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1 thermal stability of the plasma membrane of crenarchaeota.
2 rder Thermoproteales in the archaeal kingdom Crenarchaeota.
3 imental studies on S. solfataricus and other Crenarchaeota.
4 rthologous genes from free-living planktonic Crenarchaeota.
5 anch that is distinct from Euryarchaeota and Crenarchaeota.
6 derived from uncultivated, nonextremophilic Crenarchaeota.
7 m a ubiquitous component of marine plankton, Crenarchaeota.
8 ivergence, and were subsequently lost in the Crenarchaeota.
9 ents the first described symbiosis involving Crenarchaeota.
10 erature optimum of any cultivated species of Crenarchaeota.
11 fect hyperthermophilic members of the phylum Crenarchaeota.
12 on of quartet analysis of HGT for the phylum Crenarchaeota.
15 Crenarchaeota, below the bifurcation between Crenarchaeota and Euryarchaeota, or even as the sister g
17 droxybutyrate cycle emerged independently in Crenarchaeota and Thaumarchaeota, thus supporting the hy
19 nia oxidation by mesophilic and thermophilic Crenarchaeota and the widespread distribution of these o
20 onuclease type, found in N. equitans, in all Crenarchaeota, and in Methanopyrus kandleri, is able to
22 Quantitative PCR confirms that uncultivated Crenarchaeota are indeed a major microbial group in thes
25 ed, these sequences branch deeply within the Crenarchaeota, below the bifurcation between Crenarchaeo
27 icative polymerase in archaea, excluding the Crenarchaeota branch, and bear little sequence homology
28 were higher for Firmicutes, Chloroflexi and Crenarchaeota, but lower for Proteobacteria and Actinoba
29 Below the euphotic zone (> 150 m), pelagic crenarchaeota comprised a large fraction of total marine
30 metagenomic studies have revealed that such Crenarchaeota contain and express genes related to those
33 trated the ubiquity of these low-temperature Crenarchaeota in aquatic and terrestrial environments.
35 al groups (pelagic euryarchaeota and pelagic crenarchaeota) in one of the ocean's largest habitats.
37 phenotypically low modification level in the Crenarchaeota kingdom and is the only cytoplasmic small
39 l sequences, suggests that nitrifying marine Crenarchaeota may be important to global carbon and nitr
40 eota, but not in the genomes of Bacteria and Crenarchaeota, procaryotes that do not have histones.
42 Horizontal gene transfers (HGT) between four Crenarchaeota species (Metallosphaera cuprina Ar-4T, Aci
43 ila TM-1, representing the Euryarchaeota and Crenarchaeota subdomains of the Archaea, contain protein
44 ed coil domains occur in the genomes of both crenarchaeota (Sulfolobus, Pyrobaculum, Aeropyrum) and e
45 Some core metabolic genes are more common in Crenarchaeota than Euryarchaeota, up to 21% of genes hav
48 c hydroxypropionate/hydroxybutyrate cycle of Crenarchaeota that is far more energy efficient than any
49 e the determination of the first genome of a Crenarchaeota, the suggestion that horizontal gene trans
50 Considering the ubiquity and abundance of Crenarchaeota, these findings considerably challenge the
52 Autotrophic members of the Sulfolobales (crenarchaeota) use the 3-hydroxypropionate/4-hydroxybuty
53 er describe the cosmopolitan nonthermophilic Crenarchaeota, we analyzed the genome sequence of one re
54 sporter system to be widely spread among the Crenarchaeota, we propose to name it the Crenarchaeal sy
55 wo unidentified archaeal genera belonging to Crenarchaeota were also correlated to bioaccessible Mn c
56 lar tetraether lipids (BTLs) are abundant in crenarchaeota, which thrive in both thermophilic and non
57 lar surveys show that members of the kingdom Crenarchaeota within the domain Archaea represent a subs
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