ライフサイエンスコーパス: Deinococcus radiodurans

1 aRnl) from the radiation-resistant bacterium Deinococcus radiodurans.

2 the extremely radiation resistant bacterium Deinococcus radiodurans.

3 Shewanella oneidensis, Escherichia coli and Deinococcus radiodurans.

4 r the ionizing radiation-resistant bacterium Deinococcus radiodurans.

5 m the ionizing radiation-resistant bacterium Deinococcus radiodurans.

6 i, and the extremely radioresistant organism Deinococcus radiodurans.

7 ccharomyces cerevisiae, Eschericia coli, and Deinococcus radiodurans.

8 d a famously DNA damage-resistant bacterium, Deinococcus radiodurans.

9 ystallographic movie of the phytochrome from Deinococcus radiodurans.

10 sensory core of the bacteriophytochrome from Deinococcus radiodurans.

11 ly: LutC protein, encoded by ORF DR_1909, of Deinococcus radiodurans.

12 trometry and compared to a tryptic digest of Deinococcus radiodurans.

13 for 50S subunit complexes of the eubacterium Deinococcus radiodurans.

14 r, using the bacteriophytochrome (BphP) from Deinococcus radiodurans.

15 the populations approached that exhibited by Deinococcus radiodurans.

16 Escherichia coli, Thermus thermophilus, and Deinococcus radiodurans.

17 e present the crystal structure of RecF from Deinococcus radiodurans.

18 dinary radiation resistance on the bacterium Deinococcus radiodurans.

19 sis-dependent DNA strand-annealing system of Deinococcus radiodurans.

20 structure of the large ribosomal subunit of Deinococcus radiodurans.

21 Deinococcus radiodurans, a highly radioresistant and str

22 used to measure in situ Mn(II) speciation in Deinococcus radiodurans, a radiation-resistant bacteria

23 A whole-genome restriction map of Deinococcus radiodurans, a radiation-resistant bacterium

24 Deinococcus radiodurans, a radiation-resistant bacterium

25 The radiation-resistant bacterium Deinococcus radiodurans accumulates less carbonylation t

26 As an example, we use data on survival of Deinococcus radiodurans after high doses (thousands of G

27 rtholog enhances survival of the eubacterium Deinococcus radiodurans after ultraviolet irradiation.

28 certain other bacteria, such as E. coli and Deinococcus radiodurans, although the average mutation r

29 r analyzing mutations in Escherichia coli to Deinococcus radiodurans, an extremeophile with an astoni

30 We have purified the RecN protein from Deinococcus radiodurans and characterized its DNA-depend

31 ' from helix 40 of the large subunit rRNA in Deinococcus radiodurans and Escherichia coli, respective

32 einyl-tRNA synthetase from M. jannaschii and Deinococcus radiodurans and its characterization in vitr

33 herichia coli and to characterize DR_1025 of Deinococcus radiodurans and MM_0920 of Methanosarcina ma

34 ke proteins in two heterotrophic eubacteria, Deinococcus radiodurans and Pseudomonas aeruginosa.

35 proteins in the nonphotosynthetic eubacteria Deinococcus radiodurans and Pseudomonas aeruginosa.

36 coded by the radiation-resistant eubacterium Deinococcus radiodurans and show that DNA binding does n

37 In the radiation-resistant bacterium Deinococcus radiodurans and some eukaryotes, Ro has also

38 complex between the SF1B helicase RecD2 from Deinococcus radiodurans and ssDNA in the presence and ab

39 ts and genomic sequence analysis showed that Deinococcus radiodurans and Thermus thermophilus do not

40 l subunit RNAs of Haloarcula marismortui and Deinococcus radiodurans, and the small ribosomal subunit

41 e, by comparing RNAPs from Escherichia coli, Deinococcus radiodurans, and Thermus aquaticus, we show

42 present in Yersinia pestis and the other in Deinococcus radiodurans, appear to encode closely relate

43 te metabolism in the radiation-resistance of Deinococcus radiodurans are discussed.

44 When exponential-phase cultures of Deinococcus radiodurans are exposed to a 5000-Gray dose

45 taining polypeptides (Cys-polypeptides) from Deinococcus radiodurans as well as from mouse B16 melano

46 Here we show that in Synechocystis sp. and Deinococcus radiodurans, as in A. aeolicus, CCA is added

47 77) in the L1 loop of the non-discriminating Deinococcus radiodurans AspRS2 is required for tRNA(Asn)

48 crystal structure of the RecD2 helicase from Deinococcus radiodurans at 2.2-A resolution.

49 Fusing a photosensory core module of Deinococcus radiodurans bacterial phytochrome (DrBphP-PC

50 ome, using the chromophore-binding domain of Deinococcus radiodurans bacterial phytochrome assembled

51 ity by recombining the photosensor module of Deinococcus radiodurans bacterial phytochrome with the e

52 hore in the x-ray structure of a fragment of Deinococcus radiodurans bacteriophytochrome in the Pr fo

53 ino acids within the bilin-binding domain of Deinococcus radiodurans bacteriophytochrome with respect

54 sis of the chromophore-binding domain of the Deinococcus radiodurans bacteriophytochrome.

55 hesis activity by a different bacterial NOS (Deinococcus radiodurans) but not by any of the three mam

56 MarR family, regulates uricase expression in Deinococcus radiodurans by binding a shared promoter reg

57 Deinococcus radiodurans can reconstitute its genome from

58 stal structures of this D207H variant of the Deinococcus radiodurans CBD, in which His-207 is observe

59 ynthase in the radiation-resistant bacterium Deinococcus radiodurans charges tRNA with tryptophan and

60 We show applications to the analysis of Deinococcus radiodurans chromosome I, of two strains of

61 Gene Dr1184 from Deinococcus radiodurans codes for a Nudix enzyme (DR-CoA

62 ed open reading frames for the microorganism Deinococcus radiodurans, consistent with previous result

63 enome of the radiation-resistant eubacterium Deinococcus radiodurans contains an ortholog of an RNA-b

64 the extremely radiation resistant bacterium Deinococcus radiodurans contains genes for two SSB homol

65 The radiation-resistant bacterium Deinococcus radiodurans contains two DNA-binding protein

66 of Ro in the radiation-resistant eubacterium Deinococcus radiodurans contributes to survival of this

67 anges in gene expression as stationary phase Deinococcus radiodurans cultures recover from acute expo

68 ressed, and characterized a hemeprotein from Deinococcus radiodurans (D. radiodurans NO synthase, dei

69 ned nucleotide co-occurrence patterns in the Deinococcus radiodurans, D. geothermalis, and Thermus th

70 complexes of the large ribosomal subunit of Deinococcus radiodurans (D50S) with these 16-membered se

71 otein from the radiation-resistant bacterium Deinococcus radiodurans (deiNOS) associates with an unus

72 Deinococcus radiodurans (DEIRA) can survive very high do

73 Deinococcus radiodurans disproportionately favored TGA m

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

75 However, Deinococcus radiodurans Dps-1, which binds DNA with high

76 e RecA proteins of Escherichia coli (Ec) and Deinococcus radiodurans (Dr) both promote a DNA strand e

77 The resistance of Deinococcus radiodurans (Dr) to extreme doses of ionizin

78 Deinococcus radiodurans (Dr) withstands desiccation, rea

79 n enzyme from the amidohydrolase family from Deinococcus radiodurans (Dr-OPH) with homology to phosph

80 encoding prolyl-tRNA synthetase) or with the Deinococcus radiodurans DR0705 gene, the ortholog of the

81 We present high-resolution structures of Deinococcus radiodurans (Dra)Nramp in multiple conformat

82 We present high-resolution structures of Deinococcus radiodurans (Dra)Nramp in three stable confo

83 Deinococcus radiodurans (Drad), a bacterium with an extr

84 h droplets of the bacterial phytochrome from Deinococcus radiodurans (DrBphP), which is weakly fluore

85 Here, we investigate DXPS from Deinococcus radiodurans (DrDXPS), showing that it has si

86 The RecA protein of Deinococcus radiodurans (DrRecA) has a central role in g

87 The RecQ helicase from Deinococcus radiodurans (DrRecQ) is unusual among RecQ f

88 otein from the radiation-resistant bacterium Deinococcus radiodurans (DrSSB) functions as a homodimer

89 viously shown that urate is a ligand for the Deinococcus radiodurans-encoded MarR homolog HucR (hypot

90 The mutY homolog gene (mutY(Dr)) from Deinococcus radiodurans encodes a 39.4-kDa protein consi

91 Q helicase from the radioresistant bacterium Deinococcus radiodurans encodes three "Helicase and RNas

92 Four of these genomes (Deinococcus radiodurans, Escherichia coli, Haemophilus i

93 tridium sticklandii, Cytophaga hutchinsonii, Deinococcus radiodurans, Escherichia coli, Magnetospiril

94 Unlike the Haloarcula marismortui and Deinococcus radiodurans examples, the lower portion of h

95 Deinococcus radiodurans exhibits an extraordinary resist

96 of iron, Dps-1 from the radiation-resistant Deinococcus radiodurans fails to protect DNA from hydrox

97 imental data from gene expression studies on Deinococcus radiodurans following DNA damage using cDNA

98 ntial for preserving the genome integrity of Deinococcus radiodurans following treatment by gamma rad

99 New interpretations of the capacity of Deinococcus radiodurans for resistance to high doses of

100 The P5CDHs from Thermus thermophilus and Deinococcus radiodurans form trimer-of-dimers hexamers i

101 rnative sigma factors were identified in the Deinococcus radiodurans genome sequence and designated s

102 Decontamination testing of Deinococcus radiodurans, Geobacillus stearothermophilus

103 n this issue how the genome of the bacterium Deinococcus radiodurans gets reassembled after being sha

104 Deinococcus radiodurans harbors a multipartite ploid gen

105 Deinococcus radiodurans has a remarkable capacity to sur

106 mparison with other Dps proteins, Dps-1 from Deinococcus radiodurans has an extended N terminus compr

107 The MarR homolog, HucR, from Deinococcus radiodurans has been shown to repress expres

108 smidic and intrachromosomal recombination in Deinococcus radiodurans has been studied recently and ha

109 The study of natural extremophiles such as Deinococcus radiodurans has revealed much.

110 mic function-type heat shock sigma factor of Deinococcus radiodurans, has been shown to play a centra

111 genes from the radiation-resistant organism Deinococcus radiodurans have been cloned into vectors un

112 e we have identified, cloned and deleted the Deinococcus radiodurans HspR homologue, DR0934.

113 the structures of proline dehydrogenase from Deinococcus radiodurans in the oxidized state complexed

114 nformation on DXS, from Escherichia coli and Deinococcus radiodurans, in complex with the coenzyme th

115 rboxypeptidase, an S9C subfamily member from Deinococcus radiodurans, in its active and inactive stat

116 We now show that a bacteriophytochrome from Deinococcus radiodurans, incorporating biliverdin as the

117 Here, we demonstrate that the RecF of Deinococcus radiodurans interacts with DNA as an ATP-dep

118 Deinococcus radiodurans is a gram-positive bacterium res

119 Deinococcus radiodurans is a highly radiation-resistant

120 Deinococcus radiodurans is a phylogenetically deep-branc

121 The radiation-resistant Deinococcus radiodurans is a spherical bacterium protect

122 RecD2 from Deinococcus radiodurans is a superfamily 1 DNA helicase

123 Deinococcus radiodurans is an atypical diderm bacterium

124 Deinococcus radiodurans is extraordinarily resistant to

125 The bacterium Deinococcus radiodurans is extremely resistant to high l

126 Deinococcus radiodurans is extremely resistant to ionizi

127 Deinococcus radiodurans is highly resistant to radiation

128 The radiation-resistant bacterium Deinococcus radiodurans is known as the world's toughest

129 Deinococcus radiodurans is known for its remarkable abil

130 The bacterium Deinococcus radiodurans is resistant to extremely high l

131 from the extremely radioresistant bacterium Deinococcus radiodurans is the exact inverse of this est

132 Deinococcus radiodurans is unique in its ability to reco

133 by one particular family member, ISDra2 from Deinococcus radiodurans, is dramatically stimulated upon

134 o-electron microscopy (cryo-EM) structure of Deinococcus radiodurans ISDra2 TnpB in complex with its

135 Deinococcus radiodurans, known for its extraordinary DNA

136 aeal (Haloarcula marismortui) and bacterial (Deinococcus radiodurans) large ribosomal subunits have b

137 uman and two bacterial (Escherichia coli and Deinococcus radiodurans) MnSODs.

138 We report that the complex between Deinococcus radiodurans NOS (deiNOS) and an unusual tryp

139 Recent structures of Deinococcus radiodurans Nramp (DraNramp) in multiple con

140 otein in the radiation-resistant eubacterium Deinococcus radiodurans participates in ribosomal RNA (r

141 Shewanella putrefaciens, Synechocystis sp., Deinococcus radiodurans, Pasteurella multocida, and Acti

142 bridges at the dimerization interface of the Deinococcus radiodurans phytochrome (DrBphP).

143 ructure of the chromophore-binding domain of Deinococcus radiodurans phytochrome assembled with its c

144 re of the chromophore-binding domains of the Deinococcus radiodurans phytochrome at 2.1 A resolution.

145 oreceptor through structural analysis of the Deinococcus radiodurans phytochrome BphP assembled with

146 HY domain of a 57-kDa photosensory module of Deinococcus radiodurans phytochrome changes from a struc

147 ochemical, and computational analyses of the Deinococcus radiodurans phytochrome, we demonstrate that

148 ing (Pr) state, the bilin chromophore of the Deinococcus radiodurans proteobacterial phytochrome (DrB

149 Deinococcus radiodurans R1 (DEIRA) is a bacterium best k

150 Deinococcus radiodurans R1 and other members of this gen

151 e complete genome sequence of the bacterium, Deinococcus radiodurans R1 has been released.

152 ual ORFs from Shewanella oneidensis MR-1 and Deinococcus radiodurans R1 have been designed.

153 equence of the radiation-resistant bacterium Deinococcus radiodurans R1 is composed of two chromosome

154 Deinococcus radiodurans R1 is extremely resistant to bot

155 , developed to facilitate gene disruption in Deinococcus radiodurans R1, has been used to inactivate

156 in and Snf2/Rad54 helicase were reported for Deinococcus radiodurans R1, leading to the speculation t

157 e hypothetical uricase regulator (HucR) from Deinococcus radiodurans R1.

158 The RecA protein of Deinococcus radiodurans (RecA(Dr)) is essential for the

159 We show here that Deinococcus radiodurans RecD2 helicase inactivates Esche

160 Intriguingly, Deinococcus radiodurans RecO does not bind SSB-Ct and we

161 Deinococcus radiodurans represents an organism in which

162 and 200 than those for Escherichia coli and Deinococcus radiodurans, respectively.

163 Deinococcus radiodurans RNA ligase (DraRnl) is a templat

164 Deinococcus radiodurans RNA ligase (DraRnl) is the found

165 Deinococcus radiodurans RNA ligase (DraRnl) seals 3-OH/5

166 hermophilic Thermus aquaticus and mesophilic Deinococcus radiodurans RNAPs and identify the FL as an

167 Deinococcus radiodurans single-stranded (ss) DNA binding

168 The Deinococcus radiodurans SSB protein has an occluded site

169 rmined a 1.8-A-resolution x-ray structure of Deinococcus radiodurans SSB.

170 IRS24 is a DNA damage-sensitive strain of Deinococcus radiodurans strain 302 carrying a mutation i

171 on usages are characterized in the genome of Deinococcus radiodurans (strain R1).

172 equence of the radiation-resistant bacterium Deinococcus radiodurans suggests the presence of both di

173 erization of HucR, a novel MarR homolog from Deinococcus radiodurans that demonstrates phenolic sensi

174 fication of the large ribosomal subunit from Deinococcus radiodurans that exploits its association wi

175 this instrument, we employ a model system of Deinococcus radiodurans that has been engineered to expr

176 nctions have been characterized primarily in Deinococcus radiodurans, the first sequenced bacterium w

177 velopment of bioremediation strategies using Deinococcus radiodurans, the most radiation resistant or

178 ive potential lateral transfer with archaea; Deinococcus radiodurans, the most radiation-resistant mi

179 truction and characterization of recombinant Deinococcus radiodurans, the most radiation-resistant or

180 In the extremophile bacterium Deinococcus radiodurans, the outermost surface layer is

181 onuclease A and the ICAT-labeled proteome of Deinococcus radiodurans, the presence of these label-spe

182 In both animal cells and the eubacterium Deinococcus radiodurans, the Ro autoantigen, a ring-shap

183 In the only studied bacterium, Deinococcus radiodurans, the Ro ortholog Rsr functions i

184 ersal in Bacteria as t(6)A is dispensable in Deinococcus radiodurans, Thermus thermophilus, Synechocy

185 response of the genomes of cyanobacteria and Deinococcus radiodurans to ionizing radiation.

186 mplex from the radiation-resistant bacterium Deinococcus radiodurans to protect protein epitopes from

187 The ability of Deinococcus radiodurans to recover from extensive DNA da

188 The remarkable ability of bacterium Deinococcus radiodurans to survive extreme doses of gamm

189 re we report the 1.75-A crystal structure of Deinococcus radiodurans topoisomerase IB (DraTopIB), a p

190 Deinococcus radiodurans topoisomerase IB (DraTopIB), an

191 nvelope of the radiation-resistant bacterium Deinococcus radiodurans was studied by cryo-electron mic

192 y identified peptides from the microorganism Deinococcus radiodurans was used for the training of the

193 The NOS gene from one such bacterium, Deinococcus radiodurans, was cloned and expressed (deiNO

194 member of the amidohydrolase superfamily in Deinococcus radiodurans, was cloned, expressed, and puri

195 weakly promiscuous PLL scaffold (Dr0930 from Deinococcus radiodurans ), we designed an extremely effi

196 siccation- and radiation-resistant bacterium Deinococcus radiodurans, we suggest that the extraordina

197 -one ionizing radiation-sensitive strains of Deinococcus radiodurans were evaluated for their ability

198 d based on the radiation-resistant bacterium Deinococcus radiodurans, which is being engineered to ex

199 we analyzed the sHsp system of the bacterium Deinococcus radiodurans, which is resistant against vari

200 ratio found in the radioresistant bacterium Deinococcus radiodurans, with [Mn(2+)] = 1 mM.