1887

Abstract

The existence of programmed cell death in has been reported for many years. Glucose induces the death of in the absence of additional nutrients within a few hours, and the absence of active potassium uptake makes cells highly sensitive to this process. cells possess two transporters, Trk1 and Trk2, which ensure a high intracellular concentration of potassium, necessary for many physiological processes. Trk1 is the major system responsible for potassium acquisition in growing and dividing cells. The contribution of Trk2 to potassium uptake in growing cells is almost negligible, but Trk2 becomes crucial for stationary cells for their survival of some stresses, e.g. anhydrobiosis. As a new finding, we show that both Trk systems contribute to the relative thermotolerance of BY4741. Our results also demonstrate that Trk2 is much more important for the cell survival of glucose-induced cell death than Trk1, and that stationary cells deficient in active potassium uptake lose their ATP stocks more rapidly than cells with functional Trk systems. This is probably due to the upregulated activity of plasma-membrane Pma1 H-ATPase, and consequently, it is the reason why these cells die earlier than cells with functional active potassium uptake.

Funding
This study was supported by the:
  • Grantová Agentura České Republiky (Award 20/04420S)
    • Principle Award Recipient: HanaSychrova
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/content/journal/micro/10.1099/mic.0.001065
2021-06-25
2024-04-20
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References

  1. Granot D, Snyder M. Carbon source induces growth of stationary phase yeast-cells, independent of carbon source metabolism. Yeast 1993; 9:465–479 [View Article] [PubMed]
    [Google Scholar]
  2. Granot D, Levine A, Dor-Hefetz E. Sugar-induced apoptosis in yeast cells. FEMS Yeast Res 2003; 4:7–13 [View Article] [PubMed]
    [Google Scholar]
  3. Valiakhmetov AY, Kuchin AV, Suzina NE, Zvonarev AN, Shepelyakovskaya AO et al. Glucose causes primary necrosis in exponentially grown yeast Saccharomyces cerevisiae. FEMS Yeast Res 2019; 19: [View Article] [PubMed]
    [Google Scholar]
  4. Lauff DB, Santa-Maria GE. Potassium deprivation is sufficient to induce a cell death program in Saccharomyces cerevisiae. FEMS Yeast Res 2010; 10:497–507 [View Article] [PubMed]
    [Google Scholar]
  5. Arino J, Ramos J, Sychrova H. Alkali metal cation transport and homeostasis in yeasts. Microbiol Mol Biol Rev 2010; 74:95–120 [View Article] [PubMed]
    [Google Scholar]
  6. Arino J, Ramos J, Sychrova H. Monovalent cation transporters at the plasma membrane in yeasts. Yeast 2019; 36:177–193 [View Article] [PubMed]
    [Google Scholar]
  7. Durell SR, Guy HR. Structural models of the KtrB, TrkH, and Trk1,2 symporters based on the structure of the KcsA K(+) channel. Biophys J 1999; 77:789–807 [View Article] [PubMed]
    [Google Scholar]
  8. Elicharova H et al. Potassium uptake systems of Candida krusei. Yeast 2019; 36:439–448 [View Article] [PubMed]
    [Google Scholar]
  9. Petrezselyova S, Ramos J, Sychrova H. Trk2 transporter is a relevant player in K+ supply and plasma-membrane potential control in Saccharomyces cerevisiae. Folia Microbiol 2011; 56:23–28 [View Article]
    [Google Scholar]
  10. Borovikova D, Herynkova P, Rapoport A, Sychrova H et al. Potassium uptake system Trk2 is crucial for yeast cell viability during anhydrobiosis. FEMS Microbiol Lett 2014; 350:28–33 [View Article] [PubMed]
    [Google Scholar]
  11. Navarrete C, Petrezsélyová S, Barreto L, Martínez JL, Zahrádka J et al. Lack of main K+ uptake systems in Saccharomyces cerevisiae cells affects yeast performance in both potassium-sufficient and potassium-limiting conditions. FEMS Yeast Res 2010; 10:508–517 [View Article] [PubMed]
    [Google Scholar]
  12. Hoeberichts FA, Perez-Valle J, Montesinos C, Mulet JM, Planes MD et al. The role of K(+) and H(+) transport systems during glucose- and H(2)O(2)-induced cell death in Saccharomyces cerevisiae. Yeast 2010; 27:713–725 [View Article] [PubMed]
    [Google Scholar]
  13. Maresova L, Sychrova H. Applications of a microplate reader in yeast physiology research. Biotechniques 2007; 43:667–672 [View Article] [PubMed]
    [Google Scholar]
  14. Petrezselyova S, Zahradka J, Sychrova H. Saccharomyces cerevisiae BY4741 and W303-1A laboratory strains differ in salt tolerance. Fungal Biol 2010; 114:144–150 [View Article] [PubMed]
    [Google Scholar]
  15. de Alteriis E, Cartenì F, Parascandola P, Serpa J, Mazzoleni S et al. Revisiting the Crabtree/warburg effect in a dynamic perspective: A fitness advantage against sugar-induced cell death. Cell Cycle 2018; 17:688–701 [View Article] [PubMed]
    [Google Scholar]
  16. Serrano R. In vivo glucose activation of the yeast plasma membrane ATPase. FEBS Lett 1983; 156:11–14 [View Article] [PubMed]
    [Google Scholar]
  17. Barreto L, Canadell D, Petrezsélyová S, Navarrete C, Maresová L et al. A genomewide screen for tolerance to cationic drugs reveals genes important for potassium homeostasis in saccharomyces cerevisiae. Eukaryot Cell 2011; 10:1241–1250 [View Article] [PubMed]
    [Google Scholar]
  18. Caspeta L. Biofuels. Altered sterol composition renders yeast thermotolerant. Science 2014; 346:75–78 [View Article] [PubMed]
    [Google Scholar]
  19. Godinho CP, Costa R, Sá-Correia I. The ABC transporter Pdr18 is required for yeast thermotolerance due to its role in ergosterol transport and plasma membrane properties. Environ Microbiol 2021; 23:69–80 [View Article] [PubMed]
    [Google Scholar]
  20. Souza MAA, Tropia MJ, Brandao RL. New aspects of the glucose activation of the H(+)-ATPase in the yeast Saccharomyces cerevisiae. Microbiol SGM 2001; 147:2849–2855 [View Article]
    [Google Scholar]
  21. Sychrova H, Kotyk A. Conditions of activation of yeast plasma membrane ATPase. FEBS Lett 1985; 183:21–24 [View Article] [PubMed]
    [Google Scholar]
  22. Zahradka J, Sychrova H. Plasma-membrane hyperpolarization diminishes the cation efflux via Nha1 antiporter and Ena ATPase under potassium-limiting conditions. FEMS Yeast Res 2012; 12:439–446 [View Article] [PubMed]
    [Google Scholar]
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