ライフサイエンスコーパス: Sinorhizobium meliloti

1 o the sigma(54)-polymerase activator DctD of Sinorhizobium meliloti.

2 rsenic detoxification in the legume symbiont Sinorhizobium meliloti.

3 e symbiosis between alfalfa and its symbiont Sinorhizobium meliloti.

4 genome are similar to those of the symbiotic Sinorhizobium meliloti.

5 go truncatula plants grown in symbiosis with Sinorhizobium meliloti.

6 inducible within 3 h after inoculation with Sinorhizobium meliloti.

7 d factor from the alfalfa-nodulating strain, Sinorhizobium meliloti.

8 cteria, Propionibacterium freudenreichii and Sinorhizobium meliloti.

9 2308 by complementation of an exoB mutant of Sinorhizobium meliloti.

10 catula during the symbiotic interaction with Sinorhizobium meliloti.

11 eparate downstream responses to its symbiont Sinorhizobium meliloti.

12 ing of TraR in the closely related bacterium Sinorhizobium meliloti.

13 ut using the model root nodulating bacterium Sinorhizobium meliloti.

14 e-dimensional architecture of the biofilm of Sinorhizobium meliloti.

15 c interaction with the diazotropic bacterium Sinorhizobium meliloti.

16 l to form nodules following inoculation with Sinorhizobium meliloti.

17 t of the symbiotic nitrogen fixing bacterium Sinorhizobium meliloti.

18 nodulation (nod) genes in the soil bacterium Sinorhizobium meliloti.

19 of 2-aminoethylphosphonate in the bacterium Sinorhizobium meliloti 1021 is proposed based on the ana

20 m (T4SS) of the plant intracellular symbiont Sinorhizobium meliloti 1021 is required for conjugal tra

21 The nitrogen-fixing rhizobial symbiont Sinorhizobium meliloti 1021 produces acidic symbiotic ex

22 r by tri-parental mating of these genes into Sinorhizobium meliloti 1021, a strain that lacks these p

23 The gltA gene, encoding Sinorhizobium meliloti 104A14 citrate synthase, was isol

24 e of cyclic diguanylate (c-di-GMP) levels in Sinorhizobium meliloti 8530, a bacterium that does not c

25 Sinorhizobium meliloti, a gram-negative soil bacterium,

26 Sinorhizobium meliloti, a legume symbiont and Brucella a

27 Sinorhizobium meliloti, a legume symbiont, and Brucella

28 In Sinorhizobium meliloti (also known as Rhizobium meliloti

29 For Sinorhizobium meliloti (also known as Rhizobium meliloti

30 charide (LPS) plays in the symbiosis between Sinorhizobium meliloti and alfalfa has been studied for

31 e indeterminate symbiosis that forms between Sinorhizobium meliloti and alfalfa requires biosynthesis

32 In the symbiosis between Sinorhizobium meliloti and alfalfa, mutations in GlnD, t

33 root systems that have been inoculated with Sinorhizobium meliloti and are developing root nodules.

34 n is essential for the long-term survival of Sinorhizobium meliloti and Brucella abortus within acidi

35 Two related alphaproteobacteria, Sinorhizobium meliloti and Caulobacter crescentus, serve

36 is presented here that two of these species, Sinorhizobium meliloti and Caulobacter crescentus, simpl

37 Membranes of Sinorhizobium meliloti and E. coli lack this activity.

38 proteobacteria Agrobacterium tumefaciens and Sinorhizobium meliloti and found that they are located a

39 Sinorhizobium meliloti and host legumes enter into a nit

40 and functional analyses of the SOE SorT from Sinorhizobium meliloti and its cognate electron acceptor

41 A successful symbiotic relationship between Sinorhizobium meliloti and its host Medicago sativa (alf

42 effective nitrogen-fixing symbiosis between Sinorhizobium meliloti and its legume host alfalfa (Medi

43 The nitrogen-fixing symbiosis between Sinorhizobium meliloti and its leguminous host plant Med

44 ages of symbiosis between the soil bacterium Sinorhizobium meliloti and its leguminous host plant, al

45 The nitrogen-fixing symbiosis between Sinorhizobium meliloti and Medicago sativa requires comp

46 Using the Sinorhizobium meliloti and Medicago truncatula symbiotic

47 LC) legumes, such as the interaction between Sinorhizobium meliloti and Medicago, bacteroid different

48 of 2 representative proteins, SMc02148 from Sinorhizobium meliloti and PA3455 from Pseudomonas aerug

49 There exist commonalities between symbiotic Sinorhizobium meliloti and pathogenic Brucella bacteria

50 h their counterparts in the che operons from Sinorhizobium meliloti and Rhodobacter sphaeroides, and

51 ent chromosomes that have been classified as Sinorhizobium meliloti and Sinorhizobium medicae.

52 a, Vibrio cholerae, Shewanella putrefaciens, Sinorhizobium meliloti, and Caulobacter crescentus.

53 h of Medicago truncatula, its symbiosis with Sinorhizobium meliloti, and on soil microbial community

54 mus intraradices and the rhizobial bacterium Sinorhizobium meliloti as well as with the pathogenic oo

55 f the recent extension of the TspO system to Sinorhizobium meliloti, as described by Davey and de Bru

56 e were able to successfully predict sRNAs in Sinorhizobium meliloti, as well as in multiple and poorl

57 The Medicago truncatula-Sinorhizobium meliloti association is an excellent model

58 Sinorhizobium meliloti bacA mutants are symbiotically de

59 Sinorhizobium meliloti bacteria produce a signal molecul

60 also occurs in the closely related bacteria Sinorhizobium meliloti, Brucella abortus, and Ochrobactr

61 Rhizobium leguminosarum, Rhizobium etli, and Sinorhizobium meliloti but not Escherichia coli.

62 The AAA+ domain of Sinorhizobium meliloti C4-dicarboxylic acid transport pr

63 Sinorhizobium meliloti can live as a soil saprophyte and

64 Sinorhizobium meliloti can live as symbionts inside legu

65 The Nod factor of Sinorhizobium meliloti carries O-sulphate, O-acetate and

66 In Sinorhizobium meliloti, catabolite repression is influen

67 Sinorhizobium meliloti cells store excess carbon as intr

68 but similar to that measured for the related Sinorhizobium meliloti CheA.

69 tion of the one HK-two RR motif found in the Sinorhizobium meliloti chemotaxis pathway and measuring

70 e constructed a strain of the soil bacterium Sinorhizobium meliloti containing a gfp gene fused to th

71 The symbiotic nitrogen-fixing soil bacterium Sinorhizobium meliloti contains three replicons: pSymA,

72 FixL/FixJ two-component regulatory system of Sinorhizobium meliloti controls the expression of nitrog

73 In Rhizobium meliloti (Sinorhizobium meliloti) cultures, the endo-1, 3-1,4-beta

74 In Sinorhizobium meliloti, CuxR stimulates transcription of

75 Sinorhizobium meliloti dctA encodes a transport protein

76 In contrast to R. leguminosarum dctA, the Sinorhizobium meliloti dctA promoter region was found to

77 for the Mg2+-BeF3--bound receiver domain of Sinorhizobium meliloti DctD bearing amino acid substitut

78 Sinorhizobium meliloti DctD is an activator of sigma(54)

79 orms of the two-component receiver domain of Sinorhizobium meliloti DctD, a sigma(54)-dependent AAA+

80 sertion in a gene with similarity to exsH of Sinorhizobium meliloti did not nodulate the plant host P

81 the sigma(54)-dependent activator DctD from Sinorhizobium meliloti, displayed an altered DNase I foo

82 Rhizobium leguminosarum and the lpsB gene of Sinorhizobium meliloti encode protein orthologs that are

83 The soil-dwelling alpha-proteobacterium Sinorhizobium meliloti engages in a symbiosis with legum

84 Sinorhizobium meliloti enters into a symbiotic relations

85 The alpha-proteobacterium Sinorhizobium meliloti establishes a chronic intracellul

86 er UV light, colonies of Rhizobium meliloti (Sinorhizobium meliloti) exoK mutants produce a fluoresce

87 The production of the Sinorhizobium meliloti exopolysaccharide, succinoglycan,

88 Sinorhizobium meliloti ExoR regulates the production of

89 The Sinorhizobium meliloti ExoS/ChvI two-component signaling

90 in M. truncatula plants inoculated with the Sinorhizobium meliloti exoY mutant, and the M. truncatul

91 The symbiotic, nitrogen-fixing bacterium Sinorhizobium meliloti favors succinate and related dica

92 When tested for nodulation by Sinorhizobium meliloti, flavonoid-deficient roots had a

93 e sink" among the alpha-proteobacteria (e.g. Sinorhizobium meliloti), for dephosphorylating CheY-P.

94 Sinorhizobium meliloti forms symbiotic, nitrogen-fixing

95 Recently, we discovered that a Sinorhizobium meliloti gene, bluB, is necessary for DMB

96 sucrose uptake and hydrolysis, we screened a Sinorhizobium meliloti genomic library and discovered a

97 ion of nitric oxide in roots inoculated with Sinorhizobium meliloti greatly increased our understandi

98 Sinorhizobium meliloti growth inside infection threads w

99 The symbiotic nitrogen-fixing bacterium Sinorhizobium meliloti harbors a gene, SMc02396, which e

100 d RaxQ are similar to the bacterial symbiont Sinorhizobium meliloti host specificity proteins, NodP a

101 equence similarity with protein sequences of Sinorhizobium meliloti IdhA and MocA; Bacillus subtilis

102 (nod) gene expression in the soil bacterium Sinorhizobium meliloti in response to the plant-secreted

103 nd cryo-electron microscopy structure of the Sinorhizobium meliloti-infecting T4 superfamily phage Ph

104 ent of plant flotillin-like genes (FLOTs) in Sinorhizobium meliloti infection of its host legume Medi

105 fection and cortical cell division following Sinorhizobium meliloti inoculation.

106 ediate the differentiation of the bacterium, Sinorhizobium meliloti into a nitrogen-fixing bacteroid

107 development of the symbiotic soil bacterium Sinorhizobium meliloti into nitrogen-fixing bacteroids,

108 l signal referred to as Nod factor, which in Sinorhizobium meliloti is a beta-(1,4)-linked tetramer o

109 Sinorhizobium meliloti is a free-living soil bacterium w

110 Sinorhizobium meliloti is a gram-negative soil bacterium

111 Sinorhizobium meliloti is a gram-negative soil bacterium

112 Sinorhizobium meliloti is a gram-negative soil bacterium

113 Sinorhizobium meliloti is a gram-negative soil bacterium

114 Sinorhizobium meliloti is a member of the Alphaproteobac

115 Sinorhizobium meliloti is a nitrogen-fixing bacterial sy

116 Sinorhizobium meliloti is a soil bacterium capable of in

117 Sinorhizobium meliloti is a soil bacterium which can est

118 The bacterium Sinorhizobium meliloti is attracted to seed exudates of

119 The soil bacterium Sinorhizobium meliloti is capable of entering into a nit

120 We show that GroEL1 of Sinorhizobium meliloti is required for efficient infecti

121 (EPSs) by the nitrogen-fixing soil bacterium Sinorhizobium meliloti is required for efficient invasio

122 Exopolysaccharide production by Sinorhizobium meliloti is required for invasion of root

123 the gene coding for acetate kinase (ackA) in Sinorhizobium meliloti is up-regulated in response to ph

124 aying a central role during key steps of the Sinorhizobium meliloti-M. truncatula symbiotic interacti

125 We show that, in the Sinorhizobium meliloti-Medicago truncatula interaction,

126 The Sinorhizobium meliloti megaplasmid pSymA has previously

127 gy with other dioxygenases and hydrolases in Sinorhizobium meliloti, Mesorhizobium loti, and Bradyrhi

128 mbiosis with the host plant Medicago sativa, Sinorhizobium meliloti must overcome an oxidative burst

129 oying a novel two-part screen, we identified Sinorhizobium meliloti mutants that were both sensitive

130 nt, heparin-stable complexes on heteroduplex Sinorhizobium meliloti nifH DNA mismatched next to the G

131 duction system ensures that a cascade of the Sinorhizobium meliloti nitrogen fixation genes is induce

132 is the key step in the hypoxic induction of Sinorhizobium meliloti nitrogen fixation genes.

133 We tested the ability of three Sinorhizobium meliloti nod gene products to modify Nod f

134 s involved in the synthesis of an inducer of Sinorhizobium meliloti nod genes, as well as a gene asso

135 prisingly, even sulfated fungal Myc-LCOs and Sinorhizobium meliloti Nod-LCOs, having very similar str

136 Sinorhizobium meliloti nodL and nodF mutations additivel

137 Sinorhizobium meliloti NRG247 has a Fix(+) phenotype on

138 ur analyses of lipopolysaccharide mutants of Sinorhizobium meliloti offer insights into how this bact

139 t of nitrogen-fixing root nodules induced by Sinorhizobium meliloti on the model plant Medicago trunc

140 eport here the first characterization of the Sinorhizobium meliloti open reading frame SMc01113.

141 R. leguminosarum and Rhizobium etli but not Sinorhizobium meliloti or E. coli.

142 y expressed in plants exposed for 24 h to WT Sinorhizobium meliloti or to the invasion defective S. m

143 Sinorhizobium meliloti participates in a nitrogen-fixing

144 While screening for Sinorhizobium meliloti Pho regulatory mutants, a transpo

145 g system of the gram-negative soil bacterium Sinorhizobium meliloti plays an important role in the es

146 Sinorhizobium meliloti produces an exopolysaccharide cal

147 eed, eliminating SMc01113/YbeY expression in Sinorhizobium meliloti produces symbiotic and physiologi

148 The symbiotic lifestyle of Sinorhizobium meliloti requires a drastic cellular diffe

149 Sinorhizobium meliloti requires exopolysaccharides in or

150 Sinorhizobium meliloti requires ExoS/ChvI two-component

151 interaction between Medicago truncatula and Sinorhizobium meliloti results in the formation of nitro

152 c capsular polysaccharide produced by strain Sinorhizobium meliloti Rm1021 contributes to symbiosis w

153 The Sinorhizobium meliloti Rm1021 Delta glnD-sm2 mutant, whi

154 homologous regions of A. tumefaciens C58 and Sinorhizobium meliloti Rm1021 genomes.

155 The production of succinoglycan by Sinorhizobium meliloti Rm1021 is required for successful

156 ows the greatest identity to SinI (71%) from Sinorhizobium meliloti Rm1021.

157 As populations of Sinorhizobium meliloti Rm2011 were similar in bulk/disso

158 level incompatibility with the microsymbiont Sinorhizobium meliloti Rm41.

159 The nitrogen-fixing symbiont Sinorhizobium meliloti senses and responds to constantly

160 Here we report evidence that in Sinorhizobium meliloti, sensing of AHLs with acyl chains

161 include: the nitrogen-fixing plant symbionts Sinorhizobium meliloti (SINME) and Mesorhizobium loti (M

162 Proline utilization A from Sinorhizobium meliloti (SmPutA) is a 1233-residue bifunc

163 Sinorhizobium meliloti stores carbon and energy in poly-

164 bacterial symbiont of one of these species (Sinorhizobium meliloti strain Rm1021) and an opportunist

165 Sinorhizobium meliloti strains lacking BacA function are

166 mes of A. tumefaciens and the plant symbiont Sinorhizobium meliloti suggest a recent evolutionary div

167 g in the morphologically symmetric bacterium Sinorhizobium meliloti suggests that this type of cell c

168 cterial status in mutant nodules, we assayed Sinorhizobium meliloti symbiosis gene promoters (nodF, e

169 However, in the Medicago truncatula-Sinorhizobium meliloti symbiosis, incompatibility betwee

170 In the Medicago truncatula/Sinorhizobium meliloti symbiosis, the plant undergoes a

171 fixing nodules (Fix+) in Medicago truncatula-Sinorhizobium meliloti symbiosis.

172 scale metabolic model of the legume symbiont Sinorhizobium meliloti that is integrated with carbon ut

173 quenced three genes from Rhizobium meliloti (Sinorhizobium meliloti) that are involved in sulfate act

174 hm to a symbiotic nitrogen-fixing bacterium, Sinorhizobium meliloti The LDSS-P profiles that overlap

175 focused on the study of trehalose uptake by Sinorhizobium meliloti, the demonstrated approach is app

176 e and dynamics of Sma0114 from the bacterium Sinorhizobium meliloti, the first such characterization

177 First discovered in Sinorhizobium meliloti, the main response regulator CheY

178 Here we identify in Sinorhizobium meliloti, the Medicago symbiont, a cAMP-si

179 Quorum sensing (QS) in Sinorhizobium meliloti, the N-fixing bacterial symbiont

180 in the presence of the compatible bacterium Sinorhizobium meliloti, the nip mutant showed nitrogen d

181 Sinorhizobium meliloti, the nitrogen-fixing symbiont of

182 to the Rhizobiales order: the plant symbiont Sinorhizobium meliloti, the plant pathogen Agrobacterium

183 In Sinorhizobium meliloti, the production of exopolysacchar

184 In particular, in Sinorhizobium meliloti there are four groESL operons and

185 In Sinorhizobium meliloti there are two rpoH genes, four gr

186 This peptide affects Sinorhizobium meliloti transcription, translation, and c

187 y, we showed that a FadD-deficient mutant of Sinorhizobium meliloti, unable to convert free fatty aci

188 he nitro -fixing symbiosis with host plants, Sinorhizobium meliloti undergoes a profound cellular dif

189 n factors produced by the bacterial symbiont Sinorhizobium meliloti using a dual-dye ratiometric imag

190 When they are available, Sinorhizobium meliloti utilizes C(4)-dicarboxylic acids

191 at catalyzes the synthesis of PC, and Pcs in Sinorhizobium meliloti was characterized.

192 The CbcX orthologue ChoX from Sinorhizobium meliloti was similar to CbcX in these bind

193 dicago truncatula and its rhizobial symbiont Sinorhizobium meliloti, which includes more than 23,000

194 The dicarboxylate transport (Dct) system of Sinorhizobium meliloti, which is essential for a functio

195 biosis between Medicago truncatula roots and Sinorhizobium meliloti would identify regulated plant ge