Recent advances in the biocatalytic reduction of ketones and oxidation of sec-alcohols

Curr Opin Chem Biol. 2004 Apr;8(2):120-6. doi: 10.1016/j.cbpa.2004.02.005.

Abstract

To improve the efficiency and applicability of biocatalytic redox-reactions for asymmetric ketone-reduction and enantioselective alcohol-oxidation catalyzed by nicotinamide-dependent dehydrogenases/reductases, several achievements for cofactor-recycling have been made during the last two years. First, the use of hydrogenases for NADPH recycling in a two enzyme system. Second, preparative transformations with alcohol dehydrogenases coupled with NADH oxidases for NAD+/NADP+ recycling. Third, an exceptional chemo-stable alcohol dehydrogenase can efficiently use i-propanol and acetone as cosubstrates for reduction and oxidation, respectively, in a single-enzyme system. Novel carbonyl reductases and dehydrogenases derived from plant cells are particularly suited for sterically demanding substrates.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alcohols / chemistry
  • Alcohols / metabolism*
  • Bacteria / enzymology
  • Biotransformation
  • Catalysis
  • Ketones / chemistry
  • Ketones / metabolism*
  • Molecular Structure
  • Oxidation-Reduction
  • Oxidoreductases / chemistry
  • Oxidoreductases / metabolism

Substances

  • Alcohols
  • Ketones
  • Oxidoreductases