Characterization of the action of tyrosinase on resorcinols

Bioorg Med Chem. 2016 Sep 15;24(18):4434-4443. doi: 10.1016/j.bmc.2016.07.048. Epub 2016 Jul 22.

Abstract

The action of tyrosinase on resorcinol and some derivatives (4-ethylresorcinol, 2-methylresorcinol and 4-methylresorcinol) was investigated. If the catalytic cycle is completed with a reductant such as ascorbic acid or an o-diphenol such as 4-tert-butylcatechol, these compounds act as substrates of tyrosinase in all cases. The reaction can also be carried out, adding hydrogen peroxide to the medium. All the above compounds were characterized as substrates of the enzyme and their kinetic constants, KM (Michaelis constant) and kcat (catalytic constant) were determined. Measurement of the activity of the enzyme after pre-incubation with resorcinol, 4-ethylresorcinol or 4-methylresorcinol points to an apparent loss of activity at short times, which could correspond to an enzymatic inactivation process. However, if the measurements are extended over longer times, a burst is observed and the enzymatic activity is recovered, demonstrating that these compounds are not suicide substrates of the enzyme. These effects are not observed with 2-methylresorcinol. The docking results indicate that the binding of met-tyrosinase with these resorcinols occurs in the same way, but not with 2-methylresorcinol, due to steric hindrance.

Keywords: 2-Methylresorcinol; 4-Ethylresorcinol; 4-Methylresorcinol; Alternative substrate; Inhibitor; Kinetic; Resorcinol; Tyrosinase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Isomerism
  • Kinetics
  • Molecular Docking Simulation
  • Resorcinols / metabolism*
  • Substrate Specificity
  • Thermodynamics
  • Tyrosine / metabolism*

Substances

  • Resorcinols
  • Tyrosine