金黄色葡萄球菌
细菌
铜绿假单胞菌
微生物学
大肠杆菌
染色
抗菌活性
细菌细胞结构
细胞外
沙门氏菌
膜
荧光染色
化学
生物
生物化学
基因
遗传学
作者
Natalia A. Scilletta,Magdalena Pezzoni,Martín F. Desimone,Galo J. A. A. Soler‐Illia,Martín G. Bellino,Paolo N. Catalano
出处
期刊:Bio-protocol
[American Academy of Arts and Sciences]
日期:2021-01-01
卷期号:11 (2): e3887-e3887
被引量:8
标识
DOI:10.21769/bioprotoc.3887
摘要
were incubated on titania mesostructured thin film coatings for 24 h. Then, cell viability was studied considering three methods: counting of the number of colony forming units (CFU), live/dead staining, and quantification of extracellular DNA in suspension. Firstly, bacterial count was determined by the standard plate-count technique. Secondly, bacteria membrane integrity was evaluated by utilization of two fluorescent dyes, which allow distinction between live (membrane intact) and dead (membrane disrupted) bacteria. Lastly, extracellular DNA was quantified by spectrophotometry. In this manner, the three aforementioned techniques enabled the study of bacterial viability by qualitative and quantitative analyses.
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