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 sensory core of the bacteriophytochrome from Deinococcus radiodurans.

5 r the ionizing radiation-resistant bacterium Deinococcus radiodurans.

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

7 m the ionizing radiation-resistant bacterium Deinococcus radiodurans.

8 i, and the extremely radioresistant organism Deinococcus radiodurans.

9 ccharomyces cerevisiae, Eschericia coli, and Deinococcus radiodurans.

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

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

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

13 the populations approached that exhibited by Deinococcus radiodurans.

14 Escherichia coli, Thermus thermophilus, and Deinococcus radiodurans.

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

16 dinary radiation resistance on the bacterium Deinococcus radiodurans.

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

18 structure of the large ribosomal subunit of Deinococcus radiodurans.

19 Deinococcus radiodurans, a highly radioresistant and str

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

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

22 Deinococcus radiodurans, a radiation-resistant bacterium

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 Deinococcus radiodurans can reconstitute its genome from

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

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

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

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

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

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

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

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

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

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

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

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

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

66 Deinococcus radiodurans (DEIRA) can survive very high do

67 Deinococcus radiodurans disproportionately favored TGA m

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

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

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

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

72 Deinococcus radiodurans (Dr) withstands desiccation, rea

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

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

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

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

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

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

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

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

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

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

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

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

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

86 Deinococcus radiodurans exhibits an extraordinary resist

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

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

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

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

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

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

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

94 Deinococcus radiodurans has a remarkable capacity to sur

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

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

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

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

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

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

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

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

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

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

105 Deinococcus radiodurans is a highly radiation-resistant

106 RecD2 from Deinococcus radiodurans is a superfamily 1 DNA helicase

107 Deinococcus radiodurans is extraordinarily resistant to

108 The bacterium Deinococcus radiodurans is extremely resistant to high l

109 Deinococcus radiodurans is extremely resistant to ionizi

110 Deinococcus radiodurans is highly resistant to radiation

111 The bacterium Deinococcus radiodurans is resistant to extremely high l

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

113 Deinococcus radiodurans is unique in its ability to reco

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

115 Deinococcus radiodurans, known for its extraordinary DNA

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

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

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

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

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

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

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

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

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

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

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

127 Deinococcus radiodurans R1 and other members of this gen

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

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

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

131 Deinococcus radiodurans R1 is extremely resistant to bot

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

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

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

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

136 We show here that Deinococcus radiodurans RecD2 helicase inactivates Esche

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

138 Deinococcus radiodurans represents an organism in which

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

140 Deinococcus radiodurans RNA ligase (DraRnl) is a templat

141 Deinococcus radiodurans RNA ligase (DraRnl) is the found

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

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

144 Deinococcus radiodurans single-stranded (ss) DNA binding

145 The Deinococcus radiodurans SSB protein has an occluded site

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

165 Deinococcus radiodurans topoisomerase IB (DraTopIB), an

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

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

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

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

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

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

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

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