Extreme Thermophiles

Extreme thermophiles are those microorganisms whose optimal growth temperature is between 65 and 85°C.

Keywords: thermophilic environments; biodiversity; thermostable enzymes; thermophiles

Figure 1. The universally phylogenetic tree with the extreme thermophilic and hyperthermophilic lineages in bold. Examples are: 1, Thermoanaerobacter spp.; 2, Thermotoga spp.; 3, Desulfurococcus spp.; 4, Sulfolobus spp.; 5, Thermophilum spp.; 6, Thermoproteus spp.; 7, Aquifex spp.; 8, Methanopyrus spp.; 9, Methanococcus jannaschii; 10, Thermococcus spp.
Figure 2. The universal phylogenetic tree and the position of some representative extreme thermophiles.
Figure 3. Dictyoglomus thermophilium strain Rt8N2 (Patel et al., 1987, isolated from a hot spring in New Zealand (light microscopy, phase contrast; bar, 10 m). (a)–(e) Aggregation and lysis of cells during growth cycle. (a) Single cells at the early exponential growth phase. (b) Beginning of cell aggregation. (c) Coiling of cells forming a shape of a bowl. Notice that at this stage no common membrane is visible. (d) Sphere with cells arranged around the periphery. Note the visible common membrane/envelope around the cells at this stage. (e) At the stationary growth phase there is a loss of distinct cell appearance, which makes the common membrane/envelope clearly visible. Unpublished results of H. Morgan and J. Wiegel. Reproduced courtesy of H. Morgan and J. Wiegel.
Figure 4. Thermosipho, an anaerobic extreme thermophile, a bacterium that exhibits one of the highest growth temperatures among the bacteria and the special morphological feature of a toga (electron microscope preparation shadowed with platinum). Several cells (the cell bodies are marked by arrows) are enclosed in one long sheath, the toga, surrounding the cells. The toga (marked by arrowheads) becomes visible between the cells. Bar, 5 m. Reproduced courtesy of Drs Reinhard Rachel and Karl O. Stetter, University of Regensburg.
Figure 5. Thermotoga maritima, an anaerobic extreme thermophile. The electron micrograph depicts a cell shadowed with platinum. The cell is under division and therefore possess (already) two flagella. The elongated cell body is marked by an arrow; the toga surrounding the cell at both ends (or cell poles?) is marked by arrowheads. Bar, 1 m. Reproduced courtesy of Drs Reinhard Rachel and Karl O. Stetter, University of Regensburg.
Figure 6. Thermotoga maritima. Electron micrograph of an ultrathin section of a cell: the cell body is densely stained (marked by a white arrow) and intimately surrounded by a cytoplasmic membrane, which is not visible as a layered structure in this section. The cell body is loosely surrounded by the ‘toga’, which in fact is an outer membrane (marked by arrowheads). Bar, 0.5 m. Reproduced courtesy of Drs Reinhard Rachel and Karl O. Stetter, University of Regensburg.
Figure 7. Thermoanaerobacter ethanolicus. (a)–(c) Light microscopic and electron microscopic observations of strain JW 200. (a) Normal size (arrow) and longer filamentous cells that may divide to give long chains of bacteria (arrow heads; light microscopy). (b) Coccoid cell (scanning electron micrograph). The cells contain DNA and thus are not equivalent to the E. coli minicells. (c) Uneven length of dividing cells (electron micrograph); notice the incomplete cross wall formation (arrow). (d) and (e) Protuberances or autoplast type of cells (light microscopy, Normaski technique). (f) Single cell with flagella. The insert on the right shows the hexagonal pattern of the outer cell wall layer (‘S-layer’) and the insertion point of the flagellum; the insert on the left shows pili (arrows) and flagella. Bars, 0.1 m. (g) Ultrathin section showing cell envelope layers (electron micrograph). (h) Higher magnification electron micrograph of the cell envelope layers: CM, cytoplasmic membrane: D, dense layer; O, outer cell wall layer. Bar, 25 nm. (i) Electron micrograph of a cell wall from a lysed cell showing three layers: outer cell wall layer (O), dense layer (D) and an inner cell wall layer (I). Bar, 25 nm. Reproduced with permission from Wiegel and Ljungdahl 1981. Copyright © 1981 Springer-Verlag.
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 References
    Berquist PL, Gibbs MD, Morris DD et al. (1999) Molecular diversity of thermophylic cellulolytic and hemicellulolytic bacteria. FEMS Microbiology Ecology 28: 99–110.
    Blochl E, Rachel R, Burggraf S et al. (1997) Pyrolobus fumarii, gen. nov., sp. nov., represents a novel group of archaea, extending the upper temperature limit for life to 113 degrees C. Extremophiles 1: 14–21.
    Brechtel E, Matuschek M, Hellberg A et al. (1999) Cell wall of Thermoanaerobacterium thermosulfurigenes EM1: isolation of its components and attachment of the xylanase XynA. Archives of Microbiology 171: 159–165.
    book Brock TD (ed.) (1986) Thermophiles: General, Molecular and Applied Microbiology. New York: John Wiley & Sons.
    book Canganella F and Wiegel J (1993) "The potential of thermophilic Clostridia in biotechnology". In: Woods DR (ed.) The Clostridia and Biotechnology, pp. 393–429. Boston: Butterworth.
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    Driessen AJM, van de Vossenberg JLCM, Konings WN (1996) Membrane composition and ion-permeability in extremophiles. FEMS Microbiology Reviews 18: 139–148.
    Engle M, Li Y, Rainey F et al. (1996) Thermobrachium celere, gen. nov., sp. nov., a fast growing thermophilic, alkalitolerant, and proteolytic obligate anaerobe. International Journal of Systematic Bacteriology 46: 1025–1033.
    Friedrich AB and Antranikian G (1996) Keratin degradation by Fervidobacterium pennavorans, a novel thermophilic anaerobic species of the order Thermotogales. Applied and Environmental Microbiology 62: 2875–2882.
    Hreggvidsson GO, Kaiste E, Holst O et al. (1996) An extremely thermostable cellulase from the thermophilic eubacterium Rhodothermus marinus. Applied and Environmental Microbiology 62: 3047–3049.
    book Huber R and Stetter KO (1992) "The Thermogales: Hyperthermophilic and extremely thermophilic bacteria". In: Kristjansson JK (ed.) Thermophilic Bacteria, pp. 185–194. Boca Raton, FL: CRC Press.
    book Kandler O (1998) "The early diversification of life and the origin of the three domains: a proposal". In: Wiegel J and Adams MWW (eds) Thermophiles, the Keys to Molecular Evolution and the Origin of Life? pp. 19–32. London: Taylor & Francis.
    Kozianowski G, Canganella F, Rainey FA, Hippe H and Antranikian G (1997) Purification and characterization of thermostable pectate-lyases from a newly isolated thermophilic bacterium, Thermoanaerobacter italicus sp. nov. Extremophiles 1: 171–182.
    Liu S-Y, Rainey FA, Morgan HW, Mayer F and Wiegel J (1996) Thermoanaerobacterium aotearoense, sp. nov., a slightly acidophilic, anaerobic thermophile isolated from various hot springs in New Zealand and emendation of the genus Thermoanaerobacterium. International Journal of Systematic Bacteriology 46: 388–396.
    Patel BK, Morgan HW, Wiegel J and Daniel RM (1987) Isolation of an extremely thermophilic chemoorganotrophic anaerobe similar to Dictyoglomus thermophilium from New Zealand hot springs. Archives of Microbiology 147: 21–24.
    Shoham Y, Lamed R and Bayer EA (1999) The cellulose concept as an efficient microbial strategy for the degradation of insoluble polysaccharides. Trends in Microbiology 7: 275–281.
    Spooner ETC (1992) Similarities between environmental requirements for the deepest known branches of the universal phylogenetic tree and early Archaean (~3.0–3.5 Ga) whole ocean conditions. Abstracts Annual Meeting of Geological Society of America 24: A137.
    Thoma R, Schwander M, Liebl W, Kirschner K and Sterner R (1998) A histidine gene cluster of the hyperthermophile Thermotoga maritima: sequence analysis and evolutionary significance. Extremophiles 2: 379–389.
    van de Vossenberg JLCM, Ubbink-Kok T, Elferink MGL, Driessen AJM and Konings WN (1995) Ion permeability of the cytoplasmic membrane limits the maximum growth temperature of bacteria and archaea. Molecular Microbiology 18: 925–932.
    book Wächtershäuser G (1998) "The case for a hyperthermophilic, chemolithoautotrophic origin of life in an iron–sulfur world". In: Wiegel J and Adams MWW (eds) Thermophiles, the Keys to Molecular Evolution and the Origin of Life? pp. 47–58. London: Taylor & Francis.
    Wiegel J (1981) Distinction between the Gram reaction and the Gram type of bacteria. International Journal of Systematic Bacteriology 31: 88.
    book Wiegel J (1992) "The anaerobic thermophilic bacteria". In: Kristjansson JK (ed.) Thermophilic Bacteria, pp. 105–184. Boca Raton, FL: CRC Press.
    Wiegel J (1998) Anaerobic alkali-thermophiles, a novel group of extremophiles. Extremophiles 2: 257–267.
    book Wiegel J and Adams WW (eds) (1998) Thermophiles, the Keys to Molecular Evolution and the Origin of Life? London: Taylor & Francis.
    Wiegel J and Ljungdahl LG (1981) Thermoanaerobacter ethanolicus gen. nov. spec. nov., a new, extreme thermophilic, anaerobic bacterium. Archives of Microbiology 128: 343–348.
    Woese CR, Kandler O and Wheelis ML (1990) Towards a natural system of organisms: proposal for the domain Archaea, Bacteria and Eukarya. Proceedings of the National Academy of Sciences of the USA 87: 4576–4590.
 Further Reading
    book Wiegel J (1998) "Lateral gene exchange, an evolutionary mechanism for extending the upper or lower temperature limits for growth of a microorganism? A hypothesis". In: Wiegel J and Adams WW (eds) Thermophiles, the Keys to Molecular Evolution and the Origin of Life? London: Taylor & Francis.
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Wiegel, Juergen, and Canganella, Francesco(Jan 2002) Extreme Thermophiles. In: eLS. John Wiley & Sons Ltd, Chichester. http://www.els.net [doi: 10.1038/npg.els.0000392]