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 aused by reactive oxygen species produced by Rhizobium and found that hydrogen peroxide added to beni

10 is a global regulator of iron homeostasis in Rhizobium and related alpha-proteobacteria.

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

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

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

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

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

16 Rhizobium are Gram-negative bacteria that survive intrac

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

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

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

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

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

22 e symbiotic relationship between legumes and rhizobium bacteria in root nodules has a high demand for

23 Rhizobium bacteria synthesize signal molecules called No

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

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

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

27 iated with nematodes in fruit, we found that Rhizobium causes a genome instability phenotype; we obse

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

29 uccessful sym plasmid transfer between major Rhizobium chromosomal types.

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

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

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

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

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

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

36 the importance of host plants in controlling Rhizobium diversity.

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

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

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

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

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

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

43 Rhizobium etli CE3 bacteroids were isolated from Phaseol

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

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

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

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

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

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

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

51 only one non-Agrobacterium bacterial strain, Rhizobium etli CFN42, harbors a complete set of virulenc

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

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

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

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

56 Rhizobium etli modifies lipopolysaccharide (LPS) structu

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

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

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

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

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

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

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

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

65 in the carboxyltransferase domain of PC from Rhizobium etli.

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

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

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

69 Rhizobium fredii participates in a nitrogen-fixing symbi

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

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

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

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

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

75 fting studies show that while recognition of rhizobium incompatibility is root driven, bacterial excl

76 odel, free radical scavengers suppressed the Rhizobium-induced C. elegans DNA damage.

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

78 erent development stages of nodulation after rhizobium infection.

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

80 aponicus and Medicago truncatula showed that rhizobium LCOs are perceived by a heteromeric receptor c

81 orthologous LysM-type receptors to perceive rhizobium LCOs, suggesting a shared evolutionary origin

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

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

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

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

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

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

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

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

90 lly, this process can be adapted to multiple Rhizobium-legume symbioses, soil types, and environmenta

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

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

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

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

95 The Rhizobium-legume symbiosis culminates in the exchange of

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

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

98 Rhizobium-legume symbiosis provides a rich source of inf

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

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

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

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

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

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

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

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

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

108 A Rhizobium leguminosarum 3841 acpXL mutant (named here Rl

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

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

111 Rhizobium leguminosarum and Rhizobium etli contain funct

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

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

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

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

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

117 Rhizobium leguminosarum biovar viciae strain 3841 is a m

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

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

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

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

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

123 ated phosphotransferase system (PTS(Ntr)) of Rhizobium leguminosarum bv.

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

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

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

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

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

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

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

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

132 The endosymbiotic bacterium Rhizobium leguminosarum contains a single hydrogenase sy

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

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

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

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

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

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

139 Rhizobium leguminosarum is a Gram-negative bacterium tha

140 Rhizobium leguminosarum is a soil bacterium that infects

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

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

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

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

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

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

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

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

149 with those expressing R. capsulatus CcoA and Rhizobium leguminosarum RibN as bona fide copper and rib

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

151 To this end, Rhizobium leguminosarum strains nodulating sympatric spe

152 il, we simultaneously monitored 84 different Rhizobium leguminosarum strains, identifying a supercomp

153 iotic nodules with a large diversity of soil Rhizobium leguminosarum symbiovar viciae (Rlv) bacteria.

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

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

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

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

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

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

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

161 different steps of the symbiotic interaction Rhizobium leguminosarum-Trifolium repens.

162 siderophore made by the symbiotic bacterium Rhizobium leguminosarum.

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

164 orum-sensing signalling molecule produced by Rhizobium leguminosarum.

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

166 Pseudomonas brassicacearum and rhizospheric Rhizobium leguminosarum.

167 hydrolases from Burkholderia caryophylli and Rhizobium leguminosarum.

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

169 Rhizobium lipochitooligosaccharide signal molecules stim

170 Rhizobium lipopolysaccharide (LPS) contains four termina

171 Rhizobium-made Nod factors induce rapid changes in both

172 DNA damage repair pathways, suggesting that Rhizobium may cause DNA damage in C. elegans intestinal

173 Thus, Rhizobium may signal to eukaryotic hosts via reactive ox

174 In Rhizobium meliloti (Sinorhizobium meliloti) cultures, th

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

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

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

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

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

180 The Rhizobium meliloti bacA gene encodes a function that is

181 Rhizobium meliloti can occupy at least two distinct ecol

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

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

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

185 Rhizobium meliloti DctD (C4-dicarboxylate transport prot

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

187 The Rhizobium meliloti ExoK and ExsH glycanases have been pr

188 The Rhizobium meliloti exoS gene is involved in regulating t

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

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

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

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

193 Rhizobium meliloti harboring the binary system also tran

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

195 Rhizobium meliloti mutants defective in EPS production f

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

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

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

199 Rhizobium meliloti Rm1021 must be able to synthesize suc

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

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

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

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

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

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

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

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

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

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

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

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

212 egulatory role in Caulobacter crescentus and Rhizobium meliloti.

213 56 from Burkholderia cepacia, and ISRm3 from Rhizobium meliloti.

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

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

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

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

218 and homology with glucosamine synthase from Rhizobium meliloti.

219 Rhizobium melioti DctD activates transcription from the

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

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

222 Rhizobium mutations that increase both host and symbiont

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

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

225 se is influenced by polyploidy in the legume-rhizobium mutualism.

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

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

228 Rhizobium nitrogen-fixing nodule symbiosis occurs in two

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

230 The pooled correlation between rhizobium nodulation competitiveness and plant abovegrou

231 seed mass, ectomycorrhizal associations, or Rhizobium nodulation.

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

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

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

235 Legume-rhizobium pairs are often observed that produce symbioti

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

237 favour legumes that provided less benefit to rhizobium partners.

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

239 P biosynthetic gene cluster in the genome of Rhizobium Pop5, which encodes the precursor peptide and

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

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

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

243 he fructosyl amino acid binding protein from Rhizobium radiobacter (SocA), which binds to alpha-fruct

244 ipooligosaccharides (LOS) from the bacterium Rhizobium radiobacter Rv3 are structurally related to an

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

246 Rhizobium radiobacter), Ralstonia solanacearum, Xanthomo

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

248 Studies measuring rhizobium relative or absolute fitness and host benefit

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

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

251 mbioses are initiated upon the perception of rhizobium-secreted lipochitooligosaccharides (LCOs), cal

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

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

254 Rhizobium (Sinorhizobium) sp. strain NGR234 contains thr

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

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

257 ophytes (Azorhizobium caulinodans ORS571 and Rhizobium sp. IRBG74) and the well-characterized plant e

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

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

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

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

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

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

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

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

266 Rhizobium sp. strain TAL1145 degrades the Leucaena toxin

267 Therefore, while Rhizobium species are genetically isolated units within

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

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

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

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

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

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

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

275 plasmid pRiA4b and three large plasmids from Rhizobium spp.

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

277 Rhizobium strains that are capable of utilizing certain

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

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

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

281 Legume-rhizobium symbiosis contributes large quantities of fixe

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

283 The legume-rhizobium symbiosis results in nitrogen-fixing root nodu

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

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

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

287 Flavonoids play critical roles in legume-rhizobium symbiosis.

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

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

290 ression occurred exclusively during Medicago-rhizobium symbiosis.

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

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

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

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

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

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

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

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

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

300 Using Rhizobium tropici CIAT 899 and Phaseolus vulgaris as wor