Engineering the Amine Transaminase from Vibrio fluvialis towards Branched-Chain Substrates

Maika Genz, Okke Melse, Sandy Schmidt, Clare Vickers, Mark Dörr, Tom Van Den Bergh, Henk-Jan Joosten, Uwe T. Bornscheuer*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review


Chiral amines are important building blocks, especially for the pharmaceutical industry. Although amine transaminases (ATAs) are versatile enzymes to synthesize chiral amines, the wildtype enzymes do not accept ketones with two large substituents next to the carbonyl functionality. Using bioinformatic tools to design a seven-site mutant library followed by high-throughput screening, we were able to identify variants of the enzyme from Vibrio fluvialis (VF-ATA) with a widened binding pocket, as exemplified for a range of ketones. Three variants allowed the asymmetric synthesis of 2,2-dimethyl-1-phenylpropan-1-amine—not accessible by any wildtype ATA described so far. The best variant containing four mutations (L56V, W57C, F85V, V153A) gave 100 % conversion of the ketone to yield the amine with an enantiomeric excess value >99 %, notably with preference for the (R)-enantiomer. In silico modeling enabled the reconstruction of the substrate binding mode to the newly evolved pocket and, hence, allowed explanation of the experimental results.

Original languageEnglish
Pages (from-to)3199-3202
Number of pages4
Issue number20
Publication statusPublished - 20 Oct 2016
Externally publishedYes


  • amines
  • bioinformatics
  • enzyme catalysis
  • protein engineering
  • transaminases

ASJC Scopus subject areas

  • Catalysis
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry


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