Université de Toulouse; INSA, UPS, INP; LISBP, F-31077 Toulouse, France.
J Microbiol Methods. 2012 Oct;91(1):8-13. doi: 10.1016/j.mimet.2012.07.002. Epub 2012 Jul 14.
Quantification of different physiological states of Candida shehatae cells was performed by flow cytometry associated with two fluorescent probes. Propidium iodide and carboxyfluorescein diacetate acetoxymethyl ester fluorescent dyes were chosen based on data from the literature. A staining procedure, developed from the previous works was applied to the yeast. Then, the protocol was improved to fit with fermentation constraints such as no physiological interference between the staining procedure and the cells, shortest preparation time and small amounts of dyes. From this optimisation, propidium iodide was included in the sample at 8 mg/L whereas carboxyfluorescein was first diluted in Pluronic® agent and used at 3mg/L, samples were incubated for 10 min at 40°C. Repeatability and accuracy were evaluated to validate this flow cytometry procedure for viability determination.
采用流式细胞术结合两种荧光探针对谢氏念珠菌细胞的不同生理状态进行定量分析。根据文献数据,选择碘化丙啶和羧基荧光素二乙酸乙酰甲酯荧光染料。从先前的工作中开发出一种染色程序应用于酵母。然后,对方案进行了改进,以适应发酵的限制,如染色程序和细胞之间没有生理干扰、最短的准备时间和染料用量小。通过这种优化,将 8mg/L 的碘化丙啶纳入样品中,而将羧基荧光素首先在 Pluronic®试剂中稀释,然后以 3mg/L 的浓度使用,样品在 40°C 下孵育 10 分钟。为了验证该用于测定生存力的流式细胞术程序的重复性和准确性,对其进行了评估。