Chiral alcohols were produced on a large scale by developing effective
regeneration systems of nicotinamide coenzymes in bakers' yeast cells
. In the asymmetric reduction of prochiral ketones, ethanol is used in
stead of carbohydrate as the energy source for NAD(P)H regeneration. W
e propose an overall scheme for NAD(P)H regeneration from NAD(P)(+) th
rough the oxidative pathway of ethanol, In the oxidative resolution of
a racemic alcohol, NAD(+) is effectively regenerated from NADH throug
h the respiratory chain in the yeast cells. Thus, racemic 1,2-alkanedi
ols were microbially resolved on a large scale by repeating the oxidat
ive resolution and the asymmetric reduction.