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1 fect hyperthermophilic members of the phylum Crenarchaeota.
2 on of quartet analysis of HGT for the phylum Crenarchaeota.
3  thermal stability of the plasma membrane of crenarchaeota.
4 rder Thermoproteales in the archaeal kingdom Crenarchaeota.
5 imental studies on S. solfataricus and other Crenarchaeota.
6 rthologous genes from free-living planktonic Crenarchaeota.
7 anch that is distinct from Euryarchaeota and Crenarchaeota.
8  derived from uncultivated, nonextremophilic Crenarchaeota.
9 m a ubiquitous component of marine plankton, Crenarchaeota.
10 ivergence, and were subsequently lost in the Crenarchaeota.
11 ents the first described symbiosis involving Crenarchaeota.
12 erature optimum of any cultivated species of Crenarchaeota.
13 ly absent in the Desulfurococcales of phylum Crenarchaeota.
14 ives exist only in the Sulfolobales order of Crenarchaeota.
15                                          The crenarchaeota and euryarchaeota apparently differ in res
16 ervation, are found in archaea from both the Crenarchaeota and Euryarchaeota phyla.
17 Crenarchaeota, below the bifurcation between Crenarchaeota and Euryarchaeota, or even as the sister g
18 ators coded in the genomic sequences of both crenarchaeota and euryarchaeota.
19 droxybutyrate cycle emerged independently in Crenarchaeota and Thaumarchaeota, thus supporting the hy
20 subdomains, and prominent among them are the Crenarchaeota and the Euryarchaeota.
21 nia oxidation by mesophilic and thermophilic Crenarchaeota and the widespread distribution of these o
22 onuclease type, found in N. equitans, in all Crenarchaeota, and in Methanopyrus kandleri, is able to
23                                     However, Crenarchaeota, another branch of the archaea, lack FtsZ
24  Quantitative PCR confirms that uncultivated Crenarchaeota are indeed a major microbial group in thes
25  small-subunit ribosomal genes suggests that Crenarchaeota are the abundant microbial member.
26                                              Crenarchaeota are ubiquitous and abundant microbial cons
27 ed, these sequences branch deeply within the Crenarchaeota, below the bifurcation between Crenarchaeo
28 rm a coherent group rooted deeply within the Crenarchaeota branch of the domain Archaea.
29 icative polymerase in archaea, excluding the Crenarchaeota branch, and bear little sequence homology
30  were higher for Firmicutes, Chloroflexi and Crenarchaeota, but lower for Proteobacteria and Actinoba
31   Below the euphotic zone (> 150 m), pelagic crenarchaeota comprised a large fraction of total marine
32  metagenomic studies have revealed that such Crenarchaeota contain and express genes related to those
33 ting hyperthermophilic archaea of the phylum Crenarchaeota display enormous morphological and genetic
34            The numerical dominance of marine Crenarchaeota--estimated at 10(28) cells in the world's
35 sis and transport genes in major lineages of Crenarchaeota, Euryarchaeota and Thaumarchaeota.
36 were Acidobacteriota and Pseudomonadota, and Crenarchaeota for Ushkovsky.
37 trated the ubiquity of these low-temperature Crenarchaeota in aquatic and terrestrial environments.
38 ndependent methods uncovered vast numbers of Crenarchaeota in cold oxic ocean waters.
39 la and attributed DSR in this environment to Crenarchaeota in the Vulcanisaeta genus.
40 al groups (pelagic euryarchaeota and pelagic crenarchaeota) in one of the ocean's largest habitats.
41                              The fraction of crenarchaeota increased with depth, reaching 39% of tota
42 phenotypically low modification level in the Crenarchaeota kingdom and is the only cytoplasmic small
43  that unites the Thaumarchaeota-Aigarchaeota-Crenarchaeota-Korarchaeota (TACK) superphylum into a sin
44 marchaeota/"Aigarchaeota" (candidate phylum)/Crenarchaeota/Korarchaeota (TACK).
45 l sequences, suggests that nitrifying marine Crenarchaeota may be important to global carbon and nitr
46 eota, but not in the genomes of Bacteria and Crenarchaeota, procaryotes that do not have histones.
47                Our data suggest that pelagic crenarchaeota represent one of the ocean's single most a
48 Horizontal gene transfers (HGT) between four Crenarchaeota species (Metallosphaera cuprina Ar-4T, Aci
49 ila TM-1, representing the Euryarchaeota and Crenarchaeota subdomains of the Archaea, contain protein
50 ed coil domains occur in the genomes of both crenarchaeota (Sulfolobus, Pyrobaculum, Aeropyrum) and e
51 Some core metabolic genes are more common in Crenarchaeota than Euryarchaeota, up to 21% of genes hav
52                            For instance, all Crenarchaeota that are currently cultivated are sulphur-
53                         Recently, a group of Crenarchaeota that grow in non-extreme environments was
54 c hydroxypropionate/hydroxybutyrate cycle of Crenarchaeota that is far more energy efficient than any
55 e the determination of the first genome of a Crenarchaeota, the suggestion that horizontal gene trans
56    Considering the ubiquity and abundance of Crenarchaeota, these findings considerably challenge the
57 anism known; and Aeropyrum pernix, the first Crenarchaeota to be completely sequenced.
58     Autotrophic members of the Sulfolobales (crenarchaeota) use the 3-hydroxypropionate/4-hydroxybuty
59 er describe the cosmopolitan nonthermophilic Crenarchaeota, we analyzed the genome sequence of one re
60 sporter system to be widely spread among the Crenarchaeota, we propose to name it the Crenarchaeal sy
61 tribution of SMC superfamily proteins in the Crenarchaeota, we suggest that the organization of the A
62 wo unidentified archaeal genera belonging to Crenarchaeota were also correlated to bioaccessible Mn c
63 lar tetraether lipids (BTLs) are abundant in crenarchaeota, which thrive in both thermophilic and non
64 lar surveys show that members of the kingdom Crenarchaeota within the domain Archaea represent a subs