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Inhibitory effects of hinokitiol on tyrosinase activity and melanin biosynthesis and its antimicrobial activities

机译:扁柏酚对酪氨酸酶活性和黑色素生物合成的抑制作用及其抗菌活性

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The inhibitory effects of hinokitiol, a constituent of the woody oils isolated from Cupressaceae heartwood, on mushroom tyrosinase and melanin formation in B16 melanoma cells as well as its antimicrobial activity were investigated. Our results showed that hinokitiol could strongly inhibit both monophenolase activity and diphenolase activity of the enzyme and the inhibition was reversible. The IC50 values were estimated as 9.67 μM for monophenolase activity and 0.21 μM for diphenolase activity. The lag time of the monophenolase activity was not obviously lengthened by the compound. Kinetic analyses showed that the inhibition mechanism of hinokitiol was a mixed-type inhibition of the diphenolase activity. Hinokitiol effectively inhibited both cellular tyrosinase activity and melanin biosynthesis in B16 melanoma cells with significant cytotoxicity. Furthermore, it was found that hinokitiol could inhibit the proliferation of Salmonella enteritidis , Escherichia coli , Bacillus subtilis , Staphyloccocus aureus , Klebsiella pneumoniae , and Ralstonia solanacearum to different extents. This research may widen the use of hinokitiol in the fields of food preservation, depigmentation, and insecticide use.
机译:研究了从柏柏心材中分离出来的木酚类成分扁柏酚对蘑菇酪氨酸酶和B16黑色素瘤细胞黑色素形成的抑制作用及其抗菌活性。我们的结果表明,扁柏酚可以强烈抑制该酶的单酚酶活性和双酚酶活性,并且这种抑制作用是可逆的。 IC 50 的值估计单酚酶活性为9.67μm,双酚酶活性为0.21μm。该化合物没有明显延长单酚酶活性的滞后时间。动力学分析表明,扁柏酚的抑制机理是对双酚酶活性的混合型抑制。 Hinokitiol有效抑制B16黑色素瘤细胞中的细胞酪氨酸酶活性和黑色素生物合成,具有明显的细胞毒性。此外,发现酚可以不同程度地抑制肠炎沙门氏菌,大肠杆菌,枯草芽孢杆菌,金黄色葡萄球菌,肺炎克雷伯菌和青枯雷尔氏菌的增殖。这项研究可以扩大扁柏酚在食品保存,脱色和杀虫剂使用方面的用途。

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