Production of chiral alcohols from prochiral ketones by microalgal photo-biocatalytic asymmetric reduction reaction

J Ind Microbiol Biotechnol. 2012 Jun;39(6):835-41. doi: 10.1007/s10295-012-1088-y. Epub 2012 Feb 10.

Abstract

Microalgal photo-biocatalysis is a green technique for asymmetric synthesis. Asymmetric reduction of nonnatural prochiral ketones to produce chiral alcohols by microalgal photo-biocatalysis was studied in this work. Acetophenone (ACP) and ethyl acetoacetate (EAA) were chosen as model substrates for aromatic ketones and β-ketoesters, respectively. Two prokaryotic cyanophyta and two eukaryotic chlorophyta were selected as photo-biocatalysts. The results proved that nonnatural prochiral ketones can be reduced by microalgal photo-biocatalysis with high enantioselectivity. Illumination is indispensable to the photo-biocatalysis. For aromatic ketone, cyanophyta are eligible biocatalysts. For ACP asymmetric reduction reaction, about 45% yield and 97% e.e. can be achieved by the photo-biocatalysis reaction with Spirulina platensis as biocatalyst. On the contrary, chlorophyta are efficient biocatalysts for β-ketoester asymmetric reduction reaction among the four tested algae. For EAA asymmetric reduction reaction, about 70% yield and 90% e.e. can be achieved with Scenedesmus obliquus as biocatalyst. The microalgae used in this study outperformed other characterized biocatalysts such as microbial and plant cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetoacetates / metabolism
  • Acetophenones / metabolism
  • Alcohols / chemical synthesis*
  • Biocatalysis
  • Chlorophyta / metabolism*
  • Cyanobacteria / metabolism*
  • Industrial Microbiology*
  • Ketones / metabolism
  • Microalgae / metabolism*
  • Photochemical Processes

Substances

  • Acetoacetates
  • Acetophenones
  • Alcohols
  • Ketones
  • ethyl acetoacetate
  • acetophenone