Literature DB >> 3002794

Trehalase activation in yeasts is mediated by an internal acidification.

E Valle, L Bergillos, S Gascón, F Parra, S Ramos.   

Abstract

It has been reported that the addition of glucose, uncouplers and nystatin to yeast cells grown in a sugarfree medium causes trehalase activation; it has been postulated that this activation might be mediated by the depolarization of the plasma membrane. In this article the values of membrane potential and pH gradient across the plasma membrane of Saccharomyces cerevisiae have been determined under the same conditions as those in which trehalase is activated. Membrane potential was evaluated from the distribution of triphenylmethylphosphonium, the pH gradient from the distribution of benzoic acid across the plasma membrane. When the effect of several agents on the two components of the electrochemical proton gradient across the plasma membrane of ethanol-grown yeast cells were studied, under trehalase activation conditions, the following observations were made. (a) The addition of glucose activated trehalase and caused internal acidification of the cells, but had practically no effect on the membrane potential. (b) The addition of 200 mM KCl depolarized the cell membrane but did not affect the internal pH, nor trehalase activity. (c) Although carbonyl cyanide m-chlorophenylhydrazone depolarized the cells at external pH 6.0 and 7.0, it only activated trehalase at an external pH 6.0, leading to the acidification of the internal medium at this pH. (d) Nystatin caused an increase in the triphenylmethylphosphonium accumulation at external pH 6.0 and 7.0, but only activated trehalase at external pH 6.0, causing acidification of the cell interior at this pH. (e) Activation of trehalase was also observed when the internal acidification was caused by addition of a weak acid such as acetate. It is concluded that trehalase activation is mediated by an intracellular acidification and is independent of the membrane potential.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3002794     DOI: 10.1111/j.1432-1033.1986.tb09389.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  6 in total

1.  Intracellular pH in Schizosaccharomyces pombe--comparison with Saccharomyces cerevisiae.

Authors:  R S Haworth; L Fliegel
Journal:  Mol Cell Biochem       Date:  1993-07-21       Impact factor: 3.396

2.  Catabolite inactivation of isocitrate lyase from Saccharomyces cerevisiae.

Authors:  Y S López-Boado; P Herrero; S Gascón; F Moreno
Journal:  Arch Microbiol       Date:  1987-04       Impact factor: 2.552

3.  Absence of glucose-induced cAMP signaling in the Saccharomyces cerevisiae mutants cat1 and cat3 which are deficient in derepression of glucose-repressible proteins.

Authors:  J C Argüelles; K Mbonyi; L Van Aelst; M Vanhalewyn; A W Jans; J M Thevelein
Journal:  Arch Microbiol       Date:  1990       Impact factor: 2.552

4.  Enzymic analysis of the crabtree effect in glucose-limited chemostat cultures of Saccharomyces cerevisiae.

Authors:  E Postma; C Verduyn; W A Scheffers; J P Van Dijken
Journal:  Appl Environ Microbiol       Date:  1989-02       Impact factor: 4.792

5.  Requirement of one functional RAS gene and inability of an oncogenic ras variant to mediate the glucose-induced cyclic AMP signal in the yeast Saccharomyces cerevisiae.

Authors:  K Mbonyi; M Beullens; K Detremerie; L Geerts; J M Thevelein
Journal:  Mol Cell Biol       Date:  1988-08       Impact factor: 4.272

Review 6.  Physiological controls and regulation of ergot alkaloid formation.

Authors:  Z Rehácek
Journal:  Folia Microbiol (Praha)       Date:  1991       Impact factor: 2.099

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.