ライフサイエンスコーパス: hyperthermophilic

1 protein that is monomeric, well-folded, and hyperthermophilic.

2 study demonstrates coenzyme engineering of a hyperthermophilic 6PGDH and its application to high-temp

3 s islandicus rod-shaped virus 2) infects the hyperthermophilic acidophile Sulfolobus islandicus, whic

4 aracterized an archaeal antioxidant from the hyperthermophilic acidophile Sulfolobus solfataricus.

5 l mobilities differ between a mesophilic and hyperthermophilic adenylate kinase, but are strikingly s

6 nal regulator SurR of Pyrococcus furiosus, a hyperthermophilic anaerobe.

7 The cpn10 from the hyperthermophilic, ancient bacterium Aquifex aeolicus (A

8 The hyperthermophilic and anaerobic bacterium Thermotoga mar

9 family involved in heat shock regulation in hyperthermophilic and mesophilic Archaea organisms.

10 This hyperthermophilic and strictly anaerobic crenarchaeon pr

11 ogue (TP0823) for neelaredoxin, an enzyme of hyperthermophilic and sulfate-reducing anaerobes shown t

12 nt comparison of ECAK dynamics with those of hyperthermophilic Aquifex aeolicus AK (AAAK), our result

13 ) accumulates as a compatible solute in many hyperthermophilic archaea (e.g., Archaeoglobus fulgidus)

14 riginated in an extreme environment, such as hyperthermophilic archaea (Pyrococcus furiosus), are sig

15 RNA-encoding DNA analysis places many of the hyperthermophilic Archaea (species with an optimum growt

16 f structures and complete genomes of several hyperthermophilic archaea and bacteria revealed that org

17 bilizes tRNAs from thermophilic bacteria and hyperthermophilic archaea and is required for growth at

18 interaction with uracil is not restricted to hyperthermophilic archaea and that the polymerase from m

19 So far, little is known about how hyperthermophilic Archaea cope with such pyrimidine dama

20 Here we describe a consortium of three hyperthermophilic archaea enriched from a continental ge

21 Hyperthermophilic archaea grow at temperatures that dest

22 In particular, the approaches employed by hyperthermophilic archaea have been a general source of

23 f the DNA replication-associated proteins of hyperthermophilic archaea have yielded considerable insi

24 Inositol monophosphatase (EC 3.1.3.25) in hyperthermophilic archaea is thought to play a role in t

25 Hsp16.5, isolated from the hyperthermophilic Archaea Methanococcus jannaschii, is a

26 o establish the key cell-cycle parameters of hyperthermophilic archaea of the genus Sulfolobus.

27 perties when compared even to Fds from other hyperthermophilic archaea or bacteria.

28 ficity and binding mechanism of MCM from the hyperthermophilic Archaea Sulfolobus solfataricus on var

29 However, in hyperthermophilic archaea that live optimally at tempera

30 Viruses infecting hyperthermophilic archaea typically do not encode DNA po

31 quences (ISs) are abundant and widespread in hyperthermophilic archaea, but few experimental studies

32 e that the intracellular proteins of certain hyperthermophilic archaea, especially the crenarchaea Py

33 In hyperthermophilic archaea, however, TIM exists as a tetr

34 Divergence of the hyperthermophilic Archaea, Pyrococcus furiosus and Pyroc

35 d over a contiguous 16 kb region between two hyperthermophilic Archaea, Pyrococcus furiosus and Therm

36 esponses have been of particular interest in hyperthermophilic archaea, since these microbes live und

37 s of recombination involving short ssDNAs in hyperthermophilic archaea, we evaluated oligonucleotide-

38 d response mechanism that is present even in hyperthermophilic archaea.

39 enzymes in sugar and peptide fermentation of hyperthermophilic archaea.

40 ting experiments for bacteria and 90-99% for hyperthermophilic archaea.

41 like CPSase such as those present in several hyperthermophilic archaea.

42 communities dominated by several species of hyperthermophilic Archaea.

43 7d are two small chromatin proteins from the hyperthermophilic archaeabacterium Sulfolobus solfataric

44 The two recombinant hyperthermophilic archaeal [2Fe-2S] cluster-binding prot

45 Moreover, this latest example of a split hyperthermophilic archaeal DNA polymerase further illust

46 els for dNTP, ddNTP, and acyNTP selection by hyperthermophilic archaeal DNA polymerases to rationaliz

47 the parameters for dNTP incorporation by the hyperthermophilic archaeal Family B Vent DNA polymerase

48 trand RNA viruses that probably replicate in hyperthermophilic archaeal hosts and are highly divergen

49 Pyrococcus woesei (Pw) is a hyperthermophilic archaeal organism that exists under co

50 Analysis of the genome sequence of the small hyperthermophilic archaeal parasite Nanoarchaeum equitan

51 The hyperthermophilic archaeal parasite, Nanoarcheaum equita

52 first structure of a catalytic domain from a hyperthermophilic archaeal viral integrase reveals a min

53 gle-stranded (ss) DNA genome among the known hyperthermophilic archaeal viruses.

54 Archaeoglobus fulgidus, a hyperthermophilic, archaeal sulfate reducer, is one of t

55 Here, we found that the hyperthermophilic archaeaon, Pyrococcus furiosus, active

56 a voltage-dependent K+ (K(V)) channel from a hyperthermophilic archaebacterium from an oceanic therma

57 structure of adenylosuccinate lyase from the hyperthermophilic archaebacterium Pyrobaculum aerophilum

58 is work, we characterize the enzyme from the hyperthermophilic archaebacterium Pyrococcus furiosus.

59 The hyperthermophilic archaeon Acidianus ambivalens expresse

60 The hyperthermophilic archaeon Aeropyrum pernix (A. pernix)

61 m chain alcohol dehydrogenase (ADH) from the hyperthermophilic archaeon Aeropyrum pernix has been sol

62 he Aeropyrum coil-shaped virus (ACV), of the hyperthermophilic archaeon Aeropyrum pernix, with a viri

63 The hyperthermophilic archaeon Archaeoglobus fulgidus contai

64 A new carboxyl esterase, AF-Est2, from the hyperthermophilic archaeon Archaeoglobus fulgidus has be

65 The heat shock response of the hyperthermophilic archaeon Archaeoglobus fulgidus strain

66 structure of the 104 residue SRP19 from the hyperthermophilic archaeon Archaeoglobus fulgidus, desig

67 homogeneity from the soluble fraction of the hyperthermophilic archaeon Archaeoglobus fulgidus.

68 ed, expressed and purified components of the hyperthermophilic archaeon Archaeoglobus fulgidus.

69 ctures, to our knowledge, of an ACD from the hyperthermophilic archaeon Candidatus Korachaeum cryptof

70 ed by an intron in the 23 S rRNA gene of the hyperthermophilic archaeon Desulfurococcus mobilis.

71 Sulfolobus acidocaldarius is so far the only hyperthermophilic archaeon in which genetic recombinatio

72 The hyperthermophilic archaeon Methanocaldococcus jannaschii

73 MAT from the hyperthermophilic archaeon Methanococcus jannaschii (MjM

74 The hyperthermophilic archaeon Methanococcus jannaschii enco

75 The hyperthermophilic archaeon Methanococcus jannaschii enco

76 The hyperthermophilic archaeon Methanococcus jannaschii has

77 However, the hyperthermophilic archaeon Methanopyrus kandleri harbors

78 This 12.7-kDa protein from the hyperthermophilic archaeon Pyrobaculum aerophilum adopts

79 The hyperthermophilic archaeon Pyrobaculum aerophilum used 2

80 The nitrate reductase of the hyperthermophilic archaeon Pyrobaculum aerophilum was pu

81 an endonuclease III homolog, PaNth, from the hyperthermophilic archaeon Pyrobaculum aerophilum, whose

82 ation of a putative DNA glycosylase from the hyperthermophilic archaeon Pyrobaculum aerophilum, whose

83 is of intracellular disulfide bonding in the hyperthermophilic archaeon Pyrobaculum aerophilum.

84 ORFs of the recently sequenced genome of the hyperthermophilic archaeon Pyrobaculum aerophilum.

85 The hyperthermophilic archaeon Pyrobaculum islandicum uses t

86 odABC transport system, was predicted in the hyperthermophilic archaeon Pyrobaculum.

87 transcarbamoylase (OTCase) from the deep sea hyperthermophilic archaeon Pyrococcus abyssi demonstrate

88 ned the solution structure of RPP21 from the hyperthermophilic archaeon Pyrococcus furiosus ( Pfu) us

89 ngle cubane cluster ferredoxin (Fd) from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) have

90 ngle cubane cluster ferredoxin (Fd) from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) poss

91 es from Escherichia coli (EcMetAP-I) and the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-

92 ng for the methionyl aminopeptidase from the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-

93 tic studies were conducted on the POP of the hyperthermophilic archaeon Pyrococcus furiosus (Pfu) 85

94 protons of perdeuterated rubredoxin from the hyperthermophilic archaeon Pyrococcus furiosus and the m

95 The LrpA protein from the hyperthermophilic archaeon Pyrococcus furiosus belongs t

96 ylase was identified in cell extracts of the hyperthermophilic archaeon Pyrococcus furiosus by its ab

97 Cell extracts of the proteolytic, hyperthermophilic archaeon Pyrococcus furiosus contain h

98 shed membrane preparations from cells of the hyperthermophilic archaeon Pyrococcus furiosus contain h

99 The original genome annotation of the hyperthermophilic archaeon Pyrococcus furiosus contained

100 The hyperthermophilic archaeon Pyrococcus furiosus genome en

101 The hyperthermophilic archaeon Pyrococcus furiosus grows opt

102 Crystal structures of SOR from the hyperthermophilic archaeon Pyrococcus furiosus have been

103 The cytoplasmic hydrogenase (SHI) of the hyperthermophilic archaeon Pyrococcus furiosus is an NAD

104 Identification of operons in the hyperthermophilic archaeon Pyrococcus furiosus represent

105 The hyperthermophilic archaeon Pyrococcus furiosus uses carb

106 Iron is an essential element for the hyperthermophilic archaeon Pyrococcus furiosus, and many

107 a tungstopterin-containing protein from the hyperthermophilic archaeon Pyrococcus furiosus, have bee

108 nder anaerobic, reducing conditions from the hyperthermophilic archaeon Pyrococcus furiosus.

109 e rare biological form of RNA circles in the hyperthermophilic archaeon Pyrococcus furiosus.

110 e report random insertion mutagenesis in the hyperthermophilic archaeon Pyrococcus furiosus.

111 vate synthetase (PpsA) was purified from the hyperthermophilic archaeon Pyrococcus furiosus.

112 nsferase at resolutions up to 1.2 A from the hyperthermophilic archaeon Pyrococcus furiosus.

113 oreductase (NROR) has been purified from the hyperthermophilic archaeon Pyrococcus furiosus.

114 A intein located in the ATPase domain of the hyperthermophilic archaeon Pyrococcus horikoshii is stro

115 The hyperthermophilic archaeon Sulfolobus acidocaldarius exc

116 domain of life, with the discovery that the hyperthermophilic archaeon Sulfolobus has three replicat

117 II chaperonins known as rosettasomes in the hyperthermophilic archaeon Sulfolobus shibatae, are not

118 The hyperthermophilic archaeon Sulfolobus solfataricus emplo

119 The hyperthermophilic archaeon Sulfolobus solfataricus grows

120 The Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus is an

121 ce of a global gene regulatory system in the hyperthermophilic archaeon Sulfolobus solfataricus is de

122 ral modules of the homomultimeric MCM of the hyperthermophilic archaeon Sulfolobus solfataricus.

123 in chromatin structure and regulation in the hyperthermophilic archaeon Sulfolobus solfataricus.

124 noncatalytic subunit, denoted PriX, from the hyperthermophilic archaeon Sulfolobus solfataricus.

125 eavage of mRNA from an invading virus in the hyperthermophilic archaeon Sulfolobus solfataricus.

126 gh mutagenesis of the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus.

127 gh mutagenesis of the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus; Sso7

128 Pyrococcus furiosus is a hyperthermophilic archaeon that grows optimally at 100 d

129 structure of TIM from Thermoproteus tenax, a hyperthermophilic archaeon that has an optimum growth te

130 cture of the ribosomal protein L30e from the hyperthermophilic archaeon Thermococcus celer determined

131 that ribonucleotides are incorporated by the hyperthermophilic archaeon Thermococcus kodakarensis bot

132 The hyperthermophilic archaeon Thermococcus litoralis strain

133 Pyrococcus furiosus is a hyperthermophilic archaeon which grows optimally near 10

134 ncovered a putative MIG protein from another hyperthermophilic archaeon, Aeropyrum pernix.

135 ted Box C/D RNAs from Pyrococcus furiosus, a hyperthermophilic archaeon, into the nuclei of oocytes f

136 DNA in Methanothermus fervidus, a hyperthermophilic archaeon, is constrained into archaeal

137 The hyperthermophilic archaeon, Pyrococcus furiosus, was gro

138 leaves the 5' side of deoxyinosine, from the hyperthermophilic archaeon, Pyrococcus furiosus.

139 ily DNA replication polymerase (Dpo1) in the hyperthermophilic archaeon, Sulfolobus solfataricus, is

140 evolution, have not been determined for any hyperthermophilic archaeon.

141 st description of a nitrate reductase from a hyperthermophilic archaeon.

142 ution assay of homologous recombination in a hyperthermophilic archaeon.

143 ifies a putative primordial Orai sequence in hyperthermophilic archaeons.

144 The open reading frame ST0928 from a hyperthermophilic archaeron Sulfolobus tokodaii was clon

145 aracterized an unusual type IA enzyme from a hyperthermophilic archaeum, Nanoarchaeum equitans, which

146 The hyperthermophilic archeon Pyrococcus furiosus produces a

147 CopA from Archaeoglobus fulgidus is a hyperthermophilic ATPase responsible for the cellular ex

148 methanarchaeon, Methanococcus jannaschii, a hyperthermophilic, autotrophic, and strictly hydrogenotr

149 e gyrase is a DNA topoisomerase specific for hyperthermophilic bacteria and archaea.

150 merases and positive plasmid supercoiling in hyperthermophilic bacteria and archea.

151 existence of peptide-based quorum sensing in hyperthermophilic bacteria and indicate that cellular co

152 .4 A resolution, of the class I BPL from the hyperthermophilic bacteria Aquifex aeolicus (AaBPL) in i

153 ins taken from mesophilic, thermophilic, and hyperthermophilic bacteria are studied using these metho

154 In contrast, archaeal rRNA and that of hyperthermophilic bacteria differ from the rRNA of mesop

155 Our results explain the root location of hyperthermophilic bacteria in the phylogenetic tree for

156 th is more similar to that of A. aeolicus, a hyperthermophilic bacteria.

157 vated C:G content of the rRNA of archaea and hyperthermophilic bacteria.

158 Cpn10 from the deep-branching, hyperthermophilic bacterium Aquifex aeolicus (Aacpn10) s

159 onate-8-phosphate synthase (KDO8PS) from the hyperthermophilic bacterium Aquifex aeolicus differs fro

160 The hyperthermophilic bacterium Aquifex aeolicus has a MutL

161 tural features of the NtrC1 protein from the hyperthermophilic bacterium Aquifex aeolicus suggested t

162 An NAD(+)-dependent DNA ligase from the hyperthermophilic bacterium Aquifex aeolicus was cloned,

163 rt the crystal structures of GatCAB from the hyperthermophilic bacterium Aquifex aeolicus, complexed

164 he crystal structure of a homologue from the hyperthermophilic bacterium Aquifex aeolicus, that share

165 -6-phosphate dehydrogenase (tG6PDH) from the hyperthermophilic bacterium Aquifex aeolicus.

166 usA is also present in the chromosome of the hyperthermophilic bacterium Aquifex aeolicus.

167 shift assays with rRNA and proteins from the hyperthermophilic bacterium Aquifex aeolicus.

168 focus on the energy substrate traffic in the hyperthermophilic bacterium Aquifex aeolicus.

169 eport the crystal structure of TatC from the hyperthermophilic bacterium Aquifex aeolicus.

170 unknown type of protein-only RNase P in the hyperthermophilic bacterium Aquifex aeolicus: Without an

171 is of the crystal structure of MurI from the hyperthermophilic bacterium Aquifex pyrophilus, we perfo

172 us ribose-binding protein, isolated from the hyperthermophilic bacterium Thermoanaerobacter tengconge

173 RAP-PBP (open reading frame tm0322) from the hyperthermophilic bacterium Thermotoga maritima (TM0322)

174 hosphogluconate dehydrogenase (6PGDH) from a hyperthermophilic bacterium Thermotoga maritima from its

175 A thermostable endonuclease V from the hyperthermophilic bacterium Thermotoga maritima has been

176 The genome sequence of the hyperthermophilic bacterium Thermotoga maritima MSB8 pre

177 The hyperthermophilic bacterium Thermotoga maritima MSB8 was

178 ide expression patterns during growth of the hyperthermophilic bacterium Thermotoga maritima on 14 mo

179 The biochemical behavior of RNase III of the hyperthermophilic bacterium Thermotoga maritima was anal

180 The structure of RNase P protein from the hyperthermophilic bacterium Thermotoga maritima was dete

181 of proteins from one specific organism, the hyperthermophilic bacterium Thermotoga maritima, and tho

182 In the genome of the hyperthermophilic bacterium Thermotoga maritima, TM0504

183 es is apparent in the genome sequence of the hyperthermophilic bacterium Thermotoga maritima.

184 tual open reading frame in the genome of the hyperthermophilic bacterium Thermotoga maritima.

185 nt of the MI catabolic pathway in the marine hyperthermophilic bacterium Thermotoga maritima.

186 rsion dynamics in real time in ThyX from the hyperthermophilic bacterium Thermotoga maritima.

187 stallographic studies of the enzyme from the hyperthermophilic bacterium, Aquifex aeolicus.

188 tandemly repeated GTP-binding domains from a hyperthermophilic bacterium, Thermotoga maritima, was cl

189 ermatoga maritima, an evolutionarily ancient hyperthermophilic bacterium.

190 otes, was cloned from Thermotoga maritima, a hyperthermophilic bacterium.

191 CbpA is the first hyperthermophilic cellobiose phosphorylase to be charact

192 Archaea and particularly hyperthermophilic crenarchaea are hosts to many unusual

193 Hyperthermophilic crenarchaea in the genus Pyrobaculum a

194 nstrate that the Thermoproteales, a clade of hyperthermophilic Crenarchaea, lack a canonical SSB.

195 Members of the hyperthermophilic crenarchaea, that lack tubulin-like pr

196 A4 were found to be toxic for members of the hyperthermophilic crenarchaeal genus Sulfolobus.

197 es or genes that are first in operons in the hyperthermophilic crenarchaeon P. aerophilum proceeds mo

198 tion crystal structure of SurEalpha from the hyperthermophilic crenarchaeon Pyrobaculum aerophilum (P

199 and a PCNA homolog (Pa-PCNA1), both from the hyperthermophilic crenarchaeon Pyrobaculum aerophilum (T

200 ionine beta-synthase domain protein from the hyperthermophilic crenarchaeon Pyrobaculum aerophilum.

201 h10b, a member of the Sac10b family from the hyperthermophilic crenarchaeon Sulfolobus shibatae, bind

202 erial-like DnaG primase contained within the hyperthermophilic crenarchaeon Sulfolobus solfataricus (

203 The hyperthermophilic crenarchaeon Sulfolobus solfataricus P

204 erase-Like Lactonases (PLLs) family from the hyperthermophilic crenarchaeon Vulcanisaeta moutnovskia

205 NA polymerases of Sulfolobus solfataricus, a hyperthermophilic crenarchaeon.

206 ea, and an activity has been observed in the hyperthermophilic crenarchaeote Sulfolobus solfataricus.

207 Moreover, the robustness of this hyperthermophilic DH, in terms of both catalytic activit

208 architecture of this protein is uncommon for hyperthermophilic endoglucanases, and two of the four do

209 Thus, the hyperthermophilic enzyme has evolved to have optimum act

210 or directly assaying the activity of another hyperthermophilic enzyme, 1,4-beta-D-glucan glucohydrola

211 AK (ECAK) at 30 degrees C, TNAK is a unique hyperthermophilic enzyme.

212 ut the substrate specificity of two specific hyperthermophilic enzymes and the first test of some nat

213 Herein, the utilization of hyperthermophilic enzymes in a microwave reactor is repo

214 as a general explanation for the activity of hyperthermophilic enzymes.

215 neralizable approach to enzyme recycling for hyperthermophilic enzymes.

216 s been purified from native membranes of the hyperthermophilic eubacterium Aquifex aeolicus.

217 DNA-binding properties of HU from the hyperthermophilic eubacterium Thermotoga maritima are sh

218 We show here that HU from the hyperthermophilic eubacterium Thermotoga maritima HU ben

219 The hyperthermophilic eubacterium Thermotoga maritima posses

220 ort the crystal structure of FliG-C from the hyperthermophilic eubacterium Thermotoga maritima.

221 The hyperthermophilic euryarchaeon Methanococcus jannaschii

222 The hyperthermophilic euryarchaeon Methanococcus jannaschii

223 p in CoM biosynthesis, was identified in the hyperthermophilic euryarchaeon Methanococcus jannaschii.

224 Some hyperthermophilic heterotrophs in the genus Thermococcus

225 Seven hyperthermophilic heterotrophs isolated from low-tempera

226 nd molecular screens, although abundances of hyperthermophilic heterotrophs were relatively high.

227 be partly ameliorated by H(2) syntrophy with hyperthermophilic heterotrophs.

228 essure, which is significantly different for hyperthermophilic (IPPase) and mesophilic (HEWL) protein

229 sitions -40 to +1 of the gdh promoter of the hyperthermophilic marine archaea, Pyrococcus furiosus (P

230 s of this family have been identified in the hyperthermophilic marine archaeon Methanococcus jannasch

231 ha family (family B) DNA polymerase from the hyperthermophilic marine archaeon Thermococcus sp. 9 deg

232 of Thermofilum pendens, a deeply branching, hyperthermophilic member of the order Thermoproteales in

233 CopA from Archaeoglobus fulgidus is a hyperthermophilic member of this ATPase subfamily and is

234 However, a number of hyperthermophilic members of the Kingdom Crenarchaea, in

235 I focus primarily on viruses that infect hyperthermophilic members of the phylum Crenarchaeota.

236 To our knowledge, Amt proteins are the first hyperthermophilic membrane transport proteins shown to b

237 d stability from the hot-start toward modern hyperthermophilic, mesophilic, and psychrophilic organis

238 thanocaldococcus jannaschii--a deeply rooted hyperthermophilic methanogen growing only on H2 plus CO2

239 ences obtained from the obligately anaerobic hyperthermophilic methanogen M. jannaschii.

240 first structures of archaeal G1PDH from the hyperthermophilic methanogen Methanocaldococcus jannasch

241 The genome sequence of the hyperthermophilic methanogen Methanococcus jannaschii co

242 have been detected in a non-nitrogen-fixing hyperthermophilic methanogen, Methanocaldococcus jannasc

243 ata support our estimated H(2) threshold for hyperthermophilic methanogenesis at vents and highlight

244 pure culture H(2) threshold measurements for hyperthermophilic methanogenesis in low-temperature hydr

245 Here we show that ORF MJ1117 of the hyperthermophilic, methanogenic archaeon Methanocaldococ

246 of genome sequence data from mesophilic and hyperthermophilic micro-organisms has revealed a strong

247 Thermotoga maritima is a marine hyperthermophilic microorganism that degrades a wide ran

248 is a large oligomeric protein derived from a hyperthermophilic microorganism that is found near hydro

249 aled that, on a global scale, populations of hyperthermophilic microorganisms are isolated from one a

250 redicted to be particularly energy-rich, and hyperthermophilic microorganisms that broadly reflect su

251 The 16S ribosomal RNA gene of the hyperthermophilic nitrogen fixer, designated FS406-22, w

252 The family 4 uracil-DNA glycosylase from the hyperthermophilic organism Archaeoglobus fulgidus (AFUDG

253 The enzyme from Aquifex aeolicus, a hyperthermophilic organism of ancient lineage, was clone

254 minating unpaired regions in the genome of a hyperthermophilic organism.

255 Proteins from thermophilic and hyperthermophilic organisms are stable and function at h

256 Several hyperthermophilic organisms contain an unusual phosphata

257 haracterisation of this enzyme isolated from hyperthermophilic organisms has led to its adoption as a

258 ete genomes for mesophilic, thermophilic and hyperthermophilic organisms have been sequenced, vastly

259 Hyperthermophilic organisms must protect their constitue

260 Because POP is found in mesophilic and hyperthermophilic organisms, and is distributed among al

261 roteins have been characterized in extremely hyperthermophilic organisms, and most function as repres

262 ungsten, which substitutes for molybdenum in hyperthermophilic organisms, could also be ligated to mo

263 other Archaea or Bacteria, particularly the hyperthermophilic organisms.

264 used frequently in regulatory proteins from hyperthermophilic organisms.

265 ion, biosynthesis and role of fatty acids in hyperthermophilic organisms.

266 sing DNA composition bias in genomes of some hyperthermophilic organisms: simply screening for GC-ric

267 ndidates for a specific association with the hyperthermophilic phenotype.

268 used thioredoxin (Trx) folds, belongs to the hyperthermophilic protein disulfide oxidoreductase famil

269 n enzymatically active, soluble variant of a hyperthermophilic protein that is normally insoluble whe

270 utions to the folding free energy of several hyperthermophilic proteins and their mesophilic homologs

271 aken together, our results suggest that many hyperthermophilic proteins enhance electrostatic interac

272 o 100 degrees C emphasizes the importance in hyperthermophilic proteins of the specific location of i

273 tabilizing forces required for extracellular hyperthermophilic proteins to tolerate high-temperature

274 of improving the low-temperature activity of hyperthermophilic proteins, likely by facilitating the i

275 in 1998, the method has been used to create hyperthermophilic proteins, to evolve novel folded domai

276 ties similar to the natural thermophilic and hyperthermophilic proteins.

277 labile amino-acid residues (i.e. N and Q) in hyperthermophilic proteins.

278 tatic interactions are more favorable in the hyperthermophilic proteins.

279 Here, we describe three hyperthermophilic PrxQ crystal structures originally det

280 ys+1, in an intein precursor composed of the hyperthermophilic Pyrococcus abyssi PolII intein and ext

281 We report the solution NMR structures of the hyperthermophilic Pyrococcus abyssi PolII intein, which

282 idium pasteurianum (Topt = 37 degrees C) and hyperthermophilic Pyrococcus furiosus (Topt = 95 degrees

283 n to activate transcription by its conjugate hyperthermophilic RNA polymerase.

284 Here we present the NMR structure of a hyperthermophilic rubredoxin variant (PFRD-XC4) and the

285 g agent, dextran 20, on the folded states of hyperthermophilic (S16Thermo) and mesophilic (S16Meso) h

286 coli and WrbA from Archaeoglobus fulgidus, a hyperthermophilic species from the Archaea domain, shows

287 jor osmoprotecting metabolite in a number of hyperthermophilic species of archaea and bacteria.

288 d refined the structure of the mIPS from the hyperthermophilic sulfate reducer Archaeoglobus fulgidus

289 (diaphorase) activity was isolated from the hyperthermophilic sulfate-reducing anaerobe Archaeoglobu

290 Archaeoglobus fulgidus, a hyperthermophilic sulfate-reducing Archaeon, contains hi

291 inantly expressed components of SRP from the hyperthermophilic, sulfate-reducing archaeon Archaeoglob

292 onlytic temperate viruses were isolated from hyperthermophilic Sulfolobus hosts, and both viruses sha

293 loned and purified the RadA protein from the hyperthermophilic, sulphate-reducing archaeon Archaeoglo

294 ior previously observed for thermophilic and hyperthermophilic superoxide dismutases but over a lower

295 um, a facultatively aerobic nitrate-reducing hyperthermophilic (T(opt) = 100 degrees C) crenarchaeon.

296 In solution, however, and unlike other hyperthermophilic TIMs, the T.tenax enzyme exhibits an e

297 , it has been suggested that thermophilic or hyperthermophilic (Tm) enzymes have lower catalytic powe

298 Mutants created using the hyperthermophilic TnAK were found to support growth with

299 scuous natural human IgG-binding domain, the hyperthermophilic variant of protein G (HTB1), into a hi

300 , single-point core mutants of a 57-residue, hyperthermophilic variant of the B1 domain of protein G

301 We report here the structure of a hyperthermophilic virus isolated from an archaeal host f