1887

Abstract

NCIB 11883 was grown in ammonia-limited continuous culture at low dilution rate with glucose as the carbon source. Under these conditions the organism produced an extracellular succinoglucan polysaccharide and transported glucose using the same periplasmic glucose-binding proteins (GBP1 and GBP2) as during glucose-limited growth. Transition from glucose- to ammonia-limited growth was accompanied by a very rapid decrease in glucose uptake capacity, whereas the glucose-binding proteins were diluted out much more slowly ( approximately 1 h and 14 h respectively). Although the rate of glucose uptake and the concentrations of GBP1 and GBP2 were much lower during ammonia limitation, the activities of enzymes involved in the early stages of glucose metabolism and in the production of succinoglucan precursors were essentially unchanged. Glucose transport was also investigated in two new strains of which had been isolated following prolonged growth under glucose limitation. Glucose uptake by strain AR18 was significantly less repressed during ammonia limitation compared with either the original parent strain or strain AR9, and this was reflected both in its relatively high concentration of GBP1 and in its significantly higher rate of succinoglucan synthesis. Flux control analysis using 6-chloro-6-deoxy--glucose as an inhibitor of glucose transport showed that the latter was a major kinetic control point for succinoglucan production. It is concluded that glucose uptake by , particularly via the GBP1-dependent system, is only moderately repressed during ammonia-limited growth and that the organism avoids the potentially deleterious effects of accumulating excess glucose by converting the surplus into succinoglucan.

Loading

Article metrics loading...

/content/journal/micro/10.1099/00221287-134-12-3111
1988-12-01
2024-04-19
Loading full text...

Full text loading...

/deliver/fulltext/micro/134/12/mic-134-12-3111.html?itemId=/content/journal/micro/10.1099/00221287-134-12-3111&mimeType=html&fmt=ahah

References

  1. Ames G.F.-L. 1986; Bacterial periplasmic transport systems: structure, mechanism and evolution.. Annual Review of Biochemistry 55:397–425
    [Google Scholar]
  2. Beardsmore A.J., Aperghis P.N.G., Quayle J.R. 1982; Characterization of the assimilatory and dissimilatory pathways of carbon metabolism during growth of Methylophilus methylotrophus on methanol. Journal of General Microbiology 128:1423–1439
    [Google Scholar]
  3. Bergmeyer H.U. editor editor Methods of Enzymatic Analysis, 2nd edn.. 1 New York & London: Academic Press;
    [Google Scholar]
  4. Cornish A., Linton J.D., Jones C.W. 1987; The effect of growth conditions on the respiratory system of a succinoglucan-producing strain of Agrobacterium radiobacter . Journal of General Microbiology 133:2971–2978
    [Google Scholar]
  5. Cornish A., Greenwood J.A., Jones C.W. 1988; Binding-protein-dependent glucose transport by Agrobacterium radiobacter grown in glucose- limited continuous culture. Journal of General Microbiology 134:3099–3110
    [Google Scholar]
  6. Darzins A., Nixon L.L., Vanags R.I. 1985a; Cloning of Escherichia coli and Pseudomonas aeruginosa phosphoman- nose (isomerase genes and their expression in alginate-negative mutants of Pseudomonas aeruginosa . Journal of Bacteriology 164:249–267
    [Google Scholar]
  7. Darzins A., Wang S.-K., Vanags R.I., Chakrabarty A.M. 1985b; Clustering of mutations affecting alginic acid biosynthesis in mucoid Pseudomonas aeruginosa . Journal of Bacteriology 164:516–524
    [Google Scholar]
  8. Groen A.K., Wanders .R.J.A., Westerhoff H.V., Van der meer R., Tager J.M. 1982; Quantification of the contribution of various steps to the control of mitochondrial respiration. Journal of Biological Chemistry 257:2754–2757
    [Google Scholar]
  9. Higgins C.F., Haag P.D., Whalley K., Jamieson D.J. 1985; Nucleotide binding by membrane components of bacterial periplasmic binding protein-dependent transport systems. EMBO Journal 4:1033–1040
    [Google Scholar]
  10. Higgins C.F., Hiles I.D., Salmond G.P.C., Gill D.R., Downie J.A., Evans I.J., Holland I.B., Gray L., Buckel S.D., Bell A.W. 1986; A family of related ATP-binding subunits coupled to many distinct biological processes in bacteria. Nature; London: 323448–450
    [Google Scholar]
  11. Hueting S., Delang T., Tempest D.W. 1979; Energy requirement for maintenance of the transmembrane potassium gradient in Klebsiella aero- genes NCTC418: a continuous culture study. Archives of Microbiology 123:183–188
    [Google Scholar]
  12. Kell D.B., Westerhoff H.V. 1986a; Towards a rational approach to the optimization of flux in microbial transformations. Trends in Biotechnology 4:137–142
    [Google Scholar]
  13. Kell D.B., Westbrhoff H.V. 1986b; Metabolic control theory: its role in microbiology and biotechnology. FEMS Microbiology Reviews 39:305–320
    [Google Scholar]
  14. Linton J.D., Evans M., Jones D.S., Gouldney D.N. 1987a; Exocellular succinoglucan production by Agrobacterium radiobacter NCIB 11883. Journal of General Microbiology 133:2961–2969 ferent pathways of assimilationJournal of General Microbiology 132:2961–2969
    [Google Scholar]
  15. Linton J.D., Evans M., Jones D.A. 1987a; Exocellular succinoglucan production by Agrobacterium radiobacter NCIB 11883. Journal of General Microbiology 133:2961–2969
    [Google Scholar]
  16. Linton J.D., Jones D.S., Woodard S. 1987b; Factors that control the rate of exopolysaccharide production by Agrobacterium radiobacter NCIB 11883. Journal of General Microbiology 133:2979–2987
    [Google Scholar]
  17. Neijssbl O.M., Tempest D.W. 1975; The regulation of carbohydrate metabolism in Klebsiella aerogenes NCTC 418 organisms growing in chemo- stat culture. Archives of Microbiology 106:251–258
    [Google Scholar]
  18. Maxwell E.S., Kurahashi K., Kalcar H.M. 1962; Enzymes of the Leloir pathway. Methods in Enzymology 5:174–190
    [Google Scholar]
  19. Sutherland I.W. 1982; Biosynthesis of microbial exopolysaccharides. Advances in Microbial Physiology 23:79–150
    [Google Scholar]
  20. Thorne L., Tansey L., Pollock T.J. 1987; Clustering of mutations blocking synthesis of xanthan gum by Xanthomonas campestris . Journal of Bacteriology 169:3593–3600
    [Google Scholar]
  21. Walter R.P., Morris J.G., Kell D.B. 1987; The roles of osmotic stress and water activity in the inhibition of growth, glycolysis and glucose phosphotransferase system of Clostridium pasteurianum . Journal of General Microbiology 133:259–266
    [Google Scholar]
  22. Wood W.A. 1971; Assay of enzymes representative of metabolic pathways. Methods in Microbiology 6A:411–424
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/00221287-134-12-3111
Loading
/content/journal/micro/10.1099/00221287-134-12-3111
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error