Enzymatic Reaction (image will open in a new window)
Polyphenol oxidase (tyrosinase) (TY) is a bifunctional, copper-containing oxidase having both catecholase and cresolase activity (Malmström and Rydén 1968):
Jolley et al. (1974) refer to it as an oxygen and 4 electron-transferring phenol oxidase. It is responsible for browning reactions throughout the phylogenetic scale.
Although a tyrosinase from Neurospora crassa has been purified (Fling et al. 1963), most work has been done with the mushroom enzyme, even though yields and consistency are poor; its multiplicity was shown by Smith and Krueger (1962). Bouchilloux et al. (1963) obtained four enzymes. See review by Nelson and Mason (1970).
Characteristics of Polyphenol Oxidase from Mushroom:
Molecular weight: 128,000 (Duckworth and Coleman 1970).
Composition: The enzyme is a tetramer containing four gram atoms of copper per molecule (Jolley et al. 1974), and two binding sites for aromatic compounds including phenolic substrates. There is also a distinctly different binding site for oxygen, the copper site (Duckworth and Coleman 1970). The copper is probably in the cuprous state; inactivation of the enzyme is associated with increase in Cu2+. (Kertész et al. 1972). The amino acid composition has been determined. Extensive structural studies have been reported by Jolley et al. (1969); and Duckworth and Coleman (1970). See also Jolley et al. (1972, 1973, and 1974).
Optimum pH: 6.0-7.0.
Extinction coefficent: = 24.9 (immediately after purification) (Duckworth and Coleman 1970).
Inhibitors: Compounds that complex with copper. The enzyme is also inhibited competitively by benzoic acid with respect to catechol and by cyanide with respect to oxygen (Duckworth and Coleman 1970).
Activity: Polyphenol oxidase is an oxygen transferring enzyme. Besides using O2 to catalyze the dehydrogenation of catechols to orthoquinones and the orthohydroxylation of phenols to catechols, a peroxidase activity has been reported on by Strothkamp and Mason (1974). Kinetic studies have been reported by Kertész et al. (1971). See also the review by Malmström and Rydén.
Specificity: A large number of parasubstituted catechols areoxidized (Duckworth and Coleman 1970).
Stability: The lyophilized preparation is stable for 6-12 months when stored at -20°C.
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