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  • Title: Stereochemistry of NADPH leads to NADP+ transhydrogenation catalyzed by bovine heart mitochondrial pyridine dinucleotide transhydrogenase.
    Author: Wu LN, Fisher RR.
    Journal: J Biol Chem; 1982 Oct 10; 257(19):11680-3. PubMed ID: 7118903.
    Abstract:
    Bovine heart submitochondrial particle energy-linked NADH leads to NADP+ transhydrogenase also catalyzes transhydrogenation between NADPH and NADP+. The stereochemistry of hydride ion transfer in the NADH leads to NADP+ reaction involves the nicotinamide 4A locus of NADH and the 4B locus of NADPH. In this paper it is demonstrated that during NADPH leads to NADP+ transhydrogenation the NADP+ is reduced exclusively at the 4B locus and that oxidation of NADPH is predominately at the 4B locus. Reduction of [4-3H]NADP+ by NADPH yielded [4A-3H]NADPH as the only product. Oxidation of [4A-3H]NADPH by NADP+ resulted in the conversion of nearly 33% of the label into [4-3H]NADP+, whereas the oxidation of [4B-3H] NADPH yielded only about a 6.5% conversion. These data suggest that while a small portion of total energy-linked NADPH leads to NADP+ transhydrogenation results from the binding of NADPH at the NAD domain of the active site with hydride transfer to NADP+ bound at the NADP domain, most of the reaction occurs by a mechanism in which both substrates are bound sequentially at the NADP domain. It is proposed that NADPH leads to NADP+ transhydrogenation represents a partial reaction of NADH leads to NADP+ transhydrogenation which involves the participation of a reduced-enzyme intermediate.
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