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 rs of hyperthermophilic archaea of the genus Sulfolobus.

5 epressor and its overexpression is toxic for Sulfolobus.

6 estabilization of RNA secondary structure in Sulfolobus.

7 continuous cultures of the thermoacidophile Sulfolobus acidocaldarius (DSM 639).

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 bacterial cells (Methanosarcina acetivorans, Sulfolobus acidocaldarius and Pseudomonas putida) enrich

12 d GrsB, essential for GDGT ring formation in Sulfolobus acidocaldarius Both proteins are radical S-ad

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

14 ther with this system, we were able to image Sulfolobus acidocaldarius cells live to reveal tight cou

15 In Sulfolobus acidocaldarius conjugation assays, recombinan

16 ganism, we cultivated the model Crenarchaeon Sulfolobus acidocaldarius DSM639 at different combinatio

17 aii 'restored' sulphur oxidation capacity in Sulfolobus acidocaldarius DSM639, but not autotrophy, al

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

19 Sulfolobus acidocaldarius is the closest experimentally

20 317H variant of the thermostable CYP119 from Sulfolobus acidocaldarius maintains heme iron coordinati

21 efore, we determine the crystal structure of Sulfolobus acidocaldarius soluble FlaG (sFlaG), which re

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

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

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

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

26 e thermostable M/R complex from the archaeon Sulfolobus acidocaldarius using atomic force microscopy

27 Sulfolobus acidocaldarius utilizes glucose and xylose as

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

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

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

31 In the crenearchaeon Sulfolobus acidocaldarius, biosynthesis of the archaellu

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

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

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

35 and ArnB, in the thermoacidophilic archaeon Sulfolobus acidocaldarius, where they act synergisticall

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

37 ave used previously to characterize Dbh from Sulfolobus acidocaldarius.

38 ated from the thermoacidophilic crenarchaeon Sulfolobus acidocaldarius.

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

40 onents during starvation-induced motility in Sulfolobus acidocaldarius.

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

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

43 sylation is present for Pyrobaculum than for Sulfolobus and Saccharolobus pili.

44 We reveal that chromosomes of Sulfolobus archaea are organized into CID-like topologic

45 Sulfolobus are the most intensively studied members of T

46 eparation and cytokinesis are coordinated in Sulfolobus, as is the case in eukaryotes, and that two c

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

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

49 , to date, it has not been possible to image Sulfolobus cells as they grow and divide.

50 Strikingly, Sulfolobus cells that lack the S-layer component bound b

51 lymers perform distinct roles to ensure that Sulfolobus cells undergo a robust and symmetrical divisi

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

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

54 eveal the presence of distinct domains along Sulfolobus chromosomes that undergo discrete and specifi

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

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

57 many archaea, including members of the genus Sulfolobus do not encode canonical condensin.

58 Sulfolobus encodes a single-Xer homologue and its deleti

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

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

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

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

63 not display the remarkable stability of the Sulfolobus filaments in vitro.

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

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

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

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

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

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

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

71 Pili on the surface of Sulfolobus islandicus are used for many functions, and s

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

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

74 1 (SSRV1), at 2.8- angstrom resolution, and Sulfolobus islandicus filamentous virus (SIFV), at 4.0-

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

76 glycosylation previously observed in T4P of Sulfolobus islandicus is a response to an acidic environ

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

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

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

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

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

82 and genetic analyses of the paralogs within Sulfolobus islandicus supported the hypothesis that LeuR

83 We identify the resistance of Sulfolobus islandicus to Sulfolobus spindle-shaped virus

84 Here we show that the Sulfolobus islandicus type I-D Cas10d large subunit exhi

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

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

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

88 speciation in the thermoacidophilic Archaeon Sulfolobus islandicus.

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

90 Sulfolobus knockout strains that are incapable of formin

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

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

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

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

95 .7- angstrom resolution the structure of the Sulfolobus polyhedral virus 1 (SPV1), which was original

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

112 We found that KARI from archaea Sulfolobus solfataricus (Sso-KARI) is unusual in being a

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

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

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

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

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

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

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

120 The genome of Sulfolobus solfataricus and related crenarchaea contain

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

122 Sulfolobus solfataricus and the infecting virus Sulfolob

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

156 The hyperthermophilic archaeon Sulfolobus solfataricus grows optimally above 80 degrees

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

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

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

160 6 homologous proteins (MCM2-7), the archaeon Sulfolobus solfataricus has only 1 MCM protein (ssoMCM),

161 The crenarchaeon Sulfolobus solfataricus has two divergent subtypes of th

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

163 ation of structure in an intermediate in the Sulfolobus solfataricus indole-3-glycerol phosphate synt

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

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

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

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

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

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

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

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

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

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

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

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

176 Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) has

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

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

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

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

181 Sulfolobus solfataricus P2 is an aerobic crenarchaeon wh

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

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

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

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

186 The Sulfolobus solfataricus protein acetyltransferase (PAT)

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

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

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

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

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

192 Sulfolobus solfataricus SSB (SsoSSB) contains a single O

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

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

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

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

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

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

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

200 Sulfolobus solfataricus TFS1 functions as a bona fide cl

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

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

203 Previously, we demonstrated that the Sulfolobus solfataricus type III-D CRISPR complex genera

204 The crenarchaeon Sulfolobus solfataricus uses arginine to produce putresc

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

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

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

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

209 iota and Dpo4 from the archaeal thermophile Sulfolobus solfataricus We found that hpol eta and Dpo4

210 The Sulfolobus solfataricus Y-family DNA polymerase Dpo4 is

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

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

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

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

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

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

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

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

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

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

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

222 In Sulfolobus solfataricus, this complex is composed of sev

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

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

225 us work, the thermoacidophilic crenarchaeon, Sulfolobus solfataricus, was subjected to adaptive labor

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

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

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

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

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

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

232 tro using proteins derived from the archaeon Sulfolobus solfataricus.

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

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

235 protein from the hyperthermophilic archaeon Sulfolobus solfataricus.

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

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

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

239 omologous XPB proteins from the crenarchaeon Sulfolobus solfataricus.

240 ipaludis, Methanocaldococcus jannaschii, and Sulfolobus solfataricus.

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

242 imeric MCM of the hyperthermophilic archaeon Sulfolobus solfataricus.

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

244 protein from the thermoacidophilic archaeon Sulfolobus solfataricus.

245 neralized transcription in the crenarchaeote Sulfolobus solfataricus.

246 xidant from the hyperthermophilic acidophile Sulfolobus solfataricus.

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

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

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

250 onally related archaeal exosome complex from Sulfolobus solfataricus.

251 ermostable enzyme isolated from the archaeon Sulfolobus solfataricus.

252 ed PriX, from the hyperthermophilic archaeon Sulfolobus solfataricus.

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

254 purified CRISPR-associated CMR complex from Sulfolobus solfataricus.

255 ding virus in the hyperthermophilic archaeon Sulfolobus solfataricus.

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

257 ation orientation of Saccharolobus (formally Sulfolobus) solfataricus MCM on DNA.

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 ly over time, primarily from closely related Sulfolobus species.

264 romosome conformation capture experiments on 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 y the resistance of Sulfolobus islandicus to Sulfolobus spindle-shaped virus (SSV9) conferred by chro

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

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

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

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

276 In sequenced Sulfolobus strains from around the globe, one copy of ea

277 y maps of archaeal S-layers from 3 different Sulfolobus strains.

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

279 iosulphate-quinone oxidoreductase (TQO) from Sulfolobus tokodaii 'restored' sulphur oxidation capacit

280 th Bax1 from Archaeoglobus fulgidus (Af) and Sulfolobus tokodaii (St).

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

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

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 Additionally, studies using Sulfolobus were among the first to reveal striking simil

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