Asymmetric Reduction of (R)-Carvone through a Thermostable and Organic-Solvent-Tolerant Ene-Reductase

Chembiochem. 2020 Apr 17;21(8):1217-1225. doi: 10.1002/cbic.201900599. Epub 2020 Jan 7.

Abstract

Ene-reductases allow regio- and stereoselective reduction of activated C=C double bonds at the expense of nicotinamide adenine dinucleotide cofactors [NAD(P)H]. Biological NAD(P)H can be replaced by synthetic mimics to facilitate enzyme screening and process optimization. The ene-reductase FOYE-1, originating from an acidophilic iron oxidizer, has been described as a promising candidate and is now being explored for applied biocatalysis. Biological and synthetic nicotinamide cofactors were evaluated to fuel FOYE-1 to produce valuable compounds. A maximum activity of (319.7±3.2) U mg-1 with NADPH or of (206.7±3.4) U mg-1 with 1-benzyl-1,4-dihydronicotinamide (BNAH) for the reduction of N-methylmaleimide was observed at 30 °C. Notably, BNAH was found to be a promising reductant but exhibits poor solubility in water. Different organic solvents were therefore assayed: FOYE-1 showed excellent performance in most systems with up to 20 vol% solvent and at temperatures up to 40 °C. Purification and application strategies were evaluated on a small scale to optimize the process. Finally, a 200 mL biotransformation of 750 mg (R)-carvone afforded 495 mg of (2R,5R)-dihydrocarvone (>95 % ee), demonstrating the simplicity of handling and application of FOYE-1.

Keywords: Old Yellow Enzymes; biocatalysis; biotransformations; cofactor mimics; oxidoreductases; solvent stability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biocatalysis*
  • Cyclohexane Monoterpenes / chemistry*
  • Flavoproteins / metabolism*
  • Kinetics
  • NADP / metabolism
  • Oxidation-Reduction
  • Oxidoreductases / metabolism*
  • Solvents / chemistry*
  • Substrate Specificity

Substances

  • Cyclohexane Monoterpenes
  • Flavoproteins
  • Solvents
  • NADP
  • carvone
  • Oxidoreductases
  • dihydrocarvone