Activation of the plasma membrane H(+)-ATPase of Saccharomyces cerevisiae by addition of hydrogen peroxide
Language English Country Australia Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
1831983
Knihovny.cz E-resources
- MeSH
- Enzyme Activation MeSH
- Cell Membrane enzymology MeSH
- Dicyclohexylcarbodiimide pharmacology MeSH
- Diethylstilbestrol pharmacology MeSH
- Potassium metabolism MeSH
- Carbonyl Cyanide m-Chlorophenyl Hydrazone pharmacology MeSH
- Hydrogen-Ion Concentration MeSH
- NAD metabolism MeSH
- Onium Compounds MeSH
- Organophosphorus Compounds MeSH
- Oxidation-Reduction MeSH
- Hydrogen Peroxide pharmacology MeSH
- Proton-Translocating ATPases metabolism MeSH
- Buffers MeSH
- Saccharomyces cerevisiae enzymology MeSH
- Oxygen Consumption MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Dicyclohexylcarbodiimide MeSH
- Diethylstilbestrol MeSH
- Potassium MeSH
- Carbonyl Cyanide m-Chlorophenyl Hydrazone MeSH
- NAD MeSH
- Onium Compounds MeSH
- Organophosphorus Compounds MeSH
- Hydrogen Peroxide MeSH
- Proton-Translocating ATPases MeSH
- Buffers MeSH
- tetraphenylphosphonium MeSH Browser
Addition of hydrogen peroxide (greater than 10 mM) to aerated derepressed cells of S. cerevisiae in the absence of substrate caused a boost of endogenous respiration and both intra- and extracellular acidification, without any significant change in cellular ATP level. Furthermore, a hyperpolarization of the plasma membrane was indicated by an enhanced accumulation of tetraphenylphosphonium in the cells. The extracellular pH attained was as low as 3.5. The acidification could be suspended by the H(+)-ATPase inhibitors diethylstilbestrol and dicyclohexylcarbodiimide and was, in general, associated with an opposite flux of K+. K+ also stimulated the H(+)-ATPase activity in the purified plasma membrane fraction. These results are consistent with the plasma membrane H(+)-ATPase being involved in the H+ extrusion induced by H2O2 in the absence of substrate. Extended exposure of cells to H2O2 led eventually to an arrest of both respiration and ion fluxes that could be again lifted by depolarizing the plasma membrane. Along with differences in the cellular NADH/NAD+ ratio and in the participation of organic acids, this makes the H2O2-induced acidification distinct from that induced by glucose.