ライフサイエンスコーパス: Sulfolobus

1 e identity and originate from two strains of Sulfolobus.

2 crenarchaeal organisms, especially the genus Sulfolobus.

3 mporally and spatially distinct processes in Sulfolobus.

4 epressor and its overexpression is toxic for Sulfolobus.

5 rs of hyperthermophilic archaea of the genus Sulfolobus.

6 tin structure and regulation in the archaeon Sulfolobus.

7 estabilization of RNA secondary structure in Sulfolobus.

8 onucleotide-mediated transformation (OMT) in Sulfolobus acidocaldarius and Escherichia coli as a func

9 al structures of the XPD catalytic core from Sulfolobus acidocaldarius and measured mutant enzyme act

10 l context, we used ECT to image the archaeon Sulfolobus acidocaldarius and observed a distinct protei

11 Genetic transformation of Sulfolobus acidocaldarius by a multiply marked pyrE gene

12 In Sulfolobus acidocaldarius conjugation assays, recombinan

13 isolated from the thermoacidophilic archaeon Sulfolobus acidocaldarius grown at different temperature

14 hnique to show that both S. solfataricus and Sulfolobus acidocaldarius have three functional origins.

15 317H variant of the thermostable CYP119 from Sulfolobus acidocaldarius maintains heme iron coordinati

16 y dynamic and TBP from the archaeal organism Sulfolobus acidocaldarius strictly requires TFB for DNA

17 on of strains of Sulfolobus solfataricus and Sulfolobus acidocaldarius that allow the incorporation o

18 tify saci_0568 and saci_0748, two genes from Sulfolobus acidocaldarius that are highly induced upon U

19 chromatin protein from the hyperthermophile Sulfolobus acidocaldarius that severely kinks duplex DNA

20 Sulfolobus acidocaldarius utilizes glucose and xylose as

21 The 3 DNA replication origins of Sulfolobus acidocaldarius were mapped by 2D gel analysis

22 Sac7d is a small, chromatin protein from Sulfolobus acidocaldarius which induces a sharp kink in

23 chromatin protein from the hyperthermophile Sulfolobus acidocaldarius which kinks duplex DNA by appr

24 In the crenearchaeon Sulfolobus acidocaldarius, biosynthesis of the archaellu

25 bled those of the thermoacidophilic archaeon Sulfolobus acidocaldarius, despite important molecular d

26 rize prototypical superfamily ATPase FlaI in Sulfolobus acidocaldarius, showing FlaI activities in ar

27 In S. solfataricus and Sulfolobus acidocaldarius, tfb3 is one of the most highl

28 he relevance of this threat for the archaeon Sulfolobus acidocaldarius, the mode of GGCC methylation

29 ave used previously to characterize Dbh from Sulfolobus acidocaldarius.

30 ated from the thermoacidophilic crenarchaeon Sulfolobus acidocaldarius.

31 and inhibitor binding to CYP119, a P450 from Sulfolobus acidocaldarius.

32 degrees C) is near the growth temperature of Sulfolobus acidocaldarius.

33 onents during starvation-induced motility in Sulfolobus acidocaldarius.

34 in-like modification pathway in the archaeon Sulfolobus acidocaldarius.

35 of a shuttle plasmid (pJlacS) propagated in Sulfolobus acidocaldarius.

36 A crystal structure of XPD from Sulfolobus acidocaldiarius that lacks helicase domain 2

37 be distinct from previously described ISs of Sulfolobus, and one of the six could not be assigned to

38 he ESCRT machinery play an important role in Sulfolobus cell division.

39 teins are essential for DNA transfer between Sulfolobus cells and act downstream of the Ups pili syst

40 0a shows no sequence similarity to the other Sulfolobus chromatin proteins Sac7d, Sac8, Sso10b2, and

41 one of the three replication origins in the Sulfolobus chromosome remain in close proximity, the thr

42 in situ hybridisation analyses, suggest that Sulfolobus chromosomes have a significant period of post

43 Therefore, MacDinB-1 is different from the Sulfolobus DinB proteins, which are members of cluster I

44 Members of the crenarchaeal kingdom, such as Sulfolobus, divide by binary fission yet lack genes for

45 Sulfolobus encodes a single-Xer homologue and its deleti

46 We propose that the Sulfolobus ESCRT machinery is involved in viral assembly

47 We found that Sulfolobus ESCRT-III and Vps4 homologs underwent regulat

48 in, CdvA, that is responsible for recruiting Sulfolobus ESCRT-III to membranes.

49 t treatment, cells of the crenarchaeal genus Sulfolobus express Ups pili, which initiate cell aggrega

50 As a way to investigate the impact of ISs on Sulfolobus genomes, we identified seven transpositionall

51 radually eliminate the defective copies from Sulfolobus genomes.

52 ingdom Crenarchaea, including members of the Sulfolobus genus, encode homologs of the eukaryotic endo

53 iscovery that the hyperthermophilic archaeon Sulfolobus has three replication origins.

54 that Aeropyrum pernix, a distant relative of Sulfolobus, has two origins.

55 Archaea of the genus Sulfolobus have a single-circular chromosome with three

56 Recent work has established that Sulfolobus homologs of the eukaryotic ESCRT-III and Vps4

57 viruses were isolated from hyperthermophilic Sulfolobus hosts, and both viruses share the spindle-sha

58 rst application of a dehydrogenase from this Sulfolobus hyperthermophile to asymmetric synthesis and

59 ulum in moderate-temperature acidic springs, Sulfolobus in high-temperature acidic springs, and Hydro

60 spatial and temporal population structure of Sulfolobus islandicus by comparing geochemical and molec

61 the ancestor to the Sulfolobus solfataricus-Sulfolobus islandicus clade was able to metabolize pheno

62 h population-scale comparative genomics of 7 Sulfolobus islandicus genomes from 3 locations, we demon

63 ve assessed interactions between proteins of Sulfolobus islandicus rod-shaped virus 2 (SIRV2) and the

64 olobus turreted icosahedral virus (STIV) and Sulfolobus islandicus rod-shaped virus 2 (SIRV2) produce

65 ation of ORF131b (gp17) and ORF436 (gp18) of Sulfolobus islandicus rod-shaped virus 2 (SIRV2), both e

66 The nonenveloped, rod-shaped virus SIRV2 (Sulfolobus islandicus rod-shaped virus 2) infects the hy

67 have sampled a population of closely related Sulfolobus islandicus strains from Kamchatka, Russia at

68 The Sulfolobus islandicus type III-B Cmr-alpha system target

69 e archaeal species: Sulfolobus solfataricus, Sulfolobus islandicus, and Pyrococcus furiosus.

70 2) infects the hyperthermophilic acidophile Sulfolobus islandicus, which lives at 80 degrees C and p

71 speciation in the thermoacidophilic Archaeon Sulfolobus islandicus.

72 nctional characterization of a novel ATPase, Sulfolobus islandicusPilT N-terminal-domain-containing A

73 The Sulfolobus ISs also differed with respect to target-site

74 Sulfolobus knockout strains that are incapable of formin

75 Analysis of the structure of the Sulfolobus MazG points to 2-hydroxyadenosine (isoguanosi

76 Here, we selected two archaeal viruses Sulfolobus monocaudavirus 1 (SMV1) and Sulfolobus spindl

77 tion of the Ampullaviridae family as well as Sulfolobus Monocaudavirus 1 (SMV1)-related viruses.

78 Comparison with the Sulfolobus origins provides evidence for evolution of re

79 inery and assembly mechanism of the archaeal Sulfolobus pNOB8 partition system.

80 of L14e shows the greatest similarity of any Sulfolobus protein to the reported N-terminal sequence o

81 occur in the genomes of both crenarchaeota (Sulfolobus, Pyrobaculum, Aeropyrum) and euryarchaeota (M

82 n of a catalytically inactive mutant Vps4 in Sulfolobus resulted in the accumulation of enlarged cell

83 Using the archaeal Sulfolobus shibabae enzyme as an example of the class I,

84 odeled the structure of the class I archaeal Sulfolobus shibatae CCA-adding enzyme on eukaryotic poly

85 us maripaludis pili filament and an archaeal Sulfolobus shibatae flagellar filament.

86 s of Methanobacterium thermautotrophicum and Sulfolobus shibatae in its strict specificity for ATP.

87 gly, the CCA-adding enzyme from the archaeon Sulfolobus shibatae is a homodimer that forms a tetramer

88 ation), and Methanosarcina mazei topo VI and Sulfolobus shibatae topo VI (type IIB enzymes, which do

89 mily from the hyperthermophilic crenarchaeon Sulfolobus shibatae, binds to RNA in vivo.

90 e Dpo4-like enzymes from Acidianus infernus, Sulfolobus shibatae, Sulfolobus tengchongensis, Stygiolo

91 erol phosphate synthase from the thermophile Sulfolobus solfataricus (sIGPS) and the alpha subunit of

92 he indole-3-glycerol phosphate synthase from Sulfolobus solfataricus (sIGPS), was assessed by hydroge

93 of indole-3-glycerol phosphate synthase from Sulfolobus solfataricus (sIGPS).

94 ay crystal structure of an archaeal NAT from Sulfolobus solfataricus (ssNAT).

95 The acylphosphatase from Sulfolobus solfataricus (Sso AcP) is a globular protein

96 ative-like state of the acylphosphatase from Sulfolobus solfataricus (Sso AcP).

97 ed within the hyperthermophilic crenarchaeon Sulfolobus solfataricus (Sso) and compared in vitro prim

98 major chromatin proteins, Alba and Sul7d, of Sulfolobus solfataricus (Sso) on the ability of the MCM

99 e replication DNA polymerase holoenzyme from Sulfolobus solfataricus (Sso) was investigated using pre

100 re of Csa3, a CRISPR-associated protein from Sulfolobus solfataricus (Sso1445), which reveals a dimer

101 The primary DNA replication polymerase from Sulfolobus solfataricus (SsoDpo1) has been shown previou

102 yltransferase from the thermophilic archaeon Sulfolobus solfataricus (SsOGT).

103 ichromosomal maintenance (MCM) helicase from Sulfolobus solfataricus (SsoMCM) is a model for understa

104 me maintenance (MCM) complex of the archaeon Sulfolobus solfataricus (SsoMCM).

105 The crystal structure of Sulfolobus solfataricus 5'-deoxy-5'-methylthioadenosine

106 efficient heterologous expression system for Sulfolobus solfataricus ADH-10 (Alcohol Dehydrogenase is

107 The activity of ThrRS from Sulfolobus solfataricus and Halobacterium sp. NRC-1 was

108 The genome of Sulfolobus solfataricus and related crenarchaea contain

109 rk, we describe the generation of strains of Sulfolobus solfataricus and Sulfolobus acidocaldarius th

110 Sulfolobus solfataricus and the infecting virus Sulfolob

111 Using Sso7d from Sulfolobus solfataricus as the DNA binding protein, we d

112 crystal structure of the archaeal RNAP from Sulfolobus solfataricus at 3.4 A resolution, completing

113 rates, whereas the Cas4 protein SSO1391 from Sulfolobus solfataricus can cleave ssDNA in both the 5'

114 Sulfolobus solfataricus contains a membrane-associated p

115 pecies complementation of a copper-sensitive Sulfolobus solfataricus copR mutant.

116 Cas1 from both Escherichia coli and Sulfolobus solfataricus display sequence specific activi

117 We have determined structures of Sulfolobus solfataricus DNA ligase and heterotrimeric PC

118 In the absence of nicked DNA, the Sulfolobus solfataricus DNA ligase has an open, extended

119 A similar bias is seen with Sulfolobus solfataricus DNA polymerase 4, which forms a

120 the kinetics and conformational dynamics of Sulfolobus solfataricus DNA polymerase B1 (PolB1) during

121 Previous work has shown that Sulfolobus solfataricus DNA polymerase Dpo4-catalyzed by

122 The human DNA polymerase kappa homolog Sulfolobus solfataricus DNA polymerase IV (Dpo4) produce

123 Steady-state kinetics with the Y-family Sulfolobus solfataricus DNA polymerase IV (Dpo4) showed

124 specifically placed dGAP lesion catalyzed by Sulfolobus solfataricus DNA polymerase IV (Dpo4), a mode

125 dducts derived from 1-NP, can be bypassed by Sulfolobus solfataricus DNA polymerase IV (Dpo4), althou

126 sequences were determined, with the Y-family Sulfolobus solfataricus DNA polymerase IV (Dpo4), at res

127 ction pathways of a Y-family DNA polymerase, Sulfolobus solfataricus DNA polymerase IV (Dpo4), for th

128 ) adduct by a model Y-family DNA polymerase, Sulfolobus solfataricus DNA polymerase IV (Dpo4).

129 ased model to explore functional dynamics in Sulfolobus solfataricus DNA Y-family polymerase IV (DPO4

130 lication, we have detected an interaction of Sulfolobus solfataricus DnaG (SsoDnaG) with the replicat

131 the catalytic efficiency of the model enzyme Sulfolobus solfataricus Dpo4 16,000-fold.

132 the structures of the model DNA polymerases Sulfolobus solfataricus Dpo4 and Bacillus stearothermoph

133 revious work with the translesion polymerase Sulfolobus solfataricus Dpo4 showed a decrease in cataly

134 In contrast to replicative DNA polymerases, Sulfolobus solfataricus Dpo4 showed a limited decrease i

135 Our previous publication shows that Sulfolobus solfataricus Dpo4 utilizes an 'induced-fit' m

136 ing situations in structures of complexes of Sulfolobus solfataricus Dpo4, a bypass pol that favors C

137 ings to that of a model translesion DNA pol, Sulfolobus solfataricus Dpo4.

138 chanism for blunt-end additions catalyzed by Sulfolobus solfataricus Dpo4.

139 ted that Lys-110 (numbering according to the Sulfolobus solfataricus enzyme) behaves as a general aci

140 we reveal that the highly studied PolB1 from Sulfolobus solfataricus exists as a heterotrimeric compl

141 three different operons of the crenarchaeon Sulfolobus solfataricus following UV irradiation.

142 and have applied it to Escherichia coli and Sulfolobus solfataricus for genome-wide prediction of nc

143 Here, we demonstrate that Hjc from Sulfolobus solfataricus forms a physical interaction wit

144 that the three RadA paralogs encoded by the Sulfolobus solfataricus genome are expressed under norma

145 rd of the open reading frames encoded in the Sulfolobus solfataricus genome were differentially expre

146 dentified ISs in the Sulfolobus tokodaii and Sulfolobus solfataricus genomes.

147 erent from those of the archaeal thermophile Sulfolobus solfataricus growing in the same temperature

148 The hyperthermophilic archaeon Sulfolobus solfataricus grows optimally above 80 degrees

149 Here we establish that the archaeon Sulfolobus solfataricus harbors a hybrid segrosome consi

150 By contrast, Sulfolobus solfataricus has a complex CRISPR-Cas system

151 t the Cas4 protein SSO0001 from the archaeon Sulfolobus solfataricus has metal-dependent endonuclease

152 6 homologous proteins (MCM2-7), the archaeon Sulfolobus solfataricus has only 1 MCM protein (ssoMCM),

153 The crenarchaeon Sulfolobus solfataricus has two divergent subtypes of th

154 spindle-shaped virus 1 (SSV1), which infects Sulfolobus solfataricus in volcanic hot springs at 80 de

155 proach to engineer the lactonase SsoPox from Sulfolobus solfataricus into a phosphotriesterase.

156 ea possess a homo-trimeric PCNA, the PCNA of Sulfolobus solfataricus is a heterotrimer.

157 protein from the hyperthermophilic archaeon Sulfolobus solfataricus is an attractive binding scaffol

158 The thermoacidophilic archaeon Sulfolobus solfataricus is known for its metabolic versa

159 The 3 million-base pair genome of Sulfolobus solfataricus likely undergoes depurination/de

160 For example, the archaeal Sulfolobus solfataricus minichromosome maintenance (SsoM

161 The structure is a chimera of Sulfolobus solfataricus N-terminal domain and Pyrococcus

162 sm of MCM from the hyperthermophilic Archaea Sulfolobus solfataricus on various DNA substrates.

163 ide was identified from tryptic digests from Sulfolobus solfataricus P1 by liquid chromatography-tand

164 investigated the ultrastructural changes of Sulfolobus solfataricus P2 associated with infection by

165 t the Y-family DNA polymerase IV (Dpo4) from Sulfolobus solfataricus P2 can preferentially insert C o

166 alyzed by an exonuclease-deficient mutant of Sulfolobus solfataricus P2 DNA polymerase B1 (PolB1 exo-

167 Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) has

168 lysis of the products of primer extension by Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) indi

169 Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) is a

170 mechanism of DNA polymerization catalyzed by Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) is r

171 mational dynamics of the Y-family polymerase Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) usin

172 of translesion bypass of 1,N(2)-epsilondG by Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4), lea

173 The hyperthermophilic crenarchaeon Sulfolobus solfataricus P2 encodes three B-family DNA po

174 Sulfolobus solfataricus P2 is an aerobic crenarchaeon wh

175 S2), an acidophilic and aerobic thermophile (Sulfolobus solfataricus P2), and an anaerobic hypertherm

176 ase Dpo4, from the thermophilic crenarchaeon Sulfolobus solfataricus P2, offers a valuable opportunit

177 etermined the X-ray crystal structure of the Sulfolobus solfataricus PCNA1-PCNA2 heterodimer, bound t

178 onuclease and the translesion DNA polymerase Sulfolobus solfataricus pol IV were used as models to di

179 The Sulfolobus solfataricus protein acetyltransferase (PAT)

180 The Sulfolobus solfataricus Rad54 (SsoRad54) protein is a do

181 The crystal structure of Sulfolobus solfataricus RadA has been solved to a resolu

182 ite of the homologous alpha-glucosidase from Sulfolobus solfataricus resulted in a shift from hydroly

183 The archaeal homohexameric MCM helicase from Sulfolobus solfataricus serves as a model for understand

184 Y-Family DNA polymerase IV (Dpo4) from Sulfolobus solfataricus serves as a model system for euk

185 re we have produced a fusion protein between Sulfolobus solfataricus SRP54 (Ffh) and a signal peptide

186 Sulfolobus solfataricus SSB (SsoSSB) contains a single O

187 report a role for the thermophilic archaeal Sulfolobus solfataricus SSB (SsoSSB) in the presynaptic

188 We demonstrate that Sulfolobus solfataricus SSB can melt DNA containing a mi

189 Following infection of Sulfolobus solfataricus strain 2-2-12 with STIV, transcr

190 tinct for each strain, indicating that these Sulfolobus solfataricus strains have differential respon

191 scribed here focuses on the response of four Sulfolobus solfataricus strains to ionizing radiation (I

192 we have characterized the responses of three Sulfolobus solfataricus strains to UV-C irradiation, whi

193 rmined structure of a MazG-like protein from Sulfolobus solfataricus supported the unification of the

194 Sulfolobus solfataricus TFS1 functions as a bona fide cl

195 A-binding proteins from the hyperthermophile Sulfolobus solfataricus that has been associated with DN

196 Sulfolobus solfataricus ThrRS-cat was shown to synthesiz

197 Methanococcus maripaludis tRNA2(Ile) and in Sulfolobus solfataricus total tRNA, indicating its proba

198 The archaeon Sulfolobus solfataricus uses a catabolite repression-lik

199 The crenarchaeon Sulfolobus solfataricus uses arginine to produce putresc

200 differences, we have characterized Dpo4 from Sulfolobus solfataricus using the same biochemical and c

201 ctive wild-type Saccharomyces cerevisiae and Sulfolobus solfataricus Vps4 enzymes can form hexamers i

202 ative LipA from the hypothermophilic archaea Sulfolobus solfataricus was expressed in Escherichia col

203 aea, the splicing endonuclease from archaeum Sulfolobus solfataricus was found to contain two differe

204 The archaeon Sulfolobus solfataricus was sensitive to mercuric chlori

205 The Sulfolobus solfataricus Y-family DNA polymerase Dpo4 is

206 itional microorganisms (Escherichia coli and Sulfolobus solfataricus) revealed species-specific assim

207 icative and lesion bypass DNA polymerases of Sulfolobus solfataricus, a hyperthermophilic crenarchaeo

208 Orc1-1 and Orc1-3 paralogs from the archaeon Sulfolobus solfataricus, and tested their effect on orig

209 IV (Dpo4), a prototype Y-family enzyme from Sulfolobus solfataricus, can bypass 8-oxoG both efficien

210 Y-family DNA polymerases, such as Dpo4 from Sulfolobus solfataricus, can traverse a wide variety of

211 dentified splicing endonuclease homolog from Sulfolobus solfataricus, despite possessing all of the p

212 undant proteins present in the crenarchaeote Sulfolobus solfataricus, including subunits of the therm

213 polymerase Dpo4, from the archaeon bacterium Sulfolobus solfataricus, is a member of the DinB family,

214 virus that infects the hyperthermoacidophile Sulfolobus solfataricus, is one of the most well-studied

215 se (Dpo1) in the hyperthermophilic archaeon, Sulfolobus solfataricus, is shown here to possess a rema

216 nly been examined in three archaeal species: Sulfolobus solfataricus, Sulfolobus islandicus, and Pyro

217 In Sulfolobus solfataricus, this complex is composed of sev

218 In the crenarchaeon Sulfolobus solfataricus, type IV pili formation is stron

219 ructure of the CSM complex from the archaeon Sulfolobus solfataricus, using a combination of electron

220 etypal Y-family member from the thermophilic Sulfolobus solfataricus, was used to extend our kinetic

221 the third replication origin in the archaeon Sulfolobus solfataricus, we identify and characterise si

222 d two origins of replication in the archaeon Sulfolobus solfataricus, whereas a second study used a d

223 e demonstrate that the XPF endonuclease from Sulfolobus solfataricus, which is dependent on the slidi

224 lesion-bypass DNA polymerase IV (Dpo4) from Sulfolobus solfataricus, with template guanine and Watso

225 yses also predicted that the ancestor to the Sulfolobus solfataricus-Sulfolobus islandicus clade was

226 s required for pyramid formation in its host Sulfolobus solfataricus.

227 protein from the hyperthermophilic archaeon Sulfolobus solfataricus.

228 ation of an archaeal CASCADE (aCASCADE) from Sulfolobus solfataricus.

229 onally related archaeal exosome complex from Sulfolobus solfataricus.

230 ics of a model Y-family polymerase Dpo4 from Sulfolobus solfataricus.

231 h a model Y-family DNA polymerase, Dpo4 from Sulfolobus solfataricus.

232 ermostable enzyme isolated from the archaeon Sulfolobus solfataricus.

233 omologous XPB proteins from the crenarchaeon Sulfolobus solfataricus.

234 ipaludis, Methanocaldococcus jannaschii, and Sulfolobus solfataricus.

235 ns-lesion (Y-class) DNA polymerase Dpo4 from Sulfolobus solfataricus.

236 imeric MCM of the hyperthermophilic archaeon Sulfolobus solfataricus.

237 is by a model Y family polymerase, Dpo4 from Sulfolobus solfataricus.

238 protein from the thermoacidophilic archaeon Sulfolobus solfataricus.

239 neralized transcription in the crenarchaeote Sulfolobus solfataricus.

240 xidant from the hyperthermophilic acidophile Sulfolobus solfataricus.

241 -resolving enzyme; the Hje endonuclease from Sulfolobus solfataricus.

242 ion structure and properties of Sso10b2 from Sulfolobus solfataricus.

243 igh-resolution crystal structure of Hje from Sulfolobus solfataricus.

244 regulation in the hyperthermophilic archaeon Sulfolobus solfataricus.

245 e single-stranded DNA-binding protein SSB in Sulfolobus solfataricus.

246 e primase was identified in the crenarchaeon Sulfolobus solfataricus.

247 ed PriX, from the hyperthermophilic archaeon Sulfolobus solfataricus.

248 ases human Pol eta and P2 Pol IV (Dpo4) from Sulfolobus solfataricus.

249 purified CRISPR-associated CMR complex from Sulfolobus solfataricus.

250 ding virus in the hyperthermophilic archaeon Sulfolobus solfataricus.

251 ymerase (YB site) bound to PCNA and DNA from Sulfolobus solfataricus.

252 it named PriX was identified in the archaeon Sulfolobus solfataricus.

253 dic hot springs where it infects the archeon Sulfolobus solfataricus.

254 og proteins, SsoRal3, from the crenarchaeaon Sulfolobus solfataricus.

255 tro using proteins derived from the archaeon Sulfolobus solfataricus.

256 se 3, SsTop3, from the thermophilic archaeon Sulfolobus solfataricus.

257 protein from the hyperthermophilic archaeon Sulfolobus solfataricus; Sso7d-hFc was isolated from a c

258 Dpo4 and Dbh are from two closely related Sulfolobus species and are well studied archaeal homolog

259 Sac10b homologs in thermophilic Sulfolobus species are very abundant.

260 The UV-induced pili of three different Sulfolobus species had distinct morphologies, and corres

261 atterns and protein regulation levels in two Sulfolobus species in "biofilm vs planktonic" experiment

262 It infects Sulfolobus species that thrive in the acidic hot springs

263 itionally active ISs in a widely distributed Sulfolobus species, and measured their functional proper

264 ly over time, primarily from closely related Sulfolobus species.

265 g another example for pathway promiscuity in Sulfolobus species.

266 ruses Sulfolobus monocaudavirus 1 (SMV1) and Sulfolobus spindle shaped virus 2 (SSV2) owing to their

267 Sulfolobus spindle-shaped virus 1 (SSV1) and its fusello

268 to study the well-characterized fusellovirus Sulfolobus spindle-shaped virus 1 (SSV1), which infects

269 e show that bacteriophage T4, archaeal virus Sulfolobus spindle-shaped virus Kamchatka, and vaccinia

270 fforts, we report the structure of D212 from Sulfolobus spindle-shaped virus Ragged Hills.

271 ficant contributions to our understanding of Sulfolobus spindle-shaped viruses (Fuselloviridae), an i

272 The complete genome sequences of two Sulfolobus spindle-shaped viruses (SSVs) from acidic hot

273 Sulfolobus spindle-shaped viruses (SSVs), or Fuselloviri

274 f replication errors in chromosomal genes of Sulfolobus spp. demonstrate that these extreme thermoaci

275 about the threat of ectopic recombination in Sulfolobus spp. mediated by this apparently efficient ye

276 of accurate classifications from subspecies (Sulfolobus spp.) to phyla, and of preliminary rooting of

277 Unlike the heavily methylated Sulfolobus SSU RNA, Thermus contains a single ribose-met

278 rom Acidianus infernus, Sulfolobus shibatae, Sulfolobus tengchongensis, Stygiolobus azoricus and Sulf

279 al copies of the newly identified ISs in the Sulfolobus tokodaii and Sulfolobus solfataricus genomes.

280 Here, we present the crystal structure of Sulfolobus tokodaii malonyl-CoA reductase in the substra

281 me ST0928 from a hyperthermophilic archaeron Sulfolobus tokodaii was cloned and expressed in E. coli.

282 ryotic (Escherichia coli, Bacillus subtilis, Sulfolobus tokodaii, and Thermotoga maritima) and two eu

283 ystal structure of XPD from the crenarchaeon Sulfolobus tokodaii, presented here together with detail

284 putative regulator ST1710 from the archaeon Sulfolobus tokodaii.

285 Archaeal host cells infected by Sulfolobus turreted icosahedral virus (STIV) and Sulfolo

286 Host cells infected by Sulfolobus turreted icosahedral virus (STIV) have been s

287 The Sulfolobus turreted icosahedral virus (STIV) is a double

288 folobus solfataricus and the infecting virus Sulfolobus turreted icosahedral virus (STIV) is one of t

289 Microarray analysis of infection by Sulfolobus turreted icosahedral virus (STIV) revealed in

290 Sulfolobus turreted icosahedral virus (STIV) was isolate

291 Sulfolobus turreted icosahedral virus (STIV) was the fir

292 Sulfolobus turreted icosahedral virus (STIV), an archaea

293 Sulfolobus turreted icosahedral virus (STIV), isolated f

294 solfataricus P2 associated with infection by Sulfolobus turreted icosahedral virus (STIV).

295 ophilic viruses that infect archaea, such as Sulfolobus turreted icosahedral virus and halophage SH1.

296 thus, prevents establishment of a productive Sulfolobus turreted icosahedral virus infection.

297 rent work, we reveal that the archaeal virus Sulfolobus turreted icosahedral virus isolated from Yell

298 ure of the major capsid protein (MCP) of the Sulfolobus turreted icosahedral virus, an archaeal virus

299 t of Archaea, including members of the genus Sulfolobus where it plays a role in cytokinesis.

300 nuclear antigen may dictate the activity of Sulfolobus XPF in vivo.