ライフサイエンスコーパス: Methanococcus

1 n the antibiotic-insensitive archaebacterium Methanococcus.

2 proteolipid type found in eukaryotes and in Methanococcus.

3 ty between an adjacent upstream sequence and Methanococcus 16S rRNA.

4 synthase (AHAS) was cloned from the archaeon Methanococcus aeolicus.

5 consecutive helices (alpha-alpha-alpha), and Methanococcus, alternating helix-strand structures (beta

6 and function of the predicted exosome in the Methanococcus and Halobacterium lineages.

7 rent gene loss complementary to that seen in Methanococcus and Halobacterium, Thermoplasma acidophilu

8 present evidence for a "nitrogen regulon" in Methanococcus and Methanobacterium species containing ge

9 eropyrum) and euryarchaeota (Methanosarcina, Methanococcus, Archaeoglobus, Thermoplasma), with multip

10 dies of the mesophiles in the archaeal genus Methanococcus have become commonplace following the rece

11 tions found in yeast fibrillarin Nop1 to the Methanococcus homologue structure reveals that many of t

12 trophicus (MTH), and the extreme thermopiles Methanococcus igneus (MIG) and Methanococcus jannaschii

13 perthermophiles Methanococcus jannaschii and Methanococcus igneus were studied to determine whether m

14 ol to generate DIP has also been detected in Methanococcus igneus.

15 ng candidate enzymes previously evolved from Methanococcus janaschii Tyr synthetase for unnatural ami

16 hose of Haemophilus influenzae (a bacteria), Methanococcus jannaschii (an archaeon), and yeast (a euk

17 ted from ribosomes and whole-cell lysates of Methanococcus jannaschii (approximately 1,800 genes) usi

18 The crystal structure of eIF-5A from Methanococcus jannaschii (MJ eIF-5A) has been determined

19 The small heat-shock protein (sHSP) from Methanococcus jannaschii (Mj HSP16.5) forms a homomeric

20 motetrameric tRNA splicing endonuclease from Methanococcus jannaschii (MJ), indicating its role in ca

21 n of C8-substituted-nucleotides by FtsZ from Methanococcus jannaschii (Mj-FtsZ) and Bacillus subtilis

22 with that of a previously solved enzyme from Methanococcus jannaschii (MJ0109).

23 e thermopiles Methanococcus igneus (MIG) and Methanococcus jannaschii (MJA)) were characterized for t

24 a hyperthermophilic piezophilic methanogen, Methanococcus jannaschii (Mja).

25 MAT from the hyperthermophilic archaeon Methanococcus jannaschii (MjMAT) is a prototype of the n

26 from the thermophilic methanogenic archaeon Methanococcus jannaschii (Mjpri).

27 a(+)/Ca(2+)-exchange function of an NCX from Methanococcus jannaschii (NCX_Mj) and report its 1.9 ang

28 and 31 open reading frames including one in Methanococcus jannaschii .

29 teria such as Escherichia coli, archaea like Methanococcus jannaschii and animal viruses.

30 for three other I-1-Pases (from the archaea Methanococcus jannaschii and Archaeoglobus fulgidus, and

31 udy, these potential RubisCO sequences, from Methanococcus jannaschii and Archaeoglobus fulgidus, wer

32 for highly similar proteins were detected in Methanococcus jannaschii and Bacillus stearothermophilus

33 aea Methanobacterium thermoautotrophicum and Methanococcus jannaschii and in Bacillus subtilis.

34 synthetase in the genomes of Archae such as Methanococcus jannaschii and Methanobacterium thermoauto

35 he only known exceptions are the euryarchaea Methanococcus jannaschii and Methanobacterium thermoauto

36 the mechanism of cysteinyl-tRNA formation in Methanococcus jannaschii and Methanobacterium thermoauto

37 The genomic sequences of Methanococcus jannaschii and Methanobacterium thermoauto

38 residing in the transcription factor IIB of Methanococcus jannaschii and Methanocaldococcus vulcaniu

39 thermolithotrophicus, and hyperthermophiles Methanococcus jannaschii and Methanococcus igneus were s

40 s and, in part, its operon organization with Methanococcus jannaschii and Methanothermobacter thermoa

41 dehydrogenase genes, MJ1425 and MJ0490, from Methanococcus jannaschii and one from Methanothermus fer

42 rom47 Aquifex aeolicus,47 Bacillus subtilis, Methanococcus jannaschii and Pseudomonas aeruginosa that

43 screening for GC-rich regions in the AT-rich Methanococcus jannaschii and Pyrococcus furiosus genomes

44 ied in the hyperthermophilic marine archaeon Methanococcus jannaschii and shown to catalyze the final

45 FEN1 enzymes from Archaeoglobus fulgidus and Methanococcus jannaschii and the DNA polymerase I homolo

46 om several archaea, including the methanogen Methanococcus jannaschii and the sulfate-reducing archae

47 binant versions of the F and P subunits from Methanococcus jannaschii and used them in in vitro and i

48 Escherichia coli, Haemophilus influenzae and Methanococcus jannaschii are involved in 64 unique fusio

49 s of two adjacent genes in the chromosome of Methanococcus jannaschii are similar to the amino and ca

50 stal structure of a specificity subunit from Methanococcus jannaschii at 2.4-A resolution.

51 rt the crystal structure of the complex from Methanococcus jannaschii at a resolution of 3.2 A.

52 oth Methanobacterium thermoautotrophicum and Methanococcus jannaschii but is unrelated to canonical L

53 derived from the tyrosyl-tRNA synthetase of Methanococcus jannaschii can be used to genetically enco

54 The complete genomic sequencing of Methanococcus jannaschii cannot identify the gene for th

55 family, the archaeal Sulfolobus shibatae and Methanococcus jannaschii CCA-adding enzymes, are also ca

56 f the hyperthermophiles Aquifex aeolicus and Methanococcus jannaschii complement enteric amtB mutants

57 sequence of the hyperthermophilic methanogen Methanococcus jannaschii contains homologs of most genes

58 rial S. typhimurium CorA and by the archaeal Methanococcus jannaschii CorA, which bear only 12% ident

59 the structure of the DNA-binding core of the Methanococcus jannaschii DNA topoisomerase VI A subunit

60 The hyperthermophilic archaeon Methanococcus jannaschii encodes two putative transcript

61 The hyperthermophilic archaeon Methanococcus jannaschii encodes two putative transcript

62 a, Saccharomyces cerevisiae for Eukarya, and Methanococcus jannaschii for Archaea, provide the basis

63 The Methanococcus jannaschii gene MJ0671 was cloned and over

64 The Methanococcus jannaschii gene MJ1392 was cloned, and its

65 In comparisons of the entire set of Methanococcus jannaschii genes with their orthologs from

66 Comparisons with the Methanococcus jannaschii genome data underline the exten

67 One of the ORFs in the Methanococcus jannaschii genome possesses high similarit

68 The interpretation of the Methanococcus jannaschii genome will inevitably require

69 From homology searching of the Methanococcus jannaschii genome, a gene coding for an en

70 asma genitalium, Haemophilus influenzae, and Methanococcus jannaschii genomes for unidentified or mis

71 but homologous enzymes, the hyperthermophile Methanococcus jannaschii has an enzyme, DCD-DUT, that ha

72 beta-semialdehyde dehydrogenase (ASADH) from Methanococcus jannaschii has been determined to 2.3 angs

73 ble 8-oxoguanine (oxoG) DNA glycosylase from Methanococcus jannaschii has been expressed in Escherich

74 The hyperthermophilic euryarchaeon Methanococcus jannaschii has no recognizable homologues

75 The hyperthermophilic archaeon Methanococcus jannaschii has two members of this gene fa

76 Cell extracts of Methanococcus jannaschii have been shown to readily conv

77 Analyses of the F(420)s present in Methanococcus jannaschii have shown that these cells con

78 lactate synthase encoded by the ComA gene in Methanococcus jannaschii have suggested that ComA, which

79 lutionary distant alpha-crystallin domain in Methanococcus jannaschii heat-shock protein 16.5 reveals

80 ontrast to the syn conformation reported for Methanococcus jannaschii homoserine kinase.

81 The high-resolution structures of Methanococcus jannaschii HSK ternary complexes with its

82 vergence, we induced the ordered oligomer of Methanococcus jannaschii Hsp16.5 to transition to either

83 y studies of five different sHSP assemblies: Methanococcus jannaschii HSP16.5, human alphaB-crystalli

84 the complete genome sequence of the archaeon Methanococcus jannaschii in 1996.

85 We have polymerized FtsZ1 from Methanococcus jannaschii in the presence of millimolar c

86 le cassette of known structure, MJ0796, from Methanococcus jannaschii indicates that at least two bin

87 AdoMetDC from the Archaea Methanococcus jannaschii is a prototype for a recently d

88 mple, a previous putative gene (MJ1604) from Methanococcus jannaschii is now annotated as a phosphofr

89 Whereas ProRS from Methanococcus jannaschii is similar to E. coli in its ab

90 Two putative Methanococcus jannaschii isocitrate dehydrogenase genes,

91 The genome of the archaeon Methanococcus jannaschii lacks the gene for a normal cys

92 ative third catalytic residue from a related Methanococcus jannaschii LonB, also faces the solvent an

93 hosphate (in a reaction analogous to that of Methanococcus jannaschii MJ0044).

94 similarity to that of the recently reported Methanococcus jannaschii Mj0226 protein.

95 The protein product of the Methanococcus jannaschii MJ0503 gene aksA (AksA) was fou

96 old classes have been proposed: one based on Methanococcus jannaschii MJ0577 (1MJH) that binds ATP, a

97 The protein product of the Methanococcus jannaschii MJ0768 gene has been expressed

98 We studied a prototypical ABC NBD, the Methanococcus jannaschii MJ0796, using spectroscopic tec

99 h are typified by Bacillus subtilis YqeV and Methanococcus jannaschii Mj0867, and we predict that Rim

100 Methanococcus jannaschii MJ0936 is a hypothetical protei

101 The Methanococcus jannaschii MJ109 gene product, the sequenc

102 The protein product of the Methanococcus jannaschii MJ1256 gene has been expressed

103 Here,Methanococcus jannaschii MR-ATPgammaS-DNA structure reve

104 recognition model based on the structures of Methanococcus jannaschii Mre11 (MjMre11) bound to longer

105 The archaeal NCX_Mj (Methanococcus jannaschii NCX) system was used to resolve

106 onsense codon, TAG, together with orthogonal Methanococcus jannaschii or Escherichia coli tRNA/synthe

107 Methanococcus jannaschii partially retains the superoper

108 e forms part of a multidomain protein, as in Methanococcus jannaschii peptidyl-prolyl cis/trans isome

109 Both the Methanococcus jannaschii phosphoenolpyruvate synthase an

110 The protein translation apparatus of Methanococcus jannaschii possesses the unusual enzyme pr

111 The archaeal Methanococcus jannaschii ProRS is a member of the eukary

112 Studies with human and Methanococcus jannaschii ProRS, which lack a post-transf

113 A solution NMR study of a model ABC, Methanococcus jannaschii protein MJ1267, reveals that AD

114 The phylogenetic distribution of Methanococcus jannaschii proteins can provide, for the f

115 uence of the extremely thermophilic archaeon Methanococcus jannaschii provides a wealth of data on pr

116 he hyperthermophiles Thermotoga maritima and Methanococcus jannaschii resulted in fivefold higher T.

117 vely high similarity to the sequences of the Methanococcus jannaschii reverse gyrase (48% overall ide

118 y the recently solved X-ray structure of the Methanococcus jannaschii SecY complex, is a matter of co

119 changer (NCX) antiporter NCX_Mj protein from Methanococcus jannaschii shows an outward-facing conform

120 We have solved the structure of the Methanococcus jannaschii Spt4/5 complex by X-ray crystal

121 coli, and their ability to bind to human and Methanococcus jannaschii SRP RNA were determined in vitr

122 genes from the thermophilic archaeabacterium Methanococcus jannaschii that code for the putative cata

123 nucleotide triphosphate pyrophosphatase from Methanococcus jannaschii that shows a preference for pur

124 oded by bacterial genomes ranged from 8% for Methanococcus jannaschii to 37% for Mycoplasma pneumonia

125 For Methanococcus jannaschii tRNA(Pro), accuracy is difficul

126 he crystal structures of two substrate-bound Methanococcus jannaschii tyrosyl aminoacyl-tRNA syntheta

127 o alter or expand the genetic code, only the Methanococcus jannaschii tyrosyl tRNA synthetase and tRN

128 The Methanococcus jannaschii tyrosyl-transfer-RNA synthetase

129 ocedure, we apply it to the design of mutant Methanococcus jannaschii tyrosyl-tRNA synthetase (M.jann

130 Methanococcus jannaschii tyrosyl-tRNA synthetase is a mi

131 The small size of the archaebacterial Methanococcus jannaschii tyrosyl-tRNA synthetase may giv

132 We synthesized 1 and evolved a Methanococcus jannaschii tyrosyl-tRNA synthetase/tRNA(CU

133 The hyperthermophilic euryarchaeon Methanococcus jannaschii uses coenzyme M (2-mercaptoetha

134 , we demonstrate that the Thi4 ortholog from Methanococcus jannaschii uses exogenous sulfide and is c

135 of subunit H, in solution, from the archaeon Methanococcus jannaschii using multidimensional nuclear

136 MVP, a Methanococcus jannaschii voltage-gated potassium channel

137 ucture of the endonuclease from the archaeon Methanococcus jannaschii was determined to a resolution

138 In the work presented here, aIF2beta from Methanococcus jannaschii was expressed in Escherichia co

139 ease (FEN) of the hyperthermophilic archaeon Methanococcus jannaschii was expressed in Escherichia co

140 for observed IMP cyclohydrolase activity in Methanococcus jannaschii was purified and sequenced: its

141 monella serovar Typhimurium and the archaeon Methanococcus jannaschii were purified and shown to reta

142 e have investigated three such proteins from Methanococcus jannaschii with the strongest overall sequ

143 udy, a conserved archaeal gene (gi1500322 in Methanococcus jannaschii) was identified as the best can

144 Cd1 from Clostridium difficile, and Mj2 from Methanococcus jannaschii) were overproduced in Escherich

145 plasma genitalium, Synechocystis PCC6803 and Methanococcus jannaschii).

146 structure of the fibrillarin homologue from Methanococcus jannaschii, a hyperthermophile, at 1.6 A r

147 A sHSP homologue of Methanococcus jannaschii, a hyperthermophilic Archaeon,

148 structure of a small heat-shock protein from Methanococcus jannaschii, a hyperthermophilic archaeon.

149 The methanarchaeon, Methanococcus jannaschii, a hyperthermophilic, autotroph

150 the genomic sequence of the hyperthermophile Methanococcus jannaschii, addressing questions of its ph

151 Many archaebacteria, such as Methanococcus jannaschii, also contain a gene (S4) that

152 for chorismate mutase (CM) from the archaeon Methanococcus jannaschii, an extreme thermophile, was su

153 In contrast, the IMPase from Methanococcus jannaschii, an organism in which DIP does

154 tyrosyl-tRNA synthetases from S. cerevisiae, Methanococcus jannaschii, and Bacillus stearothermophilu

155 genome sequence of an autotrophic archaeon, Methanococcus jannaschii, and its 58- and 16-kilobase pa

156 Archaeoglobus fulgidus, Pyrococcus furiosus, Methanococcus jannaschii, and Methanobacterium thermoaut

157 neumoniae, Synechocystis sp. strain PCC6803, Methanococcus jannaschii, and Pyrobaculum aerophilum).

158 lap endonuclease from Archaeglobus fulgidus, Methanococcus jannaschii, and Pyrococcus furiosus, respe

159 en purified to homogeneity from the archaeon Methanococcus jannaschii, and the gene encoding it has b

160 In this report, it is shown not only that Methanococcus jannaschii, Archaeoglobus fulgidus, Methan

161 ch protein, MJ0577, from a hyperthermophile, Methanococcus jannaschii, at 1.7-A resolution.

162 The MJ1149 gene from the Archaeon, Methanococcus jannaschii, has been cloned and expressed

163 t variations were observed in (G+C)% and, in Methanococcus jannaschii, in the frequency of the dinucl

164 rophosphatase gene from the archaebacterium, Methanococcus jannaschii, introduced into E. coli, incre

165 isolated from the hyperthermophilic Archaea Methanococcus jannaschii, is a member of the small heat-

166 hose genomes have been sequenced completely (Methanococcus jannaschii, Methanobacterium thermoautotro

167 no orthologs for these genes can be found in Methanococcus jannaschii, Methanobacterium thermoautotro

168 letely sequenced and are publicly available: Methanococcus jannaschii, Methanobacterium thermoautotro

169 is sp. genome nor in the archaeal genomes of Methanococcus jannaschii, Methanobacterium thermoautotro

170 ately halophilic and non-halophilic Archaea (Methanococcus jannaschii, Methanosarcina mazei, Methanob

171 structure of the corresponding protein from Methanococcus jannaschii, MJ0158.

172 segment, RCK domain-containing channel from Methanococcus jannaschii, MjK2, by testing its general f

173 Haemophilus influenzae, Helicobacter pylori, Methanococcus jannaschii, Mycoplasma pneumoniae, M. geni

174 ations for 81 gel patterns for Homo sapiens, Methanococcus jannaschii, Pyro coccus furiosus, Shewanel

175 d metal ion, which is different from that of Methanococcus jannaschii, strongly supports an active ro

176 habditis elegans, Methanopyrus kandleri, and Methanococcus jannaschii, suggesting a conservation of i

177 ynthetic organisms, viz. the archaebacterium Methanococcus jannaschii, the eubacterium Escherichia co

178 Applied to the complete genome of Methanococcus jannaschii, the method recognized the fold

179 nd with the exception of the archaebacterium Methanococcus jannaschii, the numbers of multidrug efflu

180 ingle polypeptide of 645 amino acids, as for Methanococcus jannaschii, the Sulfolobus solfataricus SS

181 bound to full-length SRP RNA of the archaeon Methanococcus jannaschii, to eukaryotic human SRP RNA, a

182 signed open reading frame from the genome of Methanococcus jannaschii, viz., MJ0757.

183 available archaeal genome sequence, that of Methanococcus jannaschii, were analysed using the BLAST2

184 For the prolyl-tRNA synthetase (ProRS) of Methanococcus jannaschii, which activates both proline a

185 esolution (1.5-1.9 A) structures of PSP from Methanococcus jannaschii, which define the open state pr

186 rium Haemophilus influenzae and the archaeon Methanococcus jannaschii, which had been previously misi

187 of the orthogonal tyrosine pair derived from Methanococcus jannaschii, which has been used to selecti

188 ethanoarchaea Methanosarcina thermophila and Methanococcus jannaschii.

189 tified in the hyperthermophilic euryarchaeon Methanococcus jannaschii.

190 ative RNA helicase from the hyperthermophile Methanococcus jannaschii.

191 -) with phosphoserine phosphatase (PSP) from Methanococcus jannaschii.

192 was characterized from the hyperthermophile Methanococcus jannaschii.

193 ecognized in the complete genome sequence of Methanococcus jannaschii.

194 etected and purified from one such organism, Methanococcus jannaschii.

195 ng methanoarchaea M. thermoautotrophicum and Methanococcus jannaschii.

196 recombinant RNAP subunits from the archaeon Methanococcus jannaschii.

197 esence of a homolog in the archaeal organism Methanococcus jannaschii.

198 t FtsZ from the hyperthermophilic methanogen Methanococcus jannaschii.

199 characterization of the SSB of an archaeon, Methanococcus jannaschii.

200 tion with their counterparts in the archaeon Methanococcus jannaschii.

201 chocystis PCC 6803, as well as one Archaeon, Methanococcus jannaschii.

202 search open reading frames in the genome of Methanococcus jannaschii.

203 a bacterial regulatory protein, GlnK1, from Methanococcus jannaschii.

204 col challenge, and syntrophic coculture with Methanococcus jannaschii.

205 ng two 36.2-kDa subunits from the methanogen Methanococcus jannaschii.

206 was recently shown that Methanocaldococcus (Methanococcus) jannaschii and other anaerobic archaea sy

207 Although Methanocaldococcus (Methanococcus) jannaschii was the first archaeon to have

208 tor the conformations of the PAN ATPase from Methanococcus jannischii.

209 ion would predict that it would, between the Methanococcus lineage (which is the deepest of the metha

210 closely related homologue from the mesophile Methanococcus maripaludis (Mma) is nearly inert as a tra

211 e that L7Ae coelutes with partially purified Methanococcus maripaludis (Mma) RNase P activity.

212 cci, we isolated nine conditional mutants of Methanococcus maripaludis after transformation of the wi

213 An acetate-requiring mutant of Methanococcus maripaludis allowed efficient labeling of

214 Methanococcus maripaludis and Methanocaldococcus jannasc

215 ions with alternative methanogenic partners, Methanococcus maripaludis and Methanospirillum hungatei,

216 s of H(2) metabolism in the model methanogen Methanococcus maripaludis and using formate as an additi

217 equence of the 8,285-bp plasmid pURB500 from Methanococcus maripaludis C5 was determined.

218 The methanogenic archaean Methanococcus maripaludis can use ammonia, alanine, or d

219 ble, mesophilic, hydrogenotrophic methanogen Methanococcus maripaludis contains 1,722 protein-coding

220 Here we show that ThiI from the archaeon Methanococcus maripaludis contains a [3Fe-4S] cluster th

221 oacylation of the same tRNA with cysteine by Methanococcus maripaludis cysteinyl-tRNA synthetase.

222 or switch-off, in the methanogenic archaeon Methanococcus maripaludis does not involve detectable co

223 The Methanococcus maripaludis energy-conserving hydrogenase

224 Although the Methanococcus maripaludis genome lacks a gene that can b

225 roscopy, we show that an archaeal pilus from Methanococcus maripaludis has a structure entirely diffe

226 Among the archaea, Methanococcus maripaludis has the unusual ability to use

227 Here we report the crystal structure of a Methanococcus maripaludis homologue of Rce1, whose endop

228 d structures of the archaeal chaperonin from Methanococcus maripaludis in both a peptide acceptor (op

229 al structure of the archaeal chaperonin from Methanococcus maripaludis in several nucleotides bound s

230 Methanococcus maripaludis is a mesophilic archaeon that

231 Mma10b from the euryarchaeote Methanococcus maripaludis is a mesophilic member of the

232 Methanococcus maripaludis is a mesophilic species of Arc

233 Methanococcus maripaludis is a methanogenic archaeon tha

234 Methanococcus maripaludis is a strictly anaerobic, metha

235 Methanococcus maripaludis is a strictly anaerobic, metha

236 en assimilation in the methanogenic archaeon Methanococcus maripaludis is regulated by transcriptiona

237 The Methanococcus maripaludis MMP0352 protein belongs to an

238 in Hildenborough growing syntrophically with Methanococcus maripaludis on lactate were used to develo

239 d, at 3.2-A resolution, the structure of the Methanococcus maripaludis phosphoseryl-tRNA synthetase (

240 t has recently been reported for an archaeal Methanococcus maripaludis pili filament and an archaeal

241 or switch-off, in the methanogenic archaeon Methanococcus maripaludis requires both nifI(1) and nifI

242 the hydrogenotrophic, methanogenic archaeon Methanococcus maripaludis S2 using a derivative of the T

243 narum NRC-1), a hydrogenotrophic methanogen (Methanococcus maripaludis S2), an acidophilic and aerobi

244 addition, SerRS was expressed from a cloned Methanococcus maripaludis serS gene.

245 a mutational analysis of Sec biosynthesis in Methanococcus maripaludis strain Mm900.

246 We showed previously that in Methanococcus maripaludis switch-off requires at least o

247 ) in the aminoacylation reaction for the two Methanococcus maripaludis synthetases SepRS (forming Sep

248 ere we report the construction of mutants of Methanococcus maripaludis that are defective in each put

249 In Methanococcus maripaludis the electrons for this reactio

250 evels were used to determine the response of Methanococcus maripaludis to leucine limitation.

251 We have used genetic methods in Methanococcus maripaludis to study nitrogen metabolism a

252 and tRNA(Ser), we introduced mutations into Methanococcus maripaludis tRNA(Sec) to investigate how M

253 Agmatidine is also present in Methanococcus maripaludis tRNA2(Ile) and in Sulfolobus s

254 we report that during continuous culture of Methanococcus maripaludis under defined nutrient conditi

255 a source of hydrogen gas for the methanogen, Methanococcus maripaludis using a capillary assay with a

256 gar-biosynthetic proteins were identified in Methanococcus maripaludis using phylogenetic and gene cl

257 rium Desulfovibrio vulgaris and the archaeon Methanococcus maripaludis were established and followed

258 Cells of Methanococcus maripaludis were grown by using continuous

259 hod, eight independent acetate autotrophs of Methanococcus maripaludis were isolated.

260 h canonical LysRS activity was purified from Methanococcus maripaludis, and the gene that encodes thi

261 In the methanogenic archaeon Methanococcus maripaludis, growth with ammonia results i

262 y of apbC/NBP35 homologs from three archaea: Methanococcus maripaludis, Methanocaldococcus jannaschii

263 cture of FlaK, a preflagellin peptidase from Methanococcus maripaludis, solved at 3.6 A resolution.

264 omplex from the hydrogenotrophic methanogen, Methanococcus maripaludis, that contains heterodisulfide

265 Transfer RNAs from Methanococcus vannielii, Methanococcus maripaludis, the thermophile Methanococcus

266 Using the methanogenic archaeon Methanococcus maripaludis, we show that deletion of ThiI

267 This was proven for Methanococcus maripaludis, where deletion of the SepRS-e

268 ween the nif and glnK(1) promoter regions of Methanococcus maripaludis, where two operators are prese

269 to syntrophic conditions with the methanogen Methanococcus maripaludis.

270 disrupted the cysS gene (encoding CysRS) of Methanococcus maripaludis.

271 anogenesis in a hydrogenotrophic methanogen, Methanococcus maripaludis.

272 expression vectors was developed for use in Methanococcus maripaludis.

273 n) gene cluster in the methanogenic archaeon Methanococcus maripaludis.

274 unction of glnA in the methanogenic archaeon Methanococcus maripaludis.

275 onal regulation in the methanogenic Archaeon Methanococcus maripaludis.

276 , and tungsten on the diazotrophic growth of Methanococcus maripaludis.

277 hose of Escherichia, but some are closest to Methanococcus or to Synechocystis.

278 compared with their homologs from mesophilic Methanococcus species.

279 strates the utility of genetic approaches in Methanococcus that have not been widely used in the meth

280 e Methanococcus voltae (MVO), the thermopile Methanococcus thermolithotrophicus (MTH), and the extrem

281 es of adenylate kinases from the thermophile Methanococcus thermolithotrophicus and the mesophile Met

282 , Methanococcus maripaludis, the thermophile Methanococcus thermolithotrophicus, and hyperthermophile

283 In Methanococcus thermophila and Methanobacterium thermoaut

284 These organisms, Methanococcus vannielii and Clostridium sticklandii, pro

285 A source of the recombinant monofunctional Methanococcus vannielii PR-AMP cyclohydrolase has been d

286 A selenium-binding protein (SeBP) from Methanococcus vannielii was recently identified, and its

287 ctions of these cysteines in the enzyme from Methanococcus vannielii, a series of biochemical studies

288 Transfer RNAs from Methanococcus vannielii, Methanococcus maripaludis, the

289 In Methanococcus vannielii, selenium transport in the cell

290 Strain PS of Methanococcus voltae (a methanogenic, anaerobic archaeba

291 ogenic members of the Archaea: the mesophile Methanococcus voltae (Mv), the thermophile M. thermolith

292 ogenic members of the Archaea (the mesophile Methanococcus voltae (MVO), the thermopile Methanococcus

293 occus thermolithotrophicus and the mesophile Methanococcus voltae have been solved to resolutions of

294 integrative expression vectors contained the Methanococcus voltae histone promoter and multiple cloni

295 ructural analysis shows that archaebacterial Methanococcus voltae RadA(D302K) (MvRAD51(D302K)) and Hs

296 pDLT44 did not replicate in Methanococcus voltae.

297 tected by radiometric methods in extracts of Methanococcus voltae.

298 have created an insertion in the smc gene of Methanococcus voltae.

299 l genes are most closely related to those of Methanococcus, whereas the majority of operational genes