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Suicide inhibition of acetohydroxyacid synthase by hydroxypyruvate.

Journal of enzyme inhibition and medicinal chemistry (2005-05-18)
Ronald G Duggleby
ABSTRACT

Acetohydroxyacid synthase (Ec 2.2.1.6) catalyses the thiamine diphosphate-dependent reaction between two molecules of pyruvate yielding 2-acetolactacte and CO2. The enzyme will also utilise hydroxypyruvate with a k(cat) value that is 12% of that observed with pyruvate. When hydroxypyruvate is the substrate, the enzyme undergoes progressive inactivation with kinetics that are characteristic of suicide inhibition. It is proposed that the dihydroxyethyl-thiamine diphosphate intermediate can expel a hydroxide ion forming an enol that rearranges to a bound acetyl group.

MATERIALI
N° Catalogo
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Descrizione del prodotto

Sigma-Aldrich
β-Hydroxypyruvic acid, ≥95.0% (dry substance, T)
Sigma-Aldrich
Lithium β-hydroxypyruvate hydrate, ≥97.0% (calc. based on dry substance, NT)