Thiamin-diphosphate-dependent enzymes: new aspects of asymmetric C-C bond formation

Chemistry. 2002 Dec 2;8(23):5288-95. doi: 10.1002/1521-3765(20021202)8:23<5288::AID-CHEM5288>3.0.CO;2-F.

Abstract

Starting from a thorough investigation of mechanistic aspects of ThDP-dependent (ThDP = thiamin diphosphate) enzymes in combination with mutagenesis studies and a detailed substrate screening, new general synthetic methods have been developed based on Umpolung reactions by thiamin catalysis. A selective donor-acceptor concept was established leading to the first asymmetric cross-benzoin condensation, and a kinetic racemic resolution through C-C bond cleavage was developed. With these tools and in combination with protein engineering, we approached the synthesis of new chiral building blocks on a preparative scale. An outlook is given with respect to the potential of other ThDP-dependent enzymes as catalysts in asymmetric synthesis.

Publication types

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

MeSH terms

  • Aldehyde-Lyases / chemistry
  • Aldehyde-Lyases / metabolism*
  • Bacteria / enzymology
  • Bacteria / genetics
  • Carboxy-Lyases / chemistry
  • Carboxy-Lyases / metabolism*
  • Catalysis
  • Kinetics
  • Mutagenesis, Site-Directed
  • Pyruvate Decarboxylase / chemistry
  • Pyruvate Decarboxylase / metabolism*
  • Stereoisomerism
  • Structure-Activity Relationship
  • Thiamine / metabolism
  • Thiamine Pyrophosphate / chemistry
  • Thiamine Pyrophosphate / metabolism*

Substances

  • Carboxy-Lyases
  • Pyruvate Decarboxylase
  • benzoylformate decarboxylase
  • Aldehyde-Lyases
  • benzaldehyde lyase
  • Thiamine Pyrophosphate
  • Thiamine