绿茶儿茶素可猝灭细菌偶联Alexa荧光染料的荧光。

Lin Zhao, Wei Li, Shu Zhu, Sheena Tsai, Jianhua Li, Kevin J Tracey, Ping Wang, Saijun Fan, Andrew E Sama, Haichao Wang
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引用次数: 14

摘要

越来越多的证据表明,绿茶多酚儿茶素,特别是(-)-表没食子儿茶素没食子酸酯(EGCG),可以与许多蛋白质交联,并可能通过破坏微生物细胞质脂质和蛋白质而赋予广泛的抗菌活性。EGCG的剂量对致命的多微生物感染(由盲肠结扎和穿刺引起)具有保护作用,显著降低了细菌负荷,尤其是肝脏和肺部的细菌负荷。为了阐明其杀菌机制,我们测定了EGCG是否影响细菌偶联Alexa Fluor 488或594染料的荧光强度。当与未共轭的Alexa Fluor 488或594染料混合时,EGCG或类似物不影响这些染料的荧光强度。与此形成鲜明对比的是,EGCG和一些类似物(如儿茶素没食子酸酯,CG)显著降低了革兰氏阳性金黄色葡萄球菌偶联的Alexa 594和革兰氏阴性大肠杆菌偶联的Alexa 488的荧光强度。有趣的是,与乙醇共处理会破坏egcg介导的G(+)金黄色葡萄球菌的荧光猝灭,但不会破坏G(-)大肠杆菌结合的Alexa面粉染料。鉴于Alexa氟染料可以被芳香氨基酸猝灭的概念,EGCG可能通过改变微生物蛋白质的构象和功能来发挥抗菌活性是合理的。现在可以通过筛选其他可能具有抗菌活性的荧光猝灭剂来探索这种可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Green tea catechins quench the fluorescence of bacteria-conjugated Alexa fluor dyes.

Accumulating evidence suggests that Green tea polyphenolic catechins, especially the (-)-epigallocatechin gallate (EGCG), can be cross-linked to many proteins, and confer a wide range of anti-bacterial activities possibly by damaging microbial cytoplasmic lipids and proteins. At the doses that conferred protection against lethal polymicrobial infection (induced by cecal ligation and puncture), EGCG significantly reduced bacterial loads particularly in the liver and lung. To elucidate its bactericidal mechanisms, we determined whether EGCG affected the fluorescence intensities of bacteria-conjugated Alexa Fluor 488 or 594 dyes. When mixed with unconjugated Alexa Fluor 488 or 594 dyes, EGCG or analogs did not affect the fluorescence intensity of these dyes. In a sharp contrast, EGCG and some analogs (e.g., Catechin Gallate, CG), markedly reduced the fluorescence intensity of Gram-positive Staphylococcus aureus-conjugated Alexa 594 and Gram-negative Escherichia coli-conjugated Alexa 488. Interestingly, co-treatment with ethanol impaired the EGCG-mediated fluorescence quenching of the G(+) S. aureus, but not of the G(-) E. coli-conjugated Alexa Flour dyes. In light of the notion that Alexa Fluor dyes can be quenched by aromatic amino acids, it is plausible that EGCG exerts antimicrobial activities possibly by altering microbial protein conformations and functions. This possibility can now be explored by screening other fluorescence-quenching agents for possible antimicrobial activities.

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