ライフサイエンスコーパス: archaeon

1 y, the two archaeal histones present in this archaeon.

2 s fermentans is the first known cellulolytic archaeon.

3 ologous recombination in a hyperthermophilic archaeon.

4 ubunit of the archaeal aIF2 from the cognate 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 NA processing sites (PSSs) in a methanogenic archaeon.

12 involved in the one-carbon metabolism of the archaeon.

13 red HARP by horizontal gene transfer from an archaeon.

14 erved block in cobamide biosynthesis in this archaeon.

15 phylogenetics indicates that the host was an archaeon.

16 ed for an alternate mevalonate pathway in an archaeon.

17 rested ribosomes at initiation sites in this archaeon.

18 ikely the replicative DNA polymerase in this archaeon.

19 rimordial Orai sequence in hyperthermophilic archaeons.

20 e (casposase) encoded by the casposon of the archaeon Aciduliprofundum boonei Oligonucleotide duplexe

21 obium limicola, four other bacteria, and one archaeon additionally exhibit an H(+)-pumping activity i

22 The hyperthermophilic archaeon Aeropyrum pernix (A. pernix) can grow throughou

23 hydrogenase (ADH) from the hyperthermophilic archaeon Aeropyrum pernix has been solved by the multipl

24 stal structures of the ORC2 protein from the archaeon Aeropyrum pernix in complexes with ADP or a non

25 shaped virus (ACV), of the hyperthermophilic archaeon Aeropyrum pernix, with a virion architecture no

26 mobile elements, have close similarities to archaeon and eukaryotic miniature inverted repeat transp

27 s is a strictly anaerobic, methane-producing archaeon and facultative autotroph capable of biosynthes

28 cts of arsenic resistance in this halophilic archaeon and technical improvements in our capability fo

29 ndrion (a proteobacterium), and its host (an archaeon)--and carries a corollary that, over time, the

30 acterized from a hyperthermophile or from an archaeon, and the results are the first demonstration th

31 The hyperthermophilic archaeon Archaeoglobus fulgidus contains an L-Ala dehydr

32 sterase, AF-Est2, from the hyperthermophilic archaeon Archaeoglobus fulgidus has been cloned, over-ex

33 In the sulfate-reducing archaeon Archaeoglobus fulgidus it is a metal-dependent

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

37 acterial strains, as well as the piezophilic archaeon Archaeoglobus fulgidus.

38 he soluble fraction of the hyperthermophilic archaeon Archaeoglobus fulgidus.

39 nococcus jannaschii and the sulfate-reducing archaeon Archaeoglobus fulgidus.

40 The Y-family DNA polymerase Dpo4, from the archaeon bacterium Sulfolobus solfataricus, is a member

41 ed for a hyperthermophile or a nonhalophilic archaeon by using the 2,065 open reading frames (ORFs) t

42 Here we report that these proteins from the archaeon Candidatus 'Caldiarchaeum subterraneum' operate

43 wledge, of an ACD from the hyperthermophilic archaeon Candidatus Korachaeum cryptofilum.

44 ft genome sequence for the ammonia-oxidizing archaeon "Candidatus Nitrosopumilus salaria" BD31, which

45 An ammonia-oxidizing, carbon-fixing archaeon, Candidatus "Nitrosopumilus maritimus," recentl

46 oth RNase P forms from the same bacterium or archaeon could be verified in two selected cases.

47 pathways, suggesting dependence on the host archaeon Cuniculiplasma divulgatum.

48 oarchaeum limnia" BG20, an ammonia-oxidizing archaeon enriched in culture from low-salinity sediments

49 randed DNA-binding protein, FacRPA2, in this archaeon exhibited the wrapping mode.

50 ic change that distinguishes the acidophilic archaeon Ferroplasma acidarmanus fer1 from an environmen

51 erobic respiration using DMSO and TMAO in an archaeon for the first time.

52 Until recently, the only archaeon for which a bona fide origin of replication was

53 This is only the second archaeon for which PAM sequences have been determined, a

54 the first crenarchaeote and only the second archaeon found to have a transporter of the phosphotrans

55 This virus infects an archaeon Haloarcula hispanica that was isolated from a h

56 ation resistance in the extremely halophilic archaeon Halobacterium NRC-1 withstanding up to 110 J/m2

57 damage and oxidative stress responses of the archaeon Halobacterium salinarum exposed to ionizing rad

58 overy of the first sensory rhodopsins in the archaeon Halobacterium salinarum, genome projects have r

59 In the model archaeon Halobacterium salinarum, the transcription fact

60 light-induced proton pump in the halophilic archaeon Halobacterium salinarum.

61 ton pump found in the purple membrane of the archaeon Halobacterium salinarum.

62 39006, identifying how this differs from the archaeon Halobacterium salinarum.

63 ology of the TrmB metabolic GRN in the model archaeon Halobacterium salinarum.

64 of the cbiZ gene in the extremely halophilic archaeon Halobacterium sp. strain NRC-1 blocked the abil

65 The genome of the halophilic archaeon Halobacterium sp. strain NRC-1 encodes homologs

66 lyses of mutants of the extremely halophilic archaeon Halobacterium sp. strain NRC-1 showed that open

67 A cbiP mutant strain of the archaeon Halobacterium sp. strain NRC-1 was auxotrophic

68 nsive postgenomic investigation of the model archaeon Halobacterium sp. strain NRC-1, we used whole-g

69 rial CobC enzyme in the extremely halophilic archaeon Halobacterium sp. strain NRC-1.

70 noid utilization in the extremely halophilic archaeon Halobacterium sp. strain NRC-1.

71 predicted coupling in 9 gene pairs from the archaeon Haloferax volcanii and 5 gene pairs from the ba

72 ed from the serine and tyrosine tRNAs of the archaeon Haloferax volcanii are active in suppression of

73 The halophilic archaeon Haloferax volcanii encodes two related proteaso

74 at the SecD and SecF components in the model archaeon Haloferax volcanii form a cytoplasmic membrane

75 e can take place, one means prevalent in the archaeon Haloferax volcanii involves the transient forma

76 The halophilic archaeon Haloferax volcanii produces three different pro

77 The halophilic archaeon Haloferax volcanii synthesizes two different al

78 Here we use the model archaeon Haloferax volcanii to demonstrate that its endo

79 atural cell fusion ability of the halophilic archaeon Haloferax volcanii we were able to examine this

80 We show here that in the archaeon Haloferax volcanii, compaction and reorganizati

81 Starting with the model archaeon Haloferax volcanii, we reanalyze MS datasets fr

82 the main tools available for the halophilic archaeon Haloferax volcanii, which have enabled successf

83 green alga Chlamydomonas reinhardtii and the archaeon Haloferax volcanii.

84 iquitin, that form protein conjugates in the archaeon Haloferax volcanii.

85 the CRISPR-Cas I-B system of the halophilic archaeon Haloferax volcanii.

86 , we developed ribosome profiling in a model archaeon, Haloferax volcanii, elucidating, for the first

87 analysis of these proteins in the halophilic archaeon, Haloferax volcanii.

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

92 opy to study the adhesion filaments from the archaeon Ignicoccus hospitalis.

93 hat Methanobrevibacter smithii, the dominant archaeon in the human gut ecosystem, affects the specifi

94 an ancient horizontal gene transfer from an archaeon into an early Firmicute lineage.

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

97 Cysteine in this archaeon is synthesized primarily via the tRNA-dependent

98 A methanogenic archaeon isolated from deep-sea hydrothermal vent fluid

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 ants of the beta-class enzyme (Cab) from the archaeon Methanobacterium thermoautotrophicum.

102 ation of an RNA ligase from the thermophilic archaeon, Methanobacterium thermoautotrophicum.

103 ds true for the c ring from the methanogenic archaeon Methanobrevibacter ruminantium, whose c subunit

104 Certain bacteria, specifically the archaeon Methanobrevibacter smithii, have enhanced abili

105 microbes: methanogens including the dominant archaeon, Methanobrevibacter smithii, a polyphyletic gro

106 roides thetaiotaomicron and the methanogenic archaeon, Methanobrevibacter smithii.

107 trillions of microbes including a prominent archaeon, Methanobrevibacter smithii.

108 of some of these RPRs, such as that from the archaeon Methanocaldococcus jannaschii (Mja), to catalyz

109 e guanylyltransferase (CobY) enzyme from the archaeon Methanocaldococcus jannaschii (MjCobY) in compl

110 Using the Trm5 enzyme of the archaeon Methanocaldococcus jannaschii (previously MJ088

111 In the case of the methanogenic archaeon Methanocaldococcus jannaschii as well as most m

112 d catalytically active box C/D sRNP from the archaeon Methanocaldococcus jannaschii by single-particl

113 J1117 of the hyperthermophilic, methanogenic archaeon Methanocaldococcus jannaschii encodes a CobY pr

114 The hyperthermophilic archaeon Methanocaldococcus jannaschii encodes a potent

115 olation of a non-synthetase protein from the archaeon Methanocaldococcus jannaschii that was copurifi

116 The archaeon Methanocaldococcus jannaschii uses three differ

117 the structure of Dim1 from the thermophilic archaeon Methanocaldococcus jannaschii.

118 etected Pth-like activity in extracts of the archaeon Methanocaldococcus jannaschii.

119 sphoesterase (PE), and Ku from a mesophillic archaeon, Methanocella paludicola (Mpa).

120 ng (NHEJ) machinery from the closely related archaeon, Methanocella paludicola, allowed efficient Cas

121 The methanogenic archaeon Methanococcoides burtonii contains a Rubisco is

122 psychrotolerant archaea, specifically in the archaeon Methanococcoides burtonii grown at 4 and 23 deg

123 MAT from the hyperthermophilic archaeon Methanococcus jannaschii (MjMAT) is a prototype

124 n identified in the hyperthermophilic marine archaeon Methanococcus jannaschii and shown to catalyze

125 The hyperthermophilic archaeon Methanococcus jannaschii encodes two putative t

126 The hyperthermophilic archaeon Methanococcus jannaschii has two members of thi

127 both Salmonella serovar Typhimurium and the archaeon Methanococcus jannaschii were purified and show

128 Here we show that ThiI from the archaeon Methanococcus maripaludis contains a [3Fe-4S] c

129 fixation, or switch-off, in the methanogenic archaeon Methanococcus maripaludis does not involve dete

130 Nitrogen assimilation in the methanogenic archaeon Methanococcus maripaludis is regulated by trans

131 rogenase, or switch-off, in the methanogenic archaeon Methanococcus maripaludis requires both nifI(1)

132 rated for the hydrogenotrophic, methanogenic archaeon Methanococcus maripaludis S2 using a derivative

133 the bacterium Desulfovibrio vulgaris and the archaeon Methanococcus maripaludis were established and

134 In the methanogenic archaeon Methanococcus maripaludis, growth with ammonia

135 Using the methanogenic archaeon Methanococcus maripaludis, we show that deletio

136 of the group II chaperonin from methanogenic archaeon Methanococcus maripaludis.

137 However, the hyperthermophilic archaeon Methanopyrus kandleri harbors 30 (out of 34) tR

138 anipulation of the slow-growing methanogenic archaeon Methanosarcina acetivorans Introduction of both

139 aracterization of McrA from the methanogenic archaeon Methanosarcina acetivorans lacking tfuA and/or

140 Here, we study the methanogenic archaeon Methanosarcina acetivorans using assays of ATP

141 dy, the protein MA4561 from the methanogenic archaeon Methanosarcina acetivorans was originally predi

142 (TBP) homologs (TBP1, TBP2, and TBP3) in the archaeon Methanosarcina acetivorans were investigated by

143 subunits, termed Hsp60-4 and Hsp60-5, in the archaeon Methanosarcina acetivorans, which also has Hsp6

144 d the clamp loader (RFC) from the mesophilic archaeon Methanosarcina acetivorans.

145 his enzyme family from the methane-producing archaeon Methanosarcina acetivorans.

146 describe a new form of clamp loader from the archaeon Methanosarcina acetivorans.

147 n A homologs, RPA1, RPA2, and RPA3, from the archaeon Methanosarcina acetivorans.

148 Monomethylamine methyltransferase of the archaeon Methanosarcina barkeri contains a rare amino ac

149 In the methanogenic archaeon Methanosarcina barkeri Fusaro, the N5-methyl-te

150 ined onto the chromosome of the methanogenic archaeon Methanosarcina barkeri.

151 stantly related class II photolyase from the archaeon Methanosarcina mazei (MmCPDII) as well as plant

152 ading frame (ORF) Mm2058 of the methanogenic archaeon Methanosarcina mazei strain Go1 was shown in vi

153 The cbiZ gene of the methanogenic archaeon Methanosarcina mazei strain Gol was cloned, was

154 dia (overplus), in cells of the methanogenic archaeon Methanosarcina mazei.

155 phosphotransacetylase from the methanogenic archaeon Methanosarcina thermophila in complex with the

156 zyme was purified from the methane-producing archaeon Methanosarcina thermophila, and the N-terminal

157 rrihydrite to the cultures of a methanogenic archaeon, Methanosarcina barkeri (M. barkeri).

158 ophobacter fumaroxidans and the methanogenic archaeon Methanospirillum hungatei.

159 The MCM complex from the archaeon Methanother-mobacter thermautotrophicus is a mo

160 transmembrane channel protein AqpM from the archaeon Methanothermobacter marburgensis, we determined

161 ly fractionated extracts of the thermophilic archaeon Methanothermobacter thermautotrophicus (Mth).

162 Only one MCM is found in the archaeon Methanothermobacter thermautotrophicus (mtMCM),

163 terminal portion of the MCM complex from the archaeon Methanothermobacter thermautotrophicus (N-mtMCM

164 Open reading frame 48 (ORF48) in the archaeon Methanothermobacter thermautotrophicus encodes

165 licase activity of an MCM homologue from the archaeon Methanothermobacter thermautotrophicus is inhib

166 minichromosome maintenance helicase from the archaeon Methanothermobacter thermautotrophicus required

167 The Cdc6 proteins from the archaeon Methanothermobacter thermautotrophicus were pre

168 east two-hybrid screen was performed for the archaeon Methanothermobacter thermautotrophicus.

169 winding of individual DNA helicases from the archaeons Methanothermobacter thermautotrophicus (Mth) a

170 We find that histone proteins from the archaeon Methanothermus fervidus assemble on the E. coli

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

173 The marine archaeon Nanoarchaeum equitans is dependent on direct ph

174 In the parasitic archaeon Nanoarchaeum equitans, these domains occur as s

175 A (tRNA) 5' maturation, is challenged in the archaeon Nanoarchaeum equitans.

176 voidance motility response in the halophilic archaeon Natronobacterium pharaonis.

177 matching the genome of the ammonia-oxidizing archaeon Nitrosopumilus maritimus dominated the transcri

178 Here we show that the marine archaeon Nitrosopumilus maritimus encodes a pathway for

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

182 e Archaea, supporting hypotheses in which an archaeon participated in eukaryotic origins by founding

183 This methanogenic archaeon possesses two oxaloacetate-synthesizing enzymes

184 ese findings demonstrate a link between this archaeon, prioritized bacterial utilization of polysacch

185 lavoprotein (ETF) from the hyperthermophilic archaeon Pyrobaculum aerophilum The EtfABCX enzyme compl

186 The hyperthermophilic archaeon Pyrobaculum aerophilum used 20 mM Fe(III) citra

187 r disulfide bonding in the hyperthermophilic archaeon Pyrobaculum aerophilum.

188 n of PcalRG, a novel reverse gyrase from the archaeon Pyrobaculum calidifontis.

189 The hyperthermophilic archaeon Pyrobaculum islandicum uses the citric acid cyc

190 stem, was predicted in the hyperthermophilic archaeon Pyrobaculum.

191 tructure of RPP21 from the hyperthermophilic archaeon Pyrococcus furiosus ( Pfu) using conventional a

192 The Argonaute of the archaeon Pyrococcus furiosus (PfAgo) belongs to a differ

193 +)-dependent MATE from the hyperthermophilic archaeon Pyrococcus furiosus (PfMATE).

194 a coli (EcMetAP-I) and the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-II) was investigat

195 the RNase P holoenzyme from the thermophilic archaeon Pyrococcus furiosus (Pfu) and furthered our und

196 erated rubredoxin from the hyperthermophilic archaeon Pyrococcus furiosus and the mesophilic bacteriu

197 tracts of the proteolytic, hyperthermophilic archaeon Pyrococcus furiosus contain high specific activ

198 l genome annotation of the hyperthermophilic archaeon Pyrococcus furiosus contained 2,065 open readin

199 The genome of the hyperthermophile archaeon Pyrococcus furiosus encodes two transcription f

200 The hyperthermophilic archaeon Pyrococcus furiosus genome encodes three protea

201 The anaerobic archaeon Pyrococcus furiosus grows by fermenting carbohy

202 The archaeon Pyrococcus furiosus grows optimally at 100 degr

203 The model archaeon Pyrococcus furiosus grows optimally near 100 de

204 c hydrogenase (SHI) of the hyperthermophilic archaeon Pyrococcus furiosus is an NADP(H)-dependent het

205 oton-coupled MATE from the hyperthermophilic archaeon Pyrococcus furiosus Pairs of spin labels monito

206 fication of operons in the hyperthermophilic archaeon Pyrococcus furiosus represents an important ste

207 The hyperthermophilic archaeon Pyrococcus furiosus uses carbohydrates as a car

208 essential element for the hyperthermophilic archaeon Pyrococcus furiosus, and many of its iron-conta

209 pproach that confers on a microorganism (the archaeon Pyrococcus furiosus, which grows optimally on c

210 ductase I (NfnI) from the hyperthermophillic archaeon Pyrococcus furiosus.

211 ducing conditions from the hyperthermophilic archaeon Pyrococcus furiosus.

212 form of RNA circles in the hyperthermophilic archaeon Pyrococcus furiosus.

213 sertion mutagenesis in the hyperthermophilic archaeon Pyrococcus furiosus.

214 terial alcohol dehydrogenase (AdhA) into the archaeon Pyrococcus furiosus.

215 n the ATPase domain of the hyperthermophilic archaeon Pyrococcus horikoshii is strongly regulated by

216 irst step of diphthamide biosynthesis in the archaeon Pyrococcus horikoshii uses a novel iron-sulphur

217 f a glutamate transporter homologue from the archaeon Pyrococcus horikoshii, GltPh, showed that disti

218 The hyperthermophilic archaeon, Pyrococcus furiosus, was grown on maltose near

219 of deoxyinosine, from the hyperthermophilic archaeon, Pyrococcus furiosus.

220 it has acquired by lateral transfer from an archaeon related to the Methanomicrobiales, an important

221 nt extract of the membrane fraction from the archaeon S. solfataricus that had been enriched for this

222 In contrast, this archaeon's RNA polymerase and core transcription factors

223 he availability of a genetic system for this archaeon should allow subsequent elucidation of the phys

224 activator and some membrane proteins of the archaeon, suggesting that the expression of these protei

225 siological context, we used ECT to image the archaeon Sulfolobus acidocaldarius and observed a distin

226 E (PLFE) isolated from the thermoacidophilic archaeon Sulfolobus acidocaldarius grown at different te

227 ies of the thermostable M/R complex from the archaeon Sulfolobus acidocaldarius using atomic force mi

228 lus resembled those of the thermoacidophilic archaeon Sulfolobus acidocaldarius, despite important mo

229 termine the relevance of this threat for the archaeon Sulfolobus acidocaldarius, the mode of GGCC met

230 ins, ArnA and ArnB, in the thermoacidophilic archaeon Sulfolobus acidocaldarius, where they act syner

231 a ubiquitin-like modification pathway in the archaeon Sulfolobus acidocaldarius.

232 tification of a biogeographic pattern in the archaeon Sulfolobus challenges the current model of micr

233 ith the discovery that the hyperthermophilic archaeon Sulfolobus has three replication origins.

234 ongoing speciation in the thermoacidophilic Archaeon Sulfolobus islandicus.

235 The hyperthermoacidophilic archaeon Sulfolobus shibatae contains group II chaperoni

236 Intriguingly, the CCA-adding enzyme from the archaeon Sulfolobus shibatae is a homodimer that forms a

237 own as rosettasomes in the hyperthermophilic archaeon Sulfolobus shibatae, are not cytoplasmic but me

238 e DNA alkyltransferase from the thermophilic archaeon Sulfolobus solfataricus (SsOGT).

239 -chromosome maintenance (MCM) complex of the archaeon Sulfolobus solfataricus (SsoMCM).

240 The hyperthermophilic archaeon Sulfolobus solfataricus grows optimally above 8

241 Here we establish that the archaeon Sulfolobus solfataricus harbors a hybrid segros

242 show that the Cas4 protein SSO0001 from the archaeon Sulfolobus solfataricus has metal-dependent end

243 sists of 6 homologous proteins (MCM2-7), the archaeon Sulfolobus solfataricus has only 1 MCM protein

244 The Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus is an attractive bindin

245 The thermoacidophilic archaeon Sulfolobus solfataricus is known for its metabo

246 The archaeon Sulfolobus solfataricus uses a catabolite repre

247 The archaeon Sulfolobus solfataricus was sensitive to mercur

248 le extracts of the extreme acidothermophilic archaeon Sulfolobus solfataricus were incubated with [ga

249 s of the Orc1-1 and Orc1-3 paralogs from the archaeon Sulfolobus solfataricus, and tested their effec

250 oduct of open reading frame sso2387 from the archaeon Sulfolobus solfataricus, SsoPK2, displayed seve

251 on and structure of the CSM complex from the archaeon Sulfolobus solfataricus, using a combination of

252 lysis of the third replication origin in the archaeon Sulfolobus solfataricus, we identify and charac

253 identified two origins of replication in the archaeon Sulfolobus solfataricus, whereas a second study

254 ion in vitro using proteins derived from the archaeon Sulfolobus solfataricus.

255 poisomerase 3, SsTop3, from the thermophilic archaeon Sulfolobus solfataricus.

256 the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus.

257 homomultimeric MCM of the hyperthermophilic archaeon Sulfolobus solfataricus.

258 of a DPSL protein from the thermoacidophilic archaeon Sulfolobus solfataricus.

259 ture and regulation in the hyperthermophilic archaeon Sulfolobus solfataricus.

260 ase subunit named PriX was identified in the archaeon Sulfolobus solfataricus.

261 a hyperthermostable enzyme isolated from the archaeon Sulfolobus solfataricus.

262 it, denoted PriX, from the hyperthermophilic archaeon Sulfolobus solfataricus.

263 m an invading virus in the hyperthermophilic archaeon Sulfolobus solfataricus.

264 the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus; Sso7d-hFc was isolated

265 ties of a putative regulator ST1710 from the archaeon Sulfolobus tokodaii.

266 in chromatin structure and regulation in the archaeon Sulfolobus.

267 n polymerase (Dpo1) in the hyperthermophilic archaeon, Sulfolobus solfataricus, is shown here to poss

268 The archaeon TBP, from the halophile/hyperthermophile organi

269 F-hw mRNA interferase from a superhalophilic archaeon that cleaves RNA at a specific seven-base seque

270 Methanococcus maripaludis is a methanogenic archaeon that contains a high amount of protein-bound Fe

271 era sedula is an extremely thermoacidophilic archaeon that grows heterotrophically on peptides and ch

272 is not the case with Pyrococcus furiosus, an archaeon that grows optimally near 100 degrees C.

273 rom Thermoproteus tenax, a hyperthermophilic archaeon that has an optimum growth temperature of 86 de

274 Methanococcus maripaludis is a mesophilic archaeon that reduces CO2 to methane with H2 or formate

275 e homolog from Haloferax volcanii, a related archaeon that synthesizes bacterioruberins but lacks ops

276 othermobacter marburgensis is a methanogenic archaeon that thrives under anaerobic conditions at 65 d

277 The identification of an archaeon that uses ethane (C(2)H(6)) fills a gap in our

278 cing sulfate to sulfide, was dominated by an archaeon that we name 'Candidatus Argoarchaeum ethanivor

279 g sequence element from the chromosome of an archaeon, the extreme halophile Halobacterium strain NRC

280 omal protein L30e from the hyperthermophilic archaeon Thermococcus celer determined at cryo-temperatu

281 gh fidelity family-B DNA polymerase from the archaeon Thermococcus gorgonarius (Tgo-Pol), able to rep

282 racterized protein, encoded by TK1252 in the archaeon Thermococcus kodakaraensis, was shown to stably

283 NA primase complex and its subunits from the archaeon Thermococcus kodakaraensis.

284 es are incorporated by the hyperthermophilic archaeon Thermococcus kodakarensis both in vitro and in

285 ized small protein, encoded by TK0808 in the archaeon Thermococcus kodakarensis, was shown to stably

286 The hyperthermophilic archaeon Thermococcus litoralis strain NS-C, first isola

287 molecular weight TrxR from the thermophilic archaeon Thermoplasma acidophilum ( taTrxR) that is char

288 tal structure of the N-terminal MCM from the archaeon Thermoplasma acidophilum (tapMCM).

289 ues of the alpha-subunits of the CP from the archaeon Thermoplasma acidophilum are arranged such that

290 Here, we find that Cdc48 and 20S from the archaeon Thermoplasma acidophilum interact to form a fun

291 H of the A-ATPase from the thermoacidophilic Archaeon, Thermoplasma acidophilum.

292 growth changes were analyzed in a halophilic archaeon to generate a temporal model that describes the

293 cus (Methanococcus) jannaschii was the first archaeon to have its genome sequenced, little is known a

294 ing hooks empowering this widely distributed archaeon to predominate anaerobic groundwater, where it

295 sp. strain NRC-1 blocked the ability of this archaeon to salvage Cbi.

296 The archaeon was closely related to the hydrogenotrophic met

297 w of the mutations arising in a thermophilic archaeon were nucleotide substitutions in contrast to in

298 During coculture of a hydrothermal vent archaeon with a bacterial competitor, muramidase transcr

299 racterized complexity of translation in this archaeon with bacteria-like, eukarya-like, and potential

300 ucidate primary chromatin architecture in an archaeon without histones, Thermoplasma acidophilum, whi