1887

Abstract

The parasitic protist was cultured in chemostats with glucose or maltose as carbon and energy source. The maximum growth rate was about six divisions per day independent of the substrate, and the apparent for glucose was 0.375 mM. While growing on maltose, the growth rate depended linearly on the maltose concentration, indicating that in contrast to glucose metabolism a diffusion step is rate-limiting to maltose metabolism. Cultures were examined over a wide range of growth rates under four conditions: utilizing glucose or maltose as carbon and energy source, with the carbon source rate-limiting or present in excess. Cell density, cellular protein and carbohydrate content as well as residual substrate concentration in the culture fluid were measured at each steady state. The protein content was constant at 100 μg protein per cell except when was cultured under glucose limitation; in the latter case, slow-growing cells had less protein than cells grown at high rates. When growing under glucose limitation metabolism changed to become more energy efficient at growth rates exceeding about half the maximum rate. The maintenance energy at the low growth rates accounted for approximately half of the total carbon consumption, which is high in comparison to other micro-organisms. At low growth rates the yield on maltose exceeded that on glucose, when expressed in terms of carbon equivalents. The yields on maltose and glucose were equal, but much lower, when the carbon source was not rate-limiting. A comparison of the data of this study with similar studies on other organisms suggests that the high maintenance energy of may be used primarily for maintaining homeostasis of the internal conditions to enable growth and survival in the vagina.

Loading

Article metrics loading...

/content/journal/micro/10.1099/13500872-140-9-2495
1994-09-01
2024-04-23
Loading full text...

Full text loading...

/deliver/fulltext/micro/140/9/mic-140-9-2495.html?itemId=/content/journal/micro/10.1099/13500872-140-9-2495&mimeType=html&fmt=ahah

References

  1. Alderete J.F., Garza G., Smith J., Spence M. Trichomonas vaginalis-, electrophoretic analysis and heterogeneity among isolates due to high molecular weight trichomonad proteins. Exp Parasitol 1986; 61:244–251
    [Google Scholar]
  2. Benito B., Lagunas R. The low-affinity component of Saccharomyces cerevisiae maltose transport is an artifact. J Bacterial 1992; 174:3065–3069
    [Google Scholar]
  3. Bergmeyer H.U. Enzymes as biochemical reagents: hexokinase. In Methods of Engymatic Analysis 1974 Edited by Bergmeyer H.U. New York: Academic Press; p 473
    [Google Scholar]
  4. Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976; 72:248–254
    [Google Scholar]
  5. Daly J.J. The maltose metabolism of Trichomonas gallinae (Rivolta, 1878): I. Growth studies. J Parasitol 1970; 56:883–888
    [Google Scholar]
  6. Diamond L.S. The establishment of various trichomonads of animals and man in axenic cultures. J Parasitol 1957; 43:488–490
    [Google Scholar]
  7. Eisenthal R., Cornish-Bowden A. The direct linear plot. A new graphical procedure for estimating enzyme kinetic parameters. Biochem J 1974; 139:715–720
    [Google Scholar]
  8. Fouts A.C., Kraus S.J. Trichomonas vaginalis-, reevaluation of its clinical presentation and laboratory diagnosis. J Infect Dis 1980; 141:137–143
    [Google Scholar]
  9. Hochachka P.W., Somero G.N. Biochemical Adaptation 1984 Princeton, NJ: Princeton University Press;
    [Google Scholar]
  10. Lehker M.W., Alderete J.F. Properties of Trichomonas vaginalis grown under chemostat controlled growth conditions. Genitonrin Med 1990; 66:193 –199
    [Google Scholar]
  11. Lloyd D., Paget T.A. The effects of environmental factors on the metabolism of Giardia and Trichomonas. In biochemical Protozoology 1990 1991 Edited by Coombs G.H., North M.J. London: Taylor and Francis; pp 92–101
    [Google Scholar]
  12. Mack S.R., Muller M. End products of carbohydrate metabolism in Trichomonas vaginalis. Comp biochem Physiol 1980; 67B:213–216
    [Google Scholar]
  13. Mertens E., Muller M. Glucokinase and fructokinase of Trichomonas vaginalis and Tritrichomonas foetus. J Protocol 1990; 37:384–388
    [Google Scholar]
  14. Muller M. Energy metabolism of protozoa without mitochondria. Annu Rev Microbiol 1988; 42:465–488
    [Google Scholar]
  15. Muller M. Energy metabolism of anaerobic parasitic protists. In biochemical Protozoology 1991 Edited by Coombs G.H., North M.J. London: Taylor and Francis; pp 80–91
    [Google Scholar]
  16. Muller M. The hydrogenosome. J Gen Microbiol 1993; 139:2879–2889
    [Google Scholar]
  17. Read C.P. Comparative studies on the physiology of trichomonad protozoa. J Parasitol 1957; 43:385–394
    [Google Scholar]
  18. Schwartz M. The maltose regulon. In Escherichia coli and Salmonella typhimurium Cellular and Molecular biology 1987 Fidited by Neidhardt F.C. Washington, DC: American Society for Microbiology; pp 1482–1502
    [Google Scholar]
  19. Simonetti G., Simonetti N., D’Auria F.D. Glycogen medium, antitrichomonal drug activity in vaginal liquids. Drugs Exptl Clin Res 1989; 15:545–547
    [Google Scholar]
  20. Stolz P., Bocker G., Vogel R.F., Hammes W.P. Utilisation of maltose and glucose by lactobacilli isolated from sourdough. FEMS Microbiol Lett 1993; 109:237–242
    [Google Scholar]
  21. Stouthamer A.H. Energetic aspects of the growth of micro-organisms. Symp Soc Gen Microbiol 1977; 27:285–315
    [Google Scholar]
  22. Stouthamer A.H. The search for correlation between theoretical and experimental growth rates. Int Rev biochem 1979; 21:1–47
    [Google Scholar]
  23. Tempest D.W., Neijssel O.M. Growth yield values in relation to respiration. In Diversity of bacterial Respiration Systems 1 1980 Edited by Knowles C. Boca Raton, Florida: CRC Press; pp 1–31
    [Google Scholar]
  24. Tempest D.W., Neijssel O.M. The status of YATP and maintenance energy as biologically interpretable phenomena. Annu Rev Microbiol 1984; 38:459–486
    [Google Scholar]
  25. Ter Kuile B.H. Adaptation of the carbon metabolism of Trichomonas vaginalis to the nature and availability of the carbon source. Microbiology 1994; 140:2503–2510
    [Google Scholar]
  26. Ter Kuile B.H., Cook M. The kinetics of facilitated diffusion followed by enzymatic conversion of the substrate, biochim biophys Acta 1994 (in press);
    [Google Scholar]
  27. Ter Kuile B.H., Muller M. Interaction between facilitated diffusion of glucose across the plasma membrane and its metabolism in Trichomonas vaginalis. FEA1S Microbiol Lett 1993; 110:27–32
    [Google Scholar]
  28. Ter Kuile B.H., Muller M. Maltose utilization by extracellular hydrolysis followed by glucose transport in the amitochondriate eukaryote, Trichomonas vaginalis 1994 Parasitology (in press);
    [Google Scholar]
  29. Ter Kuile B.H., Opperdoes F.R. Chemostat cultures of Leishmania donovani promastigotes and Trypanosoma brucei procyclic trypomastigotes. Mol biochem Parasitol 1991; 45:171–174
    [Google Scholar]
  30. Ter Kuile B.H., Opperdoes F.R. Mutual adjustment of glucose uptake and metabolism in Trypanosoma brucei grown in the chemostat. J bacteriol 1992a; 174:1273–1279
    [Google Scholar]
  31. Ter Kuile B.H., Opperdoes F.R. Comparative physiology of two protozoan parasites, Leishmania donovani and Trypanosoma brucei, grown in chemostats. J bacteriol 1992b; 174:2929–2934
    [Google Scholar]
  32. Ter Kuile B.H., Opperdoes F.R. Uptake and turnover of glucose in Leishmania donovani. Mol biochem Parasitol 1993; 60:313–322
    [Google Scholar]
  33. Ter Kuile B.H., Wiemer E.A.C., Michels P.A.M., Opperdoes F.R. The electrochemical proton gradient in the blood-stream form of Trypanosoma brucei is dependent on the temperature. Alol biochem Parasitol 1992; 55:21–28
    [Google Scholar]
  34. Ter Kuile B.H. Glucose and proline transport in kineto-plastids. Parasitol Today 1993; 9:206–210
    [Google Scholar]
  35. Veldkamp H. Continuous Culture in Microbial Physiology and Ecology 1976 Durham, UK: Meadowfield Press;
    [Google Scholar]
  36. Zilberstein D. Adaptation of Leishmania species to an acidic environment. In biochemical Protozoology 1991 Edited by Coombs G.H., North M.J. London: Taylor and Francis; pp 349–358
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/13500872-140-9-2495
Loading
/content/journal/micro/10.1099/13500872-140-9-2495
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