PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of ambexSpringerOpen.comThis journalSubmit a manuscriptRegisterSpringerOpen.comAMB Express
 
AMB Express. 2012; 2: 11.
Published online 2012 January 31. doi:  10.1186/2191-0855-2-11
PMCID: PMC3281772
Transaminases for the synthesis of enantiopure beta-amino acids
Jens Rudat,corresponding author1 Birgit R Brucher,1 and Christoph Syldatk1
1Institute of Process Engineering in Life Sciences, Section II: Technical Biology, Karlsruhe Institute of Technology (KIT), Engler-Bunte-Ring 1, 76131 Karlsruhe, Germany
corresponding authorCorresponding author.
Jens Rudat: jens.rudat/at/kit.edu; Birgit R Brucher: birgit.brucher/at/c-lecta.de; Christoph Syldatk: christoph.syldatk/at/kit.edu
Received January 20, 2012; Accepted January 31, 2012.
Abstract
Optically pure β-amino acids constitute interesting building blocks for peptidomimetics and a great variety of pharmaceutically important compounds. Their efficient synthesis still poses a major challenge. Transaminases (also known as aminotransferases) possess a great potential for the synthesis of optically pure β-amino acids. These pyridoxal 5'-dependent enzymes catalyze the transfer of an amino group from a donor substrate to an acceptor, thus enabling the synthesis of a wide variety of chiral amines and amino acids. Transaminases can be applied either for the kinetic resolution of racemic compounds or the asymmetric synthesis starting from a prochiral substrate. This review gives an overview over microbial transaminases with activity towards β-amino acids and their substrate spectra. It also outlines current strategies for the screening of new biocatalysts. Particular emphasis is placed on activity assays which are applicable to high-throughput screening.
Keywords: transaminase, beta-amino acid, high-throughput screening, biocatalysis
Articles from AMB Express are provided here courtesy of
Springer-Verlag