详细信息
Screening of dandelion phenolic extracts and their anti-bacterial function against Escherichia coli through acting on Na+-K+ ATPase ( EI收录)
文献类型:期刊文献
英文题名:Screening of dandelion phenolic extracts and their anti-bacterial function against Escherichia coli through acting on Na+-K+ ATPase
作者:Xie, Pujun[1,2] Wang, Xiang[1,2] Huang, Lixin[1,2] Deng, Yejun[1,2] Zhang, Caihong[1,2]
第一作者:Xie, Pujun;谢普军
机构:[1] Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, National Engineering Laboratory for Biomass Chemical Utilization, Key and Open Laboratory on Forest Chemical Engineering, National Forestry and Grassland Administration, Key Laboratory of Biomass Energy and Material, Number 16 Suojin Wucun, Xuanwu District, Jiangsu Province, Nanjing City, 210042, China; [2] Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Nanjing Forestry University, Nanjing, 210037, China
年份:2024
卷号:6
期号:1
外文期刊名:Food Production, Processing and Nutrition
收录:EI(收录号:20244117177087);Scopus(收录号:2-s2.0-85205781364)
语种:英文
外文关键词:Cell membranes - Escherichia coli - Ligands - Molecular docking - Molecular dynamics
摘要:Food contamination by Escherichia coli (E. coli) is an increasing public health concern. Screening for natural plant preservatives has received increasing attention. In this study, dandelion flower phenolic extract (DFPE), with the strongest bacterial inhibition and the highest polyphenol level from various organs, was identified using HPLC and FTIR. The results showed a significant increase in extracellular ATP levels due to cellular membrane leakage in E. coli and decreased Na+-K+ ATPase activity. These behaviors were caused by representative phenolic compounds such as caffeic acid in DFPE. Molecular docking simulations were performed to reveal the mechanism of interaction between caffeic acid and Na+-K+ ATPase. This indicated that conventional hydrogen bonds, pi-anions, and pi-alkyl were involved in the interaction between them. Molecular dynamic equilibrium of the liganded ATPase complex was achieved after 20?ns. The lower values of Rg and SASA demonstrated that the liganded ATPase structure changed from a relatively loose to a tight state in the presence of caffeic acid. Overall, these findings are meaningful for screening bioactive compounds from various food-derived plant tissues using a combination of practical experimentation and molecular simulations. Graphical Abstract: (Figure presented.) ? The Author(s) 2024.
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