ライフサイエンスコーパス: thermostable

1 mostability and the DGK peptide is the least thermostable.

2 capacity to incorporate iron, and were less thermostable.

3 are monomeric, photochromic, and remarkably thermostable.

4 ow-salt buffer at pH 5.7-7.7, HDL are highly thermostable.

5 SsMTAPII is extremely thermoactive and thermostable.

6 alized by atomic force microscopy) which are thermostable.

7 nase-C for fructose but is considerably more thermostable.

8 atalytic domain of TbCet1 is extraordinarily thermostable.

9 gth F508del-CFTR was about 10 degrees C less thermostable.

10 A novel, thermostable adaptation of the coupled-enzyme assay for

11 pt, we have created a fusion consisting of a thermostable aldo-keto reductase, two alpha-helical leuc

12 matic hydrolysis, different from the case of thermostable alpha-amylase.

13 ty predictably into a completely de novo and thermostable alpha-helical barrel, which comprises seven

14 oyl group, and the subunits assembled into a thermostable (alphabeta)(3) complex.

15 We have now developed a thermostable, aluminum-adjuvant-containing formulation o

16 and biophysical characterization of the most thermostable amylosucrase identified so far, the amylosu

17 y, we show CagY(rpt2) to comprise two highly thermostable and acid-stable alpha-helical structural mo

18 The protein is highly thermostable and exhibits a clear cold unfolding transit

19 Highly thermostable and expressed at >500 mg/L E. coli culture,

20 Additionally, CelA is extremely thermostable and highly active at elevated temperatures,

21 This skilled production of highly thermostable and long-lasting rock art paint represents

22 ybrid thermophilic/mesophilic enzyme that is thermostable and more active than the wild-type thermoph

23 Astexin-3 is highly thermostable and resists unthreading after extensive hea

24 and fatty-acid glycerol esters are extremely thermostable and retain internal RNA and DNA oligonucleo

25 d a stabilizing salt bridge cluster, (ii) is thermostable and shows a folding mechanism similar to th

26 This enzyme was also found to be remarkably thermostable and was resistant to H2O2 at concentrations

27 n headpiece (HP67) harbors a highly helical, thermostable, and autonomously folding subdomain in the

28 rcSso7d-based binders are highly expressed, thermostable, and monomeric, suggesting that the hyperst

29 serpin that folds reversibly, is functional, thermostable, and polymerization resistant.

30 nstrate that the Pa-UDGa-Pa-PCNA1 complex is thermostable, and two hydrophobic amino acid residues on

31 icles that are monodispersed, biocompatible, thermostable, and water-soluble, allowing diverse membra

32 plex with 5'-overhangs, are extended using a thermostable archaeal DNA polymerase.

33 olfataricus P2 DNA polymerase IV (Dpo4) is a thermostable archaeal enzyme and a member of the error-p

34 tion of a highly efficient, promiscuous, and thermostable artificial enzyme that catalyzes a diverse

35 Here the authors show a highly efficient and thermostable artificial enzyme that catalyzes a diverse

36 plex II overproduced in Escherichia coli are thermostable as isolated, but moderately sensitive to re

37 des 1 to 754 were dimeric, with a linkage as thermostable as that between dimers of intact genomic RN

38 152S/C153S/C387S/C430A (mutant SSCSA) was as thermostable as the wild-type enzyme.

39 The 1D and 2D RIDC3 assemblies are highly thermostable as well, remaining intact at up to approxim

40 dary structure of calreticulin is remarkably thermostable at a given calcium concentration.

41 A. aeolicus PilT was shown to be a thermostable ATPase with a specific activity of 15.7 nmo

42 showed that folding of the smaller and more thermostable Azoarcus ribozyme is well described by two

43 primed template directly in a crystal of the thermostable Bacillus DNA polymerase I.

44 In particular, spectroscopic studies of thermostable bacterial NOSs have revealed key oxyheme in

45 ing, we established in vitro packaging for a thermostable bacteriophage, P23-45 of Thermus thermophil

46 A purely exo-acting thermostable beta-amylase from Clostridium thermosulfuro

47 aneous assembly as a homotrimer, producing a thermostable beta-trefoil architecture.

48 , pure symmetry in the design of a foldable, thermostable beta-trefoil fold is possible.

49 neous catalysis, yielding high-surface area, thermostable biochemical structures readily adaptable to

50 hich retains actin-binding activity, is more thermostable but, interestingly, does not exhibit the pa

51 ule with thermolabile N-terminal domains and thermostable C-terminal domains.

52 ORFs for ethanolamine utilization, thermostable carboxypeptidase, gamma glutamyl-transpepti

53 Thirty-one of 31 predicted thermostable CBH II chimeras have thermal inactivation t

54 llulases) has yielded a collection of highly thermostable CBH II chimeras.

55 The total of 15 validated thermostable CBH II enzymes have high sequence diversity

56 nucleases and proteases, this reconstituted thermostable cell-free protein synthesis system may enab

57 A bacterial thermostable cellulase, the endo-1,4-beta-D-glucanase E1

58 . fusca is a model organism for the study of thermostable cellulases and is a major degrader of plant

59 a model organism for the study of secreted, thermostable cellulases.

60 nto a set of general rules for the design of thermostable CHA circuits with high signals and low nois

61 ication processes and demonstrating superior thermostable characteristics and immunogenicity, this st

62 Biochemical and X-ray scattering studies of thermostable CheA from Thermotoga maritima determine tha

63 Eight of eight thermostable chimeras assayed hydrolyze the solid cellul

64 Selected purified thermostable chimeras hydrolyzed phosphoric acid swollen

65 eries, both cell types express predominantly thermostable class I and are critically dependent on TAP

66 To obtain thermostable clones without loss of activity, the librar

67 We demonstrate that the designed, thermostable, closed S trimer can be used in serological

68 ficant thermal resilience assessed as a high thermostable "coked" fraction in thermal carbon analysis

69 zed in recent advances in the development of thermostable, colorfast biomaterial pigments.

70 ranslated trespin forms detergent-stable and thermostable complexes with plasmin and elastase but not

71 R domain is capable of forming higher-order, thermostable complexes with VgrG, yet these assemblies f

72 an a chromogenic analog, using a continuous, thermostable coupled enzyme assay.

73 The T213A/C317H variant of the thermostable CYP119 from Sulfolobus acidocaldarius maint

74 ineered a hemoprotein biocatalyst based on a thermostable cytochrome c that directly transforms alken

75 PCR) that relied on the use of the extremely thermostable Deep Vent polymerase.

76 those in natural collagen and are remarkably thermostable, despite the absence of higher-order associ

77 The existence of a thermostable dimeric intermediate of P61A FIS was furthe

78 Here, we report that thermostable direct haemolysin (TDH), an exotoxin of the

79 Among them are the thermostable direct hemolysin (TDH) and the TDH-related

80 ar beta-hemolysin phenotype, we surmise that thermostable direct hemolysin (TDH) plays a limited role

81 mutations in S that allow the production of thermostable, disulfide-bonded S-protein trimers that ar

82 of the template, oligonucleotides, salt, and thermostable DNA ligase concentrations increased the spe

83 ted detector probes, one for each SNP, and a thermostable DNA ligase.

84 arious length initiating primers, with three thermostable DNA ligases: Thermus thermophilus (Tth), Th

85 hundreds to thousands of nucleotides by the thermostable DNA polymerase from Thermococcus litoralis

86 ion, we attempted to evolve a high-fidelity, thermostable DNA polymerase to use RNA templates efficie

87 s method to construct genes encoding a small thermostable DNA polymerase, a highly repetitive DNA seq

88 s, we previously reported the evolution of a thermostable DNA polymerase, SFM4-3, that more efficient

89 Using a thermostable DNA polymerase, SFM4-3, which was previousl

90 -binding site of the exonuclease domain of a thermostable DNA polymerase.

91 ately, the relatively high fidelities of the thermostable DNA polymerases commonly used for PCR resul

92 Thermostable DNA polymerases isolated from archaeal orga

93 II mutants suggest that, in contrast to the thermostable domains, the thermolabile domains are able

94 ification and characterization of five novel thermostable Dpo4-like enzymes from Acidianus infernus,

95 The inclusion of thermostable Dpo4-like polymerases in PCRs, therefore, a

96 the consequences of a method that utilizes a thermostable duplex-specific nuclease for reducing the h

97 ller version of N35CCG-N13), and the minimal thermostable ectodomain core of gp41 in its six-helix bu

98 fused in the helical phase onto the minimal thermostable ectodomain of gp41) is described.

99 f gp41 fused in helical phase to the minimal thermostable ectodomain of gp41, while the latter compri

100 The transformation method depends on a thermostable endogenous selection marker operating at hi

101 The thermostable endoglucanase EGPh from the hypothermophili

102 (C)-like domains of TprC and TprI are highly thermostable, endowing the full-length proteins with imp

103 omologue of ht-ADH, ps-A25Y, leads to a more thermostable enzyme and a change in the rate-determining

104 capable of enhancing the folding yield of a thermostable enzyme at elevated temperature (55 degrees

105 rmus aquaticus DNA polymerase I (Taq Pol), a thermostable enzyme commonly used for DNA amplification

106 aracoccus sp. strain DMF is a halophilic and thermostable enzyme comprising a multimeric complex of t

107 SOR is a thermostable enzyme that reduces O(2)(-) in a one-electr

108 s of Dr-OPH and have found it to be a highly thermostable enzyme, remaining active after 3 h of incub

109 Thermostable enzymes and thermophilic cell factories may

110 high power output could be achieved by using thermostable enzymes at elevated temperatures.

111 f between enzyme stability and activity with thermostable enzymes being less efficient catalysts that

112 Thermostable enzymes combine catalytic specificity with

113 Amplification was catalyzed with two thermostable enzymes for 30-60 minutes under isothermal

114 Both thermostable enzymes self-cleave at conserved serine res

115 g is a promising source of new organisms and thermostable enzymes that may be helpful in environmenta

116 ragment of DNA polymerase I, and we identify thermostable enzymes that process them efficiently at hi

117 ission maximum of 546 nm, providing a set of thermostable enzymes whose bioluminescence maxima were s

118 lic proteins is a valid strategy to engineer thermostable enzymes with significant low-temperature ac

119 The reaction employs two thermostable enzymes, BST-polymerase and duplex-specific

120 e from representing a potential reservoir of thermostable enzymes, thermophilic fungi are amenable to

121 which is also a characteristic of naturally thermostable enzymes.

122 tic potential as a source for several highly thermostable enzymes.

123 Therefore, engineered thermostable Est55 is a candidate for use with irinoteca

124 LeuT, a thermostable eubacterial NSS homolog, has been exploited

125 They are thermostable even at temperatures of up to 200 degrees C

126 a particular fold, and moreover to engineer thermostable exemplars of particular folds.

127 e on the isolation and characterization of a thermostable F420: NADPH oxidoreductase (Tfu-FNO) from T

128 Here, we demonstrate that the thermostable family B DNA polymerase from Pyrococcus fur

129 study, we first created a mutant (mtfl) of a thermostable firefly luciferase (tfl) bearing the peroxi

130 ngle soluble fusion proteins consisting of a thermostable firefly luciferase variant that catalyze ye

131 By using thermostable fluorescent probes together with this syste

132 Dathail was evolved from the extremely thermostable fluorescent proteins thermal green protein

133 S-OVA, a more thermostable form of ovalbumin (OVA), was formed from na

134 Herein, we characterize the most thermostable form of this enzyme to date, CocE-L169K/G17

135 be grouped into either a thermosensitive or thermostable fraction for both egg- and MDCK-grown virus

136 the proteolytic activity, in particular the thermostable fraction, should be considered as a target

137 for the first time, we engineered CHA to be thermostable from 37 to 60 degrees C and in consequence

138 Generating this group of diverse, thermostable fungal CBH II chimeras is the first step in

139 h an increased lifetime in human plasma, the thermostable GeoCas9 provides the foundation for improve

140 We describe the use of a thermostable glucokinase in a novel competitive fluoresc

141 ratures was developed by utilizing a "wired" thermostable glucose-6-phosphate dehydrogenase (tG6PDH)

142 ill allow high-throughput screening of other thermostable glucose-producing enzymes, including those

143 This is the first report of a thermostable glucostat from a marine hyperthermophile.

144 regulates transcription of mgfp5-ER encoding thermostable green fluorescent protein (GFP) or with a s

145 dth of cellular ligands for IFIT5 by using a thermostable group II intron reverse transcriptase for R

146 Here, we used thermostable group II intron reverse transcriptase seque

147 Here we present our observations using thermostable group II intron reverse transcriptase seque

148 ve base methylations and a highly processive thermostable group II intron reverse transcriptase to ov

149 odes DMS modifications as mismatches using a thermostable group II intron reverse transcriptase.

150 Thermostable group II intron reverse transcriptases (TGI

151 loits a novel template-switching activity of thermostable group II intron reverse transcriptases (TGI

152 tly capture acceptor RNAs or DNAs, we used a thermostable group II intron RT (TGIRT; GsI-IIC RT) that

153 ermined a crystal structure of a full-length thermostable group II intron RT in complex with an RNA t

154 Instead, it uses a new type of thermostable GTP cyclohydrolase enzyme that produces 2-a

155 g a premature termination codon in ORF1 or a thermostable hairpin in the inter-ORF spacer reduces ORF

156 functional in isolation, but together form a thermostable heterooligomeric Rca that can use both alph

157 ophilus (BstHPr) was established as the most thermostable homologue and also the homologue with highe

158 ny rationally designed proteins end up being thermostable, how to intentionally design de novo, therm

159 s basis, a H(2)-powered fuel cell with hyper-thermostable hydrogenase (SHI) as the anodic catalyst wa

160 sdAbs are small, compact, thermostable immunoglobulin elements capable of binding

161 we demonstrate that lipids render ISVPs less thermostable in a virus concentration-dependent manner.

162 esting that the GP64 trimers were relatively thermostable in the absence of the intermolecular disulf

163 ature isothermal amplification method with a thermostable invertase, we can directly transduce Middle

164 However, there is no thermostable isoamylase stable enough for simultaneous s

165 in the target gene and were ligated using a thermostable ligase enzyme only when the genomic DNA car

166 er require tedious purification steps or use thermostable ligases that can generate side products dur

167 ilus P1 lipase provides a template for other thermostable lipases, and offers insight into mechanisms

168 To that end, we investigated a thermostable LS from Aquifex aeolicus (AaLS) and found t

169 Here, we investigate the properties of the thermostable M/R complex from the archaeon Sulfolobus ac

170 and -2, respectively) were induced to form a thermostable (melting temperature, approximately 90 degr

171 The thermostable MJ1101 protein catalyzed both the acetylati

172 (WT) enzyme, several active site mutants, a thermostable mutant (12X-PTDH), and a thermostable mutan

173 ning with a previously reported red-emitting thermostable mutant and using mutagenesis techniques, we

174 acement amplification of DNA that utilizes a thermostable mutant of the phi29 polymerase.

175 nts, a thermostable mutant (12X-PTDH), and a thermostable mutant with dual cofactor specificity (NADP

176 e WT enzyme, the active site mutants, or the thermostable mutant.

177 t factor C5a receptor 1 retrieved 36% of the thermostable mutants in the top 50 prioritized mutants c

178 novel design strategy can be used to develop thermostable mutants of any protein.

179 of states profiles are similar overall, both thermostable mutants show increased populations of the v

180 The thermostable mutants tolerate short-chain detergents, su

181 sient transfection and the identification of thermostable mutants using a thermostability assay that

182 ifferent machine learning methods to predict thermostable mutations ahead of experiments.

183 A blind prediction for thermostable mutations of the complement factor C5a rece

184 Incubation of excess benzyl alcohol with thermostable N-benzyl-N-nitrosoamides at ambient tempera

185 aryotic thermophiles as source for purifying thermostable native macromolecular complexes with an emp

186 These thermostable Nbs can be rapidly produced in bulk from mi

187 t of thermostability, and the HN gene from a thermostable NDV could be engineered into a thermolabile

188 bile NDV vaccine strain for developing novel thermostable NDV vaccine.

189 Thermostable Newcastle disease virus (NDV) vaccines have

190 have cloned, expressed, and characterized a thermostable NOS homolog from the thermophilic bacterium

191 d the enzymatic hydrolysis of nylon-6 by the thermostable NylC mutant.

192 spring metagenomic sampling, and additional thermostable orthologs as a source of natural diversity,

193 ) dependent glucose dehydrogenase (GDH) is a thermostable, oxygen insensitive redox enzyme used in bi

194 I), have been analyzed in the reaction of a thermostable P450, CYP119, with meta-chloroperoxybenzoic

195 ictions, we constructed a family of 44 novel thermostable P450s with half-lives of inactivation at 57

196 ility between the A4V mutant protein and its thermostable parent (HSOD-AS), in which free cysteine re

197 activation temperatures higher than the most thermostable parent CBH II, from Humicola insolens, and

198 The recombinant Taq DNA pol/TBD is thermostable, PCR competent and able to copy repetitive

199 MBPs, including the thermostable PfuMBP, have been demonstrated to be excell

200 roscopy to determine the capsid structure of thermostable phage P74-26 to 2.8- angstrom resolution.

201 derived from thermostable virus exhibited a thermostable phenotype, and vice versa.

202 es can be reversibly switched between highly thermostable photostationary states.

203 systems are discussed, as is application of thermostable pol III to biotechnology.

204 led triggers in less than 10 min by means of thermostable polymerase and nicking endonuclease activit

205 spects of cellular metabolism that reinforce thermostable polymerase production.

206 from a library leads to the production of a thermostable polymerase.

207 imal to best support PCR amplification using thermostable polymerases of a six-letter alphabet that i

208 erase-evolution system and its use to evolve thermostable polymerases that efficiently interconvert C

209 Rutin was the most thermostable polyphenol detected in all buckwheat variet

210 Moreover, since the most thermostable prion protein types were those associated w

211 as accessible to enzymatic removal using the thermostable protease isolated from Pyrococcus furiosus.

212 A novel thermostable protease was purified from Penaeus vannamei

213 slipknot feature in the fold of a well-known thermostable protein, alkaline phosphatase.

214 folding kinetics of the structurally related thermostable protein.

215 Thermostable proteins are advantageous in industrial app

216 ein mass spectrometric methods to explore if thermostable proteins could be used to identify rendered

217 stable, how to intentionally design de novo, thermostable proteins is less clear.

218 p degrees , as has been observed for natural thermostable proteins.

219 activities at 37 degrees C with these novel thermostable proteins.

220 n more thermally altered samples, so-called 'thermostable' proteins such as osteocalcin which has bee

221 s well as four other cocrystal structures of thermostable PTDH and its variants with different ligand

222 To test the hypothesis that thermostable RCA can improve photosynthesis under elevat

223 promise to be a source of highly functional, thermostable Rca candidates for thermal fortification of

224 an acid metabolism (CAM) plants must possess thermostable Rca to support Calvin-Benson-Bassham cycle

225 es C exposure, the transgenic lines with the thermostable RCA1 variants exhibited higher photosynthet

226 Wild-type RCA1 and selected thermostable RCA1 variants were introduced into an Arabi

227 We found that Tfu-FNO is highly thermostable, reaching its highest activity at 65 degree

228 Using structural information as a guide, a thermostable recombinant chaperonin subunit was modified

229 resent studies on the production of a set of thermostable red- and green-emitting luciferase mutants

230 electrocatalytically reoxidized to NAD by a thermostable redox mediator, osmium (1,10-phenanthroline

231 dapters for next-generation sequencing using thermostable RNA ligase from Methanobacterium thermoauto

232 to a defined sequence oligonucleotide using thermostable RNA ligase.

233 The use of ultra-thermostable RNA nanoparticles to deliver chemical prodr

234 Even thermostable RNA structures are often denatured in cells

235 neered a thermostable xylanase (XynB) with a thermostable self-splicing bacterial intein to control t

236 n this paper, we use conserpin, a synthetic, thermostable serpin, as a model protein with which to in

237 The enzyme was found to be comparatively thermostable showing maximum activity at 60 degrees C fo

238 as good solvent and pH stability and is very thermostable, showing no loss of activity after incubati

239 The RbsB/AI-2 complex was thermostable since A. actinomycetemcomitans AI-2 could n

240 richia coli In conclusion, FKBP domains from thermostable SlyD proteins are highly suitable as a gene

241 The engineered biocatalyst was shown to be a thermostable, solvent tolerant, and effective cofactor-r

242 hich occurs naturally in the homologous more thermostable Sso7d.

243 01 suggest direct compound binding to a less thermostable state of NBD1.

244 ructure of a high fidelity polymerase from a thermostable strain of Bacillus stearothermophilus (Baci

245 owed by 22L (5 log10) while BSE was the most thermostable strain with low or null infectivity reducti

246 aphy, we reveal the assembly principles of a thermostable T = 4 shell topology and its catalytic ferr

247 e Engrailed homeodomain (EnHD) and is highly thermostable (T(m) > 99 degrees C vs. 52 degrees C for E

248 The upper helix is highly thermostable (T(m)>90 degrees C), forming 11 Watson-Cric

249 ding domain (TBD) into the distantly related thermostable Taq DNA polymerase at an analogous position

250 a isoform based on sequence alignment of the thermostable TaRca1-beta from wheat, OsRca-beta from ric

251 ns that direct the self-assembly of discrete thermostable tertiary structures.

252 ch of the homo-oligomers and which were more thermostable than alphaB, but less so than HSP27.

253 o engineer active P450 enzymes that are more thermostable than any previously made by chimeragenesis,

254 in dodecylmaltoside and is 13 degrees C more thermostable than beta(1)AR-m23 in nonylglucoside.

255 Ruminococcus lactaris is significantly more thermostable than CdiA-CT(EC536), and its intrinsic tRNA

256 t CspB-TB is approximately 20 degrees C more thermostable than CspB-Bs.

257 beta2 CP assembled at 105 degrees C was more thermostable than either the alpha+beta1+beta2 version a

258 H0 region is shown to be substantially less thermostable than mH0ACPb.

259 isoforms are approximately10 degrees C more thermostable than the C3 isoforms.

260 a mutant receptor that is 31 degrees C more thermostable than the wild-type receptor in dodecylmalto

261 However, the variant PCCs were less thermostable than the wild-type.

262 roteins from thermophiles are generally more thermostable than their mesophilic homologs, but little

263 uses bearing the TS09-C HN protein were more thermostable than those containing LaSota HN protein.

264 ations, unfold reversibly, and are even more thermostable than typical camelid V(H)H domains.

265 hat the purified mutants are equally or more thermostable than wild type CBS.

266 47C, which in the absence of calcium is more thermostable than wild type CjXyn10A bound to the divale

267 T1L/T3D M2 and T3D/T1L S4 ISVPs were less thermostable than wild-type ISVPs.

268 ts I189H, A282P, D143K were found to be more thermostable than wild-type TK.

269 s conducted at seven conserved motifs of the thermostable Thermotoga maritima endonuclease V to probe

270 on-PCR (qRT-PCR) assay using the recombinant thermostable Thermus thermophilus (rTth) enzyme was deve

271 NA structural motifs for the construction of thermostable three-dimensional nano-architectures that d

272 Here we reported the use of the thermostable three-way junction (3WJ) of bacteriophage p

273 97M SOSIP.664 trimers as being appropriately thermostable (Tm of 63.4 degrees C and 62.7 degrees C, r

274 se transcriptases are often not sufficiently thermostable to catalyze synthesis at temperatures high

275 This newly described thermostable topoisomerases IB should be a promising new

276 models the final fusion state thought to be thermostable trimers with six-helix bundle structure in

277 iruses by exchanging viral genes between the thermostable TS09-C strain and thermolabile LaSota strai

278 Tth111II is a thermostable Type IIGS restriction enzyme that recognize

279 ical potassium specificity of G4s, remaining thermostable under physiological ionic conditions.

280 f tetrabrachion, a bacterial protein that is thermostable up to at least 403 K (130 degrees C).

281 rmance of HDA, we have cloned and purified a thermostable UvrD helicase (Tte-UvrD) and the mutL homol

282 he keys to success were the development of a thermostable vaccine and the application of participator

283 ovel and safe vaccination platform featuring thermostable vaccine formulations.

284 ent the cocrystal structure of an engineered thermostable variant of PTDH bound to NAD(+) (1.7 A reso

285 A designed thermostable variant, generated by mutating K12 to M, wa

286 Here we report thermostable variants of CocE developed through rational

287 rimentally by mutating marginally stable and thermostable variants of cytochrome P450 BM3.

288 etergent conditions can support selection of thermostable variants of experimentally demanding GPCRs.

289 In simulations at 300 K the thermostable variants remain closer to their crystal str

290 -nitrobenzyl esterase (484 residues) and two thermostable variants that were generated by laboratory

291 ides and biomolecules in the design of their thermostable variants where the shielding mechanism can

292 escribe the engineering and improvement of a thermostable viral family A polymerase with inherent rev

293 Chimeras bearing the HN protein derived from thermostable virus exhibited a thermostable phenotype, a

294 A cryo-EM structure of the portal protein of thermostable virus P23-45, determined in situ in its pro

295 Furthermore, the newly developed thermostable virus rLS-T-HN, encoding the TS09-C HN prot

296 ernix bacilliform virus 1) is among the most thermostable viruses known; it infects a hyperthermophil

297 We purified thermostable wild type and QUAD opsins, with or without

298 Moreover, crosslinked SCRII was much more thermostable with its denaturation temperature (Tm) incr

299 The enzyme is extremely thermostable, with 50% of its initial activity retained

300 To overcome this problem, we engineered a thermostable xylanase (XynB) with a thermostable self-sp