Efficient kinetic resolution of secondary alcohols using an organic solvent-tolerant esterase in non-aqueous medium

Biotechnol Lett. 2016 Jul;38(7):1165-71. doi: 10.1007/s10529-016-2091-6. Epub 2016 Mar 30.

Abstract

Objective: To identify an esterase-mediated kinetic resolution of secondary alcohols in non-aqueous medium.

Results: An esterase, EST4, from a marine mud metagenomic library, showed high activity and enantioselectivity for the kinetic resolution of secondary alcohols in non-aqueous medium. Using 1-phenylethanol as the model alcohol, the effects of organic solvents, acyl donors, molar ratio, temperatures and biocatalyst loading on the kinetic resolution catalyzed by the EST4 whole-cell biocatalyst were investigated and optimized. The optimized methodology was effective on resolving 16 various racemic secondary alcohols in neat n-hexane, providing excellent enantiomeric excess (up to 99.9 % ee). Moreover, EST4 exhibited a strong tolerance for high substrate concentration (up to 1 M), and the optical purity of the desired secondary alcohols was kept above 99 % ee.

Conclusion: The esterase EST4 is a promising biocatalyst for the enantioselective synthesis of various alcohols and esters with interesting practical applications.

Keywords: Enantioselectivity; Esterase; High substrate concentration tolerance; Kinetic resolution; Secondary alcohols; Transesterification.

MeSH terms

  • Alcohols / chemistry
  • Alcohols / metabolism*
  • Esterases / metabolism*
  • Kinetics
  • Solvents / chemistry
  • Solvents / metabolism
  • Stereoisomerism

Substances

  • Alcohols
  • Solvents
  • Esterases