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. 1997 May;63(5):1847–1851. doi: 10.1128/aem.63.5.1847-1851.1997

Glucose transport by mixed ruminal bacteria from a cow.

H Kajikawa 1, M Amari 1, S Masaki 1
PMCID: PMC168477  PMID: 9143117

Abstract

The glucose transport of mixed ruminal bacteria harvested from a holstein cow fed 5.0 kg of Italian ryegrass and 1.5 kg of flaked corn a day was investigated. The Eadie-Hofstee plot characterized two transport systems: a high-affinity, low-velocity system and a low-affinity, high-velocity system. The former system (K(m) = 16 microM; Vmax = 2.2 nmol/min/mg of protein) is considered dominant under this feeding condition based on the glucose concentration in the rumen (< 1 mM). In light of the facts that the protonophore SF6847 and the lipophilic triphenylmethyl phosphonium ion had no effect on the high-affinity system and an artificially generated proton gradient and electrical potential across the cell membrane did not increase glucose transport, a proton motive force is not be involved in the system. On the other hand, from the facts that chlorhexidine inhibited about 90% of the high-affinity system while iodoacetate showed no significant effect, and a high phosphoenolpyruvate-dependent phosphorylation of glucose was actually shown, the phosphoenolpyruvate-dependent phosphotransferase system is considered the main system in the high-affinity system. Moreover, as shown by the facts that harmaline inhibited about 30% of the high-affinity system and the artificially generated sodium gradient across the cell membrane significantly stimulated glucose transport, this system also includes sodium symport to some degree. The high-affinity system was sensitive to a decrease in pH (< 6.5) and was inhibited by the presence of sucrose, mannose, and fructose.

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Selected References

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  1. Chen C. C., Tsuchiya T., Yamane Y., Wood J. M., Wilson T. H. Na+ (Li+)-proline cotransport in Escherichia coli. J Membr Biol. 1985;84(2):157–164. doi: 10.1007/BF01872213. [DOI] [PubMed] [Google Scholar]
  2. Chen G., Russell J. B., Sniffen C. J. A procedure for measuring peptides in rumen fluid and evidence that peptide uptake can be a rate-limiting step in ruminal protein degradation. J Dairy Sci. 1987 Jun;70(6):1211–1219. doi: 10.3168/jds.S0022-0302(87)80133-9. [DOI] [PubMed] [Google Scholar]
  3. Cook G. M., Russell J. B. Alternative strategies of 2-deoxyglucose resistance and low affinity glucose transport in the ruminal bacteria, Streptococcus bovis and Selenomonas ruminantium. FEMS Microbiol Lett. 1994 Oct 15;123(1-2):207–212. doi: 10.1111/j.1574-6968.1994.tb07223.x. [DOI] [PubMed] [Google Scholar]
  4. Dills S. S., Apperson A., Schmidt M. R., Saier M. H., Jr Carbohydrate transport in bacteria. Microbiol Rev. 1980 Sep;44(3):385–418. doi: 10.1128/mr.44.3.385-418.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Ellwood D. C., Phipps P. J., Hamilton I. R. Effect of growth rate and glucose concentration on the activity of the phosphoenolpyruvate phosphotransferase system in Streptococcus mutans Ingbritt grown in continuous culture. Infect Immun. 1979 Feb;23(2):224–231. doi: 10.1128/iai.23.2.224-231.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Franklund C. V., Glass T. L. Glucose uptake by the cellulolytic ruminal anaerobe Bacteroides succinogenes. J Bacteriol. 1987 Feb;169(2):500–506. doi: 10.1128/jb.169.2.500-506.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hamilton I. R., Ellwood D. C. Effects of fluoride on carbohydrate metabolism by washed cells of Streptococcus mutans grown at various pH values in a chemostat. Infect Immun. 1978 Feb;19(2):434–442. doi: 10.1128/iai.19.2.434-442.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hardy M. R. Monosaccharide analysis of glycoconjugates by high-performance anion-exchange chromatography with pulsed amperometric detection. Methods Enzymol. 1989;179:76–82. doi: 10.1016/0076-6879(89)79115-1. [DOI] [PubMed] [Google Scholar]
  9. Heytler P. G. Uncouplers of oxidative phosphorylation. Methods Enzymol. 1979;55:462–442. doi: 10.1016/0076-6879(79)55060-5. [DOI] [PubMed] [Google Scholar]
  10. Kornberg H. L., Reeves R. E. Inducible phosphoenolpyruvate-dependent hexose phosphotransferase activities in Escherichia coli. Biochem J. 1972 Aug;128(5):1339–1344. doi: 10.1042/bj1281339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  12. Marsh P. D., Keevil C. W., McDermid A. S., Williamson M. I., Ellwood D. C. Inhibition by the antimicrobial agent chlorhexidine of acid production and sugar transport in oral streptococcal bacteria. Arch Oral Biol. 1983;28(3):233–240. doi: 10.1016/0003-9969(83)90152-8. [DOI] [PubMed] [Google Scholar]
  13. Martin S. A. Nutrient transport by ruminal bacteria: a review. J Anim Sci. 1994 Nov;72(11):3019–3031. doi: 10.2527/1994.72113019x. [DOI] [PubMed] [Google Scholar]
  14. Martin S. A., Russell J. B. Phosphoenolpyruvate-dependent phosphorylation of hexoses by ruminal bacteria: evidence for the phosphotransferase transport system. Appl Environ Microbiol. 1986 Dec;52(6):1348–1352. doi: 10.1128/aem.52.6.1348-1352.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Martin S. A., Russell J. B. Transport and phosphorylation of disaccharides by the ruminal bacterium Streptococcus bovis. Appl Environ Microbiol. 1987 Oct;53(10):2388–2393. doi: 10.1128/aem.53.10.2388-2393.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Matin A., Veldkamp H. Physiological basis of the selective advantage of a Spirillum sp. in a carbon-limited environment. J Gen Microbiol. 1978 Apr;105(2):187–197. doi: 10.1099/00221287-105-2-187. [DOI] [PubMed] [Google Scholar]
  17. McAllister T. A., Cheng K. J., Rode L. M., Forsberg C. W. Digestion of barley, maize, and wheat by selected species of ruminal bacteria. Appl Environ Microbiol. 1990 Oct;56(10):3146–3153. doi: 10.1128/aem.56.10.3146-3153.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Moore G. A., Martin S. A. Effect of growth conditions on the Streptococcus bovis phosphoenolpyruvate glucose phosphotransferase system. J Anim Sci. 1991 Dec;69(12):4967–4973. doi: 10.2527/1991.69124967x. [DOI] [PubMed] [Google Scholar]
  19. Postma P. W., Lengeler J. W. Phosphoenolpyruvate:carbohydrate phosphotransferase system of bacteria. Microbiol Rev. 1985 Sep;49(3):232–269. doi: 10.1128/mr.49.3.232-269.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. RYAN R. K. CONCENTRATIONS OF GLUCOSE AND LOW-MOLECULAR-WEIGHT ACIDS IN THE RUMEN OF SHEEP CHANGED GRADUALLY FROM A HAY TO A HAY-PLUS-GRAIN DIET. Am J Vet Res. 1964 May;25:653–659. [PubMed] [Google Scholar]
  21. RYAN R. K. CONCENTRATIONS OF GLUCOSE AND LOW-MOLECULAR-WEIGHT ACIDS IN THE RUMEN OF SHEEP FOLLOWING THE ADDITION OF LARGE AMOUNTS OF WHEAT TO THE RUMEN. Am J Vet Res. 1964 May;25:646–652. [PubMed] [Google Scholar]
  22. Rinehart C. A., Hubbard J. S. Energy coupling in the active transport of proline and glutamate by the photosynthetic halophile Ectothiorhodospira halophila. J Bacteriol. 1976 Sep;127(3):1255–1264. doi: 10.1128/jb.127.3.1255-1264.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Russell J. B. Low-affinity, high-capacity system of glucose transport in the ruminal bacterium Streptococcus bovis: evidence for a mechanism of facilitated diffusion. Appl Environ Microbiol. 1990 Nov;56(11):3304–3307. doi: 10.1128/aem.56.11.3304-3307.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. 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]
  25. Sepúlveda F. V., Robinson J. W. Harmaline, a potent inhibitor of sodium-dependent transport. Biochim Biophys Acta. 1974 Dec 24;373(3):527–531. doi: 10.1016/0005-2736(74)90035-2. [DOI] [PubMed] [Google Scholar]
  26. Strobel H. J., Russell J. B. Non-proton-motive-force-dependent sodium efflux from the ruminal bacterium Streptococcus bovis: bound versus free pools. Appl Environ Microbiol. 1989 Oct;55(10):2664–2668. doi: 10.1128/aem.55.10.2664-2668.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Yang C. M., Russell J. B. Resistance of proline-containing peptides to ruminal degradation in vitro. Appl Environ Microbiol. 1992 Dec;58(12):3954–3958. doi: 10.1128/aem.58.12.3954-3958.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]

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