A stereoselective vanadium-dependent chloroperoxidase in bacterial antibiotic biosynthesis

J Am Chem Soc. 2011 Mar 30;133(12):4268-70. doi: 10.1021/ja201088k. Epub 2011 Mar 8.

Abstract

Halogenases catalyze reactions that introduce halogen atoms into electron-rich organic molecules. Vanadium-dependent haloperoxidases are generally considered to be promiscuous halogenating enzymes that have thus far been derived exclusively from eukaryotes, where their cellular function is often disputed. We now report the first biochemical characterization of a bacterial vanadium-dependent chloroperoxidase, NapH1 from Streptomyces sp. CNQ-525, which catalyzes a highly stereoselective chlorination-cyclization reaction in napyradiomycin antibiotic biosynthesis. This finding biochemically links a vanadium chloroperoxidase to microbial natural product biosynthesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / biosynthesis*
  • Anti-Bacterial Agents / chemistry
  • Biocatalysis
  • Chloride Peroxidase / chemistry
  • Chloride Peroxidase / metabolism*
  • Cyclization
  • Molecular Structure
  • Naphthoquinones / chemistry
  • Naphthoquinones / metabolism*
  • Stereoisomerism
  • Streptomyces / enzymology*
  • Streptomyces / genetics
  • Vanadium / metabolism*

Substances

  • Anti-Bacterial Agents
  • Naphthoquinones
  • Vanadium
  • Chloride Peroxidase