Redesigning alcohol dehydrogenases/reductases for more efficient biosynthesis of enantiopure isomers

Biotechnol Adv. 2015 Dec;33(8):1671-84. doi: 10.1016/j.biotechadv.2015.08.002. Epub 2015 Aug 28.

Abstract

Alcohol dehydrogenases/reductases predominantly catalyze the asymmetric biosynthesis of optically pure stereoisomers because of their unique chiral constitutions. The enantioselectivities of alcohol dehydrogenases/reductases are substrate- and cofactor-dependent, and therefore they usually catalyze specific reactions with high enantioselectivity under physiological conditions; this may not be suitable for asymmetric biosynthesis with non-natural substrates or non-natural cofactors, and under nonphysiological conditions. It is therefore necessary to modify alcohol dehydrogenases/reductases using various redesigning tools such as directed evolution and rational design, and their combinations, as well as engineering enzyme modules for more efficient production of "non-natural" products. In this article, progress in these aspects of alcohol dehydrogenase/reductase design is reviewed, and future challenges are discussed.

Keywords: Alcohol dehydrogenase/reductase; Chiral biosynthesis; Combination methods; Directed evolution; Enantiopure isomer; Modular engineering; Rational design.

Publication types

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

MeSH terms

  • Alcohol Dehydrogenase / chemistry
  • Alcohol Dehydrogenase / genetics*
  • Amino Acid Sequence / genetics
  • Catalysis
  • Directed Molecular Evolution*
  • Genetic Engineering / methods
  • Genetic Engineering / trends
  • Kinetics
  • Mutagenesis, Site-Directed
  • Stereoisomerism*

Substances

  • Alcohol Dehydrogenase