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Antityrosinase and antimicrobial activities of 2-phenylethanol, 2-phenylacetaldehyde and 2-phenylacetic acid
Authors:Yu-Jing Zhu  Han-Tao Zhou  Yong-Hua Hu  Jian-Yang Tang  Ming-Xing Su  Yun-Ji Guo  Qing-Xi Chen  Bo Liu
Affiliation:1. Agricultural Bio-resources Institute, Fujian Academy of Agricultural Sciences, Fuzhou, China;2. Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystems, School of Life Sciences, Xiamen University, Xiamen 361005, China;3. Key Laboratory for Chemical Biology of Fujian Province, Xiamen University, Xiamen, China
Abstract:The inhibition kinetics of 2-phenylethanol, 2-phenylacetaldehyde and 2-phenylacetic acid on the enzyme activity of mushroom tyrosinase have been investigated. The results showed that these aromatic compounds can lead to reversible inhibition of the enzyme; furthermore, 2-phenylacetaldehyde and 2-phenylacetic acid are uncompetitive inhibitors and 2-phenylethanol is a mixed-type inhibitor. The inhibition constants have been determined and the inhibiting ability was: 2-phenylacetaldehyde > 2-phenylacetic acid > 2-phenylethanol, indicating that the functional group on the benzene ring group played an important role in the inhibition of the enzyme. In addition, 2-phenylacetic acid and 2-phenylethanol were found to have effective antibacterial activities, and 2-phenylacetic acid was more effective against Escherichia coli and Ralstonia solanacearum than 2-phenylethanol, but 2-phenylacetaldehyde lacked of antibacterial activity.
Keywords:l-DOPA  l-3  4-dihydroxyphenylalanine  DMSO  dimethylsulfoxide  IC50  the inhibitor concentrations leading to 50% activity lost  MIC  the minimum inhibitory concentration  MBC  the minimum bactericidal concentration  KI  the equilibrium constant of the inhibitor combining with the free enzyme  KIS  the equilibrium constant of the inhibitor combining with the enzyme&ndash  substrate complex
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