Autoxidation of Native Oxymyoglobin
Open Access
- 1 September 1980
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 110 (1), 241-246
- https://doi.org/10.1111/j.1432-1033.1980.tb04861.x
Abstract
A complete kinetic description has been made on the pH profile for the autoxidation rate in terms of displacement of superoxide anion, O–2, from MbO2 by the entering water molecule or hydroxyl ion. Using the equation, the effect of temperature on the autoxidation rate has been studied over the pH range 4.8–12.6 in 0.1 M buffer at 15°, 25° and 35°C. The resulting thermodynamic parameters characterize the dissociation groups involved in the reaction as histidyl and tyrosyl residues. Despite the fact that each elementary process of the reaction is primarily protected against autoxidation by the high energy barrier of approximately 85–150 kJ · mol−1, the catalytic proton participates not only in decreasing the value of ΔH°≠ but also in increasing the value of ΔS°≠ to facilitate the formation of the activated complex, thereby promoting most of the autoxidation reaction of MbO2. The proton-catalyzed process is therefore of primary importance and a mechanistic detail of the reaction is discussed.This publication has 25 references indexed in Scilit:
- NMR titration curves of histidine ring protons. 11. Near-heme histidine residues of deoxy- and oxymyoglobinsBiochemistry, 1979
- Carbon monoxide and oxygen complexes of soybean leghemoglobins: pH effects upon infrared and visible spectra. Comparisons with carbon monoxide and oxygen complexes of myoglobin and hemoglobinBiochemistry, 1979
- Structure of oxymyoglobinNature, 1978
- The NO-probed detection of the heme-linked ionization group of myoglobinBiochemical and Biophysical Research Communications, 1976
- Superoxide DismutasesAnnual Review of Biochemistry, 1975
- REACTIONS OF OXYGEN WITH HEMOGLOBIN, CYTOCHROME C OXIDASE AND OTHER HEMEPROTEINS*Annals of the New York Academy of Sciences, 1975
- Infrared evidence for the mode of binding of oxygen to iron of myoglobin from heart muscleBiochemical and Biophysical Research Communications, 1974
- The mechanisms of hemoglobin autoxidation evidence for proton-assisted nucleophilic displacement of superoxide by anionsBiochemical and Biophysical Research Communications, 1974
- The Covalent Structure of Beef Heart MyoglobinEuropean Journal of Biochemistry, 1970
- The mode of attachment of the azide ion to sperm whale metmyoglobinJournal of Molecular Biology, 1964