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A stereoselective vanadium-dependent chloroperoxidase in bacterial antibiotic biosynthesis.

Journal of the American Chemical Society (2011-03-10)
Peter Bernhardt, Tatsufumi Okino, Jaclyn M Winter, Akimasa Miyanaga, Bradley S Moore
ZUSAMMENFASSUNG

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.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Chlorperoxidase aus Caldariomyces fumago, buffered aqueous suspension, ≥3,000 units/mL
Sigma-Aldrich
Chlorperoxidase aus Caldariomyces fumago, aqueous suspension, brown, >10,000 U/mL
Sigma-Aldrich
Chlorperoxidase aus Caldariomyces fumago, buffered aqueous suspension, 1,000-2,000 units/mg protein (E1%/280)