ライフサイエンスコーパス: Rhizobium

1 and in species of symbiotic nitrogen-fixing Rhizobium.

2 monly compared for studies of symbiosis with Rhizobium.

3 erable to invasion by nonfixing, saprophytic Rhizobium.

4 aperonin genes from two different species of Rhizobium.

5 a, such as Burkholderia, Herbaspirillum, and Rhizobium.

6 e B, were necessary, as previously shown for Rhizobium.

7 Plant-associated bacteria such as Rhizobium and Agrobacterium can use sucrose as a nutrien

8 s favoured alphaproteobacteria in the genera Rhizobium and Ensifer: this was confirmed by nodulation

9 Within this family, many Rhizobium and Sinorhizobium strains are nitrogen-fixing

10 onads; ClostriDB for clostridia; RhizoDB for Rhizobium and Sinorhizobium; and MycoDB, for Mycobacteri

11 acterial communities, increasing some (e.g., Rhizobium and Sphingomonas) but decreasing other (e.g.,

12 (Vogesella, Pseudomonas, Flavobacterium and Rhizobium) and anaerobic genera (Longilinea, Bellilinea,

13 onsists of the symbiosome membrane, a single rhizobium, and the soluble space between them, called th

14 Rhizobium are Gram-negative bacteria that survive intrac

15 that TOR plays a role in the recognition of Rhizobium as a symbiont.

16 f three gram-negative rhizobacterial genera: Rhizobium, Azospirillum, and Pseudomonas.

17 Symbiotic nitrogen-fixing rhizobium bacteria and arbuscular mycorrhizal fungi use

18 Symbiosis between Rhizobium bacteria and legumes leads to the formation of

19 Arbuscular mycorrhizal (AM) fungi and rhizobium bacteria are accommodated in specialized membr

20 he symbiotic association between legumes and Rhizobium bacteria can provide substantial amounts of ni

21 Rhizobium bacteria synthesize signal molecules called No

22 oybean can form symbiotic relationships with Rhizobium bacteria to fix atmospheric nitrogen.

23 n symbiosome membrane (SM) that encloses the rhizobium bacteroid.

24 o the periplasm was not limited to the genus Rhizobium, but was also observed in other proteobacteria

25 otein that is involved in autoaggregation of Rhizobium cells, biofilm formation, and adhesion to plan

26 uccessful sym plasmid transfer between major Rhizobium chromosomal types.

27 t hairs during primary host infection in the Rhizobium-clover symbiosis.

28 lla melitensis, and all sequenced strains of Rhizobium, consistent with the occurrence of long second

29 eight nodule)(-1) h(-1) of a Medicago sativa-Rhizobium consortium by continuously analyzing the amoun

30 ecruiting other microbes, such as Ensifer or Rhizobium, could facilitate delivery of DNA and proteins

31 ons indicated dominance of Sulfurospirillum, Rhizobium, Desulfovibrio and four members of the Clostri

32 y of nod genes carried by a given species of Rhizobium determines the NF structure synthesized and de

33 tiveness and cell surface characteristics of Rhizobium etli and has sequence similarity to a family o

34 of the lipid A from the plant endosymbionts Rhizobium etli and Rhizobium leguminosarum is the presen

35 The structure of the lipid A from Rhizobium etli and Rhizobium leguminosarum lipopolysacch

36 In contrast to Rhizobium etli and Rhizobium leguminosarum, the NGR234 l

37 entified in extracts of R. leguminosarum and Rhizobium etli but not Sinorhizobium meliloti or E. coli

38 l. reported that the lipopolysaccharide from Rhizobium etli CE3 bacteroids isolated from host bean ro

39 Rhizobium etli CE3 bacteroids were isolated from Phaseol

40 Lipid A of Rhizobium etli CE3 differs dramatically from that of oth

41 igosaccharides comprising the core region of Rhizobium etli CE3 lipopolysaccharide (LPS) has been elu

42 The O-antigen polysaccharide (OPS) of Rhizobium etli CE3 lipopolysaccharide (LPS) is linked to

43 The O-antigenic polysaccharide of the Rhizobium etli CE3 lipopolysaccharide (LPS) was structur

44 The Rhizobium etli CE3 O antigen is a fixed-length heteropol

45 The Rhizobium etli CE3 O antigen is a fixed-length heteropol

46 ies (A, B, C, D-1, D-2, and E) purified from Rhizobium etli CE3 were investigated by one- and two-dim

47 Rhizobium leguminosarum and Rhizobium etli contain functional lpxF orthologues, cons

48 but previous mutant analysis suggested that Rhizobium etli gene wreQ might encode this reductase.

49 nsduction, we characterized and investigated Rhizobium etli hybrid sensor ReFixL.

50 he structures of Rhizobium leguminosarum and Rhizobium etli lipid A are distinct from those found in

51 Rhizobium etli modifies lipopolysaccharide (LPS) structu

52 PS) in gel electrophoresis, the O antigen of Rhizobium etli mutant strain CE166 was apparently of nor

53 e site of the carboxyl transferase domain of Rhizobium etli pyruvate carboxylase have been determined

54 ctor in the common bean (Phaseolus vulgaris)-Rhizobium etli symbiosis.

55 trogen fixing (i.e., Azotobacter vinelandii, Rhizobium etli, and Azospirillum lipoferum) and denitrif

56 sarum, Rhizobium fredii, Rhizobium meliloti, Rhizobium etli, and Rhizobium tropici.

57 sent in extracts of Rhizobium leguminosarum, Rhizobium etli, and Sinorhizobium meliloti but not Esche

58 s) symbiotically associates with its partner Rhizobium etli, resulting in the formation of root nitro

59 ated at early stages of its interaction with Rhizobium etli.

60 between common bean (Phaseolus vulgaris) and Rhizobium etli.

61 in the carboxyltransferase domain of PC from Rhizobium etli.

62 Positive correlations between legume and rhizobium fitness imply that most ineffective rhizobia a

63 leguminosarum, Rhizobium sp. strain NGR234, Rhizobium fredii (Sinorhizobium fredii), and Agrobacteri

64 In vitro evidence indicates that Rhizobium fredii Nod factors are selectively de-N-acylat

65 Rhizobium fredii participates in a nitrogen-fixing symbi

66 e, being present in Rhizobium leguminosarum, Rhizobium fredii, Rhizobium meliloti, Rhizobium etli, an

67 The N-terminal portion of Rhizobium FtsZ polymerized in Escherichia coli and appea

68 of this investigation is to characterize the Rhizobium genes for HP degradation and transport.

69 In addition, a nonrandom distribution of Rhizobium genotypes across host plant species and sampli

70 Like the Rhizobium homolog, FtsZ(Bb) has a C-terminal region of a

71 essential for symbiotic nitrogen fixation by Rhizobium in pea nodules.

72 cysteine-rich (NCR) peptides produced in the rhizobium-infected plant cells.

73 erent development stages of nodulation after rhizobium infection.

74 pairs, as in some species of Mycoplasma and Rhizobium, is puzzling.

75 h the evolutionarily younger nitrogen-fixing Rhizobium legume symbiosis (RLS)(8) or by reverse geneti

76 Db-LNP is involved in the initiation of the Rhizobium legume symbiosis.

77 unds important in the different steps of the rhizobium-legume association.

78 mediating recognition and specificity in the Rhizobium-legume nitrogen-fixing symbiosis.

79 The nitrogen-fixing Rhizobium-legume partnership is presently the best under

80 N2-fixation by Rhizobium-legume symbionts is of major ecological and ag

81 The establishment of rhizobium-legume symbioses requires the bacterial synthe

82 ually since the discovery of nitrogen-fixing Rhizobium-legume symbioses, researchers have dreamed of

83 olyhydroxybutyrate (PHB), in maintaining the Rhizobium-legume symbioses.

84 nzyme may reduce the N2-fixing efficiency of Rhizobium-legume symbioses.

85 est that this protein may play a role in the rhizobium-legume symbiosis and/or in a related carbohydr

86 Recent studies strongly suggest that the Rhizobium-legume symbiosis coopted a signaling pathway,

87 The Rhizobium-legume symbiosis culminates in the exchange of

88 The Rhizobium-legume symbiosis involves the formation of a n

89 Development of the Rhizobium-legume symbiosis is controlled by the host pla

90 Rhizobium-legume symbiosis provides a rich source of inf

91 During the Rhizobium-legume symbiosis, bacteria enter the cells of

92 In the Rhizobium-legume symbiosis, compatible bacteria and host

93 In the Rhizobium-legume symbiosis, root nodules are the sites o

94 encode proteins known to be involved in the Rhizobium-legume symbiosis, six encode proteins with hom

95 ane compartment has also been coopted in the Rhizobium-legume symbiosis.

96 ead arbuscular mycorrhizal symbiosis and the Rhizobium-legume symbiosis.

97 ed by rhizobia, which play a key role in the rhizobium-legume symbiotic interaction.

98 g slow, tight-binding kinetics) of LpxC from Rhizobium leguminosarum (Ki = 340 nM), a Gram-negative p

99 e monoester hydrolase/phosphodiesterase from Rhizobium leguminosarum (R/PMH) both structurally and ki

100 A Rhizobium leguminosarum 3841 acpXL mutant (named here Rl

101 lysaccharide (OPS) isolated from free living Rhizobium leguminosarum 3841, a symbiont of Pisum sativu

102 Two such dual-host strains were tested: Rhizobium leguminosarum A34 in peas and beans and Bradyr

103 Rhizobium leguminosarum and Rhizobium etli contain funct

104 The structures of Rhizobium leguminosarum and Rhizobium etli lipid A are d

105 LpxE, a membrane-bound phosphatase found in Rhizobium leguminosarum and some other Gram-negative bac

106 branched-chain amino acid permease (Bra) of Rhizobium leguminosarum and the histidine permease (His)

107 The lpcC gene of Rhizobium leguminosarum and the lpsB gene of Sinorhizobi

108 The pyrE gene of Rhizobium leguminosarum biovar trifolii (Rl) was subclon

109 Rhizobium leguminosarum biovar viciae strain 3841 is a m

110 The topology NodC in the inner membrane of Rhizobium leguminosarum biovar viciae was analysed using

111 iens pathogenesis, and common nod genes from Rhizobium leguminosarum bv viciae and Rhizobium meliloti

112 suite of bioreporters has been developed in Rhizobium leguminosarum bv viciae strain 3841, and these

113 inoculated with Bradyrhizobium japonicum or Rhizobium leguminosarum bv viciae, respectively, and the

114 e-cell Raman spectra (SCRS) to differentiate Rhizobium leguminosarum bv.

115 ese/iron-type superoxide dismutase (SodA) of Rhizobium leguminosarum bv.

116 Rhizobium leguminosarum bv. trifolii 4S has a lipopolysa

117 olipooligosaccharides (CLOSs) from wild-type Rhizobium leguminosarum bv. trifolii on development of w

118 eviously, we have shown that tfxABCDEFG from Rhizobium leguminosarum bv. trifolii T24 is sufficient t

119 g this 3.1-kb fragment was used to transform Rhizobium leguminosarum bv. trifolii TA-1JH, a strain wh

120 protein product is highly homologous to the Rhizobium leguminosarum bv. viciae RhiR protein and a nu

121 NodO is a secreted protein from Rhizobium leguminosarum bv. viciae with a role in signal

122 In Rhizobium leguminosarum bv. viciae, quorum-sensing is re

123 show that a Cpn60 protein from the bacterium Rhizobium leguminosarum can function to allow E. coli gr

124 Membranes of Rhizobium leguminosarum contain a 3-deoxy-D-manno-octulo

125 The endosymbiotic bacterium Rhizobium leguminosarum contains a single hydrogenase sy

126 potential IHF binding sites adjacent to the Rhizobium leguminosarum dctA promoter.

127 e structure of the nitrogen-fixing bacterium Rhizobium leguminosarum differs from that of Escherichia

128 The lipopolysaccharide of Rhizobium leguminosarum differs from that of other Gram-

129 Lipid A from the nitrogen-fixing bacterium Rhizobium leguminosarum displays many structural differe

130 Rhizobium leguminosarum has two high-affinity Mn(2+) tra

131 lorimetry, and other methods that RapA2 from Rhizobium leguminosarum indeed exhibits a cadherin-like

132 Rhizobium leguminosarum is a Gram-negative bacterium tha

133 Rhizobium leguminosarum is a soil bacterium that infects

134 de (LPS) core of the Gram-negative bacterium Rhizobium leguminosarum is more amenable to enzymatic st

135 m the plant endosymbionts Rhizobium etli and Rhizobium leguminosarum is the presence of a proximal su

136 Rhizobium leguminosarum lipid A lacks both phosphates, b

137 Coexpression of FnLpxE and the Rhizobium leguminosarum lipid A oxidase RlLpxQ in E. col

138 The lipid A and inner core regions of Rhizobium leguminosarum lipopolysaccharide contain four

139 cture of the lipid A from Rhizobium etli and Rhizobium leguminosarum lipopolysaccharides (LPSs) lacks

140 the purification and characterization of the Rhizobium leguminosarum mannosyl transferase LpcC, which

141 The nitrogen-fixing symbiont Rhizobium leguminosarum reportedly produces at least six

142 nalysis of quorum-sensing (QS) regulation in Rhizobium leguminosarum revealed an unusual type of gene

143 P encoding EI(Ntr) of the PTS(Ntr) system in Rhizobium leguminosarum strain Rlv3841 caused a pleiotro

144 To this end, Rhizobium leguminosarum strains nodulating sympatric spe

145 e employed the rarely used heterologous host Rhizobium leguminosarum to invoke the activities of two

146 hingomonas strain S88 and the pssDE genes of Rhizobium leguminosarum were identified as encoding gluc

147 nd core regions of the lipopolysaccharide in Rhizobium leguminosarum, a nitrogen-fixing plant endosym

148 Lipid A of Rhizobium leguminosarum, a nitrogen-fixing plant endosym

149 In the N2-fixing bacterium Rhizobium leguminosarum, mutations in a homologue of ton

150 es this acyl chain is present in extracts of Rhizobium leguminosarum, Rhizobium etli, and Sinorhizobi

151 of the family Rhizobiaceae, being present in Rhizobium leguminosarum, Rhizobium fredii, Rhizobium mel

152 In contrast to Rhizobium etli and Rhizobium leguminosarum, the NGR234 lipid A contains a b

153 Pseudomonas brassicacearum and rhizospheric Rhizobium leguminosarum.

154 siderophore made by the symbiotic bacterium Rhizobium leguminosarum.

155 tein, (13)C, (15)N-labeled NodF protein from Rhizobium leguminosarum.

156 orum-sensing signalling molecule produced by Rhizobium leguminosarum.

157 t region from the homologous cpn60-1 gene of Rhizobium leguminosarum.

158 M, P), has been cloned and characterized in Rhizobium leguminosarum.

159 ation of nitrogen-fixing pea root nodules by Rhizobium leguminosarum.

160 hydrolases from Burkholderia caryophylli and Rhizobium leguminosarum.

161 n single-partner pairings of wild legume and rhizobium lineages, which prevented legume choice.

162 Rhizobium lipochitooligosaccharide signal molecules stim

163 Rhizobium lipopolysaccharide (LPS) contains four termina

164 Rhizobium-made Nod factors induce rapid changes in both

165 In Rhizobium meliloti (Sinorhizobium meliloti) cultures, th

166 , and visualized under UV light, colonies of Rhizobium meliloti (Sinorhizobium meliloti) exoK mutants

167 e have cloned and sequenced three genes from Rhizobium meliloti (Sinorhizobium meliloti) that are inv

168 er polysaccharide-secreting bacteria such as Rhizobium meliloti (succinoglycan), Xanthomonas campestr

169 As a first step, the ftsA genes of Rhizobium meliloti and Agrobacterium tumefaciens were is

170 ent of the nitrogen-fixing symbiosis between Rhizobium meliloti and its host plant, Medicago sativa (

171 During the symbiosis between the bacterium Rhizobium meliloti and plants such as alfalfa, the bacte

172 The Rhizobium meliloti bacA gene encodes a function that is

173 The function of the Rhizobium meliloti bacA gene, which is a homolog of the

174 Rhizobium meliloti can occupy at least two distinct ecol

175 As a first step in characterizing the Rhizobium meliloti cell division machinery, we tested wh

176 membrane potential depolarizing activity in Rhizobium meliloti cell-free filtrates, a plant response

177 tibodies prepared to the complex flagella of Rhizobium meliloti cross-reacted with the striated flage

178 Rhizobium meliloti DctD (C4-dicarboxylate transport prot

179 positions 3, 4, 6, 7, and 8 of this motif in Rhizobium meliloti DctD disrupted transcriptional activa

180 The Rhizobium meliloti ExoK and ExsH glycanases have been pr

181 The Rhizobium meliloti exoS gene is involved in regulating t

182 utoxidation rate on oxygen concentration for Rhizobium meliloti FixL and Aplysia kurodai myoglobin, w

183 e ferric forms of two soluble truncations of Rhizobium meliloti FixL, FixL (heme and kinase domains,

184 ferrous forms of two soluble truncations of Rhizobium meliloti FixL, FixL* and FixLN, are reported.

185 ous complexes of two deletion derivatives of Rhizobium meliloti FixL, FixLN (the heme domain) and a f

186 Rhizobium meliloti harboring the binary system also tran

187 The Rhizobium meliloti lipid A backbone, like that of Escher

188 Rhizobium meliloti mutants defective in EPS production f

189 igate interactions between E sigma54 and the Rhizobium meliloti nifH promoter.

190 ccus pyogenes HasA, Xenopus laevis DG42, and Rhizobium meliloti NodC.

191 ene, is expressed following inoculation with Rhizobium meliloti or by adding R. meliloti-produced nod

192 Rhizobium meliloti Rm1021 must be able to synthesize suc

193 Effective invasion of alfalfa by Rhizobium meliloti Rm1021 normally requires the presence

194 In Rhizobium meliloti the syrM regulatory gene positively c

195 For Sinorhizobium meliloti (also known as Rhizobium meliloti) AK631 to establish effective symbios

196 In Sinorhizobium meliloti (also known as Rhizobium meliloti), these molecules are highly modified

197 both known and novel gene fragments: 5 from Rhizobium meliloti, 13 from Myxococcus xanthus, and 3 fr

198 Brucella abortus, a mammalian pathogen, and Rhizobium meliloti, a phylogenetically related plant sym

199 ne from several of these bacteria, including Rhizobium meliloti, Brucella abortus, Agrobacterium tume

200 yme is not present in extracts of E. coli or Rhizobium meliloti, but it is readily demonstrable in me

201 t in the genomes of Pseudomonas syringae and Rhizobium meliloti, but not Neisseria meningitidis.

202 symbiotically important exopolysaccharide of Rhizobium meliloti, is composed of polymerized octasacch

203 activity is not present in Escherichia coli, Rhizobium meliloti, or the nodulation-defective mutant 2

204 s from Rhizobium leguminosarum bv viciae and Rhizobium meliloti, required for nodulation of pea (Pisu

205 n Rhizobium leguminosarum, Rhizobium fredii, Rhizobium meliloti, Rhizobium etli, and Rhizobium tropic

206 uction mechanism of the oxygen receptor from Rhizobium meliloti, RmFixL.

207 Primary expression of the Rhizobium meliloti-induced peroxidase gene rip1 occurs p

208 egulatory role in Caulobacter crescentus and Rhizobium meliloti.

209 56 from Burkholderia cepacia, and ISRm3 from Rhizobium meliloti.

210 en 18 h and 24 h after spot inoculation with Rhizobium meliloti.

211 is gene showed 50.6% identity with GltX from Rhizobium meliloti.

212 ded by flaA and flaB genes, respectively, in Rhizobium meliloti.

213 his operon is conserved in the same order in Rhizobium meliloti.

214 and homology with glucosamine synthase from Rhizobium meliloti.

215 ntrol of a promoter which is constitutive in Rhizobium meliloti.

216 Rhizobium melioti DctD activates transcription from the

217 sZ[Ml]) to 91% identity for the homolog from Rhizobium melliloti, (FtsZ[Rm1]).

218 bium nitrogen-fixing symbiosis, thousands of rhizobium microsymbionts, called bacteroids, are confine

219 Rhizobium mutations that increase both host and symbiont

220 Of 80 rhizobium mutations, 19 decrease both partners' fitness,

221 cheaters' potentially destabilize the legume-rhizobium mutualism, we lack a comprehensive review of h

222 o two other EPS regulatory proteins: ExoX of Rhizobium NGR234 and R. meliloti, and Psi of R. legumino

223 with higher plants, the N(2)-fixing symbiont Rhizobium NGR234 and the root-colonizing Burkholderia ce

224 In the legume-rhizobium nitrogen-fixing symbiosis, thousands of rhizob

225 sequence of Xenopus DG42 shows similarity to Rhizobium Nod C, Streptococcus Has A, and fungal chitin

226 The pooled correlation between rhizobium nodulation competitiveness and plant abovegrou

227 re the key signaling molecules in the legume-rhizobium nodule symbiosis.

228 r nodulation and symbiosis across a range of Rhizobium, NolR serves as a global regulatory protein.

229 y host responses even in the absence of live Rhizobium One of the earliest known host responses to NF

230 Legume-rhizobium pairs are often observed that produce symbioti

231 However, in species of Pseudomonas, Rhizobium, Paracoccus and Legionella, mutations in ccm g

232 favour legumes that provided less benefit to rhizobium partners.

233 This phage and its close relative Rhizobium phage vB_RleM_P10VF define a new group of T4 s

234 es the importance of both factors in shaping Rhizobium population dynamics.

235 ture on the evolution of N-fixation within a Rhizobium population using a mathematical model.

236 es depends upon the spatial structure of the Rhizobium populations within the soil.

237 hthalmitis caused by a ceftazidime-resistant Rhizobium radiobacter strain in a 62-year-old male.

238 lstonia gilardii, Ralstonia mannitolilytica, Rhizobium radiobacter, and Xanthomonas sp.

239 Studies measuring rhizobium relative or absolute fitness and host benefit

240 efense-like responses and/or to restrict the rhizobium release to precise cell layers.

241 e generated from Phaseolus vulgaris roots, a Rhizobium-responsive sucrose synthase of soybean and a c

242 sis of several derivatives of the lipid A of Rhizobium sin-1 has been developed.

243 Rhizobium Sin-1 LPS exerts these effects by competing wi

244 Rhizobium (Sinorhizobium) sp. strain NGR234 contains thr

245 Rhizobia (e.g. Rhizobium, Sinorhizobium, Bradyrhizobium, Mesorhizobium

246 ding: Mesorhizobium sp., Variovorax sp., and Rhizobium sp.

247 senite oxidase from the Alphaproteobacterium Rhizobium sp. NT-26 using a combination of X-ray absorpt

248 e iron, the N(2)-fixing, symbiotic bacterium Rhizobium sp. produce the cyclic trihydroxamate sideroph

249 om one of these symbiotic bacterial species, Rhizobium sp. Sin-1, significantly inhibits the synthesi

250 Rhizobium sp. strain NGR234 forms symbiotic, nitrogen-fi

251 spread, cell extracts from R. leguminosarum, Rhizobium sp. strain NGR234, Rhizobium fredii (Sinorhizo

252 The third is similar to traA of Rhizobium sp. strain NGR234, which is involved in conjug

253 of the TraR-TraM antiactivation complex from Rhizobium sp. strain NGR234.

254 Rhizobium sp. strain PDO1-076 is a plant-associated bact

255 Rhizobium sp. strain TAL1145 degrades the Leucaena toxin

256 Therefore, while Rhizobium species are genetically isolated units within

257 Within a single agricultural plot, multiple Rhizobium species can nodulate bean roots, but it is unc

258 her pcaQ is present and conserved in related Rhizobium species employed Southern hybridization and an

259 Periplasmic cyclic beta-glucans of Rhizobium species provide important functions during pla

260 The structure of the lipid-A from Rhizobium species Sin-1, a nitrogen-fixing Gram-negative

261 unity, a common symbiotic plasmid allows all Rhizobium species to engage in symbiosis with the same h

262 We found that the Rhizobium species we observed coexist with low genetic r

263 We now describe several novel Rhizobium-specific enzymes that recognize and modify (Kd

264 utative phosphogluconolactonase, and a novel Rhizobium-specific repeat element.

265 bium, Pantoea, Phyllobacterium, Polaromonas, Rhizobium, Sphingobium, and Variovorax were generated.

266 plasmid pRiA4b and three large plasmids from Rhizobium spp.

267 We prevented a normally mutualistic rhizobium strain from cooperating (fixing N(2)) by repla

268 Rhizobium strains that are capable of utilizing certain

269 or HP is unique to some Leucaena-nodulating Rhizobium strains.

270 In legume-Rhizobium symbioses, specialised soil bacteria fix atmos

271 GmbHLHm1 is important to the soybean rhizobium symbiosis because loss of activity results in

272 Legume-rhizobium symbiosis contributes large quantities of fixe

273 Nitrogen fixation in the legume-rhizobium symbiosis is a crucial area of research for mo

274 al microorganisms (flavonoid inducers of the Rhizobium symbiosis), and in defense against pathogens (

275 In the legume-rhizobium symbiosis, bacterial exopolysaccharides (EPS)

276 To investigate the legume-Rhizobium symbiosis, we isolated and studied a novel sym

277 Flavonoids play critical roles in legume-rhizobium symbiosis.

278 ess responses, hormone signaling, and legume-rhizobium symbiosis.

279 a stable symbiotic interface in both AM and rhizobium symbiosis.

280 ression occurred exclusively during Medicago-rhizobium symbiosis.

281 cts with DMI2 and is required for the legume-rhizobium symbiosis.

282 portant role in the initiation of the legume-rhizobium symbiosis.

283 bean (Phaseolus vulgaris)-Rhizobium tropici (Rhizobium) symbiotic interaction.

284 asmid-encoded and chromosomal loci of native Rhizobium, the nitrogen-fixing symbiont of legumes.

285 The access of nonfixing Rhizobium to the plant exudates associated with nodules

286 by expression of a malonyl-CoA synthase from Rhizobium trifolii allowed construction of strain delete

287 We sought to determine whether live Rhizobium trigger a rapid calcium spiking response and w

288 of TOR during the bean (Phaseolus vulgaris)-Rhizobium tropici (Rhizobium) symbiotic interaction.

289 . vulgaris plants with endosymbionts such as Rhizobium tropici and Rhizophagus irregularis.

290 dii, Rhizobium meliloti, Rhizobium etli, and Rhizobium tropici.