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Redox Report
Communications in Free Radical Research
Volume 2, 1996 - Issue 3
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Original Articles

Reaction of peroxynitrite with L-tryptophan

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Pages 173-177 | Received 01 Feb 1996, Accepted 05 Feb 1996, Published online: 13 Jul 2016
 

Summary

The reaction between peroxynitrous acid (hydrogen oxoperoxonitrate) and L-tryptophan is 130 M−1s−1 at 25°C. The pH dependence of the second-order rate constant shows a maximum at pH 5.1. The enthalpy and entropy of activation at pH 7.1 are 10.6 ± 0.4 kcal.mol−1 and -16 ± 2 cal.mol−1K−1 respectively. High-performance liquid chromatography analysis revealed a number of reaction products, two of which were identified as 5- and 6- nitrotryptophan. Hydroxytryptophans were not observed, even at low peroxynitrite concentrations where most of the peroxynitrite decays to nitrate via a first-order process. These results support the hypothesis that isomerization of protonated peroxynitrite to nitrate does not involve formation of the hydroxyl radical.

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