Two genes, rif15 and rif16, of the rifamycin biosynthetic gene cluster in Amycolatopsis mediterranei likely encode a transketolase and a P450 monooxygenase, respectively, both essential for the conversion of rifamycin SV into B

Acta Biochim Biophys Sin (Shanghai). 2011 Dec;43(12):948-56. doi: 10.1093/abbs/gmr091. Epub 2011 Oct 10.

Abstract

Amycolatopsis mediterranei produces an important antibiotic rifamycin, the biosynthesis of which involves many unusual modifications. Previous work suggested a putative P450 enzyme encoded by rif16 within the rifamycin biosynthetic gene cluster (rif) was required for the conversion of the intermediate rifamycin SV into the end product rifamycin B. In this study, we genetically proved that a putative transketolase encoded by rif15 is another essential enzyme for this conversion. Expression of merely rif15 and rif16 in a rif cluster null mutant of A. mediterranei U32 was able to convert rifamycin SV into B. However, this Rif15- and Rif16-mediated conversion was only detected in intact cells of A. meidterranei, but not in Streptomyce coelicolor or Mycobacterium smegmatis, suggesting that yet-characterized gene(s) in A. mediterranei other than those encoded by the rif cluster should be involved in this process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actinomycetaceae / metabolism*
  • Anti-Bacterial Agents / biosynthesis
  • Mixed Function Oxygenases / genetics*
  • Mixed Function Oxygenases / metabolism
  • Multigene Family / genetics
  • Rifamycins / biosynthesis*
  • Transketolase / genetics*
  • Transketolase / metabolism

Substances

  • Anti-Bacterial Agents
  • Rifamycins
  • rifamycin B
  • rifamycin SV
  • Mixed Function Oxygenases
  • Transketolase