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. 1976 Oct;128(1):157–164. doi: 10.1128/jb.128.1.157-164.1976

Stimulatory effect of lithium ion on proline transport by whole cells of Escherichia coli.

Y Kayama, T Kawasaki
PMCID: PMC232838  PMID: 185195

Abstract

The effect of monovalent cations on proline transport in whole cells of Escherichia coli K-12 has been examined. Lithium ion added to the uptake medium stimulated proline transport severalfold and K+ and Na+ were slightly effective, whereas Rb+, Cs+, and NH4+ were completely without effect. The stimulatory effect of Li+ on proline transport was not due to an increase in osmolarity of the uptake medium, and d 5 mM p-chloromercuribenzene sulfonic acid completely blocked this effect of Li+ without having any effect on the basal rate of proline transport. The Arrhenius plots for Li+-stimulated transport showed a clear transition point at 35 degrees C in addition to 20 degrees C which was also detectable in the basal transport. Lithium ion stimulated proline transport synergistically in the presence of glucose and succinate as a carbon source. The addition of 2.5 mM KCN or 0.5 mM arsenate did not inhibit this synergistic effect, although the presence of these inhibitors inhibited completely the stimulation of proline transport induced by the addition of carbon source. Carbonylcyanide m-chlorophenylhydrazone and 2,4-dinitrophenol blocked both the basal and Li+-stimulated proline transport. When membrane potential of E. coli cells was measured by the dibenzyldimethylammonium uptake method, the incubation of Li+ with the cells did not affect the preexisting membrane potential. These results suggest that Li+ stimulates proline transport by intact cells of E. coli in a manner somewhat affecting membrane component(s) different from the transport carrier of proline. It is uncertain whether the effect of Li+ is directly involved in the mechanisms of energy coupling of proline transport.

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Selected References

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  1. Altendorf K., Hirata H., Harold F. M. Accumulation of lipid-soluble ions and of rubidium as indicators of the electrical potential in membrane vesicles of Escherichia coli. J Biol Chem. 1975 Feb 25;250(4):1405–1412. [PubMed] [Google Scholar]
  2. Asghar S. S., Levin E., Harold F. M. Accumulation of neutral amino acids by Streptococcus faecalis. Energy coupling by a proton-motive force. J Biol Chem. 1973 Aug 10;248(15):5225–5233. [PubMed] [Google Scholar]
  3. Berger E. A. Different mechanisms of energy coupling for the active transport of proline and glutamine in Escherichia coli. Proc Natl Acad Sci U S A. 1973 May;70(5):1514–1518. doi: 10.1073/pnas.70.5.1514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Berger E. A., Heppel L. A. Different mechanisms of energy coupling for the shock-sensitive and shock-resistant amino acid permeases of Escherichia coli. J Biol Chem. 1974 Dec 25;249(24):7747–7755. [PubMed] [Google Scholar]
  5. Damadian R. Ion metabolism in a potassium accumulation mutant of Escherichia coli B. I. Potassium metabolism. J Bacteriol. 1968 Jan;95(1):113–122. doi: 10.1128/jb.95.1.113-122.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Drapeau G. R., Matula T. I., MacLeod R. A. Nutrition and metabolism of marine bacteria. XV. Relation of Na+-activated transport to the Na+ requirement of a marine pseudomonad for growth. J Bacteriol. 1966 Jul;92(1):63–71. doi: 10.1128/jb.92.1.63-71.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Eagon R. G., Wilkerson L. S. A potassium-dependent citric acid transport system in Aerobacter aerogenes. Biochem Biophys Res Commun. 1972 Mar 10;46(5):1944–1950. doi: 10.1016/0006-291x(72)90074-5. [DOI] [PubMed] [Google Scholar]
  8. Eddy A. A., Indge K. J., Backen K., Nowacki J. A. Interctions between potassium ions and glycine transport in the yeast Saccharomyces carlsbergensis. Biochem J. 1970 Dec;120(4):845–852. doi: 10.1042/bj1200845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Eddy A. A., Nowacki J. A. Stoicheiometrical proton and potassium ion movements accompanying the absorption of amino acids by the yeast Saccharomyces carlsbergensis. Biochem J. 1971 May;122(5):701–711. doi: 10.1042/bj1220701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Frank L., Hopkins I. Sodium-stimulated transport of glutamate in Escherichia coli. J Bacteriol. 1969 Oct;100(1):329–336. doi: 10.1128/jb.100.1.329-336.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Griniuviene B., Chmieliauskaite V., Grinius L. Energy-linked transport of permeant ions in Escherichia coli cells: evidence for membrane potential generation by proton-pump. Biochem Biophys Res Commun. 1974 Jan;56(1):206–213. doi: 10.1016/s0006-291x(74)80335-9. [DOI] [PubMed] [Google Scholar]
  12. Halpern Y. S., Barash H., Dover S., Druck K. Sodium and potassium requirements for active transport of glutamate by Escherichia coli K-12. J Bacteriol. 1973 Apr;114(1):53–58. doi: 10.1128/jb.114.1.53-58.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Harold F. M. Conservation and transformation of energy by bacterial membranes. Bacteriol Rev. 1972 Jun;36(2):172–230. doi: 10.1128/br.36.2.172-230.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Harold F. M., Papineau D. Cation transport and electrogenesis by Streptococcus faecalis. I. The membrane potential. J Membr Biol. 1972;8(1):27–44. doi: 10.1007/BF01868093. [DOI] [PubMed] [Google Scholar]
  15. Hassan H. M., MacLeod R. A. Kinetics of Na+-dependent K+ ion transport in a marine pseudomonad. J Bacteriol. 1975 Jan;121(1):160–164. doi: 10.1128/jb.121.1.160-164.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hirata H., Altendorf K., Harold F. M. Energy coupling in membrane vesicles of Escherichia coli. I. Accumulation of metabolites in response to an electrical potential. J Biol Chem. 1974 May 10;249(9):2939–2945. [PubMed] [Google Scholar]
  17. Hirata H., Altendorf K., Harold F. M. Role of an electrical potential in the coupling of metabolic energy to active transport by membrane vesicles of Escherichia coli. Proc Natl Acad Sci U S A. 1973 Jun;70(6):1804–1808. doi: 10.1073/pnas.70.6.1804. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Hirata H., Kosmakos F. C., Brodie A. F. Active transport of proline in membrane preparations from Mycobacterium phlei. J Biol Chem. 1974 Nov 10;249(21):6965–6970. [PubMed] [Google Scholar]
  19. Kashket E. R., Wilson T. H. Galactoside accumulation associated with ion movements in Streptococcus lactis. Biochem Biophys Res Commun. 1972 Nov 1;49(3):615–620. doi: 10.1016/0006-291x(72)90455-x. [DOI] [PubMed] [Google Scholar]
  20. Kashket E. R., Wilson T. H. Proton-coupled accumulation of galactoside in Streptococcus lactis 7962. Proc Natl Acad Sci U S A. 1973 Oct;70(10):2866–2869. doi: 10.1073/pnas.70.10.2866. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Kashket E. R., Wilson T. H. Protonmotive force in fermenting Streptococcus lactis 7962 in relation to sugar accumulation. Biochem Biophys Res Commun. 1974 Aug 5;59(3):879–886. doi: 10.1016/s0006-291x(74)80061-6. [DOI] [PubMed] [Google Scholar]
  22. Kawasaki T., Miyata I., Esaki K., Nose Y. Thiamine uptake in Escherichia coli. I. General properties of thiamine uptake system in Escherichia coli. Arch Biochem Biophys. 1969 Apr;131(1):223–230. doi: 10.1016/0003-9861(69)90125-8. [DOI] [PubMed] [Google Scholar]
  23. Klein W. L., Boyer P. D. Energization of active transport by Escherichia coli. J Biol Chem. 1972 Nov 25;247(22):7257–7265. [PubMed] [Google Scholar]
  24. Leive L. Studies on the permeability change produced in coliform bacteria by ethylenediaminetetraacetate. J Biol Chem. 1968 May 10;243(9):2373–2380. [PubMed] [Google Scholar]
  25. Lombardi F. J., Reeves J. P., Short S. A., Kaback H. R. Evaluation of the chemiosmotic interpretation of active transport in bacterial membrane vesicles. Ann N Y Acad Sci. 1974 Feb 18;227:312–327. doi: 10.1111/j.1749-6632.1974.tb14396.x. [DOI] [PubMed] [Google Scholar]
  26. MacLeod R. A., Thurman P., Rogers H. J. Comparative transport activity of intact cells, membrane vesicles, and mesosomes of Bacillus licheniformis. J Bacteriol. 1973 Jan;113(1):329–340. doi: 10.1128/jb.113.1.329-340.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Niven D. F., Hamilton W. A. Mechanisms of energy coupling to the transport of amino acids by Staphylococcus aureus. Eur J Biochem. 1974 May 15;44(2):517–522. doi: 10.1111/j.1432-1033.1974.tb03510.x. [DOI] [PubMed] [Google Scholar]
  28. Niven D. F., Hamilton W. A. Valinomycin-induced amino acid uptake by Staphylococcus aureus. FEBS Lett. 1973 Dec 1;37(2):244–248. doi: 10.1016/0014-5793(73)80470-3. [DOI] [PubMed] [Google Scholar]
  29. Prezioso G., Hong J. S., Kerwar G. K., Kaback H. R. Mechanisms of active transport in isolated bacterial membrane vesicles. XII. Active transport by a mutant of Escherichia coli uncoupled for oxidative phosphorylation. Arch Biochem Biophys. 1973 Feb;154(2):575–582. doi: 10.1016/0003-9861(73)90011-8. [DOI] [PubMed] [Google Scholar]
  30. SCHULTZ S. G., SOLOMON A. K. Cation transport in Escherichia coli. I. Intracellular Na and K concentrations and net cation movement. J Gen Physiol. 1961 Nov;45:355–369. doi: 10.1085/jgp.45.2.355. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Simoni R. D., Shallenberger M. K. Coupling of energy to active transport of amino acids in Escherichia coli. Proc Natl Acad Sci U S A. 1972 Sep;69(9):2663–2667. doi: 10.1073/pnas.69.9.2663. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Singer S. J., Nicolson G. L. The fluid mosaic model of the structure of cell membranes. Science. 1972 Feb 18;175(4023):720–731. doi: 10.1126/science.175.4023.720. [DOI] [PubMed] [Google Scholar]
  33. Stock J., Roseman S. A sodium-dependent sugar co-transport system in bacteria. Biochem Biophys Res Commun. 1971 Jul 2;44(1):132–138. doi: 10.1016/s0006-291x(71)80168-7. [DOI] [PubMed] [Google Scholar]
  34. Thompson J., MacLeod R. A. Functions of Na+ and K+ in the active transport of -aminoisobutyric acid in a marine pseudomonad. J Biol Chem. 1971 Jun 25;246(12):4066–4074. [PubMed] [Google Scholar]
  35. Wong P. T., Thompson J., MacLeod R. A. Nutrition and metabolism of marine bacteria. XVII. Ion-dependent retention of alpha-aminoisobutyric acid and its relation to Na+ dependent transport in a marine pseudomonad. J Biol Chem. 1969 Feb 10;244(3):1016–1025. [PubMed] [Google Scholar]

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