ライフサイエンスコーパス: thermostable

1 capacity to incorporate iron, and were less thermostable.

2 are monomeric, photochromic, and remarkably thermostable.

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

4 SsMTAPII is extremely thermoactive and thermostable.

5 alized by atomic force microscopy) which are thermostable.

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

7 atalytic domain of TbCet1 is extraordinarily thermostable.

8 activity, has NADH-specific activity, and is thermostable.

9 nerated enzymes that were substantially less thermostable.

10 This activity was found to be remarkably thermostable.

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

12 mostability and the DGK peptide is the least thermostable.

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

14 P22 tailspike is a homotrimeric, thermostable adhesin that recognizes the O-antigen lipop

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

16 In fact, the extremely thermostable alpha-amylase from B. licheniformis was fou

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

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

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

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

21 The newly available thermostable aminotransferases may have general utility

22 However, two thermostable aminotransferases were identified that cata

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

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

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

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

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

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

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

30 Centrifugal separation of the thermostable and thermolabile fractions revealed that al

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

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

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

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

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

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

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

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

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

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

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

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

43 152S/C153S/C387S/C430A (mutant SSCSA) was as thermostable as the wild-type enzyme.

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

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

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

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

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

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

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

51 expression of fusions of a coding gene for a thermostable beta-galactosidase to a number of heat shoc

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

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

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

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

56 Dpo4 is thermostable, but can also synthesize DNA at 37 degrees

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

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

59 s should facilitate the engineering of novel thermostable catalysts.

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

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

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

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

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

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

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

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

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

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

70 Eight of eight thermostable chimeras assayed hydrolyze the solid cellul

71 Selected purified thermostable chimeras hydrolyzed phosphoric acid swollen

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

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

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

75 Electron microscopy of the thermostable complex demonstrated the presence of multil

76 of free DNA and a second corresponding to a thermostable complex with a transition temperature, T(m(

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

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

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

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

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

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

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

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

85 Instead, the amount of thermostable DNA and the enthalpy ratio Delta H((stable)

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

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

88 ting primer, which are ligated together by a thermostable DNA ligase.

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

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

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

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

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

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

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

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

97 Thermostable DNA polymerases isolated from archaeal orga

98 NA sequence that cannot be copied by certain thermostable DNA polymerases.

99 fined specificities, Ptr1 and Ptr2 provide a thermostable DNA-binding platform for analysis of effect

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

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

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

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

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

105 il is stabilized both by fusion to a minimal thermostable ectodomain of gp41 and by engineered inters

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

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

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

109 The thermostable endoglucanase EGPh from the hypothermophili

110 A thermostable endonuclease V from the hyperthermophilic b

111 ped a mutation scanning method that combines thermostable EndonucleaseV (Endo V) and DNA ligase.

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

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

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

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

116 We discovered a thermostable enzyme from the archaeon Pyrococcus furiosu

117 Although this extremely thermostable enzyme has no significant sequence similari

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

119 By means of highly strand-specific thermostable enzyme Tth-based reverse-transcriptase poly

120 To determine whether BLXI behaves as a thermostable enzyme, it was expressed in Escherichia col

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

122 Thermostable enzymes and thermophilic cell factories may

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

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

125 Thermostable enzymes combine catalytic specificity with

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

127 Both thermostable enzymes self-cleave at conserved serine res

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

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

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

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

132 which is also a characteristic of naturally thermostable enzymes.

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

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

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

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

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

138 , Lam16A, from T. maritima comprise a highly thermostable family 4 CBM that binds beta-1,3- and beta-

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

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

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

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

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

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

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

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

147 the transfection activity was present at the thermostable fraction.

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

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

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

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

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

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

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

155 The thermostable GreA factors contact the 3'-end of RNA, sti

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

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

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

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

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

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

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

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

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

165 backbone conformational fluctuations in the thermostable helical subdomain, HP36, of the F-actin-bin

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

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

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

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

170 alian guanylyltransferases are intrinsically thermostable in vitro and they are unaffected by Cet1(23

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

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

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

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

175 The method adopts thermostable ligation for allele discrimination and roll

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

177 The AksF enzyme proved to be thermostable, losing only 10% of its enzymatic activity

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

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

180 The thermostable MJ1101 protein catalyzed both the acetylati

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

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

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

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

185 es, including ISVPs of a previously reported thermostable mutant, provided further insights into the

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

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

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

189 The thermostable mutants tolerate short-chain detergents, su

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

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

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

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

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

195 Thermostable Newcastle disease virus (NDV) vaccines have

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

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

198 The ligand-free receptor, solubilized in thermostable octyl glucoside micelles, exhibited a coope

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

200 rge aromatic network found in the only other thermostable P450, CYP119, thought to contribute to ther

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

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

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

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

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

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

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

208 A thermostable phosphosulfolactate phosphohydrolase (EC 3.

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

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

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

212 spects of cellular metabolism that reinforce thermostable polymerase production.

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

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

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

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

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

218 A novel thermostable protease was purified from Penaeus vannamei

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

220 folding kinetics of the structurally related thermostable protein.

221 icates disulfide bonding in stabilizing many thermostable proteins and points to novel chemical envir

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

223 Another popular theory is that thermostable proteins have more electrostatic and hydrog

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

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

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

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

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

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

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

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

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

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

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

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

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

237 modification of PCR-based methods, employing thermostable restriction enzymes to block the synthesis

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

239 to a defined sequence oligonucleotide using thermostable RNA ligase.

240 Even thermostable RNA structures are often denatured in cells

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

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

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

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

245 0977 in E. coli resulted in high levels of a thermostable single-stranded DNase activity with propert

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

247 hich occurs naturally in the homologous more thermostable Sso7d.

248 01 suggest direct compound binding to a less thermostable state of NBD1.

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

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

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

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

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

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

255 CD studies show that GTP-bound actin is less thermostable than ATP-bound actin.

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

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

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

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

260 This enzyme is more thermostable than its bacterial and archaeal homologues

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

262 ative-like, and all three variants were more thermostable than the wild-type Hsp10.

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

264 Both Arg8Nle and Arg8Aad are more thermostable than the wild-type sequence, testifying to

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

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

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

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

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

270 47C, which in the absence of calcium is more thermostable than wild type CjXyn10A bound to the divale

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

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

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

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

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

276 97M SOSIP.664 trimers as being appropriately thermostable (Tm of 63.4 degrees C and 62.7 degrees C, r

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

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

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

280 Tth111II is a thermostable Type IIGS restriction enzyme that recognize

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

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

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

284 ovel and safe vaccination platform featuring thermostable vaccine formulations.

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

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

287 Here we report thermostable variants of CocE developed through rational

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

289 Room-temperature activities of the evolved thermostable variants range from 3.5 times greater to 4.

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

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

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

293 as yielded eight generations of increasingly thermostable variants.

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

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