Population analysis of a commercial Saccharomyces cerevisiae wine yeast in a batch culture by electric particle analysis, light diffraction and flow cytometry

被引:7
|
作者
Portell, Xavier [1 ]
Ginovart, Marta [2 ]
Carbo, Rosa [1 ]
Gras, Anna [1 ]
Vives-Rego, Josep [3 ]
机构
[1] Univ Politecn Cataluna, Dept Agri Food Engn & Biotechnol, Barcelona 08860, Spain
[2] Univ Politecn Cataluna, Dept Appl Math 3, Barcelona 08860, Spain
[3] Univ Barcelona, Dept Microbiol, Fac Biol, Barcelona, Spain
关键词
yeast populations; cell size distributions; particle size analysis; light diffraction; flow cytometry; batch culture; CELL-SIZE; NONQUIESCENT CELLS; STATIONARY-PHASE; QUIESCENT; GLUCOSE; FUTURE; LEVEL;
D O I
10.1111/j.1567-1364.2010.00682.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Data from electric particle analysis, light diffraction and flow cytometry analysis provide information on changes in cell morphology. Here, we report analyses of Saccharomyces cerevisiae populations growing in a batch culture using these techniques. The size distributions were determined by electric particle analysis and by light diffraction in order to compare their outcomes. Flow cytometry parameters forward (related to cell size) and side (related to cell granularity) scatter were also determined to complement this information. These distributions of yeast properties were analysed statistically and by a complexity index. The cell size of Saccharomyces at the lag phase was smaller than that at the beginning of the exponential phase, whereas during the stationary phase, the cell size converged with the values observed during the lag phase. These experimental techniques, when used together, allow us to distinguish among and characterize the cell size, cell granularity and the structure of the yeast population through the three growth phases. Flow cytometry patterns are better than light diffraction and electric particle analysis in showing the existence of subpopulations during the different phases, especially during the stationary phase. The use of a complexity index in this context helped to differentiate these phases and confirmed the yeast cell heterogeneity.
引用
收藏
页码:18 / 28
页数:11
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