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PMID: 15296931 Published · ppublish English Journal Article Review

A new perspective on thiamine catalysis.

Current opinion in biotechnology ·Vol. 15 ·No. 4 ·2004-08-00 ·Pages 335-42

Pohl M, Sprenger GA, Müller M

Abstract

Our knowledge of thiamine-catalyzed ligase and lyase reactions has entered a new dimension. Significant achievements have been made in the field of enzymatic catalysis with the detection of hitherto unknown reaction types - extending the synthetic potential of known thiamine diphosphate (ThDP)-dependent enzymes - and the identification and characterization of new enzymes. As we learn more about ThDP-dependent enzymes, we find an ever-expanding range of reactions that they are able to catalyze and see increased amino acid sequence heterogeneity. By contrast, the three-dimensional structures of these enzymes, so far, seem to be highly similar. Non-enzymatic thiazolium and triazolium catalysts have also been developed, enhancing the scope of acyl anion chemistry.

MeSH Terms
Bacteria/metabolism Catalysis Ligases/chemistry,classification,metabolism Lyases/chemistry,classification,metabolism Multienzyme Complexes/chemistry,metabolism Signal Transduction/physiology Thiamine Pyrophosphate/chemistry,metabolism
Chemicals
Multienzyme Complexes Lyases Ligases Thiamine Pyrophosphate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pohl Martina
Institute of Molecular Enzyme Technology, University of Duesseldorf, Research Centre Juelich, 52426 Juelich, Germany. ma.pohl@fz-juelich.de
Sprenger Georg A
Müller Michael
Article Info
Journal
Current opinion in biotechnology
Abbr.
Curr Opin Biotechnol
ISSN
0958-1669
Published
2004-08-00
Pages
335-42
Language
English
Region
England
NLM ID
9100492
Subset
IM
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