Large-scale synthesis of tert-butyl (3R,5S)-6-chloro-3,5-dihydroxyhexanoate by a stereoselective carbonyl reductase with high substrate concentration and product yield

Biotechnol Prog. 2017 May;33(3):612-620. doi: 10.1002/btpr.2460. Epub 2017 Mar 24.

Abstract

To biosynthesize the (3R,5S)-CDHH in an industrial scale, a newly synthesized stereoselective short chain carbonyl reductase (SCR) was successfully cloned and expressed in Escherichia coli. The fermentation of recombinant E. coli harboring SCR was carried out in 500 L and 5000 L fermenters, with biomass and specific activity of 9.7 g DCW/L, 15749.95 U/g DCW, and 10.97 g DCW/L, 19210.12 U/g DCW, respectively. The recombinant SCR was successfully applied for efficient production of (3R,5S)-CDHH. The scale-up synthesis of (3R,5S)-CDHH was performed in 5000 L bioreactor with 400 g/L of (S)-CHOH at 30°C, resulting in a space-time yield of 13.7 mM/h/g DCW, which was the highest ever reported. After isolation and purification, the yield and d.e. of (3R,5S)-CDHH reached 97.5% and 99.5%, respectively. © 2017 American Institute of Chemical Engineers Biotechnol. Prog., 33:612-620, 2017.

Keywords: asymmetric reduction; carbonyl reductase; space-time yield; tert-butyl (3R,5S)-6-chloro-3,5-dihydroxyhexanoate; tert-butyl (S)-6-chloro-5-hydroxy-3-oxohexanoate.

MeSH terms

  • Alcohol Oxidoreductases / metabolism*
  • Bioreactors / microbiology
  • Caproates / chemistry
  • Caproates / metabolism*
  • Escherichia coli / enzymology*
  • Escherichia coli / metabolism
  • Stereoisomerism

Substances

  • Caproates
  • tert-butyl (3R, 5S) 6-chloro-dihydroxyhexanoate
  • Alcohol Oxidoreductases