Effects of yeast suspension density on the accumulation ratio of transported solutes
Language English Country Great Britain, England Media print
Document type Journal Article
PubMed
3332977
DOI
10.1002/yea.320030407
Knihovny.cz E-resources
- MeSH
- Amino Acids metabolism MeSH
- Biological Transport MeSH
- Cell Membrane metabolism MeSH
- Deoxyglucose metabolism MeSH
- Kinetics MeSH
- Hydrogen-Ion Concentration MeSH
- Yeasts growth & development metabolism ultrastructure MeSH
- Carbohydrate Metabolism * MeSH
- Proline metabolism MeSH
- Rhodotorula growth & development metabolism ultrastructure MeSH
- Saccharomyces cerevisiae growth & development metabolism ultrastructure MeSH
- Saccharomycetales growth & development metabolism ultrastructure MeSH
- Temperature MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- 6-deoxyglucose MeSH Browser
- Amino Acids MeSH
- Deoxyglucose MeSH
- Proline MeSH
The previously described effect of cell suspension density on metabolic and transport phenomena in yeast, apparently caused by inhibition by dissolved carbon dioxide, is also observed with the accumulation ratio of both sugars and amino acids where not only a kinetic but also a energetic factor comes into play. Unlike all previously measured metabolic and transport parameters, the dependence of the accumulation ratio on suspension density is not monotonic but shows a pronounced maximum in the range of 4-8 mg dry wt/ml, depending on yeast species and on cultivation conditions. In Rhodotorula gracilis and in Lodderomyces elongisporus it is not due to CO2 but is semiquantitatively related to the proton-motive force across the plasma membrane as well as to the intracellular ATP content. It is observed both in oxygen and in argon, over a wide range of pH values and of temperatures, but it is suppressed by metabolic inhibitors. It is expressed only in a range of transported solute concentrations between about 0.1 and 10 mM.
References provided by Crossref.org
Enhancement of synthesis and activity of yeast transport proteins by metabolic substrates
Dependence of the kinetics of secondary active transports in yeast on H(+)-ATPase acidification
Interaction of 2-deoxy-D-glucose and adenine with phosphate anion uptake in yeast
Uptake of L-lysine by a double mutant of Saccharomyces cerevisiae