ライフサイエンスコーパス: radiodurans

1 e crystal structure of RecF from Deinococcus radiodurans.

2 tion resistance on the bacterium Deinococcus radiodurans.

3 t DNA strand-annealing system of Deinococcus radiodurans.

4 re of a prokaryotic Ro ortholog, Rsr from D. radiodurans.

5 f the large ribosomal subunit of Deinococcus radiodurans.

6 e activity, which occurs in IR-irradiated D. radiodurans.

7 atory mechanism of aromatic catabolism in D. radiodurans.

8 e to the ionizing radiation resistance in D. radiodurans.

9 single-stranded DNA-binding protein from D. radiodurans.

10 he radiation-resistant bacterium Deinococcus radiodurans.

11 ly radiation resistant bacterium Deinococcus radiodurans.

12 of the bacteriophytochrome from Deinococcus radiodurans.

13 oneidensis, Escherichia coli and Deinococcus radiodurans.

14 ng radiation-resistant bacterium Deinococcus radiodurans.

15 tein, encoded by ORF DR_1909, of Deinococcus radiodurans.

16 ng radiation-resistant bacterium Deinococcus radiodurans.

17 xtremely radioresistant organism Deinococcus radiodurans.

18 ly 210 peaks in the pI range of 3-8.8 for D. radiodurans.

19 cerevisiae, Eschericia coli, and Deinococcus radiodurans.

20 step for further DNA repair in wild-type D. radiodurans.

21 sible for the high radiation tolerance of D. radiodurans.

22 upon rehydration compared with wild-type D. radiodurans.

23 context of severe genomic degradation in D. radiodurans.

24 compared to a tryptic digest of Deinococcus radiodurans.

25 nit complexes of the eubacterium Deinococcus radiodurans.

26 bacteriophytochrome (BphP) from Deinococcus radiodurans.

27 ons approached that exhibited by Deinococcus radiodurans.

28 still preserved in many species including D. radiodurans.

29 e transcriptional regulation of growth in D. radiodurans.

30 ting the extraordinary radioresistance of D. radiodurans.

31 coli, Thermus thermophilus, and Deinococcus radiodurans.

32 2 bridging 5 S and 23 S rRNAs) and 30 in D. radiodurans 23 S rRNA (plus 1 bridging 5 S and 23 S rRNA

33 Deinococcus radiodurans, a highly radioresistant and stress-resistan

34 ure in situ Mn(II) speciation in Deinococcus radiodurans, a radiation-resistant bacteria capable of a

35 whole-genome restriction map of Deinococcus radiodurans, a radiation-resistant bacterium able to sur

36 Deinococcus radiodurans, a radiation-resistant bacterium, contains t

37 ferroxidation may be prevented in vivo as D. radiodurans accumulates a high ratio of Mn:Fe.

38 We show that D. radiodurans accumulates very high intracellular manganes

39 mple, we use data on survival of Deinococcus radiodurans after high doses (thousands of Gy) of acute

40 nces survival of the eubacterium Deinococcus radiodurans after ultraviolet irradiation.

41 er bacteria, such as E. coli and Deinococcus radiodurans, although the average mutation rate per muta

42 mutations in Escherichia coli to Deinococcus radiodurans, an extremeophile with an astonishingly high

43 t are unable to replicate autonomously in D. radiodurans and carry homologous sequences for replaceme

44 e purified the RecN protein from Deinococcus radiodurans and characterized its DNA-dependent and DNA-

45 tails of the in vivo Mn(2+) speciation in D. radiodurans and E. coli cells and their responses to 10

46 ase substitution hotspots in rpoB in both D. radiodurans and E. coli.

47 responding sites are very similar in both D. radiodurans and E. coli.

48 40 of the large subunit rRNA in Deinococcus radiodurans and Escherichia coli, respectively, are phyl

49 ynthetase from M. jannaschii and Deinococcus radiodurans and its characterization in vitro and in viv

50 i and to characterize DR_1025 of Deinococcus radiodurans and MM_0920 of Methanosarcina mazei.

51 in two heterotrophic eubacteria, Deinococcus radiodurans and Pseudomonas aeruginosa.

52 the nonphotosynthetic eubacteria Deinococcus radiodurans and Pseudomonas aeruginosa.

53 radiation-resistant eubacterium Deinococcus radiodurans and show that DNA binding does not require i

54 he radiation-resistant bacterium Deinococcus radiodurans and some eukaryotes, Ro has also been implic

55 een the SF1B helicase RecD2 from Deinococcus radiodurans and ssDNA in the presence and absence of an

56 or ECF-derived heat shock sigma factor in D. radiodurans and that it plays a central role in the posi

57 ata indicate that DrII is the RNase II of D. radiodurans and that its structure and catalytic propert

58 the first example of expression of GFP in D. radiodurans and the first detection of GFP in a single b

59 ic sequence analysis showed that Deinococcus radiodurans and Thermus thermophilus do not possess aspa

60 was not inactivated, it was rescued from D. radiodurans and was shown to function normally in E. col

61 As of Haloarcula marismortui and Deinococcus radiodurans, and the small ribosomal subunit RNA of Ther

62 ing RNAPs from Escherichia coli, Deinococcus radiodurans, and Thermus aquaticus, we show that the fun

63 Yersinia pestis and the other in Deinococcus radiodurans, appear to encode closely related proteins.

64 significant amounts of cellular Mn(II) in D. radiodurans are bound to peptides and proteins.

65 m in the radiation-resistance of Deinococcus radiodurans are discussed.

66 en exponential-phase cultures of Deinococcus radiodurans are exposed to a 5000-Gray dose of gamma rad

67 The specificities of NTG and 5AZ in D. radiodurans are the same as those found for E. coli and

68 peptides (Cys-polypeptides) from Deinococcus radiodurans as well as from mouse B16 melanoma cells.

69 ow that in Synechocystis sp. and Deinococcus radiodurans, as in A. aeolicus, CCA is added by homologo

70 ine, serine, or valine resulted in mutant D. radiodurans AspRS2 enzymes still capable of forming Asp-

71 1 loop of the non-discriminating Deinococcus radiodurans AspRS2 is required for tRNA(Asn) recognition

72 as transformed with DNA from a library of D. radiodurans aspS2 genes with a randomized codon 77 and t

73 cture of the RecD2 helicase from Deinococcus radiodurans at 2.2-A resolution.

74 he chromophore-binding domain of Deinococcus radiodurans bacterial phytochrome assembled with its chr

75 bining the photosensor module of Deinococcus radiodurans bacterial phytochrome with the effector modu

76 logy and mutational analysis suggest that D. radiodurans bacteriophytochrome functions as a light-reg

77 x-ray structure of a fragment of Deinococcus radiodurans bacteriophytochrome in the Pr form.

78 thin the bilin-binding domain of Deinococcus radiodurans bacteriophytochrome with respect to chromoph

79 nd autofluorescent components in a single D. radiodurans bacterium.

80 The mtcA+ and mtcB+ genes of D. radiodurans, both implicated in excision repair, have be

81 ty by a different bacterial NOS (Deinococcus radiodurans) but not by any of the three mammalian NOS o

82 regulates uricase expression in Deinococcus radiodurans by binding a shared promoter region between

83 Deinococcus radiodurans can reconstitute its genome from double-stra

84 res of this D207H variant of the Deinococcus radiodurans CBD, in which His-207 is observed to form a

85 ates of D. radiodurans SSB protein in the D. radiodurans cell indicate approximately 2500-3000 dimers

86 Thus, the extreme radiation resistance of D. radiodurans cells cannot be attributed to SodA.

87 o information about such complexes within D. radiodurans cells is lacking, and the idea that they can

88 teins may confer a selective advantage to D. radiodurans cells that aids viability in environments th

89 he radiation-resistant bacterium Deinococcus radiodurans charges tRNA with tryptophan and 4-nitrotryp

90 applications to the analysis of Deinococcus radiodurans chromosome I, of two strains of Helicobacter

91 nces for replacement recombination in the D. radiodurans chromosome.

92 Gene Dr1184 from Deinococcus radiodurans codes for a Nudix enzyme (DR-CoAse) that hyd

93 o that observed in the H. marismortui and D. radiodurans complexes.

94 ing frames for the microorganism Deinococcus radiodurans, consistent with previous results for a spec

95 radiation-resistant eubacterium Deinococcus radiodurans contains an ortholog of an RNA-binding prote

96 ly radiation resistant bacterium Deinococcus radiodurans contains genes for two SSB homologs: the hom

97 D. radiodurans contains genes for two TrpRSs: the first has

98 he radiation-resistant bacterium Deinococcus radiodurans contains two DNA-binding proteins from starv

99 radiation-resistant eubacterium Deinococcus radiodurans contributes to survival of this bacterium af

100 e expression as stationary phase Deinococcus radiodurans cultures recover from acute exposure to gamm

101 However, attempts to delete D. radiodurans cysS failed, suggesting that this is an esse

102 characterized a hemeprotein from Deinococcus radiodurans (D. radiodurans NO synthase, deiNOS) whose s

103 de co-occurrence patterns in the Deinococcus radiodurans, D. geothermalis, and Thermus thermophilus g

104 he radiation-resistant bacterium Deinococcus radiodurans (deiNOS) associates with an unusual tryptoph

105 Deinococcus radiodurans (DEIRA) can survive very high doses of ioniz

106 enced >250 mutations leading to Rif(r) in D. radiodurans derived spontaneously in wild-type and uvrD

107 Deinococcus radiodurans disproportionately favored TGA more than the

108 C is most closely related to the Deinococcus radiodurans DNA pol C.

109 Therefore, we propose that D. radiodurans Dps-1 has a distinct iron-exit channel.

110 lease of Fe(2+), the crystal structure of D. radiodurans Dps-1 was determined to 2.0 Angstroms resolu

111 D.radiodurans Dps-1, the product of gene DR2263, adopts a

112 However, Deinococcus radiodurans Dps-1, which binds DNA with high affinity, f

113 ins of Escherichia coli (Ec) and Deinococcus radiodurans (Dr) both promote a DNA strand exchange reac

114 The resistance of Deinococcus radiodurans (Dr) to extreme doses of ionizing radiation

115 Deinococcus radiodurans (Dr) withstands desiccation, reactive oxygen

116 m the amidohydrolase family from Deinococcus radiodurans (Dr-OPH) with homology to phosphotriesterase

117 Construction of a D. radiodurans DR0705 deletion strain showed this gene to b

118 lyl-tRNA synthetase) or with the Deinococcus radiodurans DR0705 gene, the ortholog of the MJ1477 gene

119 nes and not by archaeal proS genes or the D. radiodurans DR0705 gene.

120 Deinococcus radiodurans (Drad), a bacterium with an extraordinary ca

121 f the bacterial phytochrome from Deinococcus radiodurans (DrBphP), which is weakly fluorescent in the

122 The RecA protein of Deinococcus radiodurans (DrRecA) has a central role in genome recons

123 The RecQ helicase from Deinococcus radiodurans (DrRecQ) is unusual among RecQ family member

124 he radiation-resistant bacterium Deinococcus radiodurans (DrSSB) functions as a homodimer in which ea

125 The D. radiodurans-encoded HU (DrHU), which binds preferentiall

126 n that urate is a ligand for the Deinococcus radiodurans-encoded MarR homolog HucR (hypothetical uric

127 utY homolog gene (mutY(Dr)) from Deinococcus radiodurans encodes a 39.4-kDa protein consisting of 363

128 rom the radioresistant bacterium Deinococcus radiodurans encodes three "Helicase and RNase D C-termin

129 D. radiodurans encodes two sHsps, termed Hsp17.7 and Hsp20.

130 tems could provide models to guide future D. radiodurans engineering efforts aimed at integrating sev

131 Four of these genomes (Deinococcus radiodurans, Escherichia coli, Haemophilus influenzae an

132 klandii, Cytophaga hutchinsonii, Deinococcus radiodurans, Escherichia coli, Magnetospirillum magnetot

133 e the Haloarcula marismortui and Deinococcus radiodurans examples, the lower portion of helix 42 in E

134 ein of D. radiodurans is ot detectable in D. radiodurans except in the setting of DNA damage and that

135 Deinococcus radiodurans exhibits an extraordinary resistance to the

136 The Mn(2+) of D. radiodurans exists predominantly as LMW complexes with n

137 synthetase and the lack of this enzyme in D. radiodurans extracts, suggests that the gatCAB genes may

138 s-1 from the radiation-resistant Deinococcus radiodurans fails to protect DNA from hydroxyl radical-m

139 from gene expression studies on Deinococcus radiodurans following DNA damage using cDNA microarrays.

140 eserving the genome integrity of Deinococcus radiodurans following treatment by gamma radiation in an

141 support the prospective use of engineered D. radiodurans for bioremediation of mixed wastes containin

142 terpretations of the capacity of Deinococcus radiodurans for resistance to high doses of ionizing rad

143 t gene clusters could be used to engineer D. radiodurans for treatment of mixed radioactive wastes by

144 Hs from Thermus thermophilus and Deinococcus radiodurans form trimer-of-dimers hexamers in solution,

145 The results show that D. radiodurans Fpg protein and its homologue E. coli Fpg pr

146 dopyrimidines are preferred substrates of D. radiodurans Fpg protein over 8-OH-Gua, whereas E. coli F

147 The D. radiodurans genome does encode a protein whose closest c

148 ation, combined with the absence from the D. radiodurans genome of genes encoding tRNA-independent as

149 a factors were identified in the Deinococcus radiodurans genome sequence and designated sig1 and sig2

150 The D. radiodurans genome sequence indicates that the organism

151 (ORFs) from the prerelease version of the D. radiodurans genome were screened for genes more closely

152 how the genome of the bacterium Deinococcus radiodurans gets reassembled after being shattered by hi

153 ed by the inability of the discriminating D. radiodurans GluRS to produce the required mischarged Glu

154 Deinococcus radiodurans has a remarkable capacity to survive exposur

155 h other Dps proteins, Dps-1 from Deinococcus radiodurans has an extended N terminus comprising 55 ami

156 The MarR homolog, HucR, from Deinococcus radiodurans has been shown to repress expression of a pr

157 ntrachromosomal recombination in Deinococcus radiodurans has been studied recently and has been found

158 -type heat shock sigma factor of Deinococcus radiodurans, has been shown to play a central role in th

159 the radiation-resistant organism Deinococcus radiodurans have been cloned into vectors under the cont

160 s examined, 20 showed topologies in which D. radiodurans homologues clearly group with eukaryotic or

161 entified, cloned and deleted the Deinococcus radiodurans HspR homologue, DR0934.

162 mobility shift assays (EMSA), we show that D.radiodurans HU (DrHU) binds preferentially only to DNA j

163 es of proline dehydrogenase from Deinococcus radiodurans in the oxidized state complexed with the pro

164 n DXS, from Escherichia coli and Deinococcus radiodurans, in complex with the coenzyme thiamine pyrop

165 that a bacteriophytochrome from Deinococcus radiodurans, incorporating biliverdin as the chromophore

166 we demonstrate that the RecF of Deinococcus radiodurans interacts with DNA as an ATP-dependent dimer

167 The evidence presented suggests that D. radiodurans' ionizing radiation resistance is incidental

168 Deinococcus radiodurans is a highly radiation-resistant bacterium th

169 RecD2 from Deinococcus radiodurans is a superfamily 1 DNA helicase that is homo

170 o that of E. coli RecA) in recA-defective D. radiodurans is described.

171 In this study, we demonstrate that Ssb in D. radiodurans is essential for cell survival.

172 Deinococcus radiodurans is extraordinarily resistant to DNA damage,

173 The bacterium Deinococcus radiodurans is extremely resistant to high levels of DNA

174 Deinococcus radiodurans is extremely resistant to ionizing radiation

175 Deinococcus radiodurans is highly resistant to radiation and mutagen

176 venger of reactive oxygen species, and as D. radiodurans is known for its remarkable resistance to DN

177 We now find that the RecA protein of D. radiodurans is ot detectable in D. radiodurans except in

178 Deinococcus (formerly Micrococcus) radiodurans is remarkable for its extraordinary resistan

179 The bacterium Deinococcus radiodurans is resistant to extremely high levels of DNA

180 tremely radioresistant bacterium Deinococcus radiodurans is the exact inverse of this established pat

181 Deinococcus radiodurans is unique in its ability to reconstitute its

182 cular family member, ISDra2 from Deinococcus radiodurans, is dramatically stimulated upon massive gam

183 ereas DraRnl is inessential for growth of D. radiodurans, its absence sensitizes the bacterium to kil

184 Deinococcus radiodurans, known for its extraordinary DNA repair capa

185 cula marismortui) and bacterial (Deinococcus radiodurans) large ribosomal subunits have been reported

186 Furthermore, detection of DrDps2 in the D. radiodurans membrane fraction suggests that the N-termin

187 y, 10 kGy irradiation causes no change in D. radiodurans Mn(2+) speciation, despite the paucity of ho

188 of product inhibition scales as ScMnSOD > D. radiodurans MnSOD > E. coli MnSOD > human MnSOD.

189 bacterial (Escherichia coli and Deinococcus radiodurans) MnSODs.

190 hemeprotein from Deinococcus radiodurans (D. radiodurans NO synthase, deiNOS) whose sequence is 34% i

191 We conclude that neither D. radiodurans nor S. flexneri RecA is functional in the ot

192 report that the complex between Deinococcus radiodurans NOS (deiNOS) and an unusual tryptophanyl-tRN

193 knockout disrupting this pathway deprives D. radiodurans of the ability to synthesize asparagine and

194 Here, we report that the D. radiodurans ortholog Rsr (Ro sixty related) functions wi

195 radiation-resistant eubacterium Deinococcus radiodurans participates in ribosomal RNA (rRNA) degrada

196 putrefaciens, Synechocystis sp., Deinococcus radiodurans, Pasteurella multocida, and Actinobacillus a

197 he chromophore-binding domain of Deinococcus radiodurans phytochrome assembled with its chromophore b

198 romophore-binding domains of the Deinococcus radiodurans phytochrome at 2.1 A resolution.

199 rough structural analysis of the Deinococcus radiodurans phytochrome BphP assembled with biliverdin (

200 nd computational analyses of the Deinococcus radiodurans phytochrome, we demonstrate that two dimeriz

201 analysis of site-directed mutants in the D. radiodurans phytochrome, we show that this bilin prefere

202 These kinetics parallel those of D. radiodurans postirradiation genome reconstitution, sugge

203 logenetic analysis shows the M. ruber and D. radiodurans prolyl RS to be more closely related to arch

204 te, the bilin chromophore of the Deinococcus radiodurans proteobacterial phytochrome (DrBphP) is hype

205 Deinococcus radiodurans R1 (DEIRA) is a bacterium best known for its

206 Deinococcus radiodurans R1 and other members of this genus are able

207 ve promoters that were amplified from the D. radiodurans R1 genome.

208 enome sequence of the bacterium, Deinococcus radiodurans R1 has been released.

209 m Shewanella oneidensis MR-1 and Deinococcus radiodurans R1 have been designed.

210 he radiation-resistant bacterium Deinococcus radiodurans R1 is composed of two chromosomes (2,648,638

211 Deinococcus radiodurans R1 is extremely resistant to both oxidative

212 anscriptional and proteomic profiles of a D. radiodurans R1 sig1 mutant and wild-type cells in respon

213 to facilitate gene disruption in Deinococcus radiodurans R1, has been used to inactivate the gene des

214 Rad54 helicase were reported for Deinococcus radiodurans R1, leading to the speculation that a frames

215 al uricase regulator (HucR) from Deinococcus radiodurans R1.

216 s were upregulated threefold or higher in D. radiodurans R1.

217 rrE to a 970-bp region on chromosome I of D. radiodurans R1.

218 D. radiodurans radiation resistance is attributed to the ac

219 ding and biological functions of DrSSB in D. radiodurans radiation resistance, we have examined the s

220 ve previously observed that expression of D. radiodurans recA in Escherichia coli appears lethal.

221 urans, there is no complementation of any D. radiodurans recA phenotype, including DNA damage sensiti

222 The unusual DNA pairing properties of the D. radiodurans RecA protein can be explained by postulating

223 The RecA protein of Deinococcus radiodurans (RecA(Dr)) is essential for the extreme radi

224 We have purified this novel D. radiodurans RecD protein and characterized its biochemic

225 results are the first indication that the D. radiodurans RecD protein has a role in DNA damage repair

226 The D. radiodurans RecD protein is a DNA helicase that unwinds

227 These results show that the D. radiodurans RecD protein is a DNA helicase with 5'-3' po

228 We show here that Deinococcus radiodurans RecD2 helicase inactivates Escherichia coli

229 In addition, the D. radiodurans RecD2 structure has aided us in deciphering

230 Like plant phytochromes, the D. radiodurans receptor covalently binds linear tetrapyrrol

231 Intriguingly, Deinococcus radiodurans RecO does not bind SSB-Ct and weakly interac

232 s can be proteolytically removed from the D. radiodurans RecQ (DrRecQ) C terminus, consistent with ea

233 reconstitution of the 10 kGy IR-shattered D. radiodurans replicons that correlates with the timing of

234 Deinococcus radiodurans represents an organism in which all systems

235 n those for Escherichia coli and Deinococcus radiodurans, respectively.

236 s that control DrRecA activity during the D. radiodurans response to gamma radiation exposure are unk

237 ribosomal proteins from H.marismortui and D.radiodurans revealed striking examples of molecular mimi

238 Deinococcus radiodurans RNA ligase (DraRnl) is a template-directed l

239 Deinococcus radiodurans RNA ligase (DraRnl) is the founding member o

240 Deinococcus radiodurans RNA ligase (DraRnl) seals 3-OH/5-PO4 nicks i

241 Thermus aquaticus and mesophilic Deinococcus radiodurans RNAPs and identify the FL as an adaptable el

242 These results expand the D. radiodurans Sig1 heat shock regulon to include 31 potent

243 Deinococcus radiodurans single-stranded (ss) DNA binding protein (Dr

244 We hypothesize that differences between D. radiodurans SSB and homotetrameric bacterial SSB protein

245 mmetry exists between the two OB folds of D. radiodurans SSB because of sequence differences between

246 The structure shows that D. radiodurans SSB comprises two OB domains linked by a bet

247 Extensive crystallographic contacts link D. radiodurans SSB dimers in an arrangement that has import

248 and-double-strand DNA junctions in vitro, D. radiodurans SSB protein has a limited capacity to displa

249 The Deinococcus radiodurans SSB protein has an occluded site size of 50

250 Quantitative estimates of D. radiodurans SSB protein in the D. radiodurans cell indic

251 -A-resolution x-ray structure of Deinococcus radiodurans SSB.

252 a DNA damage-sensitive strain of Deinococcus radiodurans strain 302 carrying a mutation in an unchara

253 he mutant gene for ddrA157, the resulting D. radiodurans strain became almost as sensitive to gamma r

254 e characterized in the genome of Deinococcus radiodurans (strain R1).

255 By comparison, D. radiodurans strains containing the same E. coli plasmids

256 cury (Hg) (II), we have generated several D. radiodurans strains expressing the cloned Hg (II) resist

257 Proteomic analysis of t(6)A(-) D. radiodurans strains revealed an induction of the proteot

258 D. radiodurans strains were also tolerant to the solvent ef

259 We have generated D. radiodurans strains with a disruption or deletion of the

260 he radiation-resistant bacterium Deinococcus radiodurans suggests the presence of both direct and ind

261 HucR, a novel MarR homolog from Deinococcus radiodurans that demonstrates phenolic sensing capabilit

262 he HspR-like global negative regulator of D. radiodurans that directly represses chaperone and protea

263 the large ribosomal subunit from Deinococcus radiodurans that exploits its association with FLAG-tagg

264 ent, we employ a model system of Deinococcus radiodurans that has been engineered to express GFP unde

265 um albumin and proteins from the organism D. radiodurans that was analyzed using gradient reversed-ph

266 ong most prokaryotes, we derived again in D. radiodurans the rpoB/Rif(r) system that we developed in

267 bioremediation strategies using Deinococcus radiodurans, the most radiation resistant organism known

268 l lateral transfer with archaea; Deinococcus radiodurans, the most radiation-resistant microorganism

269 characterization of recombinant Deinococcus radiodurans, the most radiation-resistant organism known

270 and the ICAT-labeled proteome of Deinococcus radiodurans, the presence of these label-specific produc

271 animal cells and the eubacterium Deinococcus radiodurans, the Ro autoantigen, a ring-shaped RNA-bindi

272 In the only studied bacterium, Deinococcus radiodurans, the Ro ortholog Rsr functions in heat-stres

273 e accumulation of the S. flexneri RecA in D. radiodurans, there is no complementation of any D. radio

274 teria as t(6)A is dispensable in Deinococcus radiodurans, Thermus thermophilus, Synechocystis PCC6803

275 osome recombination following exposure of D. radiodurans to 1.75 Mrad (17.5 kGy) 60Co, when the plasm

276 articipant in the intrinsic resistance of D. radiodurans to high levels of oxidative stress.

277 he biochemical details of the response of D. radiodurans to ionizing radiation are poorly understood,

278 the genomes of cyanobacteria and Deinococcus radiodurans to ionizing radiation.

279 he radiation-resistant bacterium Deinococcus radiodurans to protect protein epitopes from radiation-i

280 The ability of Deinococcus radiodurans to recover from extensive DNA damage is due

281 trongly suggest that H(4)F may be used by D. radiodurans to replace H(4)B as a redox-active cofactor

282 remarkable ability of bacterium Deinococcus radiodurans to survive extreme doses of gamma-rays (12,0

283 plasmid that contribute to the ability of D. radiodurans to survive under conditions of starvation, o

284 olog Rsr contributes to the resistance of D. radiodurans to UV irradiation.

285 the 1.75-A crystal structure of Deinococcus radiodurans topoisomerase IB (DraTopIB), a prototype of

286 Deinococcus radiodurans topoisomerase IB (DraTopIB), an exemplary me

287 TrpRS II binds tryptophan (Trp), ATP, and D. radiodurans tRNA(Trp) and catalyzes the formation of 5'

288 The recD of D. radiodurans was deleted and this mutant was shown to hav

289 peptides from the microorganism Deinococcus radiodurans was used for the training of the ANN.

290 OS gene from one such bacterium, Deinococcus radiodurans, was cloned and expressed (deiNOS) in Escher

291 he amidohydrolase superfamily in Deinococcus radiodurans, was cloned, expressed, and purified to homo

292 scuous PLL scaffold (Dr0930 from Deinococcus radiodurans ), we designed an extremely efficient organo

293 nd radiation-resistant bacterium Deinococcus radiodurans, we suggest that the extraordinary radiation

294 D. radiodurans were cultured in both natural isotopic abund

295 ctors for stable chromosomal insertion in D. radiodurans were developed.

296 g radiation-sensitive strains of Deinococcus radiodurans were evaluated for their ability to survive

297 he radiation-resistant bacterium Deinococcus radiodurans, which is being engineered to express biorem

298 the sHsp system of the bacterium Deinococcus radiodurans, which is resistant against various stress c

299 ults from multiplexed-MS/MS analysis of a D. radiodurans whole cell digest to illustrate the utility

300 Rsr binds D. radiodurans Y RNA with low nanomolar affinity, comparabl