Abstract

The viscosity test was applied to the highly active nitrous oxide reductase purified from Wolinella succinogenes to determine whether the catalytic cycle may contain a diffusion-controlled step. For this test, the benzyl viologen cation (BV +)-N 2O oxidoreductase reaction, which exhibits a k catBV/ K mBV ∼2 × 10 8 M −1 s −1 at 23°C and pH 7.1, was run in solutions of nominally nondenaturing viscogens that were used to increase microviscosity. The parameters k catN 2O and k catBV were unaffected by viscosity in the range of viscogen concentrations that were not inhibitory and where the data were well behaved. K mBV , but not K mN 2O , was observed to increase linearly with relative viscosity with a slope of 0.14 for all viscogens surveyed. The results, when considered in the context of a plausible kinetic model for the BV +-N 2O oxidoreductase reaction, suggest that one of the two one-electron reactions between BV + and enzyme is diffusion-controlled but only partially rate determining. The ratio of the second-order-rate constants for these two one-electron steps is estimated to be about 6.1, and the larger rate constant to be about 1.1 × 10 9 M −1 s −1. There would appear to be no diffusion-controlled step associated with the half-reaction which results in reduction of N 2O to N 2.

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