Biosynthesis of 9-methylstreptimidone involves a new decarboxylative step for polyketide terminal diene formation

Org Lett. 2013 Mar 15;15(6):1278-81. doi: 10.1021/ol400224n. Epub 2013 Feb 25.

Abstract

9-Methylstreptimidone is a glutarimide antibiotic showing antiviral, antifungal, and antitumor activities. Genome scanning, bioinformatics analysis, and gene inactivation experiments reveal a gene cluster responsible for the biosynthesis of 9-methylstreptimidone in Streptomyces himastatinicus. The unveiled machinery features both acyltransferase- and thioesterase-less iterative use of module 5 as well as a branching module for glutarimide generation. Impressively, inactivation of smdK leads to a new carboxylate analogue unveiling a new mechanism for polyketide terminal diene formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / metabolism*
  • Anti-Bacterial Agents / pharmacology
  • Multigene Family
  • Piperidones / chemistry
  • Piperidones / metabolism*
  • Piperidones / pharmacology
  • Polyenes / chemical synthesis
  • Polyenes / chemistry*
  • Polyketides / chemistry
  • Polyketides / metabolism
  • Streptomyces / genetics*
  • Streptomyces / metabolism

Substances

  • Anti-Bacterial Agents
  • Piperidones
  • Polyenes
  • Polyketides
  • 9-methylstreptimidone
  • glutarimide