Literature DB >> 2853110

The stoichiometry of tyrosinase-catalyzed oxidation of 4-hydroxyanisole.

J W Dobrucki1, P A Riley.   

Abstract

Oxygen utilisation during tyrosinase-catalysed oxidation of 4-hydroxyanisole was investigated using an electron spin resonance technique which employs quantitative changes in the characteristics of the electron spin resonance spectrum of the spin label 3-carbamoyl-2,5-dihydro-2,2,5-5-tetramethyl-1-H-pyridoyl-1-ylox y (CTPO) to follow changes in the oxygen concentration. Reaction mixtures containing mushroom tyrosinase (15 micrograms ml-1) and differing initial concentrations of 4-hydroxyanisole in aerated phosphate buffer at pH 6.8 were incubated at room temperature. The ratio of utilisation of oxygen was found to be in approximately 1:1 molar ratio with the initial 4-hydroxyanisole concentration in the reaction mixture between 50 and 200 mumol/l 4-hydroxyanisole. The results are consistent with the stoichiometry of oxygen utilisation being accounted for by the oxidation of 4-hydroxyanisole to anisyl quinone.

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Year:  1988        PMID: 2853110     DOI: 10.3109/10715768809066898

Source DB:  PubMed          Journal:  Free Radic Res Commun        ISSN: 8755-0199


  1 in total

1.  Oxidation of monohydric phenol substrates by tyrosinase. An oximetric study.

Authors:  S Naish-Byfield; P A Riley
Journal:  Biochem J       Date:  1992-11-15       Impact factor: 3.857

  1 in total

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