抗菌肽
乳酸链球菌素
巨芽孢杆菌
抗菌剂
细菌
细胞内
行动方式
膜
黄色微球菌
细菌素
肽
生物
微生物学
生物化学
镧系元素
化学
金黄色葡萄球菌
遗传学
作者
Xiaoqi Wang,Roy A. M. van Beekveld,Yang Xu,Anish Parmar,Sanjit Das,Ishwar Singh,Eefjan Breukink
标识
DOI:10.1016/j.bbamem.2023.184160
摘要
Antimicrobial peptides (AMPs) commonly target bacterial membranes and show broad-spectrum activity against microorganisms. In this research we used three AMPs (nisin, epilancin 15×, [R4L10]-teixobactin) and tested their membrane effects towards three strains (Staphylococcus simulans, Micrococcus flavus, Bacillus megaterium) in relation with their antibacterial activity. We describe fluorescence and luminescence-based assays to measure effects on membrane potential, intracellular pH, membrane permeabilization and intracellular ATP levels. The results show that our control peptide, nisin, performed mostly as expected in view of its targeted pore-forming activity, with fast killing kinetics that coincided with severe membrane permeabilization in all three strains. However, the mechanisms of action of both Epilancin 15× as well as [R4L10]-teixobactin appeared to depend strongly on the bacterium tested. In certain specific combinations of assay, peptide and bacterium, deviations from the general picture were observed. This was even the case for nisin, indicating the importance of using multiple assays and bacteria for mode of action studies to be able to draw proper conclusions on the mode of action of AMPs.
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