Since the first discovery of old yellow enzyme 1 (OYE1) from Saccharomyces pastorianus in
1932, biocatalytic asymmetric reduction of activated alkenes by OYEs has become a …

The stereoselective reduction of alkenes conjugated to electron-withdrawing groups by ene-
reductases has been extensively applied to the commercial preparation of fine chemicals …

Native and promiscuous catalytic activities of flavin-dependent Old Yellow Enzymes (OYEs)
reported to date are initiated by the reduced flavin upon electron transfer. As a rare …

Old yellow enzymes (OYEs) have been proven as powerful biocatalysts for the asymmetric
reduction of activated alkenes. Fungi appear to be valuable sources of OYEs, but most of the …

Abstract Old Yellow Enzymes (OYEs) selectively reduce carbon‑carbon double bonds of a
broad range of substrates with excellent stereoselectivity. Current challenges of their …

oxophytodienoate reductase 3 (OPR3) is a key enzyme in the biosynthesis of jasmonoyl-L-
isoleucine, the receptor-active form of jasmonic acid and crucial signaling molecule in plant …

Asymmetric reduction of (R)‐carvone and ketoisophorone by an engineered ene‐reductase
from Galdieria sulphuraria (GsOYE) combined with glucose dehydrogenase for NADPH …

Aiming at expanding the biocatalytic toolbox of ene-reductase enzymes, we decided to
explore photosynthetic extremophile microorganisms as unique reservoir of (new) …

Aiming at expanding the portfolio of Old Yellow Enzymes (OYEs), which have been
systematically studied to be employed in the chemical and pharmaceutical industries as …

The asymmetric reduction of α, β-unsaturated compounds conjugated with electron-
withdrawing group by ene-reductases (ERs) is a valuable method for the synthesis of …