Crenarchaeota

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Crenarchaeota
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Archaea Sulfolobus infected with specific virus STSV-1.
Scientific classification
Domain:
Kingdom:
Superphylum:
Phylum:
"Crenarchaeota"

Garrity & Holt 2002
Class
Synonyms
  • non "Crenarchaeota" Cavalier-Smith 2002
  • Eocyta
  • Eocytes
  • Thermoproteaeota Oren et al. 2015
  • "Thermoproteota" Whitman 2018

The Crenarchaeota (also known as Crenarchaea or eocytes) are archaea that have been classified as a phylum of the Archaea domain. [1] [2] [3] Initially, the Crenarchaeota were thought to be sulfur-dependent extremophiles but recent studies have identified characteristic Crenarchaeota environmental rRNA indicating the organisms may be the most abundant archaea in the marine environment. [4] Originally, they were separated from the other archaea based on rRNA sequences; other physiological features, such as lack of histones, have supported this division, although some crenarchaea were found to have histones. [5] Until recently all cultured Crenarchaea had been thermophilic or hyperthermophilic organisms, some of which have the ability to grow at up to 113 °C. [6] These organisms stain Gram negative and are morphologically diverse, having rod, cocci, filamentous and oddly-shaped cells. [7]

Contents

Sulfolobus

One of the best characterized members of the Crenarcheota is Sulfolobus solfataricus . This organism was originally isolated from geothermally heated sulfuric springs in Italy, and grows at 80 °C and pH of 2–4. [8] Since its initial characterization by Wolfram Zillig, a pioneer in thermophile and archaean research, similar species in the same genus have been found around the world. Unlike the vast majority of cultured thermophiles, Sulfolobus grows aerobically and chemoorganotrophically (gaining its energy from organic sources such as sugars). These factors allow a much easier growth under laboratory conditions than anaerobic organisms and have led to Sulfolobus becoming a model organism for the study of hyperthermophiles and a large group of diverse viruses that replicate within them.

Marine species

Beginning in 1992, data were published that reported sequences of genes belonging to the Crenarchaea in marine environments. [9] , [10] Since then, analysis of the abundant lipids from the membranes of Crenarchaea taken from the open ocean have been used to determine the concentration of these “low temperature Crenarchaea” (See TEX-86). Based on these measurements of their signature lipids, Crenarchaea are thought to be very abundant and one of the main contributors to the fixation of carbon .[ citation needed ] DNA sequences from Crenarchaea have also been found in soil and freshwater environments, suggesting that this phylum is ubiquitous to most environments. [11]

In 2005, evidence of the first cultured “low temperature Crenarchaea” was published. Named Nitrosopumilus maritimus , it is an ammonia-oxidizing organism isolated from a marine aquarium tank and grown at 28 °C. [12]

Eocyte hypothesis Eocyte hypothesis.png
Eocyte hypothesis

Eocyte hypothesis

The eocyte hypothesis proposed in the 1980s by James Lake suggests that eukaryotes emerged within the prokaryotic eocytes. [14]

One possible piece of evidence supporting a close relationship between Crenarchaea and eukaryotes is the presence of a homolog of the RNA polymerase subunit Rbp-8 in Crenarchea but not in Euryarchaea [15]

See also

Related Research Articles

Nanoarchaeota Phylum of archaea

Nanoarchaeota are a phylum of the Archaea. This phylum currently has only one representative, Nanoarchaeum equitans.

Korarchaeota Phylum of archaea

In taxonomy, the Korarchaeota are a phylum of the Archaea. The name is derived from the Greek noun koros or kore, meaning young man or young woman, and the Greek adjective archaios which means ancient. They are also known as Xenarchaeota.

The Thermoprotei is a class of the Crenarchaeota.

Mollicutes is a class of bacteria distinguished by the absence of a cell wall. The word "Mollicutes" is derived from the Latin mollis, and cutis. Individuals are very small, typically only 0.2–0.3 μm in size and have a very small genome size. They vary in form, although most have sterols that make the cell membrane somewhat more rigid. Many are able to move about through gliding, but members of the genus Spiroplasma are helical and move by twisting. The best-known genus in the Mollicutes is Mycoplasma.

In taxonomy, the Halobacteriaceae are a family of the Halobacteriales in the domain Archaea. Halobacteriaceae represent a large part of halophilic Archaea, along with members in two other methanogenic families, Methanosarcinaceae and Methanocalculaceae. The family consists of many diverse genera that can survive extreme environmental niches. Most commonly, Halobacteriaceae are found in hypersaline lakes and can even tolerate sites polluted by heavy metals. They include neutrophiles, acidophiles, alkaliphiles, and there have even been psychrotolerant species discovered. Some members have been known to live aerobically, as well as anaerobically, and they come in many different morphologies. These diverse morphologies include rods in genus Halobacterium, cocci in Halococcus, flattened discs or cups in Haloferax, and other shapes ranging from flattened triangles in Haloarcula to squares in Haloquadratum, and Natronorubrum. Most species of Halobacteriaceae are best known for their high salt tolerance and red-pink pigmented members, but there are also non-pigmented species and those that require moderate salt conditions. Some species of Halobacteriaceae have been shown to exhibit phosphorus solubilizing activities that contribute to phosphorus cycling in hypersaline environments. Techniques such as 16S rRNA analysis and DNA-DNA hybridization have been major contributors to taxonomic classification in Halobacteriaceae, partly due to the difficulty in culturing halophilic Archaea.

In taxonomy, the Thermoplasmata are a class of the Euryarchaeota.

In taxonomy, Thermoproteus is a genus of the Thermoproteaceae. These prokaryotes are thermophilic sulphur-dependent organisms related to the genera Sulfolobus, Pyrodictium and Desulfurococcus. They are hydrogen-sulphur autotrophs and can grow at temperatures of up to 95 °C.

Methanococcus is a genus of coccoid methanogens of the family Methanococcaceae. They are all mesophiles, except the thermophilic M. thermolithotrophicus and the hyperthermophilic M. jannaschii. The latter was discovered at the base of a “white smoker” chimney at 21°N on the East Pacific Rise and it was the first archaeal genome to be completely sequenced, revealing many novel and eukaryote-like elements.

Methanomicrobia Class of archaea

In the taxonomy of microorganisms, the Methanomicrobia are a class of the Euryarchaeota.

In the taxonomy of microorganisms, the Methanomicrobiales are an order of the Methanomicrobia. Methanomicrobiales are strictly carbon dioxide reducing methanogens, using hydrogen or formate as the reducing agent. As seen from the phylogenetic tree based on 'The All-Species Living Tree' Project the family Methanomicrobiaceae is highly polyphyletic within the Methanomicrobiales.

Sulfolobales Order of archaea

In taxonomy, the Sulfolobales are an order of the Thermoprotei.

Thermococcales Order of archaea

In taxonomy, the Thermococcales are an order of microbes within the Thermococci. The species within the Thermococcales are used in laboratories as model organisms. All these species are strict anaerobes and can ferment sugars as sources of carbon, but they also need elemental sulfur.

In taxonomy, the Thermoproteales are an order of the Thermoprotei. They are the only organisms known to lack the SSB proteins, instead possessing the protein ThermoDBP that has displaced them. The rRNA genes of these organisms contain multiple introns, which can be homing endonuclease encoding genes, and their presence can impact the binding of "universal" 16S rRNA primers often used in environmental sequencing surveys.

In taxonomy, the Methanocorpusculaceae are a family of microbes within the order Methanomicrobiales. It contains exactly one genus, Methanocorpusculum. The species within Methanocorpusculum were first isolated from anaerobic digesters and anaerobic wastewater treatment plants. In the wild, they prefer freshwater environments. Unlike many other methanogenic archaea, they do not require high temperatures or extreme salt concentrations to live and grow.

In taxonomy, the Methanomicrobiaceae are a family of the Methanomicrobiales.

Methanosarcinaceae Family of archaea

In taxonomy, the Methanosarcinaceae are a family of the Methanosarcinales.

Methanospirillaceae are a family of microbes within Methanomicrobiales.

Pseudomonas avellanae is a Gram-negative plant pathogenic bacterium. It is the causal agent of bacterial canker of hazelnut. Based on 16S rRNA analysis, P. avellanae has been placed in the P. syringae group. This species was once included as a pathovar of Pseudomonas syringae, but following DNA-DNA hybridization, it was instated as a separate species. Following ribotypical analysis Pseudomonas syringae pv. theae was incorporated into this species.

George E. Fox

George Edward Fox is an astrobiologist, a Professor Emeritus and researcher at the University of Houston. He is an elected fellow of the American Academy of Microbiology, the American Association for the Advancement of Science, American Institute for Medical and Biological Engineering and the International Astrobiology Society. Fox received his B.A. degree in 1967, and completed his Ph.D. degree in 1974; both in chemical engineering at Syracuse University.

In taxonomy, Methanocalculus is a genus of the Methanomicrobiales. It contains four species:

References

  1. See the NCBI webpage on Crenarchaeota
  2. C.Michael Hogan. 2010. Archaea. eds. E.Monosson & C.Cleveland, Encyclopedia of Earth. National Council for Science and the Environment, Washington DC.
  3. Data extracted from the "NCBI taxonomy resources". National Center for Biotechnology Information . Retrieved 2007-03-19.
  4. Madigan M; Martinko J, eds. (2005). Brock Biology of Microorganisms (11th ed.). Prentice Hall. ISBN   978-0-13-144329-7.
  5. Cubonova L, Sandman K, Hallam SJ, Delong EF, Reeve JN (2005). "Histones in Crenarchaea". Journal of Bacteriology. 187 (15): 5482–5485. doi:10.1128/JB.187.15.5482-5485.2005. PMC   1196040 . PMID   16030242.
  6. Blochl E, Rachel R, Burggraf S, Hafenbradl D, Jannasch HW, Stetter KO (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 (1): 14–21. doi:10.1007/s007920050010. PMID   9680332. S2CID   29789667.
  7. Garrity GM, Boone DR, eds. (2001). Bergey's Manual of Systematic Bacteriology Volume 1: The Archaea and the Deeply Branching and Phototrophic Bacteria (2nd ed.). Springer. ISBN   978-0-387-98771-2.
  8. Zillig W, Stetter KO, Wunderl S, Schulz W, Priess H, Scholz I (1980). "The Sulfolobus-"Caldariellard" group: Taxonomy on the basis of the structure of DNA-dependent RNA polymerases". Arch. Microbiol. 125 (3): 259–269. doi:10.1007/BF00446886. S2CID   5805400.
  9. Fuhrman JA, McCallum K, Davis AA (1992). "Novel major archaebacterial group from marine plankton". Nature. 356 (6365): 148–9. Bibcode:1992Natur.356..148F. doi:10.1038/356148a0. PMID   1545865. S2CID   4342208.
  10. DeLong EF (1992). "Archaea in coastal marine environments". Proc Natl Acad Sci USA. 89 (12): 5685–9. Bibcode:1992PNAS...89.5685D. doi:10.1073/pnas.89.12.5685. PMC   49357 . PMID   1608980.
  11. Barns SM, Delwiche CF, Palmer JD, Pace NR (1996). "Perspectives on archaeal diversity, thermophily and monophyly from environmental rRNA sequences". Proc Natl Acad Sci USA. 93 (17): 9188–93. Bibcode:1996PNAS...93.9188B. doi:10.1073/pnas.93.17.9188. PMC   38617 . PMID   8799176.
  12. Könneke M, Bernhard AE, de la Torre JR, Walker CB, Waterbury JB, Stahl DA (2005). "Isolation of an autotrophic ammonia-oxidizing marine archaeon". Nature. 437 (7058): 543–6. Bibcode:2005Natur.437..543K. doi:10.1038/nature03911. PMID   16177789. S2CID   4340386.
  13. Cox, C. J.; Foster, P. G.; Hirt, R. P.; Harris, S. R.; Embley, T. M. (2008). "The archaebacterial origin of eukaryotes". Proc Natl Acad Sci USA. 105 (51): 20356–61. Bibcode:2008PNAS..10520356C. doi:10.1073/pnas.0810647105. PMC   2629343 . PMID   19073919.
  14. (UCLA) The origin of the nucleus and the tree of life Archived 2003-02-07 at archive.today
  15. Kwapisz, M; Beckouët, F; Thuriaux, P (2008). "Early evolution of eukaryotic DNA-dependent RNA polymerases". Trends Genet. 24 (5): 211–5. doi:10.1016/j.tig.2008.02.002. PMID   18384908.

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