Transport properties of membrane vesicles from Acholeplasma laidlawii. III. Evidence of active nature of glucose transport
Language English Country United States Media print
Document type Journal Article
PubMed
1193497
DOI
10.1007/bf02891708
Knihovny.cz E-resources
- MeSH
- Acholeplasma laidlawii metabolism MeSH
- Biological Transport, Active drug effects MeSH
- Amobarbital pharmacology MeSH
- Anaerobiosis MeSH
- Cell Membrane metabolism MeSH
- Depression, Chemical MeSH
- Fructose metabolism MeSH
- Glucose metabolism MeSH
- Maltose metabolism MeSH
- Rotenone pharmacology MeSH
- Uncoupling Agents pharmacology MeSH
- Subcellular Fractions MeSH
- Sulfhydryl Reagents pharmacology MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Amobarbital MeSH
- Fructose MeSH
- Glucose MeSH
- Maltose MeSH
- Rotenone MeSH
- Uncoupling Agents MeSH
- Sulfhydryl Reagents MeSH
Membrane vesicles obtained from Acholeplasma laidlawii accumulate glucose as well as maltose and fructose against their concentration gradient in the absence of exogenous energy sources. Glucose uptake by membrane vesicles is inhibited by anaerobiosis and by electron transfer inhibitors, such as rotenone and amytal, but not by 2-heptyl-4-hydroxyquinoline N-oxide, antimycin A, cyanide and azide. Rotenone, cyanide and amytal also produce a rapid efflux of glucose from the membrane vesicles. Arsenate, oligomycin and N,N'-dicyclohexylcarbodimide do not inhibit glucose transport. Transport of glucose is markedly inhibited by proton conductors such as CCCP and pentachlorophenol. It is concluded that glucose transport can be driven by a high-energy state of the membrane or by the membrane potential.
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