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1 s fermentans is the first known cellulolytic archaeon.
2 ologous recombination in a hyperthermophilic archaeon.
3 ubunit of the archaeal aIF2 from the cognate archaeon.
4 phylogenetics indicates that the host was an archaeon.
5 of chaperonin subunits ever described for an archaeon.
6 ecific aminopeptidase to be purified from an archaeon.
7 s is a strictly anaerobic, methane-producing archaeon.
8 the existence of a salvaging pathway in this archaeon.
9 ot been determined for any hyperthermophilic archaeon.
10 for the conservation of this property in an archaeon.
11 involved in the one-carbon metabolism of the archaeon.
12 erved block in cobamide biosynthesis in this archaeon.
13 ed for an alternate mevalonate pathway in an archaeon.
14 NA processing sites (PSSs) in a methanogenic archaeon.
15 ikely the replicative DNA polymerase in this archaeon.
16 red HARP by horizontal gene transfer from an archaeon.
17 y, the two archaeal histones present in this archaeon.
18 rimordial Orai sequence in hyperthermophilic archaeons.
19 e (casposase) encoded by the casposon of the archaeon Aciduliprofundum boonei Oligonucleotide duplexe
20 obium limicola, four other bacteria, and one archaeon additionally exhibit an H(+)-pumping activity i
22 hydrogenase (ADH) from the hyperthermophilic archaeon Aeropyrum pernix has been solved by the multipl
23 stal structures of the ORC2 protein from the archaeon Aeropyrum pernix in complexes with ADP or a non
24 shaped virus (ACV), of the hyperthermophilic archaeon Aeropyrum pernix, with a virion architecture no
25 mobile elements, have close similarities to archaeon and eukaryotic miniature inverted repeat transp
26 s is a strictly anaerobic, methane-producing archaeon and facultative autotroph capable of biosynthes
27 cts of arsenic resistance in this halophilic archaeon and technical improvements in our capability fo
28 ndrion (a proteobacterium), and its host (an archaeon)--and carries a corollary that, over time, the
29 acterized from a hyperthermophile or from an archaeon, and the results are the first demonstration th
30 icroorganisms, including one eukaryote, four archaeons, and 11 eubacteria, have been completely seque
32 sterase, AF-Est2, from the hyperthermophilic archaeon Archaeoglobus fulgidus has been cloned, over-ex
34 ely with that from the protein Af1503 of the archaeon Archaeoglobus fulgidus or the Tsr receptor.
35 heat shock response of the hyperthermophilic archaeon Archaeoglobus fulgidus strain VC-16 was studied
36 104 residue SRP19 from the hyperthermophilic archaeon Archaeoglobus fulgidus, designated as Af19, was
39 The Y-family DNA polymerase Dpo4, from the archaeon bacterium Sulfolobus solfataricus, is a member
40 ed for a hyperthermophile or a nonhalophilic archaeon by using the 2,065 open reading frames (ORFs) t
41 ransport system for corrinoids and that this archaeon can synthesize cobamides de novo under aerobic
42 Here we report that these proteins from the archaeon Candidatus 'Caldiarchaeum subterraneum' operate
44 ft genome sequence for the ammonia-oxidizing archaeon "Candidatus Nitrosopumilus salaria" BD31, which
50 oarchaeum limnia" BG20, an ammonia-oxidizing archaeon enriched in culture from low-salinity sediments
52 ic change that distinguishes the acidophilic archaeon Ferroplasma acidarmanus fer1 from an environmen
56 the first crenarchaeote and only the second archaeon found to have a transporter of the phosphotrans
59 ation resistance in the extremely halophilic archaeon Halobacterium NRC-1 withstanding up to 110 J/m2
60 damage and oxidative stress responses of the archaeon Halobacterium salinarum exposed to ionizing rad
61 -driven proton pump bacteriorhodopsin in the archaeon Halobacterium salinarum requires coordinate syn
62 overy of the first sensory rhodopsins in the archaeon Halobacterium salinarum, genome projects have r
69 of the cbiZ gene in the extremely halophilic archaeon Halobacterium sp. strain NRC-1 blocked the abil
71 lyses of mutants of the extremely halophilic archaeon Halobacterium sp. strain NRC-1 showed that open
73 nsive postgenomic investigation of the model archaeon Halobacterium sp. strain NRC-1, we used whole-g
76 ed from the serine and tyrosine tRNAs of the archaeon Haloferax volcanii are active in suppression of
78 at the SecD and SecF components in the model archaeon Haloferax volcanii form a cytoplasmic membrane
82 atural cell fusion ability of the halophilic archaeon Haloferax volcanii we were able to examine this
83 the genetically and biochemically tractable archaeon Haloferax volcanii were cloned, providing the t
88 under wide pH range from a square halophilic archaeon, Haloquadratum walsbyi (HwBR), was solved in tw
89 genes, polarity in operon expression in this archaeon has been established by both microarray hybridi
90 arly relevant for S. acidocaldarius, as this archaeon has natural competence for OMT, encodes no MutS
91 c model for a flagellar-like filament of the archaeon Ignicoccus hospitalis from a reconstruction at
93 hat Methanobrevibacter smithii, the dominant archaeon in the human gut ecosystem, affects the specifi
95 rom Pyrococcus furiosus, a hyperthermophilic archaeon, into the nuclei of oocytes from the aquatic fr
96 f modifications in t+rRNAs in the halophilic archaeon is surprisingly low when compared with other Ar
99 ent uranium, the extremely thermoacidophilic archaeon Metallosphaera prunae, originally isolated from
100 ve genes of the carbon fixation cycle of the archaeon Metallosphaera sedula, which grows autotrophica
101 resolvases from the moderately thermophilic archaeon Methanobacterium thermoautotrophicum and demons
102 iated with the cobY gene of the methanogenic archaeon Methanobacterium thermoautotrophicum strain Del
105 ds true for the c ring from the methanogenic archaeon Methanobrevibacter ruminantium, whose c subunit
107 microbes: methanogens including the dominant archaeon, Methanobrevibacter smithii, a polyphyletic gro
110 of some of these RPRs, such as that from the archaeon Methanocaldococcus jannaschii (Mja), to catalyz
111 e guanylyltransferase (CobY) enzyme from the archaeon Methanocaldococcus jannaschii (MjCobY) in compl
114 d catalytically active box C/D sRNP from the archaeon Methanocaldococcus jannaschii by single-particl
115 J1117 of the hyperthermophilic, methanogenic archaeon Methanocaldococcus jannaschii encodes a CobY pr
117 olation of a non-synthetase protein from the archaeon Methanocaldococcus jannaschii that was copurifi
122 ng (NHEJ) machinery from the closely related archaeon, Methanocella paludicola, allowed efficient Cas
124 psychrotolerant archaea, specifically in the archaeon Methanococcoides burtonii grown at 4 and 23 deg
126 n identified in the hyperthermophilic marine archaeon Methanococcus jannaschii and shown to catalyze
129 both Salmonella serovar Typhimurium and the archaeon Methanococcus jannaschii were purified and show
131 fixation, or switch-off, in the methanogenic archaeon Methanococcus maripaludis does not involve dete
132 Nitrogen assimilation in the methanogenic archaeon Methanococcus maripaludis is regulated by trans
133 rogenase, or switch-off, in the methanogenic archaeon Methanococcus maripaludis requires both nifI(1)
134 rated for the hydrogenotrophic, methanogenic archaeon Methanococcus maripaludis S2 using a derivative
135 the bacterium Desulfovibrio vulgaris and the archaeon Methanococcus maripaludis were established and
139 anipulation of the slow-growing methanogenic archaeon Methanosarcina acetivorans Introduction of both
140 aracterization of McrA from the methanogenic archaeon Methanosarcina acetivorans lacking tfuA and/or
142 dy, the protein MA4561 from the methanogenic archaeon Methanosarcina acetivorans was originally predi
143 (TBP) homologs (TBP1, TBP2, and TBP3) in the archaeon Methanosarcina acetivorans were investigated by
144 subunits, termed Hsp60-4 and Hsp60-5, in the archaeon Methanosarcina acetivorans, which also has Hsp6
149 Monomethylamine methyltransferase of the archaeon Methanosarcina barkeri contains a rare amino ac
152 stantly related class II photolyase from the archaeon Methanosarcina mazei (MmCPDII) as well as plant
153 ading frame (ORF) Mm2058 of the methanogenic archaeon Methanosarcina mazei strain Go1 was shown in vi
156 phosphotransacetylase from the methanogenic archaeon Methanosarcina thermophila in complex with the
157 n(II)-containing carbonic anhydrase from the archaeon Methanosarcina thermophila suggests that a very
158 zyme was purified from the methane-producing archaeon Methanosarcina thermophila, and the N-terminal
161 transmembrane channel protein AqpM from the archaeon Methanothermobacter marburgensis, we determined
162 ly fractionated extracts of the thermophilic archaeon Methanothermobacter thermautotrophicus (Mth).
164 terminal portion of the MCM complex from the archaeon Methanothermobacter thermautotrophicus (N-mtMCM
166 licase activity of an MCM homologue from the archaeon Methanothermobacter thermautotrophicus is inhib
167 minichromosome maintenance helicase from the archaeon Methanothermobacter thermautotrophicus required
170 winding of individual DNA helicases from the archaeons Methanothermobacter thermautotrophicus (Mth) a
171 d that the ungapped genome of the ARMAN-like archaeon Mia14 has lost key metabolic pathways, suggesti
172 phile Halobacterium salinarum, a salt-loving archaeon, mounts a specific response to scavenge iron fo
177 matching the genome of the ammonia-oxidizing archaeon Nitrosopumilus maritimus dominated the transcri
179 rt a cupredoxin isolated from the nitrifying archaeon Nitrosopumilus maritimus SCM1, called Nmar1307,
180 tivorans strain C2A is a marine methanogenic archaeon notable for its substrate utilization, genetic
181 lic, strictly hydrogenotrophic, methanogenic archaeon of ancient lineage isolated from a deep-sea hyd
183 e Archaea, supporting hypotheses in which an archaeon participated in eukaryotic origins by founding
185 ese findings demonstrate a link between this archaeon, prioritized bacterial utilization of polysacch
186 12.7-kDa protein from the hyperthermophilic archaeon Pyrobaculum aerophilum adopts a novel fold cons
192 tructure of RPP21 from the hyperthermophilic archaeon Pyrococcus furiosus ( Pfu) using conventional a
194 a coli (EcMetAP-I) and the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-II) was investigat
195 yl aminopeptidase from the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-II; EC 3.4.11.18)
196 the RNase P holoenzyme from the thermophilic archaeon Pyrococcus furiosus (Pfu) and furthered our und
197 We discovered a thermostable enzyme from the archaeon Pyrococcus furiosus (Pfu), which increases yiel
198 erated rubredoxin from the hyperthermophilic archaeon Pyrococcus furiosus and the mesophilic bacteriu
199 tracts of the proteolytic, hyperthermophilic archaeon Pyrococcus furiosus contain high specific activ
200 l genome annotation of the hyperthermophilic archaeon Pyrococcus furiosus contained 2,065 open readin
207 c hydrogenase (SHI) of the hyperthermophilic archaeon Pyrococcus furiosus is an NADP(H)-dependent het
208 fication of operons in the hyperthermophilic archaeon Pyrococcus furiosus represents an important ste
210 essential element for the hyperthermophilic archaeon Pyrococcus furiosus, and many of its iron-conta
211 pproach that confers on a microorganism (the archaeon Pyrococcus furiosus, which grows optimally on c
217 n the ATPase domain of the hyperthermophilic archaeon Pyrococcus horikoshii is strongly regulated by
218 irst step of diphthamide biosynthesis in the archaeon Pyrococcus horikoshii uses a novel iron-sulphur
219 f a glutamate transporter homologue from the archaeon Pyrococcus horikoshii, GltPh, showed that disti
222 it has acquired by lateral transfer from an archaeon related to the Methanomicrobiales, an important
223 nt extract of the membrane fraction from the archaeon S. solfataricus that had been enriched for this
225 he availability of a genetic system for this archaeon should allow subsequent elucidation of the phys
226 activator and some membrane proteins of the archaeon, suggesting that the expression of these protei
227 siological context, we used ECT to image the archaeon Sulfolobus acidocaldarius and observed a distin
228 E (PLFE) isolated from the thermoacidophilic archaeon Sulfolobus acidocaldarius grown at different te
229 lus resembled those of the thermoacidophilic archaeon Sulfolobus acidocaldarius, despite important mo
230 termine the relevance of this threat for the archaeon Sulfolobus acidocaldarius, the mode of GGCC met
233 tification of a biogeographic pattern in the archaeon Sulfolobus challenges the current model of micr
237 Intriguingly, the CCA-adding enzyme from the archaeon Sulfolobus shibatae is a homodimer that forms a
238 own as rosettasomes in the hyperthermophilic archaeon Sulfolobus shibatae, are not cytoplasmic but me
239 re of citrate synthase from the thermophilic Archaeon Sulfolobus solfataricus (optimum growth tempera
244 show that the Cas4 protein SSO0001 from the archaeon Sulfolobus solfataricus has metal-dependent end
245 sists of 6 homologous proteins (MCM2-7), the archaeon Sulfolobus solfataricus has only 1 MCM protein
246 The Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus is an attractive bindin
250 le extracts of the extreme acidothermophilic archaeon Sulfolobus solfataricus were incubated with [ga
251 s of the Orc1-1 and Orc1-3 paralogs from the archaeon Sulfolobus solfataricus, and tested their effec
252 oduct of open reading frame sso2387 from the archaeon Sulfolobus solfataricus, SsoPK2, displayed seve
253 on and structure of the CSM complex from the archaeon Sulfolobus solfataricus, using a combination of
254 lysis of the third replication origin in the archaeon Sulfolobus solfataricus, we identify and charac
255 identified two origins of replication in the archaeon Sulfolobus solfataricus, whereas a second study
266 the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus; Sso7d-hFc was isolated
269 n polymerase (Dpo1) in the hyperthermophilic archaeon, Sulfolobus solfataricus, is shown here to poss
272 F-hw mRNA interferase from a superhalophilic archaeon that cleaves RNA at a specific seven-base seque
273 Methanococcus maripaludis is a methanogenic archaeon that contains a high amount of protein-bound Fe
274 era sedula is an extremely thermoacidophilic archaeon that grows heterotrophically on peptides and ch
276 rom Thermoproteus tenax, a hyperthermophilic archaeon that has an optimum growth temperature of 86 de
277 Methanococcus maripaludis is a mesophilic archaeon that reduces CO2 to methane with H2 or formate
278 e homolog from Haloferax volcanii, a related archaeon that synthesizes bacterioruberins but lacks ops
279 othermobacter marburgensis is a methanogenic archaeon that thrives under anaerobic conditions at 65 d
280 g sequence element from the chromosome of an archaeon, the extreme halophile Halobacterium strain NRC
281 omal protein L30e from the hyperthermophilic archaeon Thermococcus celer determined at cryo-temperatu
282 gh fidelity family-B DNA polymerase from the archaeon Thermococcus gorgonarius (Tgo-Pol), able to rep
283 racterized protein, encoded by TK1252 in the archaeon Thermococcus kodakaraensis, was shown to stably
285 es are incorporated by the hyperthermophilic archaeon Thermococcus kodakarensis both in vitro and in
286 ized small protein, encoded by TK0808 in the archaeon Thermococcus kodakarensis, was shown to stably
288 molecular weight TrxR from the thermophilic archaeon Thermoplasma acidophilum ( taTrxR) that is char
290 ues of the alpha-subunits of the CP from the archaeon Thermoplasma acidophilum are arranged such that
291 Here, we find that Cdc48 and 20S from the archaeon Thermoplasma acidophilum interact to form a fun
293 growth changes were analyzed in a halophilic archaeon to generate a temporal model that describes the
294 cus (Methanococcus) jannaschii was the first archaeon to have its genome sequenced, little is known a
295 ing hooks empowering this widely distributed archaeon to predominate anaerobic groundwater, where it
297 enhancing effects, (i) acyclic analogs, (ii) archaeon variants and (iii) specific dyes, appear to act
298 w of the mutations arising in a thermophilic archaeon were nucleotide substitutions in contrast to in
299 During coculture of a hydrothermal vent archaeon with a bacterial competitor, muramidase transcr
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