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Published on: February 15, 2019
Inhibition of mushroom-tyrosinase by aloe extract
A Yagi1, T Kanbara, N Morinobu
1Faculty of Pharmaceutical Sciences, Fukuyama University, Fukuyama, Hiroshima, 729-02, Japan.
Abstract:
Inhibition by ALOE extracts of L-dopa oxidation by mushroom-tyrosinase was examined. 2''- O-Feruloylaloesin and aloesin at concentrations of 0.4 microM showed inhibition of 27 and 30%, respectively. Lineweaver-Burk plots of the concentration of L-dopa in the absence and presence of 2''- O-feruloylaloesin, 0.4 and 0.8 microM, showed that this compound inhibits mushroom-tyrosinase noncompetitively. The K (i) value obtained was 8.5 x 10 (-5) M. 2''- O-Feruloylaloesin and aloesin contents were analyzed by a reversed-phase HPLC, and their seasonal variations were observed.
Insights
Aloe extracts, including 2''-O-Feruloylaloesin and aloesin, effectively inhibit mushroom-tyrosinase, a key enzyme in L-dopa oxidation. These compounds show non-competitive inhibition, with seasonal variations in their content.
Area of Science:
- Biochemistry
- Enzymology
- Natural Product Chemistry
Background:
- Tyrosinase enzymes catalyze the oxidation of L-dopa, a crucial step in melanin biosynthesis.
- Mushroom-tyrosinase is a widely studied model enzyme for investigating tyrosinase inhibitors.
- Aloe extracts are known for various bioactive compounds with potential enzymatic inhibitory properties.
Purpose of the Study:
- To investigate the inhibitory effects of Aloe extracts on L-dopa oxidation by mushroom-tyrosinase.
- To characterize the mode of inhibition of key Aloe compounds on mushroom-tyrosinase.
- To analyze the seasonal variation of active compounds in Aloe extracts.
Main Methods:
- Enzyme inhibition assays using L-dopa as substrate and mushroom-tyrosinase.
- Kinetic analysis using Lineweaver-Burk plots to determine inhibition type and constants.
- Reversed-phase High-Performance Liquid Chromatography (HPLC) for quantification of active compounds.
Main Results:
- Aloe extracts, specifically 2''-O-Feruloylaloesin and aloesin, demonstrated significant inhibition of mushroom-tyrosinase.
- 2''-O-Feruloylaloesin exhibited non-competitive inhibition with a K(i) value of 8.5 x 10^-5 M at 0.4 and 0.8 microM concentrations.
- Seasonal variations in the content of 2''-O-Feruloylaloesin and aloesin were observed in the analyzed Aloe extracts.
Conclusions:
- 2''-O-Feruloylaloesin and aloesin are potent inhibitors of mushroom-tyrosinase, acting via a non-competitive mechanism.
- The findings suggest potential applications of these Aloe compounds in controlling enzymatic browning or as therapeutic agents.
- Understanding the seasonal variability of these compounds is important for consistent extraction and application.
