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Thiamine-Based Enzymes for Biotransformations

  1. Martina Pohl1,
  2. Dörte Gocke1,
  3. Michael Müller2

Published Online: 15 JUL 2010

DOI: 10.1002/9783527628698.hgc028

Handbook of Green Chemistry

Handbook of Green Chemistry

How to Cite

Pohl, M., Gocke, D. and Müller, M. 2010. Thiamine-Based Enzymes for Biotransformations. Handbook of Green Chemistry. 3:75–114.

Author Information

  1. 1

    Heinrich-Heine-Universität Düsseldorf, Institut für Molekulare Enzymtechnologie, Jülich, Germany

  2. 2

    Albert-Ludwigs-Universität Freiburg, Institut für Pharmazeutische Wissenschaften, Freiburg, Germany

Publication History

  1. Published Online: 15 JUL 2010

Chiral and prochiral alpha-oxyfunctionalized compounds, in particular carboxylic acids, aldehydes, ketones, alcohols, are indispensable building blocks for asymmetric synthesis. 2-Hydroxy ketones encompassing a chiral and prochiral center are therefore versatile building blocks for organic synthesis, as they can be easily transformed into other functionalities, such as diols, epoxides, amino alcohols and diamines. The review describes the current state of the art concerning thiamine diphosphate-dependent enzymes, which catalyze the formation of chiral 2-hydroxy ketones.

Keywords: thiamine; diphosphate; enzymes; biotransformation; carboligation; structure–function relationships; pyruvate decarboxylase; benzoylformate decarboxylase; benzaldehyde lyase