Hydroxylation of p-substituted phenols by tyrosinase: Further insight into the mechanism of tyrosinase activity

• Published in: Biochemical and biophysical research communications Vol. 424; no. 2; pp. 228 - 233
• Main Authors: Muñoz-Muñoz, Jose Luis, Berna, Jose, García-Molina, María del Mar, Garcia-Molina, Francisco, Garcia-Ruiz, Pedro Antonio, Varon, Ramon, Rodriguez-Lopez, Jose N., Garcia-Canovas, Francisco
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 27.07.2012
• Subjects: 60 APPLIED LIFE SCIENCES; Agaricales - enzymology; AQUEOUS SOLUTIONS; BENZENE; CARBON; CHEMICAL SHIFT; COPPER COMPLEXES; DEUTERIUM; FLUORINE IONS; Hammett equation; HYDROXIDES; HYDROXYLATION; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; ISOTOPE EFFECTS; Isotopic effect; Kinetics; Monophenol Monooxygenase - chemistry; Monophenols; OXIDATION; Oxidoreductases - chemistry; PEROXIDES; PH VALUE; PHENOL; Phenols - chemistry; PHOSPHORUS IONS; SOLVENTS; Steady-state; STEADY-STATE CONDITIONS; SUBSTRATES; TYROSINASE; Hammett equation; Monophenols; Steady-state; Tyrosinase; Isotopic effect
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2012.06.074

► The action the copper complexes and tyrosinase on phenols is equivalent. ► Isotope effect showed that nucleophilic attack to copper atom may be the slower step. ► The value of ρ (Hammett constant) supports an electrophilic aromatic substitution. ► Data obtained in steady state pH 7 conditions support the mechanism of Scheme 1SM. A study of the monophenolase activity of tyrosinase by measuring the steady state rate with a group of p-substituted monophenols provides the following kinetic information: kcatm and the Michaelis constant, KMm. Analysis of these data taking into account chemical shifts of the carbon atom supporting the hydroxyl group (δ) and σp+, enables a mechanism to be proposed for the transformation of monophenols into o-diphenols, in which the first step is a nucleophilic attack on the copper atom on the form Eox (attack of the oxygen of the hydroxyl group of C-1 on the copper atom) followed by an electrophilic attack (attack of the hydroperoxide group on the ortho position with respect to the hydroxyl group of the benzene ring, electrophilic aromatic substitution with a reaction constant ρ of −1.75). These steps show the same dependency on the electronic effect of the substituent groups in C-4. Furthermore, a study of a solvent deuterium isotope effect on the oxidation of monophenols by tyrosinase points to an appreciable isotopic effect. In a proton inventory study with a series of p-substituted phenols, the representation of kcatfn/kcatf0 against n (atom fractions of deuterium), where kcatfn is the catalytic constant for a molar fraction of deuterium (n) and kcatf0 is the corresponding kinetic parameter in a water solution, was linear for all substrates. These results indicate that only one of the proton transfer processes from the hydroxyl groups involved the catalytic cycle is responsible for the isotope effects. We suggest that this step is the proton transfer from the hydroxyl group of C-1 to the peroxide of the oxytyrosinase form (Eox). After the nucleophilic attack, the incorporation of the oxygen in the benzene ring occurs by means of an electrophilic aromatic substitution mechanism in which there is no isotopic effect.