1887

Abstract

More than 40 isolates of a novel, ubiquitous, proteolytic, moderately alkaliphilic, thermophilic obligate anaerobe were obtained from geothermally and anthropogenically heated environments and mesobiotic environments located on three continents. Whole-cell protein sodium dodecyl sulfate gel electrophoresis revealed that most of these organisms are very similar. Eight of the isolates were characterized in detail; this analysis included 16S ribosomal DNA sequence analysis. The cells of those organisms are (depending on the isolate) 0.5 to 0.8 μm in diameter and 1.5 to 13 μm long, exhibit tumbling motility, and have a positive Gram stain reaction. The temperature range for growth is 43° to 75°C (optimum temperature, 66°C), and the pH range for growth is 5.4 to 9.5 (optimum pH, 8.2); the shortest doubling time is around 10 min. Yeast extract is required for growth, and (depending on the strain) glucose, sucrose, fructose, galactose, and ribose are utilized. The fermentation products from glucose in the presence of yeast extract are CO, H, acetate, formate, and ethanol. The G+C content is 30 to 31 mol%. On the basis of these properties, which differentiate these strains from all alkalitolerant thermophiles described previously, and the results of a comparison of the 16S ribosomal DNA sequences of these organisms with previously described sequences, we propose that our isolates be placed in a single species of the new genus ; strain JW/YL-NZ35 is the type strain of the the type species, .

Loading

Article metrics loading...

/content/journal/ijsem/10.1099/00207713-46-4-1025
1996-10-01
2024-04-16
Loading full text...

Full text loading...

/deliver/fulltext/ijsem/46/4/ijs-46-4-1025.html?itemId=/content/journal/ijsem/10.1099/00207713-46-4-1025&mimeType=html&fmt=ahah

References

  1. Ausubel F. M., Brent R., Kingston R. E., Moore D. D., Seidman J. G., Smith J. A., Struhl K. 1989 Current protocols in molecular biology. 2.4.1–2.4.5 Wiley Interscience; New York:
    [Google Scholar]
  2. Beuscher N., Mayer F., Gottschalk G. 1974; Citrate lyase from Rhodopseudomonas gelatinosa: purification, electron microscopy and subunit structure. Arch. Microbiol 100:307–328
    [Google Scholar]
  3. Collins M. D., Lawson P. A., Willems A., Cordoba J. J., Fernandez-Garayzabal J., Garcia P., Cai J., Hippe H., Farrow J. A. E. 1994; The phylogeny of the genus Clostridium., proposal of five new genera and eleven new species combinations. Int. J. Syst. Bacteriol 44:812–826
    [Google Scholar]
  4. De Soete G. 1983; A least squares algorithm for fitting additive trees to proximity data. Psychometrika 48:621–626
    [Google Scholar]
  5. Engle M., Li Y., Woese C., Wiegel J. 1995; Isolation and characterization of a novel alkali tolerant thermophile, Anaerobranca horikoshii gen. nov., sp. nov. Int. J. Syst. Bacteriol 45:454–461
    [Google Scholar]
  6. Felsenstein J. 1993 PHYLIP (phylogeny inference package), version 3.5c University of Washington; Seattle:
    [Google Scholar]
  7. Frasca J. M., Parks V. R. 1965; A routine technique for double-staining ultra thin sections using uranyl and lead salts. J. Cell Biol 25:157–161
    [Google Scholar]
  8. Freier D., Mothershed C. P., Wiegel J. 1988; Characterization of Clostridium thermocellum JW-20. Appl. Environ. Microbiol 54:204–211
    [Google Scholar]
  9. Grant W. D., Mwatha W. E., Jones B. E. 1990; Alkaliphiles: ecology, diversity and applications. FEMS Microbiol. Rev 75:255–270
    [Google Scholar]
  10. Horikoshi K. 1990 Microorganisms in alkaline environments Kodansha; Tokyo:
    [Google Scholar]
  11. Jukes T. H., Cantor C. R. 1969 Evolution of protein molecules. 21–132 Munro H. N.ed Mammalian protein metabolism Academic Press, Inc.; New York:
    [Google Scholar]
  12. Kellenberger E., Ryter A., Seachaud J. 1958; Electron microscope study of DNA-containing plasma. II. Vegetative and mature phage DNA as compared with normal bacterial nucleosides in different physiological states. J. Biophys. Biochem. Cytol 4:72–678
    [Google Scholar]
  13. Kroll R. G. 1990 Alkaliphiles. 55–92 Edwards C.ed Microbiology of extreme environments McGraw-Hill; New York:
    [Google Scholar]
  14. Li Y., Engle M., Weiss N., Mandelco L., Wiegel J. 1994; Clostridium thermoalcaliphilum sp. nov., an anaerobic thermotolerant facultative alkaliphile. Int. J. Syst. Bacteriol 43:111–118
    [Google Scholar]
  15. Li Y., Mandelco L., Wiegel J. 1993; Isolation and characterization of a moderately thermophilic alkaliphile, Clostridium paradoxum sp. nov. Int. J. Syst. Bacteriol 43:450–460
    [Google Scholar]
  16. Lotz W., Mayer F. 1979; Isolation and characterization of a bacteriophage tail-like bacteriocin from a strain of Rhizobium. J. Virol 9:160–173
    [Google Scholar]
  17. Lowe S. E., Jain M. K., Zeikus J. G. 1993; Biology, ecology, and biotechnological applications of anaerobic bacteria adapted to environmental stresses in temperature, pH, salinity, or substrates. Microbiol. Rev 57:451–509
    [Google Scholar]
  18. Maidak B. L., Larsen N., McCaughey M. J., Overbeek R., Olsen G. J., Fogel K., Blandy J., Woese C. R. 1994; The Ribosomal Database Project. Nucleic Acids Res 22:3485–3487
    [Google Scholar]
  19. Mesbah M., Premachandran U., Whitman W. B. 1989; Precise measurement of the G+C content of deoxyribonucleic acid by high-performance liquid chromatography. Int. J. Syst. Bacteriol 39:159–167
    [Google Scholar]
  20. Nielsen P., Fritze D., Priest F. G. 1995; Phenetic diversity of alkaliphilic Bacillus strains: proposal for nine new species. Microbiology 141:1745–1761
    [Google Scholar]
  21. Nielsen P., Rainey F. A., Outtrup H., Priest F. G., Fritze D. 1994; Comparative 16S rDNA sequence analysis of some alkaliphilic bacilli and the establishment of a sixth rRNA group within the genus Bacillus. FEMS Microbiol. Lett 117:61–65
    [Google Scholar]
  22. Patel B. K. C., Monk C., Littleworth H., Morgan H. W., Daniel R. M. 1987; Clostridium fervidus sp. nov., a new chemoorganotrophic acetogenic thermophile. Int. J. Syst. Bacteriol 37:123–126
    [Google Scholar]
  23. Rainey F. A., Dorsch M., Morgan H. W., Stackebrandt E. 1992; 16S rDNA analysis of Spirochaeta thermophila. its phylogenetic position and implications for the systematics of the order Spirochaetales. Syst. Appl. Microbiol 15:197–202
    [Google Scholar]
  24. Rainey F. A., Ward N. L., Morgan H. W., Toalster R., Stackebrandt E. 1993; Phylogenetic analysis of anaerobic thermophilic bacteria: aid for their reclassification. J. Bacteriol 175:4772–4779
    [Google Scholar]
  25. Saitou N., Nei M. 1987; The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol. Biol. Evol 4:406–425
    [Google Scholar]
  26. Spurr A. R. 1969; A low-viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastruct. Res 25:31–43
    [Google Scholar]
  27. Valentine R. C., Shapiro B. M., Stadman E. R. 1968; Regulation of glutamine synthetase. XII. Electron microscopy of the enzyme from E. coli. Biochemistry 7:2143–2152
    [Google Scholar]
  28. Walther-Mauruschat A., Aragno M., Mayer F., Schlegel H. G. 1977; Micromorphology of Gram-negative hydrogen bacteria. II. Cell envelope, membranes, and cytoplasmic inclusions. Arch. Microbiol 114:101–110
    [Google Scholar]
  29. Walther-Mauruschat A., Mayer F. 1978; Isolation and characterization of polysheaths, phage tail-like defective bacteriophages of Alcaligenes eutrophus H16. J. Gen. Virol 41:239–254
    [Google Scholar]
  30. Whitman W. B., Shieh J., Sohn S., Caras D. S., Premachandran U. 1986; Isolation and characterization of 22 mesophilic methanococci. Syst. Appl. Microbiol 7:235–240
    [Google Scholar]
  31. Wiegel J. 1992 The anaerobic thermophilic bacteria. 105–184 Christjansson J. K.ed Thermophilic bacteria CRC Press; Boca Raton, Fla:
    [Google Scholar]
  32. Wiegel J., Ljundahl L. G., Rawson J. R. 1979; Isolation from soil and properties of the extreme thermophile Clostridium thermohydrosulfuricum. J. Bacteriol 139:800–810
    [Google Scholar]
  33. Wiegel J., Quandt L. 1982; Determination of the Gram type using the reaction between polymyxin B and lipopolysaccharides of the outer cell wall of whole bacteria. J. Gen. Microbiol 128:2261–2270
    [Google Scholar]
  34. Zhilina T. N., Zavarzin G. A. 1994; Alkaliphilic anaerobic community at pH 10. Curr. Microbiol 29:109–112
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/ijsem/10.1099/00207713-46-4-1025
Loading
/content/journal/ijsem/10.1099/00207713-46-4-1025
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