Rapid oxidation of dl-selenomethionine by peroxynitrite

Abstract

Peroxynitrite, the reaction product of nitric oxide and superoxide, rapidly oxidizes dl-selenomethionine (MetSe) with overall second-order kinetics, first-order in peroxynitrite and first-order in MetSe. The oxidation of MetSe by peroxynitrite goes by two competing mechanisms. The first produces ethylene by what we propose to be a one-electron oxidation of MetSe. In the second mechanism, MetSe undergoes a two-electron oxidation that gives methionine selenoxide (MetSeO); the apparent second-order rate constant, k 2(app) for this process is (2.4 ±0.1 × 10 3 M −1s −1 at pH 7.4 and 25°C. The kinetic modeling of the experimental data suggests that both peroxynitrous acid (k 2 = 20,460 ± 440 M −1s −1 at 25°C) and the peroxynitrite anion (k 2 = 200 ± 170 M −1s −1 at 25°C) are involved in the second-order reaction leading to selenoxide. These rate constants are 10-to 1,000-fold higher than those for the reactions of methionine (Met) with peroxynitrite. With increasing concentrations of MetSe at pH 7.4, the yield of ethylene decreases, while that of MetSe  O increases, suggesting that the reactions leading to ethylene and selenoxide have different kinetic orders. These results are analogous to those we previously reported for methionine and 2-keto-4-thiomethylbutanoic acid (KTBA), where ethylene is produced in a first-order reaction and sulfoxide in a second-order reaction. Therefore, we suggest that the reaction of peroxynitrite with MetSe involves a mechanism similar to that we proposed for Met, in which an activated intermediate of peroxynitrous acid (HOONO*) is the one-electron oxidant and reacts with first-order kinetics and ground-state peroxynitrite is the two-electron oxidant and reacts with second-order kinetics.