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. 1994 Mar;176(5):1303–1308. doi: 10.1128/jb.176.5.1303-1308.1994

Electrogenic glutamine uptake by Peptostreptococcus anaerobius and generation of a transmembrane potential.

B J Beck 1, J B Russell 1
PMCID: PMC205193  PMID: 8113169

Abstract

Peptostreptococcus anaerobius converted glutamine stoichiometrically to ammonia and pyroglutamic acid, and the Eadie-Hofstee plot of glutamine transport was biphasic. High-affinity, sodium-dependent glutamine transport (affinity constant [Kt] of 1.5 microM) could be driven by the chemical gradient of sodium, and more than 20 mM sodium was required for half-maximal velocity. High-affinity glutamine transport was not stimulated or inhibited by a membrane potential (delta psi). Low-affinity glutamine transport had a rate which was directly proportional to the external glutamine concentration, required less than 100 microM sodium, and was inhibited strongly by a delta psi. Cells which were treated with N,N-dicyclohexylcarbodiimide to inhibit the F1F0 ATPase still generated a delta psi but did so only if the external glutamine concentration was greater than 15 mM. Low-affinity glutamine uptake could not be saturated by as much as 200 mM glutamine, but glutamine-1 accounts for only a small fraction of the total glutamine at physiological pH values (pH 6 to 7). On the basis of these results, it appeared that the low-affinity glutamine transport was an electrogenic mechanism which was converting a chemical gradient of glutamine-1 into a delta psi. Other mechanisms of delta psi generation (electrogenic glutamine-pyroglutamate or -ammonium exchange) could not be demonstrated.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ahmed S., Booth I. R. Quantitative measurements of the proton-motive force and its relation to steady state lactose accumulation in Escherichia coli. Biochem J. 1981 Dec 15;200(3):573–581. doi: 10.1042/bj2000573. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Anantharam V., Allison M. J., Maloney P. C. Oxalate:formate exchange. The basis for energy coupling in Oxalobacter. J Biol Chem. 1989 May 5;264(13):7244–7250. [PubMed] [Google Scholar]
  3. Caldwell D. R., Hudson R. F. Sodium, an obligate growth requirement for predominant rumen bacteria. Appl Microbiol. 1974 Mar;27(3):549–552. doi: 10.1128/am.27.3.549-552.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chen G. J., Russell J. B. Fermentation of peptides and amino acids by a monensin-sensitive ruminal Peptostreptococcus. Appl Environ Microbiol. 1988 Nov;54(11):2742–2749. doi: 10.1128/aem.54.11.2742-2749.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cook G. M., Russell J. B. The glutamine cyclotransferase reaction of Streptococcus bovis: a novel mechanism of deriving energy from non-oxidative and non-reductive deamination. FEMS Microbiol Lett. 1993 Aug 1;111(2-3):263–268. doi: 10.1111/j.1574-6968.1993.tb06396.x. [DOI] [PubMed] [Google Scholar]
  6. Loubiere P., Salou P., Leroy M. J., Lindley N. D., Pareilleux A. Electrogenic malate uptake and improved growth energetics of the malolactic bacterium Leuconostoc oenos grown on glucose-malate mixtures. J Bacteriol. 1992 Aug;174(16):5302–5308. doi: 10.1128/jb.174.16.5302-5308.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lundin A., Thore A. Comparison of methods for extraction of bacterial adenine nucleotides determined by firefly assay. Appl Microbiol. 1975 Nov;30(5):713–721. doi: 10.1128/am.30.5.713-721.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Maloney P. C., Ambudkar S. V., Anatharam V., Sonna L. A., Varadhachary A. Anion-exchange mechanisms in bacteria. Microbiol Rev. 1990 Mar;54(1):1–17. doi: 10.1128/mr.54.1.1-17.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Molenaar D., Bosscher J. S., ten Brink B., Driessen A. J., Konings W. N. Generation of a proton motive force by histidine decarboxylation and electrogenic histidine/histamine antiport in Lactobacillus buchneri. J Bacteriol. 1993 May;175(10):2864–2870. doi: 10.1128/jb.175.10.2864-2870.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Olsen E. B., Russell J. B., Henick-Kling T. Electrogenic L-malate transport by Lactobacillus plantarum: a basis for energy derivation from malolactic fermentation. J Bacteriol. 1991 Oct;173(19):6199–6206. doi: 10.1128/jb.173.19.6199-6206.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Paster B. J., Russell J. B., Yang C. M., Chow J. M., Woese C. R., Tanner R. Phylogeny of the ammonia-producing ruminal bacteria Peptostreptococcus anaerobius, Clostridium sticklandii, and Clostridium aminophilum sp. nov. Int J Syst Bacteriol. 1993 Jan;43(1):107–110. doi: 10.1099/00207713-43-1-107. [DOI] [PubMed] [Google Scholar]
  12. Poolman B., Molenaar D., Smid E. J., Ubbink T., Abee T., Renault P. P., Konings W. N. Malolactic fermentation: electrogenic malate uptake and malate/lactate antiport generate metabolic energy. J Bacteriol. 1991 Oct;173(19):6030–6037. doi: 10.1128/jb.173.19.6030-6037.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Russell J. B., Strobel H. J., Chen G. J. Enrichment and isolation of a ruminal bacterium with a very high specific activity of ammonia production. Appl Environ Microbiol. 1988 Apr;54(4):872–877. doi: 10.1128/aem.54.4.872-877.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Russell J. B., Strobel H. J., Driessen A. J., Konings W. N. Sodium-dependent transport of neutral amino acids by whole cells and membrane vesicles of Streptococcus bovis, a ruminal bacterium. J Bacteriol. 1988 Aug;170(8):3531–3536. doi: 10.1128/jb.170.8.3531-3536.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Russell J. B., Strobel H. J. Effect of ionophores on ruminal fermentation. Appl Environ Microbiol. 1989 Jan;55(1):1–6. doi: 10.1128/aem.55.1.1-6.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Russell J. B., Strobel H. J., Martin S. A. Strategies of nutrient transport by ruminal bacteria. J Dairy Sci. 1990 Oct;73(10):2996–3012. doi: 10.3168/jds.S0022-0302(90)78987-4. [DOI] [PubMed] [Google Scholar]
  17. Smith D. G., Russell W. C., Ingledew W. J., Thirkell D. Hydrolysis of urea by Ureaplasma urealyticum generates a transmembrane potential with resultant ATP synthesis. J Bacteriol. 1993 Jun;175(11):3253–3258. doi: 10.1128/jb.175.11.3253-3258.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]

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