Korarchaeota | |
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Scanning electron micrograph of the Obsidian Pool enrichment culture, showing Korarchaeota. | |
Scientific classification | |
Domain: | |
Kingdom: | |
Superphylum: | |
Phylum: | "Korarchaeota" Barns et al. 1996 |
Class: | "Korarchaeia" Rinke et al. 2020 [1] |
Order: | "Korarchaeales" Petitjean et al. 2015 [2] |
Family: | "Korarchaeaceae" Rinke et al. 2020 |
Species | |
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Synonyms | |
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The Korarchaeota is a proposed phylum within the Archaea. [3] 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. [4] They are also known as Xenarchaeota. The name is equivalent to Candidatus Korarchaeota, and they go by the name Xenarchaeota or Xenarchaea as well. [5]
The Korarchaeota are a proposed phylum in the domain, Archaea. [6] They are thought to have diverged relatively early in the genesis of Archaea and are among the deep-branching lineages. [6] Korarchaeota are also known as Xenarchaeota. Korarchaeaota, along with Thaumarchaeota, Aigarchaeota, Crenarchaeota, belong to the superphylum called TACK. [7] The evolutionary link between Asgard archaea and Korarchaeota of TACK (Thaumarchaeota, Aigarchaeota, Crenarchaeota, Korarchaeota) is yet unknown. [7]
The first member of Korarchaeota to have its genome reconstructed was Korarchaeum crypotfilum, which was found in a hot spring in Yellowstone National Park and described in 2008. [8] Since then only a few Korarchaeal genomes have been described. [9] To check for Korarchaeota, samples from a variety of hot springs in Iceland and Kamchatka were gathered. According to the samples and analysis, the Icelandic samples contained about 87 distinct 16S ribosomal nucleic acid sequences, whereas the Kamchatkan samples contained about 33. [10]
Based on protein sequences and phylogenetic analysis of conserved single genes, the Korarchaeote was identified as a “deep archaeal lineage” with a possible relationship to the Crenarchaeota. [11] Furthermore, given the known genetic makeup of archaea, the Korarchaeota may have preserved a set of biological traits that correspond to the earliest known archaeal form. [11]
Analysis of their 16S rRNA gene sequences suggests that they are a deeply branching lineage that does not belong to the main archaeal groups, Thermoproteota and Euryarchaeota. [12] Analysis of the genome of one korarchaeote that was enriched from a mixed culture revealed a number of both Crenarchaeota- and Euryarchaeota-like features and supports the hypothesis of a deep-branching ancestry. [13]
The currently accepted taxonomy is based on the List of Prokaryotic names with Standing in Nomenclature (LPSN) and National Center for Biotechnology Information (NCBI).
Listed below are the known species of Korarcheota [14] Candidatus Korarchaeota
A strain of Korarchaeum cryptofilum was cultivated from an enrichment culture from a hot spring in Yellowstone National Park, USA and described in 2008. [13] The cells are long and needle-shaped, which gave the species its name, alluding to its "cryptical filaments". This organism lacks the genes for purine nucleotide biosynthesis and thus relies on environmental sources to meet its purine requirements. [17]
Korarchaeota are a proposed phylum within the domain, Archaea, and therefore exhibit characteristics such as having a cell wall without peptidoglycan, as well as lipid membranes that are ether-linked. [18] They have a surface layer of paracrystalline protein. [19] This surface layer, known as the S-layer, is densely packed and consists of 1-2 proteins form various lattice structures and are most likely what maintains the cells’ structural integrity. [18] [19] They are typically rod-shaped, however, it has been found that this morphology can change to be thicker-shaped in the presence of higher sodium dodecyl sulfate (SDS) concentrations. [20] Korarchaeota cells have an ultrathin filamentous morphology that may vary in length. [6] They typically average 15 μm in length and 0.16 μm in diameter but can be seen up to 100 μm long. [20] Some Archaea can fix carbon dioxide through the 3-hydroxypropionate/4-hydroxybutyrate pathway into organic compounds [21]
Korarcheota have only been found in hydrothermal environments ranging from terrestrial, including hot springs [6] [22] to marine, including shallow hydrothermal vents and deep-sea hydrothermal vents. [23] Previous research has shown greater diversity of Korarchaea found in terrestrial hot springs compared to marine environments. [23] Korarchaeota have been found in nature in only low abundances. [24] [25] [26] Korarcheota likely originated in marine environments and then adapted to terrestrial ones. [27]
Geographically, Korarcheota have been found in a variety of locations around the world including Japan, Yellowstone National Park, the Gulf of California, Iceland and Russia. [18] [23]
Korarchaeota are thermophiles, having been found living in conditions of up to 128 degrees Celsius. [23] The lowest temperature they have been found in is 52 degrees Celsius. [18] While they have frequently been observed living in acidic conditions, they have also been found living in conditions up to a pH of 10. [28] [23]
Researchers have identified a virus that can potentially infect Korarcheota. [29]
Carl Richard Woese was an American microbiologist and biophysicist. Woese is famous for defining the Archaea in 1977 through a pioneering phylogenetic taxonomy of 16S ribosomal RNA, a technique that has revolutionized microbiology. He also originated the RNA world hypothesis in 1967, although not by that name. Woese held the Stanley O. Ikenberry Chair and was professor of microbiology at the University of Illinois Urbana–Champaign.
The three-domain system is a taxonomic classification system that groups all cellular life into three domains, namely Archaea, Bacteria and Eukarya, introduced by Carl Woese, Otto Kandler and Mark Wheelis in 1990. The key difference from earlier classifications such as the two-empire system and the five-kingdom classification is the splitting of Archaea from Bacteria as completely different organisms. It has been challenged by the two-domain system that divides organisms into Bacteria and Archaea only, as Eukaryotes are considered as a clade of Archaea.
Nanoarchaeota is a proposed phylum in the domain Archaea that currently has only one representative, Nanoarchaeum equitans, which was discovered in a submarine hydrothermal vent and first described in 2002.
The Thermoproteota are prokaryotes that have been classified as a phylum of the Archaea domain. Initially, the Thermoproteota were thought to be sulfur-dependent extremophiles but recent studies have identified characteristic Thermoproteota environmental rRNA indicating the organisms may be the most abundant archaea in the marine environment. 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. Until recently all cultured Thermoproteota had been thermophilic or hyperthermophilic organisms, some of which have the ability to grow at up to 113°C. These organisms stain Gram negative and are morphologically diverse, having rod, cocci, filamentous and oddly-shaped cells.
Euryarchaeota is a phylum of archaea. Euryarchaeota are highly diverse and include methanogens, which produce methane and are often found in intestines, halobacteria, which survive extreme concentrations of salt, and some extremely thermophilic aerobes and anaerobes, which generally live at temperatures between 41 and 122 °C. They are separated from the other archaeans based mainly on rRNA sequences and their unique DNA polymerase.
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The Thermoprotei is a class of the Thermoproteota.
In prokaryote nomenclature, Candidatus is used to name prokaryotic taxa that are well characterized but yet-uncultured. Contemporary sequencing approaches, such as 16S ribosomal RNA sequencing or metagenomics, provide much information about the analyzed organisms and thus allow to identify and characterize individual species. However, the majority of prokaryotic species remain uncultivable and hence inaccessible for further characterization in in vitro study. The recent discoveries of a multitude of candidate taxa has led to candidate phyla radiation expanding the tree of life through the new insights in bacterial diversity.
Halobacteriales are an order of the Halobacteria, found in water saturated or nearly saturated with salt. They are also called halophiles, though this name is also used for other organisms which live in somewhat less concentrated salt water. They are common in most environments where large amounts of salt, moisture, and organic material are available. Large blooms appear reddish, from the pigment bacteriorhodopsin. This pigment is used to absorb light, which provides energy to create ATP. Halobacteria also possess a second pigment, halorhodopsin, which pumps in chloride ions in response to photons, creating a voltage gradient and assisting in the production of energy from light. The process is unrelated to other forms of photosynthesis involving electron transport; however, and halobacteria are incapable of fixing carbon from carbon dioxide.
Aciduliprofundum is a genus of the Euryarchaeota.
In taxonomy, Methanohalophilus is a genus of the Methanosarcinaceae.
Halorubrum is a genus in the family Halorubraceae. Halorubrum species are usually halophilic and can be found in waters with high salt concentration such as the Dead Sea or Lake Zabuye.
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The Nitrososphaerota are a phylum of the Archaea proposed in 2008 after the genome of Cenarchaeum symbiosum was sequenced and found to differ significantly from other members of the hyperthermophilic phylum Thermoproteota. Three described species in addition to C. symbiosum are Nitrosopumilus maritimus, Nitrososphaera viennensis, and Nitrososphaera gargensis. The phylum was proposed in 2008 based on phylogenetic data, such as the sequences of these organisms' ribosomal RNA genes, and the presence of a form of type I topoisomerase that was previously thought to be unique to the eukaryotes. This assignment was confirmed by further analysis published in 2010 that examined the genomes of the ammonia-oxidizing archaea Nitrosopumilus maritimus and Nitrososphaera gargensis, concluding that these species form a distinct lineage that includes Cenarchaeum symbiosum. The lipid crenarchaeol has been found only in Nitrososphaerota, making it a potential biomarker for the phylum. Most organisms of this lineage thus far identified are chemolithoautotrophic ammonia-oxidizers and may play important roles in biogeochemical cycles, such as the nitrogen cycle and the carbon cycle. Metagenomic sequencing indicates that they constitute ~1% of the sea surface metagenome across many sites.
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The two-domain system is a biological classification by which all organisms in the tree of life are classified into two big domains, Bacteria and Archaea. It emerged from development of knowledge of archaea diversity and challenges to the widely accepted three-domain system that defines life into Bacteria, Archaea, and Eukarya. It was preceded by the eocyte hypothesis of James A. Lake in the 1980s, which was largely superseded by the three-domain system, due to evidence at the time. Better understanding of archaea, especially of their roles in the origin of eukaryotes through symbiogenesis with bacteria, led to the revival of the eocyte hypothesis in the 2000s. The two-domain system became more widely accepted after the discovery of a large group (superphylum) of archaea called Asgard in 2017, which evidence suggests to be the evolutionary root of eukaryotes, implying that eukaryotes are members of the domain Archaea.