Epoxidation of conjugated CC-bonds and sulfur-oxidation of thioethers mediated by NADH:FMN-dependent oxidoreductases
Nicole Jasmin Mueller,Clemens Stueckler,Melanie Hall,Peter Macheroux,Kurt Faber
Organic & Biomolecular Chemistry Pub Date : 01/26/2009 00:00:00 , DOI:10.1039/B819057G
Abstract

Three FMN-dependent oxidoreductases, YcnD and YhdA from Bacillus subtilis and Lot6p from Saccharomyces cerevisiae, oxidised α,β-unsaturated carbonyl compounds and a thioether, respectively, to furnish the corresponding racemic epoxides or sulfoxide, respectively. The mechanism of this enzyme-mediated (rather than enzyme-catalysed) oxidation was shown to proceed via the NADH-dependent reduction of O2, forming H2O2, which acted as oxidant in a spontaneous (non-enzymatic) fashion.

Graphical abstract: Epoxidation of conjugated C [[double bond, length as m-dash]] C-bonds and sulfur-oxidation of thioethers mediated by NADH:FMN-dependent oxidoreductases