Journal of the American Chemical Society 2011-03-30

A stereoselective vanadium-dependent chloroperoxidase in bacterial antibiotic biosynthesis.

Peter Bernhardt, Tatsufumi Okino, Jaclyn M Winter, Akimasa Miyanaga, Bradley S Moore

Index: J. Am. Chem. Soc. 133(12) , 4268-70, (2011)

Full Text: HTML

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.

Related Compounds

Structure Name/CAS No. Articles
Chloroperoxidase, from Caldariomyces fumago Structure Chloroperoxidase, from Caldariomyces fumago
CAS:9055-20-3