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Elemental Composition of Extremely Alkaliphilic Anaerobic Bacteria

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Abstract

The contents of several chemical elements were assessed in the haloalkaliphilic acetogenic bacterium Natroniella acetigena and the alkaliphilic sulfate-reducing bacterium Desulfonatronum lacustre using X-ray microanalysis, stereoscanning microscopy, and mass spectrometry. The organisms were found to differ significantly in their relative contents of S, K, P, and Cl. The P/S ratio in cells of the alkaliphilic bacteria incubated in mineral media at different pH was pH-dependent. With a pH increase from 9 to 10, potassium extrusion from cells was observed, suggesting that secondary K+/H+ antiport activity accounts for the homeostasis of cytosolic pH. Deenergization of bacterial cells in the presence of inhibitors and ionophores results in specific changes in the P/S ratio, which may be considered an indicator of the cell energetic state. In Natroniella acetigena, the content of intracellular Cl was directly proportional to the NaCl concentration in the medium. Some metals were shown to be necessary for the N. acetigena viability; the requirement for Ni and Co was absolute. Although little demand for Mg was characteristic of the bacteria studied, their growth was stimulated by an increase in Mg concentration, and the cell resistance to lysis was enhanced.

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REFERENCES

  1. Zavarzin, G.A., Zhilina, T.N., and Kevbrin, V.V., The Alkaliphilic Microbial Community and Its Functional Diversity, Mikrobiologiya, 1999, vol. 68, no. 5, pp. 579–599.

    Google Scholar 

  2. Zavarzin, G.A. and Zhilina, T.N., Anaerobic Chemotrophic Alkaliphiles, Journey to Diverse Microbial Worlds, Seckbach, J., Ed., Dordrecht: Kluwer Academic, 2000, pp. 191–208.

    Google Scholar 

  3. Zhilina, T.N., Zavarzin, G.A., Detkova, E.N., and Rainey, F.A., Natroniella acetigena gen. nov., sp. nov., an Extremely Haloalkalophilic, Homoacetic Bacterium: A New Member of Haloanaerobiales, Curr. Microbiol., 1996, vol. 32, pp. 320–326.

    Google Scholar 

  4. Pikuta, E.V., Zhilina, T.N., Zavarzin, G.A., Kostrikina, N.A., Osipov, G.A., and Rainey, F.A., Desulfonatronovibrio lacustre gen. nov., sp. nov.: A New Alkaliphilic Sulfate-Reducing Bacterium Utilizing Ethanol, Mikrobiologiya, 1998, vol. 67, no. 1, pp. 127–135.

    Google Scholar 

  5. Nikitin, D.I., Sorokin, V.V., Pitryuk, I.A., and Nikitina, E.S., Elemental Composition of Cells of Bacteria Belonging to Various Taxa, Prikl. Biokhim. Mikrobiol., 1998, vol. 34, no. 2, pp. 180–182.

    Google Scholar 

  6. Fagerbakke, K.M., Norland, S., and Heldal, M., The Inorganic Ion Content of Native Aquatic Bacteria, Can. J. Microbiol., 1999, vol. 45, pp. 301–311.

    Google Scholar 

  7. Reznikov, A.A., Mulikovskaya, E.P., and Sokolov, I.Yu., Metody analiza prirodnykh vod (Methods for the Analysis of Natural Waters), Moscow: Nedra.

  8. Metals and Microorganisms, Hughes, M.N. and Poole, R.K., Eds., London: Chapman and Hall, 1989.

    Google Scholar 

  9. Ni, S., Boone, J.E., and Boone, D.R., Potassium Extrusion by the Moderately Halophilic and Alkaliphilic Methanogen Methanolobus taylorii GS-16 and Homeostasis of Cytosolic pH, J. Bacteriol., 1994, vol. 176, no. 23, pp. 7274–7279.

    Google Scholar 

  10. Tisa, L.S., Calcium Transport by Frankia sp. Strain EAN1pec, Curr. Microbiol., 1998, vol. 37, pp. 12–16.

    Google Scholar 

  11. Pusheva, M.A., Pitryuk, A.V., and Zavarzin, G.A., Na+-and H+-Dependent ATP Synthesis in Extremely Alkaliphilic Anaerobes, Dokl. Akad. Nauk, 2000, vol. 374, no. 6, pp. 833–835.

    Google Scholar 

  12. Roéler, M. and Müller, V., Quantitative and Physiological Analyses of Chloride Dependence of Growth of Halobacillus halophilus, Appl. Environ. Microbiol., 1998, vol. 64, no. 10, pp. 3813–3817.

    Google Scholar 

  13. Murray, T., Popham, D.L., and Setlow, P., Bacillus subtilis Cells Lacking Penicillin-Binding Protein 1 Require Increased Levels of Divalent Cations for Growth, J. Bacteriol., 1998, vol. 180, no. 17, pp. 4555–4563.

    Google Scholar 

  14. Tindall, B.J., Mills, A.A., and Grant, W.D., An Alkalophilic Red Halophilic Bacterium with a Low Magnesium Requirement from a Kenyan Soda Lake, J. Gen. Microbiol., 1980, vol. 116, pp. 257–260.

    Google Scholar 

  15. Braus-Stromeyer, S.A., Schnappauf, G., Braus, G.H., Göner, A.S., and Drake, H.L., Carbonic Anhydrase in Acetobacterium woodii and Other Acetogenic Bacteria, J. Bacteriol., 1997, vol. 179, no. 22, pp. 7197–7200.

    Google Scholar 

  16. Pusheva, M.A., Berestovskaya, Yu.Y., and Borodulina, N.P., The Effect of Nickel on the Metabolism of Homoacetic Bacteria, Mikrobiologiya, 1989, vol. 58, no. 2, pp. 206–211.

    Google Scholar 

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Pitryuk, A.V., Pusheva, M.A. & Sorokin, V.V. Elemental Composition of Extremely Alkaliphilic Anaerobic Bacteria. Microbiology 71, 24–30 (2002). https://doi.org/10.1023/A:1017990030860

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