Kinetic, Fluorescence Spectroscopy and Molecular Docking Studies of Tyrosinase Inhibition by Ellagic Acid

被引:0
|
作者
Ni D. [1 ]
Jiang X. [2 ]
Tang Y. [2 ]
He S. [2 ]
Yang Y. [1 ]
机构
[1] College of Science, Central South University of Forestry and Technology, Changsha
[2] College of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha
来源
Shipin Kexue/Food Science | 2024年 / 45卷 / 02期
关键词
ellagic acid; inhibition mechanism; molecular docking; mushroom tyrosinase; spectroscopic analysis;
D O I
10.7506/spkx1002-6630-20230411-097
中图分类号
学科分类号
摘要
In this study, inhibition kinetics, fluorescence spectroscopy and molecular docking simulation were used to systematically investigate the inhibitory effect and mechanism of EA on mushroom tyrosinase. The in vitro study and kinetic results showed that EA significantly inhibited tyrosinase activity with a half maximal inhibitory concentration (IC50) of 0.05 mg/mL in a reversible mixed-type manner; the binding constant KI was smaller than KIS, indicating that EA bound more tightly to the free enzyme than to the enzyme-substrate complex. The fluorescence of tyrosinase was quenched statically by EA, and they combined to generate a complex through a spontaneous endothermal process, with hydrophobic interaction being the main force; there was only one binding site or class of binding sites. Simultaneous and three-dimensional fluorescence spectroscopy analysis showed that EA increased the polarity of the microenvironment of tyrosinase, decreased the hydrophobicity, and brought the Trp residues of tyrosinase closer to the binding site. Molecular docking simulation analysis further complemented and validated the above results by showing visually that EA was a mixed-type tyrosinase inhibitor, binding to the free enzyme or enzyme-substrate complex mainly through hydrophobic interactions and hydrogen bonding, ultimately leading to reduced enzyme activity. This study is of reference significance for the application of EA as a preservative in the food industry. © 2024 Chinese Chamber of Commerce. All rights reserved.
引用
收藏
页码:104 / 112
页数:8
相关论文
共 29 条
  • [1] ZOLGHADRI S, BAHRAMI A, HASSAN-KHAN M T, Et al., A comprehensive review on tyrosinase inhibitors, Journal of Enzyme Inhibition and Medicinal Chemistry, 34, 1, pp. 279-309, (2019)
  • [2] FERNANDES M S, KERKAR S., Microorganisms as a source of tyrosinase inhibitors: a review, Annals of Microbiology, 67, 4, pp. 343-358, (2017)
  • [3] MASUM M N, YAMAUCHI K, MITSUNAGA T., Tyrosinase inhibitors from natural and synthetic sources as skin-lightening agents, Reviews in Agricultural Science, 7, pp. 41-58, (2019)
  • [4] LIN M Z, CHAI W M, OUYANG C, Et al., Antityrosinase mechanism of omeprazole and its application on the preservation of fresh-cut Fuji apple, International Journal of Biological Macromolecules, 117, pp. 538-545, (2018)
  • [5] WU Y, CHOI M H, LI J, Et al., Mushroom cosmetics: the present and future, Cosmetics, 3, 3, (2016)
  • [6] WEN Y T, ZHANG Y J, ZHANG X L, Et al., Inhibition of albendazole and 2-(2-aminophenyl)-1H-benzimidazole against tyrosinase: mechanism, structure-activity relationship, and anti-browning effect, Journal of the Science of Food and Agriculture, 103, 6, pp. 2824-2837, (2023)
  • [7] BENSAAD L A, KIM K H, QUAH C C, Et al., Anti-inflammatory potential of ellagic acid, gallic acid and punicalagin A&B isolated from Punica granatum, BMC Complementary and Alternative Medicine, 17, pp. 1-10, (2017)
  • [8] pp. 351-355, (2014)
  • [9] YANG H L, LIN C P, GOWRISANKAR Y V, Et al., The anti-melanogenic effects of ellagic acid through induction of autophagy in melanocytes and suppression of UVA-activated α-MSH pathways via Nrf2 activation in keratinocytes, Biochemical Pharmacology, 185, (2021)
  • [10] SOLIMINE J, GARO E, WEDLER J, Et al., Tyrosinase inhibitory constituents from a polyphenol enriched fraction of rose oil distillation wastewater, Fitoterapia, 108, pp. 13-19, (2016)