Literature DB >> 1835495

Induction of increased thermotolerance in Saccharomyces cerevisiae may be triggered by a mechanism involving intracellular pH.

P J Coote1, M B Cole, M V Jones.   

Abstract

Incubation of Saccharomyces cerevisiae at sub-lethal temperatures results in an increase in thermotolerance. This process is dependent not only on the sub-lethal temperature but also on the duration of sub-lethal heating. This indicates that the mechanism inducing thermotolerance is a time/temperature dose response. Other factors that induce thermotolerance include exposure to ethanol, sorbic acid and low external pH values. These factors induce thermotolerance after incubation in the presence of protein synthesis inhibitors, and they are all known to affect the intracellular pH (pHi). The acquisition of increased thermotolerance is minimal with sub-lethal heating under neutral external pH conditions. However, when the external pH is reduced to 4.0 the level of induced thermotolerance increases to a maximum value. Using a specific ATPase inhibitor, diethylstilboestrol (DES), ATPase activity was shown to be essential for the cell to survive heat stress. In addition, measurement of acid efflux, or ATPase activity, revealed that proton pumping from the cell increased by approximately 50% at sublethal temperatures that induce thermotolerance. This work has clearly implicated pHi perturbation as the triggering mechanism conferring thermotolerance on S. cerevisiae.

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Year:  1991        PMID: 1835495     DOI: 10.1099/00221287-137-7-1701

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  20 in total

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2.  Environmental suppression of Neurospora crassa cot-1 hyperbranching: a link between COT1 kinase and stress sensing.

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3.  Cytotoxic and genotoxic consequences of heat stress are dependent on the presence of oxygen in Saccharomyces cerevisiae.

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4.  The freeze-thaw stress response of the yeast Saccharomyces cerevisiae is growth phase specific and is controlled by nutritional state via the RAS-cyclic AMP signal transduction pathway.

Authors:  J I Park; C M Grant; P V Attfield; I W Dawes
Journal:  Appl Environ Microbiol       Date:  1997-10       Impact factor: 4.792

5.  Activation of plasma membrane H(+)-ATPase and expression of PMA1 and PMA2 genes in Saccharomyces cerevisiae cells grown at supraoptimal temperatures.

Authors:  C A Viegas; P B Sebastião; A G Nunes; I Sá-Correia
Journal:  Appl Environ Microbiol       Date:  1995-05       Impact factor: 4.792

Review 6.  Stress response of yeast.

Authors:  W H Mager; P M Ferreira
Journal:  Biochem J       Date:  1993-02-15       Impact factor: 3.857

7.  Inhibitory action of a truncated derivative of the amphibian skin peptide dermaseptin s3 on Saccharomyces cerevisiae.

Authors:  P J Coote; C D Holyoak; D Bracey; D P Ferdinando; J A Pearce
Journal:  Antimicrob Agents Chemother       Date:  1998-09       Impact factor: 5.191

8.  Isolation and characterization of acetic acid-tolerant galactose-fermenting strains of Saccharomyces cerevisiae from a spent sulfite liquor fermentation plant.

Authors:  T Lindén; J Peetre; B Hahn-Hägerdal
Journal:  Appl Environ Microbiol       Date:  1992-05       Impact factor: 4.792

9.  Monitoring stress-related genes during the process of biomass propagation of Saccharomyces cerevisiae strains used for wine making.

Authors:  Roberto Pérez-Torrado; Jose M Bruno-Bárcena; Emilia Matallana
Journal:  Appl Environ Microbiol       Date:  2005-11       Impact factor: 4.792

10.  Activity of the plasma membrane H(+)-ATPase and optimal glycolytic flux are required for rapid adaptation and growth of Saccharomyces cerevisiae in the presence of the weak-acid preservative sorbic acid.

Authors:  C D Holyoak; M Stratford; Z McMullin; M B Cole; K Crimmins; A J Brown; P J Coote
Journal:  Appl Environ Microbiol       Date:  1996-09       Impact factor: 4.792

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