溴化乙锭
流出
大肠杆菌
化学
微生物学
细菌外膜
膜
细菌
内膜
肉汤微量稀释
生物
最小抑制浓度
抗生素
生物化学
生物物理学
细胞分裂
抗生素耐药性
细菌细胞结构
分子生物学
抗药性
金融时报
细胞
ATP结合盒运输机
突变体
基因
DNA
作者
Enrico Casalone,Tiziano Vignolini,Laura Braconi,Lucia Gardini,Marco Capitanio,Francesco S. Pavone,Silvia Dei,Elisabetta Teodori
出处
期刊:Future Microbiology
[Future Medicine]
日期:2020-07-01
卷期号:15 (11): 987-999
被引量:3
标识
DOI:10.2217/fmb-2019-0296
摘要
Aim: To investigate the action mechanism of 1-benzyl-1,4-diazepane (1-BD) as efflux pump inhibitor (EPI) in Escherichia coli mutants: ΔacrAB or overexpressing AcrAB and AcrEF efflux pumps. Materials & methods: Effect of 1-BD on: antibiotic potentiation, by microdilution method; membrane functionality, by fluorimetric assays; ethidium bromide accumulation, by fluorometric real-time efflux assay; AcrB expression, by quantitative photoactivated localization microscopy. Results: 1-BD decreases the minimal inhibitory concentration of levofloxacin and other antibiotics and increase ethidium bromide accumulation in E. coli overexpressing efflux pumps but not in the ΔacrAB strain. 1-BD increases membranes permeability, without sensibly affecting inner membrane polarity and decreases acrAB transcription. Conclusion: 1-BD acts as an EPI in E. coli with a mixed mechanism, different from that of major reference EPIs.
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