Optimization of labeling and localizing bacterial membrane and nucleus with FM4-64 and Hoechst dyes
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Supported by the National Science Foundation of China (31171248),by the Key Project of China National Programs for Fundamental Research and Development (2014CB744405) and by the Hebei Province Science and Technology Plan Projects[14236602D-3(2014)]

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    Abstract:

    Abstract:[Objective]To observe cell membrane and nucleus in bacteria for subcellular localization.[Methods]FM4-64 and Hoechst were dyed that can label cell membrane and nucleus,respectively. Both dyes were used to co-stain the membranes and nucleus of eight bacterial strains ( Escherichia coli,Staphylococcus aureus,Pseudomonas aeruginosa,Klebsiella pneumoniae,Yersinia pestis,Legionella pneumonia,Vibrio cholerae and Bacillus anthracis). E.coli was dyed with different dye concentrations and times and then observed by confocal fluorescence microscopic imaging.[Results]Fluorescence intensity of cell membrane and nucleus is affected by dye concentrations and times. The optimal conditions were determined as follows: staining cell membrane with 20 μg/mL FM4-64 for 1 min and cell nucleus with 20 μg/mL Hoechst for 20 min.Gram-negative bacteria were dyed better than gram-positive bacteria with FM4-64dye.[Conclusion]FM4-64 and Hoechst can be used to stain membrane and nucleus in different types of bacteria.Co-staining bacterial membrane and nucleus provides the reference to observe cell structure in prokaryotes for studying subcellular localization.

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Jing Wang, Yanping Han, Ruifu Yang, Xingxu Zhao. Optimization of labeling and localizing bacterial membrane and nucleus with FM4-64 and Hoechst dyes. [J]. Acta Microbiologica Sinica, 2015, 55(8): 1068-1073

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History
  • Received:December 19,2014
  • Revised:February 27,2015
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  • Online: July 27,2015
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