A structure-activity relationship study of flavonoids as inhibitors of E. coli by membrane interaction effect

被引:162
|
作者
Wu, Ting [1 ]
He, Mengying [1 ]
Zang, Xixi [1 ]
Zhou, Ying [1 ]
Qiu, Tianfu [1 ]
Pan, Siyi [1 ]
Xu, Xiaoyun [1 ]
机构
[1] Huazhong Agr Univ, Minist Educ, Key Lab Environm Correlat Dietol, Wuhan 430070, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Flavonoids; Antibacterial activity; E; coli; Membrane interaction; Fluorescence polarization; QSAR; ANTIBACTERIAL ACTIVITY; ANTIMICROBIAL ACTIVITY; STAPHYLOCOCCUS-AUREUS; MOLECULAR-STRUCTURE; QSAR; FLUIDITY; PROTEIN;
D O I
10.1016/j.bbamem.2013.07.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Flavonoids exhibit a broad range of biological activities including antibacterial activity. However, the mechanism of their antibacterial activity has not been fully investigated. The antibacterial activity and membrane interaction of 11 flavonoids (including 2 polymethoxyflavones and 4 isoflavonoids) against Escherichia coli were examined in this study. The antibacterial capacity was determined as flavonoids > polymethoxyflavones > isoflavonoids. Using fluorescence, it was observed that the 5 flavonoids rigidified the liposomal membrane, while the polymethoxyflavones and isoflavonoids increased membrane fluidity. There was a significant positive correlation between antibacterial capacity and membrane rigidification effect of the flavonoids. A quantitative structure activity relationship (QSAR) study demonstrated that the activity of the flavonoid compounds can be related to molecular hydrophobicity (CLogP) and charges on C atom at position3 (C3). The QSAR model could be used to predict the antibacterial activity of flavonoids which could lead to natural compounds having important use in food and medical industry. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:2751 / 2756
页数:6
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