1. Oxygen was taken up rapidly when pyruvate was added to mixtures of pyridoxamine and Mn2+ ions after lag periods that were shortened by peroxidase (donor–hydrogen peroxide oxidoreductase, EC 184.108.40.206). 2. The total oxygen uptake was proportional to the pyridoxamine added and was accompanied by the disappearance of pyridoxamine; the pyruvate acted catalytically and hydrogen peroxide was not formed. 3. At pH6 more than half the pyridoxamine that disappeared was accounted for as pyridoxal and ammonia; it is suggested that the primary reaction is the oxidative deamination of the pyridoxamine. 4. Results were similar when α-oxobutyrate or glyoxylate were substituted for pyruvate, except that the reactions were slower and the yield of pyridoxal less. 5. The oxidative decarboxylations of α-oxoglutarate and phenylpyruvate are catalysed by Mn2+ ions and these reactions are activated by peroxidase; pyridoxamine increased both the rates and total oxygen uptakes in these reactions, and ammonia was produced. 6. The lag periods in the oxidation of mixtures of pyridoxamine and α-oxo acids, catalysed by Mn2+ ions, were also shortened by traces of colloidal manganese dioxide. 7. It is suggested that the activating effect of peroxidase depends on its catalysis of manganese oxidation.
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Research Article| July 01 1972
The oxidation of Schiff bases of pyridoxamine with α-oxo acids by manganous ions and peroxidase
Biochem J (1972) 128 (3): 701–709.
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J. M. Hill; The oxidation of Schiff bases of pyridoxamine with α-oxo acids by manganous ions and peroxidase. Biochem J 1 July 1972; 128 (3): 701–709. doi: https://doi.org/10.1042/bj1280701
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