Delobel P, Pradal M, Blondin B, Tesniere C
INRA, UMR1083, Sciences pour l'Oenologie, Montpellier, France SupAgro, UMR1083, Sciences pour l'Oenologie, Montpellier, France.
Lett Appl Microbiol. 2012 Nov;55(5):338-44. doi: 10.1111/j.1472-765X.2012.03301.x. Epub 2012 Sep 11.
To show that in anaerobic fermentation with limiting lipid nutrients, cell preparation impacts the viability assessment of yeast cells, and to identify the factors involved.
Saccharomyces cerevisiae viability was determined using propidium iodide staining and the flow cytometry. Analyses identified intact cells, dead cells and, under certain conditions, the presence of a third subpopulation of apparently damaged cells. This intermediate population could account for up to 40% of the entire cell population. We describe, analyse and discuss the effects of different solutions for cell resuspension on the respective proportion of these three populations, in particular that of the intermediate population. We show that this intermediate cell population forms in the absence of Ca(2+)/Mg(2+).
Cell preparation significantly impacts population viability assessment by FCM. The intermediate population, revealed under certain conditions, could be renamed as 'fragile cells'. For these cells, Ca(2+) and Mg(2+) reduce cell membrane permeability to PI.
This is the first study that analyses and discusses the factors influencing the formation of an intermediate population when studying viability in yeast alcoholic fermentation. With a wider application in biological research, this study provides important support to the relatively new questioning of propidium iodide staining as a universal cell death indicator.
证明在脂质营养受限的厌氧发酵中,细胞制备会影响酵母细胞的活力评估,并确定其中涉及的因素。
使用碘化丙啶染色和流式细胞术测定酿酒酵母的活力。分析确定了完整细胞、死亡细胞,以及在某些条件下存在的第三个明显受损细胞亚群。这个中间群体可能占整个细胞群体的40%。我们描述、分析并讨论了不同细胞重悬溶液对这三个群体各自比例的影响,特别是中间群体的比例。我们表明,这个中间细胞群体是在没有Ca(2+)/Mg(2+)的情况下形成的。
细胞制备显著影响通过流式细胞术进行的群体活力评估。在某些条件下显示出的中间群体可重新命名为“脆弱细胞”。对于这些细胞,Ca(2+)和Mg(2+)可降低细胞膜对PI的通透性。
这是第一项在研究酵母酒精发酵活力时分析和讨论影响中间群体形成因素的研究。随着在生物学研究中的更广泛应用,本研究为将碘化丙啶染色作为通用细胞死亡指标这一相对较新的质疑提供了重要支持。