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PMID: 4324804 Published · ppublish English Journal Article

Efflux and the steady state in alpha-methylglucoside transport in Escherichia coli.

Journal of bacteriology ·Vol. 106 ·No. 2 ·1971-05-00 ·Pages 362-8

Winkler HH

Abstract

Efflux and the steady state in a group translocation system, the alpha-methylglucoside (alphaMG) transport system, were investigated. The maximum intracellular level of alpha-methylglucoside is a function of a steady state. There is no inhibition of alphaMG influx as the intracellular pool of alphaMG, and alpha-methylglucoside-6-phosphate (alphaMGP) rises. This steady state has three components: alphaMG influx, action of an alphaMGP phosphatase, and alphaMG efflux. The phosphatase is the rate-limiting step (half-time = 5.0 min); thus, the true efflux rate (half-time = 2.0 min) cannot be simply measured from the kinetics of alphaMG loss from the cell. Under our steady-state conditions the percentage of intracellular radioactivity present as alphaMGP was 71%. Under conditions of zero influx, after an efflux of 12 min the percentage present as alphaMGP fell to 55%. However, when fluoride was present during the efflux period, the percentage of the sugar as alphaMGP increased to about 85%. Fluoride greatly inhibits both influx and phosphatase activity (half-time = 50 min). The efflux of alphaMG from the cell is apparently also fluoride-sensitive but to a lesser extent (half-time = 4.1 min). These data are summarized in a model describing the three components of the steady-state and effect of fluoride.

MeSH Terms
Azides/pharmacology Carbon Isotopes Computers Culture Media Electron Transport/drug effects Escherichia coli/analysis,drug effects,enzymology,growth & development,metabolism Filtration Fluorides/pharmacology Glycerol Glycosides/analysis,metabolism Methylation Models, Theoretical Phosphates/analysis Phosphoric Monoester Hydrolases/antagonists & inhibitors,metabolism Water/analysis
Chemicals
Azides Carbon Isotopes Culture Media Glycosides Phosphates Water Phosphoric Monoester Hydrolases Glycerol Fluorides
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Winkler H H
References (15)
15 references, click to expand
  1. The role of energy coupling in the transport of beta-galactosides by Escherichia coli.
    J Biol Chem. 1966 May 25;241(10):2200-11 PMID: 5330114
  2. A hexose-phosphate transport system in Escherichia coli.
    Biochim Biophys Acta. 1966 Mar 28;117(1):231-40 PMID: 5330662
  3. Inhibition of beta-galactoside transport by substrates of the glucose transport system in Escherichia coli.
    Biochim Biophys Acta. 1967;135(5):1030-51 PMID: 4863902
  4. The accumulation of glucose 6-phosphate from glucose and its effect in an Escherichia coli mutant lacking phosphoglucose isomerase and glucose 6-phosphate dehydrogenase.
    J Biol Chem. 1968 Dec 25;243(24):6451-7 PMID: 4302393
  5. Transmembrane effects of beta-galactosides on thiomethyl-beta-galactoside transport in Escherichia coli.
    Biochim Biophys Acta. 1969 Mar 11;173(2):234-44 PMID: 4886866
  6. Regulation of sugar transport in isolated bacterial membrane preparations from Escherichia coli.
    Proc Natl Acad Sci U S A. 1969 Jul;63(3):724-31 PMID: 4899873
  7. Compartmentation in the induction of the hexose-6-phosphate transport system of Escherichia coli.
    J Bacteriol. 1970 Feb;101(2):470-5 PMID: 4905309
  8. The glucose effect and the relationship between glucose permease, acid phosphatase, and glucose resistance.
    Cold Spring Harb Symp Quant Biol. 1961;26:261-76 PMID: 13890281
  9. Effect of metabolic activity on the glucose permease of bacterial cells.
    Proc Natl Acad Sci U S A. 1962 Oct 15;48:1759-65 PMID: 13963905
  10. Substrate specificity of a glucose permease of Escherichia coli.
    J Bacteriol. 1962 Nov;84:877-81 PMID: 13982383
  11. STUDIES ON THE GLUCOSE-TRANSPORT SYSTEM IN ESCHERICHIA COLI WITH ALPHA-METHYLGLUCOSIDE AS SUBSTRATE.
    Biochim Biophys Acta. 1963 Nov 15;78:505-15 PMID: 14088780
  12. THE GLUCOSE PERMEASE SYSTEM IN BACTERIA.
    Biochim Biophys Acta. 1964 Mar 30;79:337-50 PMID: 14163518
  13. PHOSPHATE BOUND TO HISTIDINE IN A PROTEIN AS AN INTERMEDIATE IN A NOVEL PHOSPHO-TRANSFERASE SYSTEM.
    Proc Natl Acad Sci U S A. 1964 Oct;52:1067-74 PMID: 14224387
  14. Mutants of Escherichia coli requiring methionine or vitamin B12.
    J Bacteriol. 1950 Jul;60(1):17-28 PMID: 15436457
  15. TURBIDITY CHANGE DURING GLUCOSE PERMEATION IN ESCHERICHIA COLI.
    J Bacteriol. 1963 May;85:1141-9 PMID: 14044007
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1971-05-00
Pages
362-8
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC285105
Subset
IM
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