Literature DB >> 6089881

Intracellular pH distribution and transmembrane pH profile of yeast cells.

J Slavík, A Kotyk.   

Abstract

The pH-dependent fluorescence excitation of fluorescein located intracellularly and in the vicinity of cells of the yeast Saccharomyces cerevisiae and Endomyces magnusii was used to obtain local pH values at a linear resolution 0.2 micron. Cells suspended in water or in a diluted (5 mM) acidic buffer had a relatively alkaline interior (about 7.0-7.5) with pH decreasing gradually toward the periphery and further out through the cell wall to the value of the bulk solution. In slightly alkaline weak buffers the cells also showed an alkaline center and a slightly acidic ring-shaped area, but the peripheral region close to the membrane was again alkaline with pH increasing toward the bulk solution. The heterogeneity of intracellular pH was reduced or nearly abolished in starved or antimycin-treated cell. Suspension of cells in strong (200 mM) buffer resulted within 15-20 min in a nearly homogeneous pH pattern throughout the cell, attaining pH values of 5.5-7.5, depending on the pH of the buffer. Addition of glucose with concomitant pH decrease of the extracellular medium did not change appreciably the intracellular pattern for 20-30 min, except with diethylstilbestrol (inhibitor of proton-extruding ATPase) when the cell became more acidic. It appears that the delta pH measurements between the cell as a whole and the bulk solution (as are used for the calculation of the electrochemical potential of protons in proton-driven transports) are not substantiated, the probable pH difference across the plasma membrane being substantially smaller than previously supposed.

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Year:  1984        PMID: 6089881     DOI: 10.1016/0005-2728(84)90129-4

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  10 in total

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2.  A possible role of intracellular isoelectric focusing in the evolution of eukaryotic cells and multicellular organisms.

Authors:  Jaroslav Flegr
Journal:  J Mol Evol       Date:  2009-08-18       Impact factor: 2.395

3.  Analysis of Fungal Pellets by UV-Visible Spectrum Diffuse Reflectance Spectroscopy.

Authors:  D Lestan; H Podgornik; A Perdih
Journal:  Appl Environ Microbiol       Date:  1993-12       Impact factor: 4.792

4.  The H(+)-ATPase in the plasma membrane of Saccharomyces cerevisiae is activated during growth latency in octanoic acid-supplemented medium accompanying the decrease in intracellular pH and cell viability.

Authors:  C A Viegas; P F Almeida; M Cavaco; I Sá-Correia
Journal:  Appl Environ Microbiol       Date:  1998-02       Impact factor: 4.792

5.  Dependence of thermodynamic efficiency of proton pumps on frequency of oscillatory concentration of ATP.

Authors:  M Schell; K Kundu; J Ross
Journal:  Proc Natl Acad Sci U S A       Date:  1987-01       Impact factor: 11.205

6.  Alkaline pH, membrane potential, and magnesium cations are negative modulators of purine nucleotide inhibition of H+ and Cl- transport through the uncoupling protein of brown adipose tissue mitochondria.

Authors:  P Jezek; J Houstĕk; Z Drahota
Journal:  J Bioenerg Biomembr       Date:  1988-10       Impact factor: 2.945

7.  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

8.  Dependence of the kinetics of secondary active transports in yeast on H(+)-ATPase acidification.

Authors:  A Kotyk
Journal:  J Membr Biol       Date:  1994-02       Impact factor: 1.843

9.  Mitochondrial DNA of Endomyces (Dipodascus) magnusii.

Authors:  P Griac; J Nosek
Journal:  Curr Genet       Date:  1993 May-Jun       Impact factor: 3.886

10.  2,2-Diphenyl-1-picrylhydrazyl as a screening tool for recombinant monoterpene biosynthesis.

Authors:  James Byh Behrendorff; Claudia E Vickers; Panagiotis Chrysanthopoulos; Lars K Nielsen
Journal:  Microb Cell Fact       Date:  2013-08-23       Impact factor: 5.328

  10 in total

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