynthesis and the downstream genes, dptG, dptH, dptI and dptJ predicted to encode a conserved protein of unknown function, a thioesterase, a methyltransferase (MTase) and a tryptophan 2,3‐dioxygenase respectively. Deletion of dptGHIJ reduced overall lipopeptide yield and led to production of a series of novel A21978C analogues containing Glu12 instead of 3mGlu12. Complementation by only dptI, or its S. coelicolor homologue, glmT, restored the biosynthesis of the 3mGlu‐containing compounds in the mutant. Compared with A21978C, the Glu12‐containing derivatives were less active against Staphylococcus aureus. Further genetic analyses showed that members of the dptGHIJ locus cooperatively contributed to optimal A21978C production; deletion of dptH, dptI or dptJ genes reduced the yield significantly, while expression of dptIJ or dptGHIJ from the strong ermEp* promoter substantially increased lipopeptide production. The results indicate that these genes play important roles in the biosynthesis of daptomycin, and that dptI encodes a Glu MTase.