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果糖嗪,一种具有抗菌活性的多羟基烷基吡嗪:对极耐热大肠杆菌的抑制机制

Fructosazine, a Polyhydroxyalkylpyrazine with Antimicrobial Activity: Mechanism of Inhibition against Extremely Heat Resistant Escherichia coli.

作者信息

Bhattacherjee Abhishek, Hrynets Yuliya, Betti Mirko

机构信息

Department of Agricultural, Food and Nutritional Science, University of Alberta , 410 Agriculture/Forestry Centre, Edmonton, AB T6G 2P5 Canada.

出版信息

J Agric Food Chem. 2016 Nov 16;64(45):8530-8539. doi: 10.1021/acs.jafc.6b03755. Epub 2016 Nov 2.

Abstract

Fructosazine is a polyhydroxyalkylpyrazine recently reported to have antimicrobial activity against heat-resistant Escherichia coli AW 1.7. This study investigated fructosazine's antimicrobial mechanism of action and compared it to that of riboflavin. Fructosazine-acetic acid was effective in permeabilizing the outer membrane based on an evaluation of bacterial membrane integrity using 1-N-phenyl-1-naphthylamine and propidium iodide. The uptake of fructosazine by E. coli was pH-dependent with a greater uptake at pH 5 compared to pH 7 for all times throughout 16 h, except 2, 3, and 10 h. Fructosazine generates O, which is partially why it damages E. coli. DNA fragmentation was confirmed by fluorescence microscopy, and the fructosazine-acetic acid was the second most intense treatment after riboflavin-acetic acid. Electron microscopy revealed membrane structural damage by fructosazine at pH 5 and 7. This study provides evidence that fructosazine exerts antimicrobial action by permeabilizing the cell membrane, damaging membrane integrity, and fragmenting DNA.

摘要

果糖嗪是一种多羟基烷基吡嗪,最近有报道称其对耐热大肠杆菌AW 1.7具有抗菌活性。本研究调查了果糖嗪的抗菌作用机制,并将其与核黄素的抗菌作用机制进行了比较。基于使用1-N-苯基-1-萘胺和碘化丙啶对细菌膜完整性的评估,果糖嗪-乙酸可有效使外膜通透。大肠杆菌对果糖嗪的摄取具有pH依赖性,在16小时内的所有时间里,除了2、3和10小时外,pH 5时的摄取量均高于pH 7时。果糖嗪会产生氧,这是其损害大肠杆菌的部分原因。通过荧光显微镜确认了DNA片段化,果糖嗪-乙酸是仅次于核黄素-乙酸的第二强烈处理。电子显微镜显示,在pH 5和7时,果糖嗪会破坏膜结构。本研究提供了证据表明,果糖嗪通过使细胞膜通透、破坏膜完整性和使DNA片段化来发挥抗菌作用。

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