From Infogalactic: the planetary knowledge core
(Redirected from Thermophilous)
Jump to: navigation, search
Thermophiles produce some of the bright colors of Grand Prismatic Spring, Yellowstone National Park

A thermophile is an organism — a type of extremophile — that thrives at relatively high temperatures, between 41 and 122 °C (106 and 252 °F).[1][2] Many thermophiles are archaea. Thermophilic eubacteria are suggested to have been among the earliest bacteria.[3]

Thermophiles are found in various geothermally heated regions of the Earth, such as hot springs like those in Yellowstone National Park (see image) and deep sea hydrothermal vents, as well as decaying plant matter, such as peat bogs and compost.

Unlike other types of bacteria, thermophiles can survive at much hotter temperatures, whereas other bacteria would be damaged and sometimes killed if exposed to the same temperatures.

Professor Zachary Studniberg, from Cambridge University, wrote in his book 'The Function of Extremophiles' that they are the most unique organism on the planet in terms of their contribution to modern life.

As a prerequisite for their survival, thermophiles contain enzymes that can function at high temperatures. Some of these enzymes are used in molecular biology (for example, heat-stable DNA polymerases for PCR), and in washing agents.

"Thermophile" is derived from the Greek: θερμότητα (thermotita), meaning heat, and Greek: φίλια (philia), love.


Thermophiles are classified into obligate and facultative thermophiles: Obligate thermophiles (also called extreme thermophiles) require such high temperatures for growth, whereas facultative thermophiles (also called moderate thermophiles) can thrive at high temperatures, but also at lower temperatures (below 50 °C (122 °F)). Hyperthermophiles are particularly extreme thermophiles for which the optimal temperatures are above 80 °C (176 °F).

Bacteria within the Alicyclobacillus genus are acidophilic thermophiles, which can cause contamination in fruit juice drinks.[4]

A colony of thermophiles in the outflow of Mickey Hot Springs, Oregon, the water temperature is approximately 60 °C (140 °F).

Thermophiles, meaning heat-loving, are organisms with an optimum growth temperature of 50 °C (122 °F) or more, a maximum of up to 70 °C (158 °F) or more, and a minimum of about 40 °C (104 °F), but these are only approximate. Some extreme thermophiles (hyperthermophiles) require a very high temperature (80 to 105 °C (176 to 221 °F)) for growth. Their membranes and proteins are unusually stable at these extremely high temperatures. Thus, many important biotechnological processes use thermophilic enzymes because of their ability to withstand intense heat.

Many of the hyperthermophiles Archea require elemental sulfur for growth. Some are anaerobes that use the sulfur instead of oxygen as an electron acceptor during cellular respiration. Some are lithotrophs that oxidize sulfur to sulfuric acid as an energy source, thus requiring the microorganism to be adapted to very low pH (i.e., it is an acidophile as well as thermophile). These organisms are inhabitants of hot, sulfur-rich environments usually associated with volcanism, such as hot springs, geysers, and fumaroles. In these places, especially in Yellowstone National Park, zonation of microorganisms according to their temperature optima occurs. Often, these organisms are colored, due to the presence of photosynthetic pigments.

Thermophile versus mesophile

Thermophiles can be discriminated from mesophiles from genomic features. For example, the GC content levels in the coding regions of some signatures genes were consistently identified as correlated with the temperature range condition when the association analysis was applied to mesophilic and thermophilic organisms regardless of their phylogeny, oxygen requirement, salinity, or habitat conditions.[5]

Gene transfer and genetic exchange

Sulfolobus solfataricus and Sulfolobus acidocaldarius are hyperthermophilic archaea. When these organisms are exposed to the DNA damaging agents UV irradiation, bleomycin or mitomycin C, species-specific cellular aggregation is induced.[6][7] In S. acidocaldarius, UV-induced cellular aggregation mediates chromosomal marker exchange with high frequency.[7] Recombination rates exceed those of uninduced cultures by up to three orders of magnitude. Frols et al.[6][8] and Ajon et al.[7](2011) hypothesized that cellular aggregation enhances species-specific DNA transfer between Sulfolobus cells in order to provide increased repair of damaged DNA by means of homologous recombination. Van Wolferen et al.,[9] in discussing DNA exchange in the hyperthermophiles under extreme conditions, noted that DNA exchange likely plays a role in repair of DNA via homologous recombination. They suggested that this process is crucial under DNA damaging conditions such as high temperature. Also it has been suggested that DNA transfer in Sulfolobus may be a primitive form of sexual interaction similar to the more well-studied bacterial transformation systems that are associated with species-specific DNA transfer between cells leading to homologous recombinational repair of DNA damage [see Transformation (genetics)].

See also


  1. Madigan MT; Martino JM (2006). Brock Biology of Microorganisms (11th ed.). Pearson. p. 136. ISBN 0-13-196893-9.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  2. Takai T; et al. (2008). "Cell proliferation at 122°C and isotopically heavy CH4 production by a hyperthermophilic methanogen under high-pressure cultivation" (PDF). PNAS. 105 (31): 10949–51. Bibcode:2008PNAS..10510949T. doi:10.1073/pnas.0712334105. PMC 2490668. PMID 18664583.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  3. Horiike T; Miyata D; Hamada K; et al. (January 2009). "Phylogenetic construction of 17 bacterial phyla by new method and carefully selected orthologs". Gene. 429 (1–2): 59–64. doi:10.1016/j.gene.2008.10.006. PMC 2648810. PMID 19000750.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  4. G. L. Pettipher, M. E. Osmundson, J. M. Murphy. Methods for the detection and enumeration of Alicyclobacillus acidoterrestris and investigation of growth and production of taint in fruit juice and fruit juice-containing drinks. Letters in Applied Microbiology. Volume 24, Issue 3, pages 185–189, March 1997.
  5. Zheng H; Wu H (December 2010). "Gene-centric association analysis for the correlation between the guanine-cytosine content levels and temperature range conditions of prokaryotic species". BMC Bioinformatics. 11: S7. doi:10.1186/1471-2105-11-S11-S7. PMC 3024870. PMID 21172057.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  6. 6.0 6.1 >Fröls S; Ajon M; Wagner M; Teichmann D; Zolghadr B; Folea M; et al. (November 2008). "UV-inducible cellular aggregation of the hyperthermophilic archaeon Sulfolobus solfataricus is mediated by pili formation". Mol. Microbiol. 70 (4): 938–52. doi:10.1111/j.1365-2958.2008.06459.x. PMID 18990182.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  7. 7.0 7.1 7.2 Ajon M; Fröls S; van Wolferen M; Stoecker K; Teichmann D; Driessen AJ; et al. (November 2011). "UV-inducible DNA exchange in hyperthermophilic archaea mediated by type IV pili". Mol. Microbiol. 82 (4): 807–17. doi:10.1111/j.1365-2958.2011.07861.x. PMID 21999488.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  8. Fröls S; White MF; Schleper C (February 2009). "Reactions to UV damage in the model archaeon Sulfolobus solfataricus". Biochem. Soc. Trans. 37 (Pt 1): 36–41. doi:10.1042/BST0370036. PMID 19143598.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  9. van Wolferen M; Ajon M; Driessen AJ; Albers SV (July 2013). "How hyperthermophiles adapt to change their lives: DNA exchange in extreme conditions". Extremophiles. 17 (4): 545–63. doi:10.1007/s00792-013-0552-6. PMID 23712907.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>

External links