节点文献

苯甲醛族化合物抑制蘑菇酪氨酸酶活力的研究

Studies on Mushroom Tyrosinase Activity Inhibited by Benzaldehyde Family Compounds

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 黄璜刘晓丹陈清西

【Author】 HUANG Huang, LIU Xiaodan, CHEN Qingxi(School of Life Science, Xiamen University, Xiamen 361005, China)

【机构】 厦门大学生命科学学院厦门大学生命科学学院 福建厦门361005福建厦门361005福建厦门361005

【摘要】 报道几种苯甲醛族化合物对蘑菇酪氨酸酶催化L 多巴氧化反应活力的影响以及抑制作用机理.研究结果表明,苯甲醛族化合物对酶的效应表现为可逆抑制作用,苯甲醛及其m 和p 甲氧基取代物表现为非竞争性抑制,而o 位、m 位和p 位羟基取代物表现为竞争性抑制.通过测定酶活力下降50%的抑制剂浓度(IC50)和抑制常数来比较抑制剂作用的强度,探讨不同取代基团对抑制作用的影响.提出抑制剂与酶分子的作用模型.

【Abstract】 Tyrosinase (1.14.18.1) is a metalloenzyme oxidase which catalyzes two distinct reactions of melanin synthesisthe hydroxylation of a monophenol and the oxidation of odiphenol to the corresponding oquinone. Lots of benzaldehyde family can inhibit the enzyme activity for the oxidation of LDOPA. In the present paper, the inhibition kinetics and mechanism of benzaldehyde family compounds on the enzyme for the oxidation of LDOPA were studied. The results show that the inhibition of tyrosinase by benzaldehyde family is a reversible reaction with remaining enzyme activity. The inhibitory mechanism of benzaldehyde, mmethoxybenzaldehyde and pmethoxybenzaldehyde belongs to being noncompetitive while that of ohydroxybenzaldehyde, mhydroxybenzaldehyde and phydroxybenzaldehyde belongs to being competitive. The equilibrium constants for those inhibitors binding with the enzyme were determined.

【基金】 福建省自然科学基金(B0110002);教育部留学回国人员科研启动基金资助项目
  • 【文献出处】 厦门大学学报(自然科学版) ,Journal of Xiamen University(Natural Science) , 编辑部邮箱 ,2003年01期
  • 【分类号】S609.3
  • 【被引频次】66
  • 【下载频次】465
节点文献中: 

本文链接的文献网络图示:

本文的引文网络