O-18 Kinetic Isotope Effects Reveal An Associative Transition State For Phosphite Dehydrogenase Catalyzed Phosphoryl Transfer
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY(2018)
摘要
Phosphite dehydrogenase (PTDH) catalyzes an unusual phosphoryl transfer reaction in which water displaces a hydride leaving group. Despite extensive effort, it remains unclear whether PTDH catalysis proceeds via an associative or dissociative mechanism. Here, primary H-2 and secondary O-18 kinetic isotope effects (KIEs) were determined and used together with computation to characterize the transition state (TS) catalyzed by a thermostable PTDH (17X-PTDH). The large, normal O-18 KIEs suggest an associative mechanism. Various transition state structures were computed within a model of the enzyme active site and H-2 and O-18 KIEs were predicted to evaluate the accuracy of each TS. This analysis suggests that 17X-PTDH catalyzes an associative process with little leaving group displacement and extensive nucleophilic participation. This tight TS is likely a consequence of the extremely poor leaving group requiring significant P-O bond formation to expel the hydride. This finding contrasts with the dissociative TSs in most phosphoryl transfer reactions from phosphate mono- and diesters.
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关键词
kinetic isotope effects,catalyzed
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