A soluble alpha-ketoisocaproate oxygenase from rat liver catalyzes the decarboxylation and hydroxylation of alpha-ketoisocaproate to form beta-hydroxyisovalerate. The source of oxygen (O2 or H2O) enzymatically incorporated into beta-hydroxyisovalerate was investigated using 18O2 and H218O. Greater than 92% of the carboxyl groups of beta-hydroxyisovaleric acid contained 1 18O atom from 18O2 and 15% of the beta-hydroxyl oxygens of beta-hydroxyisovaleric acid contained 18O from 18O2. Since some oxygen of the beta-hydroxyl group is derived from O2 and since others have shown a rapid H2O in equilibrium ROH exchange for similar reactions, we conclude that both of the oxygens of beta-hydroxyisovaleric acid are derived from O2 and that exchange of water oxygen with the beta-hydroxyl group of beta-hydroxyisovaleric acid must occur with an intermediate of the reaction. Thus, the alpha-ketoisocaproate oxygenase would be a dioxygenase. A mechanism consistent with the 18O experiments and other properties of the enzyme is proposed.
No takes yet. Share an insight, caveat, or question.
Sabourin et al. (1982) studied this question.
Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context: