1990
DOI: 10.1021/bp00002a007
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A Method To Disperse Aggregates of a Flocculent Yeast for Photometric Analysis

Abstract: Strategies to disperse aggregates so the cells remain in suspension long enough to take stable absorbance readings are studied. The optical density of highly flocculating yeasts, such as Saccharomyces cerevisiae ATCC 26603, drops because of cells settling to the bottom in less than 1 min. It presents a problem in using turbidimetric measurement for cell density estimate. Dilution of the yeast samples with sodium salts in a wide range of concentrations (10 mM to 1 M) disperses the aggregates, whereas dilution w… Show more

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Cited by 3 publications
(3 citation statements)
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“…This fact did not compromise our data analysis. According to Castellon‐Vogel and Menawat (2008), aggregation of yeasts is a problem in using turbidimetric methods. Jin and Speers (1998) explained that it can occur because of many factors, such as lectin‐like cell–cell interactions, electrostatic interactions of the fungal components and the presence of cell wall proteins.…”
Section: Discussionmentioning
confidence: 99%
“…This fact did not compromise our data analysis. According to Castellon‐Vogel and Menawat (2008), aggregation of yeasts is a problem in using turbidimetric methods. Jin and Speers (1998) explained that it can occur because of many factors, such as lectin‐like cell–cell interactions, electrostatic interactions of the fungal components and the presence of cell wall proteins.…”
Section: Discussionmentioning
confidence: 99%
“…The cultures were grown for 3 days at 22˚C, washed, diluted, and spread onto SC-Ura, and SC-His-Ura (for Ty1his3-AI) or YEPD + Geneticin (G418; 200 μg/ml for Ty1neo-AI) (ThermoFisher, Waltham MA) plates. To minimize flocculence, 0.25 M NaCl was used for cell washes and dilutions prior to plating [80]. The frequency of Ty1 mobility is defined as the number His + Ura + or G418 R colonies divided by the number of Ura + colonies per ml of culture.…”
Section: Ty1 Mobilitymentioning
confidence: 99%
“…The cultures were grown for 3 days at 22°C, washed, diluted, and spread onto SC-Ura, and SC-His-Ura (for Ty1 his3-AI ) or YEPD + Geneticin (G418; 200 μg/ml for Ty1 neo-AI ) (ThermoFisher, Waltham MA) plates. To minimize flocculence, 0.25 M NaCl was used for cell washes and dilutions prior to plating (Castellon-Vogel and Menawat 1990). The frequency of Ty1 mobility is defined as the number His + Ura + or G418 R colonies divided by the number of Ura + colonies per ml of culture.…”
Section: Methodsmentioning
confidence: 99%