Abstract
Thiamin diphosphate (ThDP), the vitamin B1 coenzyme, is an excellent representative of coenzymes, which carry out electrophilic catalysis by forming a covalent complex with their substrates. The function of ThDP is to greatly increase the acidity of two carbon acids by stabilizing their conjugate bases, the ylide/C2-carbanion of the thiazolium ring and the C2α-carbanion (or enamine) once the substrate binds to ThDP. In recent years, several ThDP-bound intermediates on such pathways have been characterized by both solution and solid-state (X-ray) methods. Prominent among these advances are X-ray crystallographic results identifying both oxidative and non-oxidative intermediates, rapid chemical quench followed by NMR detection of a several intermediates which are stable under acidic conditions, and circular dichroism detection of the 1′,4′-imino tautomer of ThDP in some of the intermediates. Some of these methods also enable the investigator to determine the rate-limiting step in the complex series of steps.
Original language | English (US) |
---|---|
Pages (from-to) | 190-215 |
Number of pages | 26 |
Journal | Bioorganic Chemistry |
Volume | 33 |
Issue number | 3 |
DOIs | |
State | Published - Jun 2005 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Molecular Biology
- Drug Discovery
- Organic Chemistry
Keywords
- 1′,4′-imino tautomer
- Benzoylformate decarboxylase
- C2α-carbanion or enamine
- Circular dichroism
- Pyruvate dehydrogenase complex
- Thiamin diphosphate
- Yeast pyruvate decarboxylase
- Ylide/C2-carbanion