Sequential enzymatic epoxidation involved in polyether lasalocid biosynthesis

J Am Chem Soc. 2012 May 2;134(17):7246-9. doi: 10.1021/ja301386g. Epub 2012 Apr 20.

Abstract

Enantioselective epoxidation followed by regioselective epoxide opening reaction are the key processes in construction of the polyether skeleton. Recent genetic analysis of ionophore polyether biosynthetic gene clusters suggested that flavin-containing monooxygenases (FMOs) could be involved in the oxidation steps. In vivo and in vitro analyses of Lsd18, an FMO involved in the biosynthesis of polyether lasalocid, using simple olefin or truncated diene of a putative substrate as substrate mimics demonstrated that enantioselective epoxidation affords natural type mono- or bis-epoxide in a stepwise manner. These findings allow us to figure out enzymatic polyether construction in lasalocid biosynthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / metabolism*
  • Cloning, Molecular
  • Epoxy Compounds / chemistry
  • Epoxy Compounds / metabolism*
  • Ethers / chemistry
  • Ethers / metabolism
  • Lasalocid / chemistry
  • Lasalocid / metabolism*
  • Oxygenases / genetics
  • Oxygenases / metabolism*
  • Rhodococcus / enzymology*
  • Rhodococcus / genetics
  • Rhodococcus / metabolism

Substances

  • Anti-Bacterial Agents
  • Epoxy Compounds
  • Ethers
  • Oxygenases
  • dimethylaniline monooxygenase (N-oxide forming)
  • Lasalocid