Abstract
We have established a simple kinetic model applicable to the enzyme cycling reaction for the determination of 3α-hydroxysteroids. This reaction was conducted under the reversible catalytic function of a single 3α-hydroxysteroid dehydrogenase (3α-HSD) with nucleotide cofactors, thio-NAD + (one of the NAD + analogues) for the oxidation of 3α-hydroxysteroids and NADH for the reduction of 3-oxosteroids. This model was constructed based on the reaction mechanism of 3α-HSD, following an ordered bi–bi mechanism with cofactor binding first, under the assumption that the respective enzyme-cofactor complexes were distributed according to the initial ratio of thio-NAD + to NADH by the rapid equilibrium of both enzyme-cofactor complexes. The cycling rate in the new kinetic model could be expressed with the dissociation constants of enzyme-cofactor complexes and the initial concentrations of cofactors and enzyme. The cycling rate was verified by a comparison with the experimental data using 3α-HSD from Pseudomonas sp. B-0831. The results showed that the experimental data corresponded well with the results obtained from the kinetic model.
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