ライフサイエンスコーパス: mesophilic

1 ted Ascaris suum ova in six laboratory-scale mesophilic (35 degrees C) anaerobic digesters processing

2 bed reactors (51-56 degrees C) followed by a mesophilic (36.5 degrees C) anaerobic filter.

3 A low-cost approach for enhancing mesophilic (37 degrees C) anaerobic digestion (AD) of or

4 Escherichia coli but showed no similarity to mesophilic ACS-type enzymes.

5 ere able to design more stable variants of a mesophilic adenylate kinase with only the sequence infor

6 this is analogous to previous findings with mesophilic ADH at 25 degrees C.

7 l tables for the reference identification of mesophilic aeromonads.

8 ich are soil-transmitted human pathogens, in mesophilic anaerobic digestion processes.

9 er of resource recovery technologies such as mesophilic anaerobic digestion to developing world setti

10 technologies (air drying, aerobic digestion, mesophilic anaerobic digestion, thermophilic anaerobic d

11 Our results reveal the potential of mesophilic anaerobic sludges as seed material for sulfur

12 The suitability of mesophilic anaerobic sludges as the inoculum for sulfur-

13 ~3700 mg/kg and maintained the sludge under mesophilic, anaerobic conditions for 24 h.

14 ately more activated by temperature than the mesophilic analog.

15 DeltaDeltaGu = 6.9 kcal/mol) compared to its mesophilic analogue CenAP30.

16 rmophile Pyrococcus furiosus (PfRd), and its mesophilic analogue Clostridium pasteurianum (CpRd), are

17 Although most eukaryotic TBPs are mesophilic and adapted to physiological conditions of te

18 the chromogenic data with concentrations of mesophilic and Enterobacteriaceae.

19 he primary mode of salt stabilization of the mesophilic and halophilic DHFRs appears to be through pr

20 l system to compare the effect of salts on a mesophilic and halophilic enzyme.

21 ce in the salt-dependent binding behavior of mesophilic and halophilic TBPs to DNA may be due to the

22 ally observed salt-dependent DNA-binding for mesophilic and halophilic TBPs, and suggest that the dis

23 ral kinetic steps, and to differ between the mesophilic and hyper-thermophilic proteins.

24 in a range of 5 to 90 degrees C for a set of mesophilic and hyperstable enzyme variants.

25 The fast, local mobilities differ between a mesophilic and hyperthermophilic adenylate kinase, but a

26 rative analysis of genome sequence data from mesophilic and hyperthermophilic micro-organisms has rev

27 Because POP is found in mesophilic and hyperthermophilic organisms, and is distr

28 reover, the single-subunit pyruvate ORs from mesophilic and moderately thermophilic bacteria and from

29 aeolicus (Aacpn10) shows high homology with mesophilic and other thermophilic cpn10 sequences, excep

30 prokaryotes that live at lower temperatures (mesophilic and psychrophilic Archaea and Bacteria).

31 tomic structures with citrate synthases from mesophilic and psychrophilic organisms has indicated the

32 Lower counts of mesophilic and psychrotrophic bacteria (1-2 log CFU/g) w

33 From a pair of highly homologous mesophilic and thermophilic adenylate kinases, we genera

34 first obtained evidence that four different mesophilic and thermophilic archaeal RNase P holoenzymes

35 e evolutionary history between RNases H from mesophilic and thermophilic bacteria.

36 This configuration was tested at both mesophilic and thermophilic conditions.

37 The discovery of ammonia oxidation by mesophilic and thermophilic Crenarchaeota and the widesp

38 bases are incorporated into DNA by selected mesophilic and thermophilic DNA polymerases and the resu

39 or real-time single-molecule measurements of mesophilic and thermophilic enzymes at 70 degrees C.

40 agreement with other comparative studies of mesophilic and thermophilic enzymes.

41 ampled locations in the lake, including both mesophilic and thermophilic habitats, had multiple virop

42 itionally, comparisons between corresponding mesophilic and thermophilic motif pairs provide key bioc

43 ermined through global sequence alignment of mesophilic and thermophilic motif pairs, which are ident

44 e find that mitochondrial carriers from both mesophilic and thermophilic organisms exhibit poor stabi

45 ic homologue to the previously characterized mesophilic and thermophilic pair.

46 Pairwise comparisons of homologous mesophilic and thermophilic proteins can help to identif

47 t differences in packing density between the mesophilic and thermophilic proteins.

48 ight-harvesting antennae can be regulated in mesophilic and thermophilic red algae.

49 cts influence the unfolding kinetics of both mesophilic and thermophilic rubredoxins, these findings

50 proach to identify and compare corresponding mesophilic and thermophilic sequence motifs between all

51 ed with homologous enzymes from a variety of mesophilic and thermophilic sources.

52 aled reductions in agonistic activity during mesophilic and thermophilic treatment but significant in

53 ility of the patties, delaying total aerobic mesophilic, and lactic acid bacteria growth, especially

54 e hot-start toward modern hyperthermophilic, mesophilic, and psychrophilic organisms illustrates acti

55 bacteria, that also occur in some species of mesophilic archaea and in the endosymbiotic organelles o

56 at shock regulation in hyperthermophilic and mesophilic Archaea organisms.

57 is a dimeric enzyme in eucarya, bacteria and mesophilic archaea.

58 iding a comprehensive investigation of these mesophilic archaea.

59 p (PCNA) and the clamp loader (RFC) from the mesophilic archaeon Methanosarcina acetivorans.

60 Methanococcus maripaludis is a mesophilic archaeon that reduces CO2 to methane with H2

61 to KGOR has been previously purified from a mesophilic archaeon, but the molecular properties of T.

62 re also homologous to the dimeric POR from a mesophilic archaeon, Halobacterium halobium (21% identit

63 nother well characterized AroQ class CM, the mesophilic AroQp domain from E. coli.

64 HB8 DNA ligase (Tth DNA ligase) differs from mesophilic ATP-dependent DNA ligases in three ways: (i)

65 cold shock protein (Bc-Csp) differs from the mesophilic Bacillus subtilis cold shock protein B (Bs-Cs

66 nd 1.38 log CFU/g reduction of total aerobic mesophilic bacteria (TAMB) counts.

67 tinguishes itself from nitrate reductases of mesophilic bacteria and archaea by its very high specifi

68 ated compounds and K(1)-value and microbial (mesophilic bacteria and Enterobacteriaceae) analyses wer

69 in these organisms is markedly lower than in mesophilic bacteria and eukaryotes.

70 On the tenth day of storage, total aerobic mesophilic bacteria and mould and yeast counts were stat

71 hilic archaea, two thermophilic bacteria, 17 mesophilic bacteria and two eukaryotic species were anal

72 composition to filamentous viruses infecting mesophilic bacteria but is distinguished by in vivo asse

73 ly, the sHSP confers a survival advantage on mesophilic bacteria by preventing protein aggregation at

74 occur in DNA polymerase III holoenzyme from mesophilic bacteria including delta-delta' interaction,

75 RlmO homologues are primarily found in mesophilic bacteria related to T. thermophilus.

76 that all homotetrameric L-asparaginases from mesophilic bacteria utilize a common ping-pong mechanism

77 st+mold during 12days of storage while total mesophilic bacteria was decreased during 6days of storag

78 characterized Cas9 proteins are derived from mesophilic bacteria, and canonical Cas9 systems are chal

79 contrast to many polymerization ATPases from mesophilic bacteria, ATP binding is not required for Pil

80 Here, we describe two pAgos from mesophilic bacteria, Clostridium butyricum (CbAgo) and L

81 Aerobic mesophilic bacteria, Enterobacteriaceae, yeast and mold

82 y developed Cas9 homologs all originate from mesophilic bacteria, making them susceptible to degradat

83 in contrast to replicative polymerases from mesophilic bacteria, Tth holoenzyme is efficient only at

84 mon to known peptide-signalling molecules in mesophilic bacteria, was strongly upregulated in the co-

85 It occurs in mesophilic bacteria, yeast, and thermophilic archaea.

86 Mesophilic bacteria, yeast, mold and pathogenic Enteroba

87 a maritima, and those of close homologs from mesophilic bacteria.

88 hermophilic bacteria differ from the rRNA of mesophilic bacteria.

89 is waterline contamination by heterotrophic mesophilic bacteria.

90 ing), which has previously been described in mesophilic bacteria.

91 MalQ represents the first example of a mesophilic bacterial amylomaltase with known structure a

92 he hyperthermophilic archaeal enzyme and the mesophilic bacterial enzyme, structural modifications mu

93 nt in Escherichia coli RNase R and in 88% of mesophilic bacterial genera analyzed, but absent from th

94 same relative order and spacing found in the mesophilic bacterial proteins.

95 Mesophilic bacterial proteomes contain a small number (0

96 characteristics of the conserved domains of mesophilic bacterial response regulators, and the C-term

97 ic archaeon Pyrococcus furiosus (Pf) and the mesophilic bacterium Clostridium pasteurianum (Cp) were

98 ophilic archaeon Pyrococcus furiosus and the mesophilic bacterium Clostridium pasteurianum.

99 eesC for the beta-glucosidase (abg) from the mesophilic bacterium, Agrobacterium faecalis.

100 vestigated the growth of Escherichia coli, a mesophilic bacterium, as a function of pressure (P) and

101 te synthase (AS) from Serratia marcescens, a mesophilic bacterium, has been solved in the presence of

102 e transport proteins shown to be active in a mesophilic bacterium.

103 values) dynamics for a continually operated mesophilic bioreactor and highlight the enormous potenti

104 requency (44%) than those generated from the mesophilic BsAK (6%), and selected TnAK mutants compleme

105 Why do mesophilic cells die around 50 degrees C?

106 of Clostridium cellulovorans, an anaerobic, mesophilic, cellulolytic bacterium, was characterized.

107 the cold-active trypsin into a variant with mesophilic characteristics without changing the amino ac

108 eld observations of relative abundances: the mesophilic clade grows optimally at temperatures 16 degr

109 cum and C. josui, they seem to be typical of mesophilic clostridia, indicating that the large gene cl

110 in, rubredoxin (MW = 7500 Da), from both the mesophilic Clostridium pasteurianum (Topt = 37 degrees C

111 en in simulations of the reduced form of the mesophilic Clostridium pasteurianum rubredoxin at 295 K,

112 rthermore, the samples from thermophilic and mesophilic codigesters had different DOM composition in

113 otein, CspB-TB that has the same core as the mesophilic cold shock protein CspB-Bs from Bacillus subt

114 unfold a homologous pair of thermophilic and mesophilic cold shock proteins at high temperatures.

115 drothermal conditions, is precipitated under mesophilic conditions by the metabolically versatile str

116 g arsenic-bearing sediments under anaerobic, mesophilic conditions in minimal media with acetate as t

117 ine residue might play a role in adaption to mesophilic conditions.

118 this energetic pathway has not been shown in mesophilic conditions.

119 od to alleviate ammonia toxicity effect in a mesophilic continuously stirred-tank reactor (CSTR) oper

120 pproximately 5 kcal/mol more stable than its mesophilic counterpart as judged from equilibrium denatu

121 ns, which unfold much more slowly than their mesophilic counterparts, T.thermophilus RNase H folds an

122 al peptide motifs that are absent from their mesophilic counterparts.

123 more compact and more hydrophobic than their mesophilic counterparts.

124 nces between this thermophilic phage and its mesophilic counterparts.

125 ic organisms are often more rigid than their mesophilic counterparts.

126 ally in a fundamentally different way to its mesophilic counterparts.

127 res and greater thermosensitivity than their mesophilic counterparts.

128 lity for thermophilic enzymes than for their mesophilic counterparts.

129 comparison of themophilic enzymes with their mesophilic counterparts.

130 ivation enthalpies and entropies) from their mesophilic counterparts.

131 ound were: (1) a disulfide bond not found in mesophilic counterparts; (2) an increased number of surf

132 ch other and close to reported midpoints for mesophilic cpn10 proteins.

133 d to the ancestral precursor of contemporary mesophilic CPSases.

134 kinetics and cellular characteristics of the mesophilic crenarchaeon 'Candidatus Nitrosopumilus marit

135 the reaction center and antenna system from mesophilic cyanobacteria, including red chlorophylls and

136 re of the PSI-IsiA complex isolated from the mesophilic cyanobacterium Synechocystis sp. PCC 6803.

137 s between thermophilic Thermus aquaticus and mesophilic Deinococcus radiodurans RNAPs and identify th

138 secondary treatment and the later anaerobic mesophilic digestion of the sludge.

139 Five DNA polymerases were investigated: mesophilic DNA polymerase I large (Klenow) fragment, 3'-

140 thermophilus ribonuclease H compared to its mesophilic E. coli homolog.

141 spectrometry (HDX-MS) has been applied to a mesophilic (E. coli) dihydrofolate reductase under condi

142 report the characterization of two different mesophilic EF-Tu orthologs, one from Escherichia coli, a

143 suggested by a comparison with a homologous mesophilic enzyme (55% identity), NAD(+)-dependent alcoh

144 ntersubunit linkages of the thermophilic and mesophilic enzyme Bacillus subtilis chorismate mutase su

145 nfolding (DeltaSu) of 0.55 kcal/(mol*K); the mesophilic enzyme CenAP30 had a Tm of 56.4 degrees C, a

146 ydrofolate reductases, namely the monomeric, mesophilic enzyme from E. coli (EcDHFR) and the dimeric,

147 ingly, we also present a hybrid thermophilic/mesophilic enzyme that is thermostable and more active t

148 inding and activity less frequently than the mesophilic enzyme, although these differences may manife

149 mately eight times higher than that based on mesophilic enzymes at the same temperature.

150 al similarity between this cellulase and the mesophilic enzymes serves to highlight features that may

151 obiose and beta-1-galactosylphingosine) with mesophilic enzymes.

152 aptive role in catalysis by thermophilic and mesophilic enzymes.

153 nit displayed much higher stability than the mesophilic equivalent and its iron-sulfur cluster remain

154 er promoter escape efficiency than RNAP from mesophilic Escherichia coli.

155 tionship between stability and activity in a mesophilic esterase.

156 ryotic organisms, including thermophilic and mesophilic eubacteria as well as archaebacteria, the hum

157 Comparison of these structures with those of mesophilic family 12 cellulases in complex with inhibito

158 arison of the structure of Tl Fd to those of mesophilic ferredoxins reveals that Tl Fd possesses the

159 enhanced thermostability of PH75 relative to mesophilic filamentous bacteriophages.

160 with the same symmetry (class II) as in the mesophilic filamentous phages Pf1 and Pf3.

161 nt is not apparent in capsid subunits of the mesophilic filamentous phages, fd, Pf1, and Pf3, previou

162 that consist primarily of bacteria that are mesophilic for temperature and xerotolerance (including

163 Previously, a mesophilic form of HDA (mHDA) utilizing the Escherichia

164 dominant (per)chlorate-reducing bacteria in mesophilic freshwater environments.

165 The most abundant beta-glucosidase in the mesophilic fungus Hypocrea jecorina is HjCel3A, which hy

166 urpassed the conventional system utilizing a mesophilic G6PDH (mG6PDH) from Leuconostoc mesenteroides

167 and V482L) in closely related homologs from mesophilic haloarchaea.

168 Methylomonas methanica MC09 is a mesophilic, halotolerant, aerobic, methanotrophic member

169 different for hyperthermophilic (IPPase) and mesophilic (HEWL) proteins.

170 The mesophilic hFoB is very unstable and requires approximat

171 For the mesophilic HLADH described herein, an opposite trend is

172 As in mesophilic holoenzymes, in the presence of a primed DNA

173 e from Thermus thermophilus, compared to its mesophilic homolog from Escherichia coli, is elucidated

174 and close to half that of its highly similar mesophilic homolog, subtilisin SSII, indicating that the

175 yperthermostable protein was compared to its mesophilic homologs and analyzed for differences in the

176 several hyperthermophilic proteins and their mesophilic homologs are calculated.

177 d to survive extreme temperatures with their mesophilic homologs are likely to provide valuable infor

178 ophilic sequences are more likely than their mesophilic homologs to have deletions in exposed loop re

179 s are generally more thermostable than their mesophilic homologs, but little is known about the evolu

180 ened thermophilic proteins relative to their mesophilic homologs.

181 = 7 geometry despite being twice as large as mesophilic homologs.

182 m folding of a thermophilic ribozyme and its mesophilic homologue by using hydroxyl radical protectio

183 enobacter thermophilus (Ht cyt c552) and its mesophilic homologue from Pseudomonas aeruginosa (Pa cyt

184 iors of the ion pairs when engineered into a mesophilic homologue to increase stability, in silico mu

185 ng temperature (T(m)) similar to that of the mesophilic homologue yet also has a surprisingly low Del

186 The mesophilic homologue, BBL, was less stable than the ther

187 compared to previously published data for a mesophilic homologue, Escherichia coli ribonuclease HI (

188 When it is compared with its mesophilic homologue, L30e from yeast, a number of struc

189 ermophilic protein is similar to that of its mesophilic homologue, with a proportional increase in st

190 three hyperthermophilic proteins with their mesophilic homologues and find that hydration effects pr

191 teins are significantly higher than those of mesophilic homologues at 30 degrees C; thus, heptamer th

192 ns are significantly more compact than their mesophilic homologues, while no particular interaction t

193 show pronounced structural differences from mesophilic homologues.

194 gies of mutant cores based on cores found in mesophilic homologues.

195 are considerably greater than those of their mesophilic homologues.

196 onal thermodynamics between thermophilic and mesophilic homologues.

197 proteins are very similar to those of their mesophilic homologues.

198 ydrogenase (HtADH) closely resembles that of mesophilic horse liver alcohol dehydrogenase (HLADH).

199 een cloned and expressed at high levels in a mesophilic host (Escherichia coli) as a soluble tetramer

200 genes encoding hyperthermophilic enzymes in mesophilic hosts have improved the availability of high-

201 enome sequence of the genetically tractable, mesophilic, hydrogenotrophic methanogen Methanococcus ma

202 ed wild type cellobiohydrolases (Cel7A) from mesophilic Hypocrea jecorina and thermophilic Rasamsonia

203 Although most pseudomonads are mesophilic in nature, isolates such as the Antarctic Pse

204 replacements allowed us to develop the first mesophilic in vitro protein splicing system as well as s

205 led us to demonstrate in vitro splicing of a mesophilic intein containing all wild-type catalytic res

206 olII intein is significantly more rigid than mesophilic inteins, which may contribute to the higher o

207 hat required for equivalent fermentations by mesophilic lactic acid bacteria.

208 Ts with more than 5 rings, in sediments from mesophilic marine environments (sea surface temperature,

209 euryarchaeote Methanococcus maripaludis is a mesophilic member of the Sac10b family.

210 d has identical topology to those of the two mesophilic members of the family whose structures have b

211 fferential features for distinguishing other mesophilic members of the genus.

212 from thermoadapted homologs into an exemplar mesophilic membrane protein, and demonstrated significan

213 ene isolation, while in vivo genetics in the mesophilic methanococci can provide the experimental sys

214 that the physiological role of Mma10b in the mesophilic methanococci is greatly diverged from that of

215 aschii are compared with their homologs from mesophilic Methanococcus species.

216 ore the function of all three enzymes in the mesophilic methanogen Methanosarcina mazei.

217 stress genes in the hsp70(dnaK) locus of the mesophilic, methanogenic archaeon Methanosarcina mazeii.

218 sly identified on the archaellins of related mesophilic methanogens, Methanococcus voltae and Methano

219 ophilic archaea and that the polymerase from mesophilic Methanosarcina acetivorans shows identical be

220 was lower than corresponding estimates from mesophilic microorganisms, primarily because of a low ra

221 ve been measured for enzymes from a range of mesophilic microorganisms.

222 a coli cytoplasmic membrane and membranes of mesophilic microorganisms.

223 ilic model organism distantly related to the mesophilic model organism E. coli.

224 plays much faster relaxation dynamics than a mesophilic model protein, hen egg white lysozyme (HEWL),

225 g for the t+rRNA modification enzymes in the mesophilic moderate halophile Haloferax volcanii.

226 t a given temperature than the corresponding mesophilic (Ms) enzymes, because the thermophilic enzyme

227 gnal typical of the so-called Ni-C center of mesophilic NiFe-hydrogenases.

228 Methylophaga thiooxydans is a mesophilic, obligately halophilic bacterium that is capa

229 ins were extant proteins from psychrophilic, mesophilic, or thermophilic organisms.

230 rences in dynamics between homologs from the mesophilic organism E. coli and the thermophilic organis

231 This is the first report of a single mesophilic organism that can grow while catalyzing the o

232 tral thioredoxins in the context of a modern mesophilic organism.

233 essential part of genome per replication for mesophilic organisms and one to two mutations per genome

234 entical to those of corresponding mutants of mesophilic organisms encompassing a broad phylogenetic r

235 f orthologous proteins from thermophilic and mesophilic organisms found that most highly correlated f

236 (CPSase) resembling the enzyme found in all mesophilic organisms nor a carbamate kinase-like CPSase

237 ins by hybridizing EIC from thermophilic and mesophilic organisms, and we characterize the resulting

238 ant similarity with those of prolidases from mesophilic organisms, but the enzyme differs from them i

239 te data obtained in a dozen thermophilic and mesophilic organisms.

240 very similar to rpsL mutations identified in mesophilic organisms.

241 ly distant F-type motors of thermophilic and mesophilic origins, and they differ only in the magnitud

242 a to state transitions were observed only in mesophilic P. cruentum with mobile phycobilisomes, and t

243 origin of its stability by comparing it with mesophilic P450s with known structures.

244 The biochemical characterization of mesophilic pAgo proteins paves the way for their use for

245 its closest phylogenetic neighbor Frankia, a mesophilic plant endosymbiont and soil dweller.

246 Here, using novel genome data from the mesophilic Porphyridium cruentum and Calliarthron tuberc

247 In mesophilic prokaryotes, the DNA-binding protein HU parti

248 s H that display the desired thermophilic or mesophilic properties, as defined by their DeltaC(p) val

249 tein (CspB-TB) that has the core residues of mesophilic protein from Bacillus subtilis(CspB-Bs) and a

250 ction under conditions that render a typical mesophilic protein inactive.

251 xcluded-volume effect, the resistance of the mesophilic protein to heat-induced unfolding increased i

252 icient method to confer thermostability to a mesophilic protein.

253 the folding of the thermophilic but not the mesophilic protein.

254 unusually high thermodynamic stability for a mesophilic protein.

255 Both thermophilic and mesophilic proteins are maximally stable around room tem

256 ource organisms, homologous thermophilic and mesophilic proteins have similar stabilities.

257 suggesting that hybridizing thermophilic and mesophilic proteins is a valid strategy to engineer ther

258 ndidates likely to confer thermostability to mesophilic proteins through optimization of surface elec

259 ilies containing homologous thermophilic and mesophilic proteins which show reversible two-state fold

260 acity of unfolding (DeltaC(p)) than found in mesophilic proteins, is emerging from the recent literat

261 e thermodynamic profiles of thermophilic and mesophilic proteins.

262 erature regimes, than RdCp and other typical mesophilic proteins.

263 us aculeatinus and A. sclerotiicarbonarius); mesophilic/psychrotolerant bacteria under diverse, solut

264 pgraded to average CH4 content of 89% in the mesophilic reactor and 85% in the thermophilic.

265 ly prove phycobilisome mobility in two model mesophilic red alga strains, Porphyridium cruentum and R

266 that the origin of these complex families in mesophilic red algae may have contributed to their adapt

267 Cyanidiophytina and the broadly distributed mesophilic red algae.

268 ons have an important regulatory function in mesophilic red algae; however, in thermophilic red algae

269 We demonstrate that a rich mesophilic red algal gene repertoire is crucial for test

270 and the ultimate folding transitions in the mesophilic ribozyme become linked into a single transiti

271 hich one to three motifs of a 255-nucleotide mesophilic ribozyme were substituted with the correspond

272 Unlike the case of the mesophilic rubredoxin from Clostridium pasteurianum (RdC

273 states of hyperthermophilic (S16Thermo) and mesophilic (S16Meso) homologs of the ribosomal protein S

274 in the size of the active site loops at the mesophilic ScOMPDC and the thermophilic MtOMPDC.

275 The 19-residue phosphate gripper loop of the mesophilic ScOMPDC is much larger than the nine-residue

276 An extension of this approach to a mesophilic soil environment also reveals high levels of

277 omologous enzymes from hyperthermophilic and mesophilic sources.

278 Thus, the mesophilic species B. subtilis and E. coli share the sam

279 Methanococcus maripaludis is a mesophilic species of Archaea capable of producing metha

280 n extant thermophilic species than in extant mesophilic species, supporting the idea that the LUA liv

281 dsrA analyses and likely contributing to the mesophilic SRR measured.

282 we have used directed evolution to convert a mesophilic subtilisin-like protease from Bacillus sphaer

283 d-type and far surpasses those of homologous mesophilic subtilisins.

284 activation energy (100-160 kJ mol(-1)) than mesophilic sulfate reduction (30-60 kJ mol(-1)), which m

285 vibrio desulfuricans G20) is a Gram-negative mesophilic sulfate-reducing bacterium (SRB), known to co

286 ndent DNA-binding behavior of halophilic and mesophilic TBPs by using a combined molecular mechanics/

287 concentration, the opposite is observed for mesophilic TBPs.

288 warming will mostly impact ecosystems in the mesophilic temperature range, we conclude that as microb

289 ng activity of the T. thermophilus enzyme at mesophilic temperatures do so by reconfiguring the local

290 nd evaluated using short oligonucleotides at mesophilic temperatures.

291 l structure of CYP119 compared with the five mesophilic templates.

292 Recently the complete genomes for mesophilic, thermophilic and hyperthermophilic organisms

293 ree wild-type cold shock proteins taken from mesophilic, thermophilic, and hyperthermophilic bacteria

294 Here we examine mesophilic to thermophilic AOM in hydrothermal sediments

295 the same as the recognition sequence of the mesophilic Type II restriction endonuclease MaeII.

296 we describe the first genome sequence from a mesophilic, unicellular red alga, Porphyridium purpureum

297 rences in protein structure for enzymes from mesophilic vs thermophilic sources.

298 trace and its relative frequency of usage in mesophilic vs. thermophilic eubacteria.

299 ted denitrification temperature responses to mesophilic with concurrent community shifts, and anammox

300 lic responses to pressure of live cells from mesophilic yeast and bacterial strains, as well as the p