At high temperatures, chlorophyll is degraded and therefore photosynthetic organisms cannot exist (Rothschild & Mancinelli 2001). Consequently, another problem facing thermophiles is finding an alternative source of nutrition. For example, Pyrolobus fumarii is a microbe that grows on the walls of deep-sea hydrothermal vents and can propagate in temperatures up to 113°C (Blöchl et al 1997). (P.fumarii was previously the most extreme thermophile known until the discovery of ‘Strain 121’(Kashefi & Lovley 2003), which increased the upper temperature limit for life to 121°C). P.fumarii is a chemoautotroph and synthesises its own food from surrounding chemicals, such as hydrogen.
The existence of thermophiles has significant implications for the possibility of life elsewhere in the solar system. It expands the prospect that life can exist in extremely hot extraterrestrial environments, such as those predicted on Jupiter’s moon, Io. This satellite is heated by tidal activities from Jupiter and possesses numerous active volcanoes on its surface (Lopes et al 2004). Also, findings of chemoautotrophs have dashed the ideas that energy from the Sun is a requirement for life. It is now known that communities, such as those found at deep-sea hydrothermal vents, can thrive by exclusively using inorganic compounds as energy sources (Lutz & Kennish 1993). This opens the mind to the possibility that life may exist in the sub-surface of planets elsewhere in the solar system (Schulze-Makuch & Irwin 2001, Pirajno & Van Kranendonk 2005).
Psychrophiles are organisms that exist in extreme cold environments. These extremophiles have an optimal growth at approximately 15°C or lower (Morita 1975). Such temperatures are detrimental to most organisms because membranes lose integrity and enzyme activity decreases (Somero 1995). Furthermore, the formation of ice crystals can cause severe structural cell damage. However, research over the past 25 years has shown that psychrophiles are well-adapted to their cool environments.
Psychrophile membranes are made largely from unsaturated lipids which enhance membrane fluidity at low temperatures (Russell 1997). Also, they have enzymes adapted to operate at near freezing temperatures (Gerday et al 2000). For example Polaromonas vacuolata, found in Antarctic sea ice, optimally multiplies at temperatures of 4°C (Irgens et al 1996). However, above 12°C it will cease to reproduce because its enzymes have adapted to function over a lower temperature range. To prevent ice crystal damage, some psychrophiles produce cyroprotectants (such as glycerol), which effectively lower a cell’s freezing point, allowing it to maintain flexibility in low temperatures (Krembs et al 2002).
Contrary to thermophiles, photosynthetic psychrophiles, such as Chlamydomonas nivalis (also known as ‘red snow’ due to the colouration it creates), are able to photosynthesise at near to freezing temperatures (Williams et al 2003). This provides extremophile communities with a possible energy source in extremely cold environments.
Recently there have been discoveries of lakes (kept liquid by pressure) under the ice sheet of Antartica, and it is speculated that extremophiles may exist in these hidden waters (Gavaghan 2002). This would have significant implications for extraterrestrial life since conditions predicted for these lakes may be similar to those believed to be present underneath the ice crust of Europa, another of Jupiter’s moons (Kargel et al 2000). Using these Earth lakes, life detection techniques could be refined before venturing into the solar system, hence increasing the success of extraterrestrial life searches.
Halophiles are extremophiles that thrive in salty environments, such as salt lakes, salterns and the Dead Sea. At these locations organisms become very dehydrated as they lose water through their cell walls by osmosis (Rothschild & Mancinelli 2001). However, research over the past 25 years has revealed how halophiles avoid this fate. Halophilic algae, such as Dunaliella salina, and bacteria balance the external osmotic pressure by producing compatible solutes such as glycerol (Galinski 1993). Halobacterium (Archaea) achieve the same effect using a molecular pump to exclude sodium ions from the cell, whilst accumulating potassium ions within the cell (Speelmans et al 1995).
Discoveries of halophiles are important in the search for life elsewhere, particularly concerning the Meridiani Planum plains of Mars. After discoveries of evaporates containing high sodium chloride concentrations, these plains are a hypothesised previous salt lake, perhaps once home to halophiles (Litchfield 1998).
Piezophiles are organisms that thrive under great pressure. Pressure is problematic to life as it compresses biomolecules to fatal levels (Mozhaev et al 1996). However, research over the last 25 years has discovered that piezophiles are adapted to tolerate these effects. For example, piezophile membranes are largely made from unsaturated lipids which help circumvent problems caused by high pressure (Yano et al 1998). Also a study by Sharma et al (2002) showed that even bacteria not adapted to high-pressure, such as Escherichia coli, can tolerate pressures equivalent to those experienced at 160km under water.
Piezophiles (and pressure tolerant bacteria) are important in the search for extraterrestrial life as it allows for the possibility of organisms thriving in high-pressure conditions elsewhere in the solar system such as the sub-surface of planets. Therefore, although space missions have detected no life on the surface of planets (Klein 1999), there is a possibility for the existence of sub-surface organisms.
To conclude, until relatively recently there has been limited knowledge regarding Earth’s extreme environments. As our exploration continues we realise our view as to what forms of life might take is constrained. Nevertheless, before venturing out into the unknown to discover extraterrestrial life, it would perhaps be wise to continue studying these exotic areas closer to home. Extremophiles provide us with a template for life on other planets, and encourage us to broaden our perspective of where life may exist. With an expanded idea of the necessities for life, coupled with further study of extremophiles, improvements in exploration and analytical technology can be made; effectively arming ourselves with the tools required for a successful extraterrestrial life search. By opening our minds to novel possibilities and refining our expertise, we may soon find life elsewhere in the solar system, as predicted long ago by our ancient predecessors.
References:
Adams, M.W.W., Perler, F.B. & Kelly, R.M. (1995) Extremozymes: Expanding the Limits of Biocatalysis. Nature Biotechnology, 13, 662 – 668.
Anderson, A.W., Nordon, H.C., Cain, R.F., Parrish, G. & Duggan, D. (1956) Studies on a radio-resistant micrococcus. I. Isolation, morphology, cultural characteristics, and resistance to gamma radiation. Food Technology, 10, 575-578.
Blöchl, E., Rachel, R., Burggraf, S., Hafenbradl, D., Jannasch, H.W. & Stetter, K.O. (1997) Pyrolobus fumarii , gen. and sp. nov., represents a novel group of archaea, extending the upper temperature limit for life to 113°C. Extremophiles, 1, 14-21.
Brake, M. (2006) On the plurality of inhabited worlds: a brief history of extraterrestrialism. International Journal of Astrobiology, 5, 99-107.
Brock, T.D. & Freeze, H. (1969) Thermus aquaticus, gen. and sp. nov., a Nonsporulating Extreme Thermophile. Journal of Bacteriology, 98, 289–297.
Brock, T.D. (1986) General, Molecular and Applied Microbiology. Wiley, New York.
Galinski, E. A. 1993. Compatible solutes of halophilic eubacteria: molecular principles, water-solute interactions, stress protection. Experientia 49: 487-496..
Gavaghan, H. (2002) Life in the Deep Freeze. Nature, 415, 828-830.
Gerday, C., Aittaleb, M., Bentahir, M., Chessa, J.P., Claverie, P., Collins, T., D’Amico, S., Dumont, J., Garsoux, G., Georlette, D., Hoyoux, A., Lonhienne, T., Meuwis, M.A. & Feller, G. (2000). Cold-adapted enzymes: from fundamentals to biotechnology. Trends in Biotechnology, 18, 103-107.
Forterre, P., Confalonieri, F., Charbonnier, F. & Duguet, M. (1995). Speculations on the origin of life and thermophily - review of available information on reverse gyrase suggests that hyperthermophilic prokaryotes are not so primitive. Origins of Life and Evolution of the Biosphere 25, 235-249.
Irgens, R.L., Gosink, J.J. & Staley, J.T. (1996) Polaromonas vacuolata gen. nov., sp. nov., a Psychrophilic, Marine, Gas Vacuolate Bacterium from Antarctica. International Journal of Systematic Bacteriology, 46, 822-826.
Kargel, J.S., Kaye, J.Z., Head, J.W., Marion, G.M., Sassen, R., Crowley, J.K., Ballesteros, O.P., Grant, S.A. & Hogenboom, D.L. (2000) Europa's Crust and Ocean: Origin, Composition, and the Prospects for Life. Icarus, 148, 226 -265.
Kashefi, K. & Lovley, D.R. (2003) Extending the Upper Temperature Limit for Life. Science, 301, 934.
Klein, H.P. (1999) Did Viking Discover Life on Mars? , 29, 625-631.
Krembs, C., Eicken, H., Junge, K., and Deming, J.W. (2002) High concentrations of exopolymeric substances in Arctic winter sea ice: implications for the polar ocean carbon cycle and cryoprotection of diatoms. Deep Sea Research, 49, 2163–2181.
Litchfield, C. D. (1998) Surrvival Strategies for Microorganisms: Hypersaline Environments and Their Relevance to Life on Early Mars. Meteoritics and Planetary Science, 33, 813-819.
Lopes, R.M.C, Kamp, L.W., Smythe, W.D., Mouginis-Mark, P., Kargel, J., Radebaugh, J., Turtle, E.P., Perry, J., Williams, D.A., Carlson, R.W., Douté, S. & the Galileo NIMS and SSI Teams (2004) Lava Lakes on Io: Observations of Io's Volcanic Activity from Galileo NIMS During the 2001 Fly-bys. Icarus, 169, 140–174.
Lutz R.A. & M.J. Kennish. (1993) Ecology of Deep-Sea Hydrothermal Vent Communities: a Review. Reviews of Geophysics, 31, 241-242.
Macelroy, R.D. (1974) Some comments on the evolution of extremophiles. Biosystems, 6, 74–75.
Marguet, E. & Forterre, P. (1998) Protection of DNA by salts against thermodegradation at temperatures typical for hyperthermophiles. Extremophiles, 2, 115–122.
McElhaney, R.N. (1976) The biological significance of alterations in the fatty acid composition of microbial membrane lipids in response to changes in environmental temperature. In Extreme Environments: Mechanisms of Microbial Adaptation, Academic Press, New York, 255-281.
Morita, RY. (1975) Psychrophilic bacteria. Bacteriological Review, 39, 144-167.
Mozhaev, V.V., Heremans, H., Frank, J., Masson, P., Balny, C. (1996) High pressure effects on protein structure and function. Proteins Structure Function and Genetics, 24, 81-91.
Papagiannis, M.D. (1984) A historical introduction to the search for extraterrestrial life - The search for extraterrestrial life: Recent developments. Proceedings of the Symposium, June, 18-21.
Pirajno, F. & Van Kranendonk, M.J. (2005) Review of hydrothermal processes and systems on Earth and implications for Martian analogues. Australian Journal of Earth Sciences, 52, 329-351.
Rieseberg, L.H., Raymond, O., Rosenthal, D.M., Lai, Z., Livingstone, K., Nakazato, T., Durphy, J.L., Schwarzbach, A.E., Donovan, L.A. & Lexer, C. (2003) Major ecological transitions in wild sunflowers facilitated by hybridization. Science, 301, 1211-1216.
Rothschild, L.J. & Mancinelli, R.L. (2001) Life in extreme environments. Nature, 409, 1092-1101.
Russell, N.J. (1997) Psychrophilic bacteria—Molecular adaptations of membrane lipids. Comparative biochemistry and physiology A, 118, 489-493.
Saiki, R.K., Gelfand, D.H., Stoffel, S., Scharf, S.J., Higuchi, R., Horn, G.T., Mullis, K.B., Erlich, H.A. (1988) . , 239, 487–91.
Satyanarayana1,T., Raghukumar, C. & Shivaji, S. (2005) Extremophilic microbes: Diversity and perspectives. Current science, 89, 78-90.
Schulze-Makuch, D. & Irwin, L.N. (2001) Alternative Energy Sources Could Support Life on Europa. Transactions American Geophysical Union, 82, 150-153.
Sharma, A., Scott, J.H., Cody, G.D., Fogel, M.L., Hazen, R.M., Hemley, R.J. & Huntress, W.T. (2002) Microbial Activity at Gigapascal Pressures. Science, 295, 1514-1516.
Somero, G.N. (1995) Proteins and temperature. Annual Review of Physiology, 57, 43-68.
Speelmans, G., Poolman, B. & Konings, W.N. (1995) Na+ as coupling ion in energy transduction in extremophilic Bacteria and Archaea. World Journal of Microbiology and Biotechnology, 11, 58-70.
Williams, W.E., Gorton, H.L. & Vogelmann, T.C. (). . , 100, 562–566.
Yano, Y., Nakayama, A., Ishihara, K. & Saito, H. (1998) Adaptive Changes in Membrane Lipids of Barophilic Bacteria in Response to Changes in Growth Pressure. Applied and Environmental Microbiology, 64, 479-485.