Preparation of reduced bovine Cu, Zn superoxide dismutase
- 1 July 1985
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 229 (1) , 87-90
- https://doi.org/10.1042/bj2290087
Abstract
N.m.r. and e.p.r. were used to measure the oxidation state of copper in Cu, Zn superoxide dismutase treated with reducing agents such as NaBH4, K4Fe(CN)6, Na2S2O4 and H2O2. The activity and the electrophoretic pattern of the treated enzyme were also studied. On the basis of the reducing ability and of the absence of inactivating effects, NaBH4 was the most suitable reducer of those tested. Some characteristics of the reduction of superoxide dismutase by NaBH4 were further investigated. The results obtained indicate that NaBH4 can be used to prepare, in a few minutes, solutions of completely reduced enzyme without any apparent change of the activity and of the structure.This publication has 11 references indexed in Scilit:
- Generation of superoxide ion in human red blood cell lysates.Journal of Biological Chemistry, 1984
- An NMR study of the oxidation state of Cu,Zn superoxide dismutase in human red blood cellsBiochemical and Biophysical Research Communications, 1984
- The binding of copper ions to copper-free bovine superoxide dismutase. Copper distribution in protein samples recombined with less than stoicheiometric copper ion/protein ratiosBiochemical Journal, 1977
- Interaction of bovine erythrocyte superoxide dismutase with hydrogen peroxide. Inactivation of the enzymeBiochemistry, 1975
- Polarographic determination of superoxide dismutaseAnalytical Biochemistry, 1975
- Bovine erythrocyte superoxide dismutase. Subunit structure and sequence location of the intrasubunit disulfide bond.1974
- pH dependence of the nuclear magnetic relaxation rate of solvent water protons in solutions of bovine superoxide dismutaseBiochimica et Biophysica Acta (BBA) - Protein Structure, 1974
- Reduction and inactivation of superoxide dismutase by hydrogen peroxideBiochemical Journal, 1974
- The mechanism of action of superoxide dismutase from pulse radiolysis and electron paramagnetic resonance. Evidence that only half the active sites function in catalysisBiochemical Journal, 1974
- Superoxide DismutaseJournal of Biological Chemistry, 1969