Asymmetric synthesis of optically active methyl-2-benzamido-methyl-3-hydroxy-butyrate by robust short-chain alcohol dehydrogenases from Burkholderia gladioli. Academic Article uri icon

Overview

abstract

  • Three short-chain alcohol dehydrogenases from Burkholderia gladioli were discovered for their great potential in the dynamic kinetic asymmetric transformation of methyl 2-benzamido-methyl-3-oxobutanoate, and their screening against varied organic solvents and substrates. This is the first report of recombinant enzymes capable of achieving this reaction with the highest enantio- and diastereo-selectivity.

publication date

  • August 7, 2015

Research

keywords

  • Alcohol Dehydrogenase
  • Benzamides
  • Burkholderia gladioli
  • Hydroxybutyrates

Identity

Scopus Document Identifier

  • 84937232526

Digital Object Identifier (DOI)

  • 10.1039/c5cc04652a

PubMed ID

  • 26140446

Additional Document Info

volume

  • 51

issue

  • 61