Asymmetric bioreduction of C=C bonds using enoate reductases OPR1, OPR3 and YqjM: enzyme-based stereocontrol

Melanie Hall, Clemens Stueckler, Heidemarie Ehammer, Eva Maria Pointner, Gustav Oberdorfer, Karl Gruber, Bernhard Hauer, Rainer Stuermer, Wolfgang Kroutil, Peter Macheroux, Kurt Faber

Publikation: Beitrag in einer FachzeitschriftArtikel

Abstract

Three cloned enoate reductases from the “old yellow enzyme” family of flavoproteins were investigated in the asymmetric bioreduction of activated alkenes. 12‐Oxophytodienoate reductase isoenzymes OPR1 and OPR3 from Lycopersicon esculentum (tomato), and YqjM from Bacillus subtilis displayed a remarkably broad substrate spectrum by reducing α,β‐unsaturated aldehydes, ketones, maleimides and nitroalkenes. The reaction proceeded with absolute chemoselectivity – only the conjugated CC bond was reduced, while isolated olefins and carbonyl groups remained intact – with excellent stereoselectivities (ees up to >99%). Upon reduction of a nitroalkene, the stereochemical outcome could be determined via choice of the appropriate enzyme (OPR1 versus OPR3 or YqjM), which furnished the corresponding enantiomeric nitroalkanes in excellent ee. Molecular modelling suggests that this “enzyme‐based stereocontrol” is caused by subtle differences within the active site geometries.
Originalspracheenglisch
Seiten (von - bis)411-418
FachzeitschriftAdvanced Synthesis & Catalysis
Jahrgang350
Ausgabenummer3
DOIs
PublikationsstatusVeröffentlicht - 2008

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