Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1994 Jun;176(11):3177–3187. doi: 10.1128/jb.176.11.3177-3187.1994

Halotolerance of Methanobacterium thermoautotrophicum delta H and Marburg.

R Ciulla 1, C Clougherty 1, N Belay 1, S Krishnan 1, C Zhou 1, D Byrd 1, M F Roberts 1
PMCID: PMC205486  PMID: 8195071

Abstract

Methanobacterium thermoautotrophicum delta H and Marburg were adapted to grow in medium containing up to 0.65 M NaCl. From 0.01 to 0.5 M NaCl, there was a lag before cell growth which increased with increasing external NaCl. The effect of NaCl on methane production was not significant once the cells began to grow. Intracellular solutes were monitored by nuclear magnetic resonance (NMR) spectroscopy as a function of osmotic stress. In the delta H strain, the major intracellular small organic solutes, cyclic-2,3-diphosphoglycerate and glutamate, increased at most twofold between 0.01 and 0.4 M NaCl and decreased when the external NaCl was 0.5 M. M. thermoautotrophicum Marburg similarly showed a decrease in solute (cyclic-2,3-diphosphoglycerate, 1,3,4,6-tetracarboxyhexane, and L-alpha-glutamate) concentrations for cells grown in medium containing > 0.5 M NaCl. At 0.65 M NaCl, a new organic solute, which was visible in only trace amounts at the lower NaCl concentrations, became the dominant solute. Intracellular potassium in the delta H strain, detected by atomic absorption and 39K NMR, was roughly constant between 0.01 and 0.4 M and then decreased as the external NaCl increased further. The high intracellular K+ was balanced by the negative charges of the organic osmolytes. At the higher external salt concentrations, it is suggested that Na+ and possibly Cl- ions are internalized to provide osmotic balance. A striking difference of strain Marburg from strain delta H was that yeast extract facilitated growth in high-NaCl-containing medium. The yeast extract supplied only trace NMR-detectable solutes (e.g., betaine) but had a large effect on endogenous glutamate levels, which were significantly decreased. Exogenous choline and glycine, instead of yeast extract, also aided growth in NaCl-containing media. Both solutes were internalized with the choline converted to betaine; the contribution to osmotic balance of these species was 20 to 25% of the total small-molecule pool. These results indicate that M. thermoautotrophicum shows little changes in its internal solutes over a wide range of external NaCl. Furthermore, they illustrate the considerable differences in physiology in the delta H and Marburg strains of this organism.

Full text

PDF
3177

Selected References

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

  1. Balch W. E., Fox G. E., Magrum L. J., Woese C. R., Wolfe R. S. Methanogens: reevaluation of a unique biological group. Microbiol Rev. 1979 Jun;43(2):260–296. doi: 10.1128/mr.43.2.260-296.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. 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 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
  3. Brown A. D. Microbial water stress. Bacteriol Rev. 1976 Dec;40(4):803–846. doi: 10.1128/br.40.4.803-846.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cover W. H., Martinez R. J., Rittenberg S. C. Permeability of the boundary layers of Bdellovibrio bacteriovorus 109J and its bdelloplasts to small hydrophilic molecules. J Bacteriol. 1984 Feb;157(2):385–390. doi: 10.1128/jb.157.2.385-390.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Csonka L. N. Physiological and genetic responses of bacteria to osmotic stress. Microbiol Rev. 1989 Mar;53(1):121–147. doi: 10.1128/mr.53.1.121-147.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Daniels L., Belay N., Rajagopal B. S. Assimilatory reduction of sulfate and sulfite by methanogenic bacteria. Appl Environ Microbiol. 1986 Apr;51(4):703–709. doi: 10.1128/aem.51.4.703-709.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Eisenreich W., Bacher A. Biosynthesis of methanofuran in Methanobacterium thermoautotrophicum. J Biol Chem. 1992 Sep 5;267(25):17574–17580. doi: 10.1515/pteridines.1994.5.1.8. [DOI] [PubMed] [Google Scholar]
  8. Evans J. N., Raleigh D. P., Tolman C. J., Roberts M. F. 13C NMR spectroscopy of Methanobacterium thermoautotrophicum. Carbon fluxes and primary metabolic pathways. J Biol Chem. 1986 Dec 15;261(35):16323–16331. [PubMed] [Google Scholar]
  9. Evans J. N., Tolman C. J., Kanodia S., Roberts M. F. 2,3-Cyclopyrophosphoglycerate in methanogens: evidence by 13C NMR spectroscopy for a role in carbohydrate metabolism. Biochemistry. 1985 Oct 8;24(21):5693–5698. doi: 10.1021/bi00342a001. [DOI] [PubMed] [Google Scholar]
  10. Evans J. N., Tolman C. J., Roberts M. F. Indirect observation by 13C NMR spectroscopy of a novel CO2 fixation pathway in methanogens. Science. 1986 Jan 31;231(4737):488–491. doi: 10.1126/science.3079919. [DOI] [PubMed] [Google Scholar]
  11. Gorkovenko A., Roberts M. F., White R. H. Identification, Biosynthesis, and Function of 1,3,4,6-Hexanetetracarboxylic Acid in Methanobacterium thermoautotrophicum DeltaH. Appl Environ Microbiol. 1994 Apr;60(4):1249–1253. doi: 10.1128/aem.60.4.1249-1253.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Jones W. J., Nagle D. P., Jr, Whitman W. B. Methanogens and the diversity of archaebacteria. Microbiol Rev. 1987 Mar;51(1):135–177. doi: 10.1128/mr.51.1.135-177.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Kanodia S., Roberts M. F. Methanophosphagen: Unique cyclic pyrophosphate isolated from Methanobacterium thermoautotrophicum. Proc Natl Acad Sci U S A. 1983 Sep;80(17):5217–5221. doi: 10.1073/pnas.80.17.5217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kogut M., Russell N. J. Life at the limits. Considerations on how bacteria can grow at extremes of temperature and pressure, or with high concentrations of ions and solutes. Sci Prog. 1987;71(283 Pt 3):381–399. [PubMed] [Google Scholar]
  15. Lai M. C., Sowers K. R., Robertson D. E., Roberts M. F., Gunsalus R. P. Distribution of compatible solutes in the halophilic methanogenic archaebacteria. J Bacteriol. 1991 Sep;173(17):5352–5358. doi: 10.1128/jb.173.17.5352-5358.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Measures J. C. Role of amino acids in osmoregulation of non-halophilic bacteria. Nature. 1975 Oct 2;257(5525):398–400. doi: 10.1038/257398a0. [DOI] [PubMed] [Google Scholar]
  17. Patel G. B., Roth L. A. Effect of sodium chloride on growth and methane production of methanogens. Can J Microbiol. 1977 Jul;23(7):893–897. doi: 10.1139/m77-131. [DOI] [PubMed] [Google Scholar]
  18. Roberts M. F., Lai M. C., Gunsalus R. P. Biosynthetic pathways of the osmolytes N epsilon-acetyl-beta-lysine, beta-glutamine, and betaine in Methanohalophilus strain FDF1 suggested by nuclear magnetic resonance analyses. J Bacteriol. 1992 Oct;174(20):6688–6693. doi: 10.1128/jb.174.20.6688-6693.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Robertson D. E., Noll D., Roberts M. F. Free amino acid dynamics in marine methanogens. beta-Amino acids as compatible solutes. J Biol Chem. 1992 Jul 25;267(21):14893–14901. [PubMed] [Google Scholar]
  20. Robertson D. E., Noll D., Roberts M. F., Menaia J. A., Boone D. R. Detection of the osmoregulator betaine in methanogens. Appl Environ Microbiol. 1990 Feb;56(2):563–565. doi: 10.1128/aem.56.2.563-565.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Robertson D. E., Roberts M. F., Belay N., Stetter K. O., Boone D. R. Occurrence of beta-glutamate, a novel osmolyte, in marine methanogenic bacteria. Appl Environ Microbiol. 1990 May;56(5):1504–1508. doi: 10.1128/aem.56.5.1504-1508.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Robertson D. E., Roberts M. F. Organic osmolytes in methanogenic archaebacteria. Biofactors. 1991 Jan;3(1):1–9. [PubMed] [Google Scholar]
  23. Sastry M. V., Robertson D. E., Moynihan J. A., Roberts M. F. Enzymatic degradation of cyclic 2,3-diphosphoglycerate to 2,3-diphosphoglycerate in Methanobacterium thermoautotrophicum. Biochemistry. 1992 Mar 24;31(11):2926–2935. doi: 10.1021/bi00126a012. [DOI] [PubMed] [Google Scholar]
  24. Seely R. J., Fahrney D. E. A novel diphospho-P,P'-diester from Methanobacterium thermoautotrophicum. J Biol Chem. 1983 Sep 25;258(18):10835–10838. [PubMed] [Google Scholar]
  25. Seely R. J., Fahrney D. E. Levels of cyclic-2,3-diphosphoglycerate in Methanobacterium thermoautotrophicum during phosphate limitation. J Bacteriol. 1984 Oct;160(1):50–54. doi: 10.1128/jb.160.1.50-54.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Shporer M., Civan M. M. Pulsed nuclear magnetic resonance study of 39K within halobacteria. J Membr Biol. 1977 May 12;33(3-4):385–400. doi: 10.1007/BF01869525. [DOI] [PubMed] [Google Scholar]
  27. Sowers K. R., Robertson D. E., Noll D., Gunsalus R. P., Roberts M. F. N epsilon-acetyl-beta-lysine: an osmolyte synthesized by methanogenic archaebacteria. Proc Natl Acad Sci U S A. 1990 Dec;87(23):9083–9087. doi: 10.1073/pnas.87.23.9083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Springer C. S., Jr Measurement of metal cation compartmentalization in tissue by high-resolution metal cation NMR. Annu Rev Biophys Biophys Chem. 1987;16:375–399. doi: 10.1146/annurev.bb.16.060187.002111. [DOI] [PubMed] [Google Scholar]
  29. Sprott G. D., Jarrell K. F. K+, Na+, and Mg2+ content and permeability of Methanospirillum hungatei and Methanobacterium thermoautotrophicum. Can J Microbiol. 1981 Apr;27(4):444–451. doi: 10.1139/m81-067. [DOI] [PubMed] [Google Scholar]
  30. Tolman C. J., Kanodia S., Roberts M. F., Daniels L. 31P-NMR spectra of methanogens: 2,3-cyclopyrophosphoglycerate is detectable only in methanobacteria strains. Biochim Biophys Acta. 1986 May 29;886(3):345–352. doi: 10.1016/0167-4889(86)90169-2. [DOI] [PubMed] [Google Scholar]
  31. Zeikus J. G., Wolfe R. S. Methanobacterium thermoautotrophicus sp. n., an anaerobic, autotrophic, extreme thermophile. J Bacteriol. 1972 Feb;109(2):707–715. doi: 10.1128/jb.109.2.707-713.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES