Hematoxylin, an Alternative Substrate of Tyrosinase

Author:

Crous Chantalle1,Swart Ivanke A.1,Pretorius Judey2,van der Kooy Frank1ORCID,Petzer Jacobus P.ORCID,Petzer AnélORCID

Affiliation:

1. Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa

2. Biomedical Emporium, Pretoria, South Africa

Abstract

AbstractMushroom tyrosinase from Agaricus bisporus (abTYR) is often used during the development of tyrosinase inhibitors for medicinal and cosmetic purposes. In the search for novel tyrosinase inhibitors, this study identified hematoxylin as an alternative substrate for abTYR. The interaction of hematoxylin with abTYR was investigated through spectrophotometric and chromatographic analyses. The results showed that hematoxylin acted as an abTYR substrate and exhibited Michaelis–Menten kinetic behaviour at concentrations below 1.25 mM. The substrate properties of hematoxylin were similar to the natural tyrosinase substrate, L-3,4-dihydroxyphenylalanine (L-DOPA), with regards to Km, while Vmax was eightfold lower. The main oxidation product formed during the reaction of abTYR with hematoxylin was identified as hematein. This is the first report of the interaction of hematoxylin with abTYR.

Funder

Biomedical Emporium

Publisher

Georg Thieme Verlag KG

Reference13 articles.

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