Dicarbanonaborates in yeast respiration and membrane transport
Language English Country England, Great Britain Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Adenosine Triphosphate metabolism MeSH
- Biological Transport, Active drug effects MeSH
- Borates pharmacology MeSH
- Proton-Translocating ATPases metabolism MeSH
- Saccharomyces cerevisiae drug effects metabolism physiology MeSH
- Oxygen Consumption drug effects MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Adenosine Triphosphate MeSH
- Borates MeSH
- Proton-Translocating ATPases MeSH
Two derivatives of carborates, sodium 5,6-dichloro-7,8-dicarbanonaborate (CB-Cl) and sodium 5-mercapto-7,8-dicarbanonaborate (CB-SH) were found to inhibit endogenous as well as glucose-induced respiration of the yeast Saccharomyces cerevisiae. Both substances slightly increased endogenous acid production, were neutral toward H(+)-ATPase-associated acidification but pronouncedly inhibited the K(+)-stimulated acidification. The same effects were observed also with an ATPase-deficient mutant of the yeast. The ATP-hydrolyzing activity of yeast plasma membranes in vitro was severely reduced. The membrane potential was substantially increased toward more negative values. The H(+)-symporting uptake of glutamic acid was considerably decreased, that of adenine was diminished much less. The effects of the dicarbanonaborates are obviously pleiotropic but their inhibition of ATP hydrolysis and of uptake of H(+)-symported substances, on the one hand, and absolute lack of effect on ATPase-catalyzed acidification, on the other, pose an unresolved problem.
References provided by Crossref.org
Effects of the Fenton reagent on transport in yeast
Two forms of yeast plasma membrane H(+)-ATPase: comparison of yield and effects of inhibitors
Extracellular acidification by Saccharomyces cerevisiae in normal and in heavy water