Thermophile

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, though they can be bacteria or fungi. Thermophilic eubacteria are suggested to have been among the earliest bacteria.[3]

Thermophiles produce some of the bright colors of Grand Prismatic Spring, Yellowstone National Park

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.

Thermophiles can survive at high temperatures, whereas other bacteria or archaea would be damaged and sometimes killed if exposed to the same temperatures.

The enzymes in thermophiles function at high temperatures. Some of these enzymes are used in molecular biology, for example the Taq polymerase used in PCR. "Thermophile" is derived from the Greek: θερμότητα (thermotita), meaning heat, and Greek: φίλια (philia), love.

Classification

Thermophiles can be classified in various ways. One classification sorts these organisms according to their optimal growth temperatures:[4]

  1. Simple thermophiles: 50–64 °C (122-147.2 °F)
  2. Extreme thermophiles 65–79 °C (149-174.2 °F)
  3. Hyperthermophiles 80 °C and beyond, but not < 50 °C. (176+ °F)

In a related classification, thermophiles are sorted as follows:

  1. Facultative thermophiles (also called moderate thermophiles) can thrive at high temperatures, but also at lower temperatures (below 50 °C (122 °F)), whereas
  2. Obligate thermophiles (also called extreme thermophiles) require such high temperatures for growth.
  3. Hyperthermophiles are particularly extreme thermophiles for which the optimal temperatures are above 80 °C (176 °F).
A colony of thermophiles in the outflow of Mickey Hot Springs, Oregon, the water temperature is approximately 60 °C (140 °F).

Many of the hyperthermophilic Archaea require elemental sulfur for growth. Some are anaerobes that use the sulfur instead of oxygen as an electron acceptor during cellular respiration (anaerobic). Some are lithotrophs that oxidize sulphur to create 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. These organisms are often 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 signature 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]

Fungal thermophiles

Fungi are the only group of organisms in the Eukarya kingdom that can survive at temperature ranges of 50–60 °C.[6] Thermophilic fungi have been reported from a number of habitats, with most of them belonging to the fungal order Sordariales.[7] Thermophilic fungi have great biotechnological potential due to their ability to produce industrial-relevant thermostable enzymes, in particular for the degradation of plant biomass.[8]

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.[9][10] In S. acidocaldarius, UV-induced cellular aggregation mediates chromosomal marker exchange with high frequency.[10] Recombination rates exceed those of uninduced cultures by up to three orders of magnitude. Frols et al.[9][11] and Ajon et al.[10](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.,[12] 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

References
  1. Madigan MT; Martino JM (2006). Brock Biology of Microorganisms (11th ed.). Pearson. p. 136. ISBN 0-13-196893-9.
  2. Takai T; et al. (2008). "Cell proliferation at 122°C and isotopically heavy CH4 production by a hyperthermophilic methanogen under high-pressure cultivation". PNAS. 105 (31): 10949–51. Bibcode:2008PNAS..10510949T. doi:10.1073/pnas.0712334105. PMC 2490668. PMID 18664583.
  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.
  4. Stetter, K. (2006). "History of discovery of the first hyperthermophiles". Extremophiles. 10 (5): 357–362. doi:10.1007/s00792-006-0012-7. PMID 16941067. S2CID 36345694.
  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.
  6. Rajasekaran, A. K.; Maheshwari, R. (1993-09-01). "Thermophilic fungi: An assessment of their potential for growth in soil". Journal of Biosciences. 18 (3): 345–354. doi:10.1007/BF02702992. ISSN 0973-7138.
  7. Patel, Hardi; Rawat, Seema (2021), "Thermophilic fungi: Diversity, physiology, genetics, and applications", New and Future Developments in Microbial Biotechnology and Bioengineering, Elsevier, pp. 69–93, retrieved 2022-06-02
  8. van den Brink, Joost; Facun, Kryss; de Vries, Michel; Stielow, J. Benjamin (December 2015). "Thermophilic growth and enzymatic thermostability are polyphyletic traits within Chaetomiaceae". Fungal Biology. 119 (12): 1255–1266. doi:10.1016/j.funbio.2015.09.011. ISSN 1878-6146.
  9. 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" (PDF). Mol. Microbiol. 70 (4): 938–52. doi:10.1111/j.1365-2958.2008.06459.x. PMID 18990182.
  10. 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" (PDF). Mol. Microbiol. 82 (4): 807–17. doi:10.1111/j.1365-2958.2011.07861.x. PMID 21999488.
  11. 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.
  12. 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. S2CID 5572901.
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