Deracemization of amino acids by coupling transaminases of opposite stereoselectivity

Eul Soo Park, Jong Shik Shin

Research output: Contribution to journalArticle

10 Citations (Scopus)


Biocatalytic deracemization of amino acids without relying on oxidase-based deamination of an unwanted enantiomer was demonstrated by coupling a-and w-transaminases displaying opposite stereoselectivity. This strategy employs isopropylamine and a keto acid as cosubstrates and is free of generation of hydrogen peroxide which is troublesome in the conventional oxidase-based methods.

Original languageEnglish
Pages (from-to)3505-3509
Number of pages5
JournalAdvanced Synthesis and Catalysis
Issue number17
Publication statusPublished - 2014 Nov 24

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Deracemization of amino acids by coupling transaminases of opposite stereoselectivity'. Together they form a unique fingerprint.

  • Cite this