ライフサイエンスコーパス: thermophilic

1 89% in the mesophilic reactor and 85% in the thermophilic.

2 We operated six thermophilic (55 degrees C) bioreactors to test how the

3 The gram-positive, thermophilic, acetogenic bacterium Moorella thermoacetic

4 The recently discovered thermophilic acidobacterium Candidatus Chloracidobacteri

5 We identified peptidoglycan from thermophilic acidophilic bacteria (Alicyclobacillus acid

6 ysis of the recently sequenced genome of the thermophilic actinomycete Thermobifida fusca revealed an

7 that organisms develop diverse strategies of thermophilic adaptation by using, to a varying degree, t

8 ma) relied in their evolutionary strategy of thermophilic adaptation on "sequence-based" mechanism of

9 m a pair of highly homologous mesophilic and thermophilic adenylate kinases, we generated a series of

10 ynamics are investigated in two mutants of a thermophilic alcohol dehydrogenase (ht-ADH): Y25A (at th

11 tic parameters in relation to the homologous thermophilic alcohol dehydrogenase (htADH) from Bacillus

12 A tetrameric thermophilic alcohol dehydrogenase from Bacillus stearot

13 function of temperature in two variants of a thermophilic alcohol dehydrogenase: W87F and W87F:H43A.

14 ransfer step catalyzed by a series of mutant thermophilic alcohol dehydrogenases (ht-ADH), presenting

15 The thermophilic alga C. merolae thrives in extreme environm

16 Naegleria fowleri is a climate-sensitive, thermophilic ameba found in the environment, including w

17 Naegleria fowleri is a climate-sensitive, thermophilic ameba found in warm, freshwater lakes and r

18 iter, is the highest reported thus far for a thermophilic anaerobe, although further improvements are

19 gain insights into mannan degradation by the thermophilic anaerobic bacterium Caldanaerobius polysacc

20 oxidation activator protein (CooA) from the thermophilic anaerobic bacterium Carboxydothermus hydrog

21 ing Thermoanaerobacterium saccharolyticum, a thermophilic anaerobic bacterium that ferments xylan and

22 Clostridium thermocellum is a thermophilic anaerobic bacterium that rapidly solubilize

23 ith 100 mM of [2-(13)C] sodium acetate under thermophilic anaerobic conditions.

24 s and intI1 decreased in all microcosms, but thermophilic anaerobic digestion, alkaline stabilization

25 c digestion, mesophilic anaerobic digestion, thermophilic anaerobic digestion, pasteurization, and al

26 g insight into the physiology and ecology of thermophilic anaerobic methanotrophy and suggesting that

27 ial capability, and acetotrophic pathways in thermophilic anaerobic reactors.

28 The host, Marinitoga piezophila is a thermophilic, anaerobic and piezophilic bacterium isolat

29 ) (ATCC BAA-2073, JCM 16842) is an extremely thermophilic, anaerobic bacterium capable of hydrolyzing

30 Clostridium thermocellum DSM1313 is a thermophilic, anaerobic bacterium with some of the highe

31 We began with the thermophilic, anaerobic, cellulolytic bacterium Caldicel

32 Marinitoga piezophila KA3 is a thermophilic, anaerobic, chemoorganotrophic, sulfur-redu

33 e candidate SAM-I riboswitches isolated from thermophilic and cryophilic bacteria.

34 lap between quinone compositions of distinct thermophilic and halophilic archaea and bacteria may ind

35 lic homologue, BBL, was less stable than the thermophilic and hyper-thermophilic variants (E3BD and P

36 Proteins from thermophilic and hyperthermophilic organisms are stable

37 etal uptake behavior previously observed for thermophilic and hyperthermophilic superoxide dismutases

38 Furthermore, the samples from thermophilic and mesophilic codigesters had different DO

39 ere performed to unfold a homologous pair of thermophilic and mesophilic cold shock proteins at high

40 res distinguish intersubunit linkages of the thermophilic and mesophilic enzyme Bacillus subtilis cho

41 P and plays an adaptive role in catalysis by thermophilic and mesophilic enzymes.

42 thermal growth rate data obtained in a dozen thermophilic and mesophilic organisms.

43 the evolutionarily distant F-type motors of thermophilic and mesophilic origins, and they differ onl

44 ndant in crenarchaeota, which thrive in both thermophilic and nonthermophilic environments, with wide

45 upport the notions that Precambrian life was thermophilic and that proteins can evolve from substrate

46 Here we examine mesophilic to thermophilic AOM in hydrothermal sediments recovered fro

47 sed to show a dramatic preference in certain thermophilic archaea and bacteria for disulfide bonds wi

48 ethods the number of viruses identified from thermophilic Archaea and Bacteria is still very small.

49 oses the process of allopatric speciation in thermophilic Archaea and brings us closer to a generaliz

50 Two thermophilic archaea, strain PK and strain MG, were isol

51 In thermophilic archaea, the HerA helicase and NurA nucleas

52 In thermophilic archaea, the Mre11 and Rad50 genes cluster

53 ole in thermostabilization compared with the thermophilic archaea.

54 eotide binding to the HerA-NurA complex from thermophilic archaea.

55 or the repair of double-strand DNA breaks in thermophilic archaea.

56 evidence that four different mesophilic and thermophilic archaeal RNase P holoenzymes, reconstituted

57 Here we report a role for the thermophilic archaeal Sulfolobus solfataricus SSB (SsoSS

58 re, we report the structure of Dim1 from the thermophilic archaeon Methanocaldococcus jannaschii.

59 ted in vitro the RNase P holoenzyme from the thermophilic archaeon Pyrococcus furiosus (Pfu) and furt

60 studies on the DNA alkyltransferase from the thermophilic archaeon Sulfolobus solfataricus (SsOGT).

61 2, and the topoisomerase 3, SsTop3, from the thermophilic archaeon Sulfolobus solfataricus.

62 a novel, low molecular weight TrxR from the thermophilic archaeon Thermoplasma acidophilum ( taTrxR)

63 e characterization of an RNA ligase from the thermophilic archaeon, Methanobacterium thermoautotrophi

64 t exploits protein engineering to "humanise" thermophilic archeal surrogate proteins as targets for s

65 conditions that allow direct comparison to a thermophilic (B. stearothermophilus) ortholog, Ec-DHFR a

66 Thermophilic Bacillus altitudinis immobilized nanodiamon

67 utant subcomplex of the F(1)-ATPase from the thermophilic Bacillus PS3 (TF(1)), free of endogenous nu

68 The catalytic chemistry of the thermophilic Bacillus stearothermophilus alcohol dehydro

69 uridine at position 54 stabilizes tRNAs from thermophilic bacteria and hyperthermophilic archaea and

70 the physiology and biochemistry of anaerobic thermophilic bacteria and, more lately, to anaerobic fun

71 r instance with a cluster of sulfur-reducing thermophilic bacteria coming together irrespective of th

72 Phenol hydroxylase gene cloning from the thermophilic bacteria Geobacillus thermoglucosidasius wa

73 Extremely thermophilic bacteria of the genus Caldicellulosiruptor

74 esent the crystal structure of BamD from the thermophilic bacteria Rhodothermus marinus refined to 2.

75 very stable members of this superfamily from thermophilic bacteria to use as robust engineerable part

76 e cases of operon differences occurred among thermophilic bacteria, suggesting a much higher incidenc

77 the isolated HisF TIM barrel domain from the thermophilic bacteria, Thermotoga maritima, enabled an N

78 med on Escherichia coli RecA and RecA from a thermophilic bacteria, Thermus thermophilus.

79 history between RNases H from mesophilic and thermophilic bacteria.

80 cycle of F1-ATPase, mostly based on F1 from thermophilic bacteria.

81 ive features as F1 from Escherichia coli and thermophilic bacteria.

82 c bacterial genera analyzed, but absent from thermophilic bacteria.

83 A search of five thermophilic bacterial genomes identified a coded amino

84 by species in the noncellulosomal, extremely thermophilic bacterial genus Caldicellulosiruptor.

85 res of the large terminase nuclease from the thermophilic bacteriophage G20c show that it is most sim

86 Here, we show that photosystem I from a thermophilic bacterium and cytochrome-c(6) can, in combi

87 Thermobifida fusca is a moderately thermophilic bacterium and holds high biocatalytic poten

88 ve determined the structure of NusB from the thermophilic bacterium Aquifex aeolicus and studied the

89 temperatures, we sequenced the genome of the thermophilic bacterium Caldanaerobius polysaccharolyticu

90 The thermophilic bacterium Caldicellulosiruptor bescii uses

91 The genome of the extremely thermophilic bacterium Caldicellulosiruptor kronotskyens

92 ystal structures of a Group III CPN from the thermophilic bacterium Carboxydothermus hydrogenoformans

93 dihydrofolate reductase from the moderately thermophilic bacterium Geobacillus stearothermophilus (B

94 Here, we show that the Cas9 protein from the thermophilic bacterium Geobacillus stearothermophilus (G

95 cterized a thermostable NOS homolog from the thermophilic bacterium Geobacillus stearothermophilus (g

96 a nisin analog encoded on the genome of the thermophilic bacterium Geobacillus thermodenitrificans N

97 hosphogluconate dehydrogenase (6PGDH) from a thermophilic bacterium Moorella thermoacetica with rever

98 xide/oxygen binding (H-NOX) protein from the thermophilic bacterium Thermoanaerobacter tengcongensis,

99 teractions of SmpB.SsrA orthologues from the thermophilic bacterium Thermoanaerobacter tengcongensis.

100 glC ORF encoding a beta-glucosidase from the thermophilic bacterium Thermobifida fusca and inserted i

101 An ArsI ortholog, TcArsI, from the thermophilic bacterium Thermomonospora curvata was expre

102 an extensive and diverse sugar kinome in the thermophilic bacterium Thermotoga maritima.

103 n of gene expression during infection of the thermophilic bacterium Thermus thermophilus HB8 with the

104 T4P and natural transformation of DNA in the thermophilic bacterium Thermus thermophilus requires a u

105 ntibiotic-resistant mutants of the extremely thermophilic bacterium Thermus thermophilus, a species w

106 sis of replication fidelity in the extremely thermophilic bacterium Thermus thermophilus.

107 interacting mutations in the ribosome of the thermophilic bacterium Thermus thermophilus.

108 he dioxygen complex of the NOS enzyme from a thermophilic bacterium, Geobacillus stearothermophilus (

109 s (ECs) of RNA polymerase from the extremely thermophilic bacterium, Thermus thermophilus.

110 nteract with one another to generate extreme thermophilic behavior and are responsible for approximat

111 hat three residues in the active site of the thermophilic beta-1,4-xylanase from Nonomuraea flexuosa

112 d to ferment milk to obtain yogurt belong to thermophilic, bile-sensitive species of lactic acid bact

113 enes creates unprecedented opportunities for thermophilic bioalcohol production.

114 Thermophilic Bst DNA polymerase had the highest specific

115 gment, 3'-->5' exo(-) Klenow DNA polymerase, thermophilic Bst DNA polymerase large fragment, Thermina

116 Thermostable enzymes and thermophilic cell factories may afford economic advantag

117 s by the Firmicutes and Bacteroidetes in the thermophilic cellulolytic consortia is proposed.

118 ocellum wild-type strain YS is an anaerobic, thermophilic, cellulolytic bacterium capable of directly

119 Clostridium thermocellum is an anaerobic, thermophilic, cellulolytic, and ethanogenic bacterium.

120 These values reflect the thermophilic characteristics of the UVrABC nuclease comp

121 icus UBT1 has been described as a moderately thermophilic chemolithoautotroph with a novel nitrogenas

122 The thermophilic chemolithotroph, Aquifex aeolicus, expresse

123 ntigs from an in situ-enriched cellulolytic, thermophilic community.

124 rich source for additional investigations of thermophilic composting microbiology.

125 Under thermophilic conditions (60 degrees C), T. pseudethanoli

126 to microcrystalline cellulose under aerobic, thermophilic conditions using green waste compost as the

127 At thermophilic conditions, a higher efficiency of CH4 prod

128 artial pressure between 0.25 and 1 atm under thermophilic conditions.

129 re specifically adapted to switchgrass under thermophilic conditions.

130 figuration was tested at both mesophilic and thermophilic conditions.

131 hows high homology with mesophilic and other thermophilic cpn10 sequences, except for a 25-residue C-

132 The Y-family DNA polymerase Dpo4, from the thermophilic crenarchaeon Sulfolobus solfataricus P2, of

133 overy of ammonia oxidation by mesophilic and thermophilic Crenarchaeota and the widespread distributi

134 enomes of the two closely related freshwater thermophilic cyanobacteria Synechococcus sp. strain JA-3

135 re we describe a novel pair of Phys from two thermophilic cyanobacteria, Synechococcus sp. OS-A and O

136 ly available crystal structures of PSII from thermophilic cyanobacteria.

137 The genomes of two closely related thermophilic cyanobacterial isolates, designated Synecho

138 Deep sequencing of a thermophilic cyanobacterial population and analysis of t

139 e discovered a tetrameric form of PSI in the thermophilic cyanobacterium Chroococcidiopsis sp TS-821

140 agnesium chelatase H subunit, ChlH, from the thermophilic cyanobacterium Thermosynechococcus elongatu

141 ize the cyanobacteriochrome Tlr0924 from the thermophilic cyanobacterium Thermosynechococcus elongatu

142 highly active dimeric b(6)f complex from the thermophilic cyanobacterium Thermosynechococcus elongatu

143 complex of oxygenic photosynthesis from the thermophilic cyanobacterium, Mastigocladus laminosus, an

144 sis of the cytochrome b(6)f complex from the thermophilic cyanobacterium, Mastigocladus laminosus, in

145 cally improve the orientation of PSII from a thermophilic cyanobacterium, Thermosynechococcus elongat

146 Unfolding thermodynamics of a thermophilic cytochrome c552 from Hydrogenobacter thermo

147 tions in the substrate binding region of the thermophilic cytochrome P450 enzyme CYP119.

148 nd finally, how he extended these studies to thermophilic desert ants in other deserts of the world,

149 centered on Cataglyphis have rendered these thermophilic desert ants model organisms in the study of

150 are either unchanged or more flexible in the thermophilic DHFR from B. stearothermophilus.

151 y (HDX-MS) as a function of temperature in a thermophilic dihydrofolate reductase from Bacillus stear

152 rmincola ferriacetica is a recently isolated thermophilic, dissimilatory Fe(III)-reducing, Gram-posit

153 rporated into DNA by selected mesophilic and thermophilic DNA polymerases and the resulting primer ex

154 In planta expression of a thermophilic endoglucanase (AcCel5A) reduces recalcitran

155 milar communities were observed in companion thermophilic enrichments on insoluble wheat arabinoxylan

156 ORFs from other organisms living in the same thermophilic environment to produce the type strain of P

157 cus primase may represent an adaptation to a thermophilic environment.

158 supporting the idea that the LUA lived in a thermophilic environment.

159 nzyme from E. coli (EcDHFR) and the dimeric, thermophilic enzyme from Thermotoga maritima (TmDHFR).

160 of 0.96) with the relative activity of this thermophilic enzyme.

161 ponding mesophilic (Ms) enzymes, because the thermophilic enzymes are less flexible (assuming that fl

162 ion in mesophiles can be aided by the use of thermophilic enzymes as starting points for protein desi

163 ngle-molecule measurements of mesophilic and thermophilic enzymes at 70 degrees C.

164 ons presume that the reduced dynamics of the thermophilic enzymes is the reason for their reduced cat

165 g kinetic stabilization as observed for some thermophilic enzymes.

166 d oligonucleotide, an [alpha-(32)P]dNTP, and thermophilic enzymes.

167 idues, in contrast with previously described thermophilic enzymes.

168 studies of RNA polymerases (RNAPs) from the thermophilic eubacteria Thermus aquaticus (Taq) and Ther

169 ttle is known about nucleoid organization in thermophilic eubacteria.

170 -GlcNAc cycling enzymes in the genome of the thermophilic eubacterium Thermobaculum terrenum.

171 ved crystal structures of free CRM1 from the thermophilic eukaryote Chaetomium thermophilum.

172 e, these genomes are the first described for thermophilic eukaryotes and the first complete telomere-

173 nced by structural adaptations specific to a thermophilic existence.

174 obacter pseudethanolicus 39E (ATCC 33223), a thermophilic, Fe(III)-reducing, and fermentative bacteri

175 cyanobacterium Synechocystis PCC6803 and the thermophilic, fermentative bacterium Pelotomaculum therm

176 ponse to the nonconserved E77 present in the thermophilic Fpg sequences used for the crystallography

177 ntral nervous system infection caused by the thermophilic free-living ameba Naegleria fowleri.

178 potential reservoir of thermostable enzymes, thermophilic fungi are amenable to manipulation using cl

179 e we describe and compare the genomes of two thermophilic fungi, Myceliophthora thermophila and Thiel

180 the junction-resolving enzyme GEN1 from the thermophilic fungus Chaetomium thermophilum and expresse

181 res of the separase protease domain from the thermophilic fungus Chaetomium thermophilum, alone or co

182 e most stable parent, CBH II enzyme from the thermophilic fungus Humicola insolens, which suggests th

183 estigated two related Dicer enzymes from the thermophilic fungus Sporotrichum thermophile.

184 Thermophilic fungus Thermoascus aurantiacus (CBMAI 756)

185 We characterized a novel BVMO from the thermophilic fungus Thermothelomyces thermophila, determ

186 n, which binds the motor heavy chain, from a thermophilic fungus.

187 gh resolution structure was determined for a thermophilic glutamate transporter.

188 rAB is a heterodimeric ABC exporter from the thermophilic Gram-negative eubacterium Thermus thermophi

189 complex, and the reaction center (RC) in the thermophilic green phototrophic bacterium Chloroflexus a

190 ne boundary, while trans-Arctic dispersal in thermophilic groups may have been limited to the early E

191 e because it is halophilic, alkaliphilic and thermophilic, growing optimally at 3.5 M Na(+), pH(55 de

192 s in the lake, including both mesophilic and thermophilic habitats, had multiple virophage genotypes.

193 ion/proton antiporters in the genome of this thermophilic haloalkaliphile.

194 mined the crystal structure of DGGR from the thermophilic heterotrophic archaea Thermoplasma acidophi

195 and high temperature unfolding kinetics of a thermophilic homolog, Thermobifida fusca protease A (TFP

196 t thermal constraints by adding a moderately thermophilic homologue to the previously characterized m

197 o has a surprisingly low DeltaC(p), like the thermophilic homologue.

198 end the frontier of metabolic engineering in thermophilic hosts, have the potential to significantly

199 cterized the conformational stability of the thermophilic HPr proteins using thermal and solvent dena

200 c complementation of yeast with prokaryotic, thermophilic IGPS.

201 P. horikoshii ligase is thermophilic in vitro, with optimal adenylyltransferase

202 -hairpin that is unique in the structures of thermophilic inteins.

203 experimental biogas plant composed of three thermophilic leach bed reactors (51-56 degrees C) follow

204 etate formation at different OLRs within the thermophilic leach bed reactors as well as a negligible

205 umber of organisms with photoautotrophic and thermophilic lifestyles.

206 while the folding core region determines the thermophilic-like behavior of this family of proteins, t

207 th the termination of conditions required by thermophilic lineages.

208 Archaea such as Metallosphaera sedula are thermophilic lithoautotrophs that occupy unusually acidi

209 y enhancing the mechanistic understanding of thermophilic lithoautotrophy.

210 ly been solved to 3.0-A resolution using the thermophilic Mastigocladus laminosus whose genome has no

211 Agr-type cyclic peptide to be produced by a thermophilic member of the Firmicutes.

212 genome of strain Exiguobacterium sp. AT1b, a thermophilic member of the genus Exiguobacterium whose r

213 autotrophicus, two strictly hydrogenotrophic thermophilic methanogens.

214 studies that have suggested that, in certain thermophilic microbes, disulfide bonds play a key role i

215 tabilizing intracellular proteins in certain thermophilic microbes.

216 izing beta-1,4-galactosidase activity from a thermophilic microbial community lysate.

217 45 degrees C) resulted in the emergence of a thermophilic microbial community specialized in fermenta

218 The alpha-galactosidase AgaA from the thermophilic microorganism Geobacillus stearothermophilu

219 The use of thermophilic microorganisms as biocatalysts for electrom

220 iments of the Guaymas Basin are inhabited by thermophilic microorganisms, including anaerobic methane

221 cations of phenotype arrays to anaerobic and thermophilic microorganisms, use of the plates in stress

222 (Moapa coriacea) is a critically endangered thermophilic minnow native to the Muddy River ecosystem

223 Thermus thermophilus is a thermophilic model organism distantly related to the mes

224 anosarcina mazei Go1 A-ATP synthase, and the thermophilic motor alpha3beta3gamma, from Geobacillus st

225 site loops at the mesophilic ScOMPDC and the thermophilic MtOMPDC.

226 Clostridium thermocellum is a thermophilic, obligately anaerobic, gram-positive bacter

227 ect numerous redox enzymes, particularly for thermophilic ones, which can generate NAD(P)H reacted wi

228 two mutations per genome per replication for thermophilic ones.

229 In particular, it has been suggested that thermophilic or hyperthermophilic (Tm) enzymes have lowe

230 to design RNases H that display the desired thermophilic or mesophilic properties, as defined by the

231 Here we report that P450s derived from a thermophilic organism and containing an iridium porphyri

232 [a]P-N2-dG (G*), by UvrABC nuclease from the thermophilic organism Bacillus caldotenax was investigat

233 from the mesophilic organism E. coli and the thermophilic organism T. thermophilus.

234 :quinone oxidoreductase (complex I) from the thermophilic organism Thermus thermophilus HB8 has been

235 Cel7A from the thermophilic organism was moderately more activated by t

236 hydrofolate reductase (DHFR) from a moderate thermophilic organism, Bacillus stearothermophilus, has

237 first structure for a monomeric DHFR from a thermophilic organism, indicating a high degree of conse

238 rium did not fix nitrogen and probably was a thermophilic organism.

239 plain the high optimal growth temperature in thermophilic organisms and are in excellent quantitative

240 Proteins from thermophilic organisms are able to function under condit

241 ochondrial carriers from both mesophilic and thermophilic organisms exhibit poor stability in mild de

242 coming limitations include sourcing CAs from thermophilic organisms, using protein engineering to evo

243 proteins from psychrophilic, mesophilic, or thermophilic organisms.

244 grees C, which is more akin to proteins from thermophilic organisms.

245 the previously characterized mesophilic and thermophilic pair.

246 Interglacial deposits contain thermophilic palms suggesting warm and wet climates.

247 For the most part, thermophilic patterns in the genome and proteome of A. c

248 DNA binding and cleavage using TerL from the thermophilic phage P74-26.

249 bacterial RNAP-binding proteins encoded by a thermophilic phage.

250 g point, Bryant et al. have discovered a new thermophilic phototroph from a poorly characterized bact

251 genus Caldicellulosiruptor contains the most thermophilic, plant biomass-degrading bacteria isolated

252 This composting exhibits a sustained thermophilic profile (50 degrees C to 75 degrees C), whi

253 ), we discovered three related proteins from thermophilic prokaryotes, which we grouped into a novel

254 hioarsenate species transformation by (hyper)thermophilic prokaryotes.

255 terise the transition state for folding of a thermophilic protein at the relatively high temperature

256 The slower unfolding of the thermophilic protein could be attributed to ion pair for

257 The moderately thermophilic protein has a melting temperature (T(m)) si

258 on of the MD trajectories indicates that the thermophilic protein samples conformations productive fo

259 low the same unfolding pathway, but with the thermophilic protein showing much slower unfolding.

260 capacity upon unfolding (DeltaC(p)) for the thermophilic protein.

261 behaviors to those in the simulation of the thermophilic protein.

262 derstand the origin of enhanced stability in thermophilic proteins by analyzing thermodynamic data fo

263 ise comparisons of homologous mesophilic and thermophilic proteins can help to identify the energetic

264 structural features normally associated with thermophilic proteins such as an increase in salt bridge

265 re to understand the dynamical properties of thermophilic proteins under pressure.

266 d state is encoded in the sequences of these thermophilic proteins, we subjected the RNase H from Chl

267 idual structure in the unfolded state of the thermophilic proteins.

268 d to differ between the mesophilic and hyper-thermophilic proteins.

269 cellulase enzyme, an endoglucanase from the thermophilic Pyrococcus horikoshii.

270 Cel7A) from mesophilic Hypocrea jecorina and thermophilic Rasamsonia emersonii and two variants of th

271 ow fiber membrane (HFM) module in continuous thermophilic reactors, CO did not inhibit the process ev

272 was almost no phycobilisome mobility in the thermophilic red alga Cyanidium caldarium that was not c

273 unction in mesophilic red algae; however, in thermophilic red algae, this process is replaced by nonp

274 antennae can be regulated in mesophilic and thermophilic red algae.

275 stablishes a system to comprehensively study thermophilic replisomes and evolutionary links between a

276 emical attractants E. coli exhibits a steady thermophilic response, the magnitude of which decreases

277 ormational basis for reduced activity of the thermophilic ribonuclease HI enzyme from Thermus thermop

278 y important when using crystal structures of thermophilic ribosomes to interpret genetic results from

279 vable that phenotypes of mutations affecting thermophilic ribosomes, for instance, will be influenced

280 In this work, we describe the ability of the thermophilic RNA ligase MthRnl from Methanobacterium the

281 In reported structures of thermophilic RNA polymerase, the G1249 residue is locate

282 Thermobifida fusca is a moderately thermophilic soil bacterium that belongs to Actinobacter

283 he genome of Heliobacterium modesticaldum, a thermophilic species belonging to this unique group of p

284 ectra (MALDI-TOF-MS) of cell lysates of five thermophilic species of Campylobacter: jejuni, coli, lar

285 served composition of the same set in extant thermophilic species than in extant mesophilic species,

286 roteins have been analyzed from a variety of thermophilic species, suggesting different structural fe

287 sed as abrupt shifts to regimes dominated by thermophilic species.

288 se trends in SRR, members of the potentially thermophilic, spore-forming, Desulfotomaculum were detec

289 inated by a single phylotype affiliated with thermophilic sulfate reducers belonging to Firmicutes.

290 Thermophilic sulfate reduction, however, had a higher ac

291 Dpo4, an archetypal Y-family member from the thermophilic Sulfolobus solfataricus, was used to extend

292 Sac10b homologs in thermophilic Sulfolobus species are very abundant.

293 ferences in the catalytic parameters between thermophilic Thermus aquaticus and mesophilic Deinococcu

294 RNA polymerase (RNAP) from thermophilic Thermus aquaticus is characterized by highe

295 tro at high temperature, making it the first thermophilic topoisomerase IB characterized so far.

296 (rRNA and tRNAs) in A. cellulolyticus showed thermophilic traits suggesting the importance of adaptat

297 Synechococcus OS-B', a thermophilic unicellular cyanobacterium, recently isolat

298 ease of ordered water molecules and, for the thermophilic variant, a relaxation of monomer-tertiary s

299 less stable than the thermophilic and hyper-thermophilic variants (E3BD and POB, respectively).

300 the novel genomes, one belongs to a putative thermophilic virus infecting the bacterium Hydrogenobacu