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表没食子儿茶素没食子酸酯及相关植物多酚作为细菌II型脂肪酸合酶的FabG和FabI还原酶抑制剂的评估

Evaluation of epigallocatechin gallate and related plant polyphenols as inhibitors of the FabG and FabI reductases of bacterial type II fatty-acid synthase.

作者信息

Zhang Yong-Mei, Rock Charles O

机构信息

Protein Science Division, Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

出版信息

J Biol Chem. 2004 Jul 23;279(30):30994-1001. doi: 10.1074/jbc.M403697200. Epub 2004 May 7.

Abstract

Epigallocatechin gallate (EGCG) is the major component of green tea extracts and possesses antibacterial, antiviral, and antitumor activity. Our study focused on validating the inhibition of the bacterial type II fatty acid synthesis system as a mechanism for the antibacterial effects of EGCG and related plant polyphenols. EGCG and the related tea catechins potently inhibited both the FabG and FabI reductase steps in the fatty acid elongation cycle with IC(50) values between 5 and 15 microm. The presence of the galloyl moiety was essential for activity, and EGCG was a competitive inhibitor of FabI and a mixed type inhibitor of FabG demonstrating that EGCG interfered with cofactor binding in both enzymes. EGCG inhibited acetate incorporation into fatty acids in vivo, although it was much less potent than thiolactomycin, a validated fatty acid synthesis inhibitor, and overexpression of FabG, FabI, or both did not confer resistance. A panel of other plant polyphenols was screened for FabG/FabI inhibition and antibacterial activity. Most of these inhibited both reductase steps, possessed antibacterial activity, and inhibited cellular fatty acid synthesis. The ability of the plant secondary metabolites to interfere with the activity of multiple NAD(P)-dependent cellular processes must be taken into account when assessing the specificity of their effects.

摘要

表没食子儿茶素没食子酸酯(EGCG)是绿茶提取物的主要成分,具有抗菌、抗病毒和抗肿瘤活性。我们的研究重点是验证抑制细菌II型脂肪酸合成系统作为EGCG及相关植物多酚抗菌作用的一种机制。EGCG和相关的茶儿茶素能有效抑制脂肪酸延长循环中的FabG和FabI还原酶步骤,IC50值在5至15微摩尔之间。没食子酰基部分的存在对活性至关重要,EGCG是FabI的竞争性抑制剂和FabG的混合型抑制剂,表明EGCG干扰了这两种酶中辅因子的结合。EGCG在体内抑制乙酸盐掺入脂肪酸,尽管其效力远低于已证实的脂肪酸合成抑制剂硫内酯霉素,并且FabG、FabI或两者的过表达均未赋予抗性。对一组其他植物多酚进行了FabG/FabI抑制和抗菌活性筛选。其中大多数抑制了两个还原酶步骤,具有抗菌活性,并抑制细胞脂肪酸合成。在评估植物次生代谢产物作用的特异性时,必须考虑它们干扰多种依赖NAD(P)的细胞过程活性的能力。

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