Biosynthesis of depudecin, a metabolite of Nimbya scirpicola

Biosci Biotechnol Biochem. 2000 Feb;64(2):244-7. doi: 10.1271/bbb.64.244.

Abstract

Feeding experiments of labeled acetates to Nimbya scirpicola proved the carbon origin of the straight-chain polyketide, depudecin. Differential hydrogen exchange of the 2H label originating from 2H labeled acetate along the polyketide chain occurred. In particular, the deuterium of an epoxide methine at C-3 was lost to a substantial extent in the formation of depudecin.

MeSH terms

  • Alkadienes / chemistry
  • Alkadienes / metabolism*
  • Epoxy Compounds / chemistry
  • Epoxy Compounds / metabolism*
  • Fatty Alcohols / chemistry
  • Fatty Alcohols / metabolism*
  • Fermentation
  • Fungi / growth & development
  • Fungi / metabolism*
  • Magnetic Resonance Spectroscopy

Substances

  • Alkadienes
  • Epoxy Compounds
  • Fatty Alcohols
  • depudecin