Saccharomyces cerevisiae BY4741 and W303-1A laboratory strains differ in salt tolerance
Language English Country Netherlands Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20960970
DOI
10.1016/j.funbio.2009.11.002
PII: S1878-6146(09)00236-0
Knihovny.cz E-resources
- MeSH
- Biological Transport MeSH
- Cell Membrane metabolism physiology MeSH
- Potassium metabolism pharmacology MeSH
- Species Specificity MeSH
- Homeostasis MeSH
- Hygromycin B pharmacology MeSH
- Cations MeSH
- Lithium metabolism pharmacology MeSH
- Membrane Potentials MeSH
- Mutation MeSH
- Gene Expression Regulation, Fungal MeSH
- Saccharomyces cerevisiae Proteins genetics metabolism MeSH
- Saccharomyces cerevisiae classification genetics growth & development physiology MeSH
- Sodium metabolism pharmacology MeSH
- Salt Tolerance physiology MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Potassium MeSH
- Hygromycin B MeSH
- Cations MeSH
- Lithium MeSH
- Saccharomyces cerevisiae Proteins MeSH
- Sodium MeSH
Saccharomyces cerevisiae yeast cells serve as a model to elucidate the bases of salt tolerance and potassium homeostasis regulation in eukaryotic cells. In this study, we show that two widely used laboratory strains, BY4741 and W303-1A, differ not only in cell size and volume but also in their relative plasma-membrane potential (estimated with a potentiometric fluorescent dye diS-C3(3) and as Hygromycin B sensitivity) and tolerance to alkali-metal cations. W303-1A cells and their mutant derivatives lacking either uptake (trk1 trk2) or efflux (nha1) systems for alkali-metal cations are more tolerant to toxic sodium and lithium cations but also more sensitive to higher external concentrations of potassium than BY4741 cells and their mutants. Moreover, our results suggest that though the two strains do not differ in the total potassium content, the regulation of intracellular potassium homeostasis is probably not the same in BY4741 and W303-1A cells.
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