膜流动性
膜
劳丹
细菌
细胞膜
细菌细胞结构
生物物理学
枯草芽孢杆菌
生物
化学
生物化学
遗传学
作者
Michaela Wenzel,Norbert O. E. Vischer,Henrik Strahl,Leendert W. Hamoen
出处
期刊:Bio-protocol
[Bio-Protocol]
日期:2018-01-01
卷期号:8 (20)
被引量:43
标识
DOI:10.21769/bioprotoc.3063
摘要
Membrane fluidity is a key parameter of bacterial membranes that undergoes quick adaptation in response to environmental challenges and has recently emerged as an important factor in the antibacterial mechanism of membrane-targeting antibiotics. The specific level of membrane fluidity is not uniform across the bacterial cell membrane. Rather, specialized microdomains associated with different cellular functions can exhibit fluidity values that significantly deviate from the average. Assessing changes in the overall membrane fluidity and formation of membrane microdomains is therefore pivotal to understand both the functional organization of the bacterial cell membrane as well as antibiotic mechanisms. Here we describe how two fluorescent membrane dyes, laurdan and DiIC12, can be employed to assess membrane fluidity in living bacteria. We focus on Bacillus subtilis, since this organism has been relatively well-studied with respect to membrane domains. However, we also describe how these assays can be adapted for other bacteria such as Staphylococcus aureus and Streptococcus pneumoniae.
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