ライフサイエンスコーパス: nitrogen-fixing

1 ial strains, most of which are known to have nitrogen fixing abilities, have similar psbA orthologs.

2 differences and similarities that govern the nitrogen-fixing ability of unicellular diazotrophic cyan

3 gen fixation research has been to expand the nitrogen-fixing ability to major cereal crops.

4 , to produce plants with superior biological nitrogen-fixing ability).

5 e the presence and absence of cyanobacterial nitrogen-fixing ability.

6 ocystis sp. PCC 6803 and in the filamentous, nitrogen-fixing Anabaena sp. PCC 7120 is stimulated thro

7 leases are essential to the establishment of nitrogen-fixing and phosphate-delivering arbuscular myco

8 ive genus-level phylogenetic analysis of the nitrogen-fixing angiosperms based on three plastid loci.

9 ifI(1) and nifI(2) in the nif operons of all nitrogen-fixing Archaea and some anaerobic Bacteria sugg

10 irements and suggests that an ancestor was a nitrogen-fixing autotroph.

11 introduction into cereal crops of either the nitrogen fixing bacteria or the nitrogenase enzyme respo

12 al root mucilage has been found that harbors nitrogen fixing bacteria that are attracted to the carbo

13 ules where plant cells are fully packed with nitrogen fixing bacteria.

14 oculation experiment designed to explore how nitrogen-fixing bacteria (rhizobia) adapt to legumes.

15 ethod we analyzed soybean plants infected by nitrogen-fixing bacteria and uninfected plants to invest

16 t of the lipopolysaccharide O-antigen of the nitrogen-fixing bacteria Bradyrhizobium sp. BTAi1 and sp

17 Moreover, nitrogen-fixing bacteria can recognize and colonize thes

18 Nitrogen-fixing bacteria catalyze the reduction of dinit

19 lateral organs that form on roots, and house nitrogen-fixing bacteria collectively called rhizobia.

20 he symbiotic association between legumes and nitrogen-fixing bacteria collectively known as rhizobia

21 have coevolved symbiotic relationships with nitrogen-fixing bacteria in nitrogen limited environment

22 For example, methanotrophic and nitrogen-fixing bacteria may benefit the plant host by p

23 ell cytoskeleton precedes symbiotic entry of nitrogen-fixing bacteria within the host plant roots.

24 eneficial plant microbes (mycorrhizal fungi, nitrogen-fixing bacteria), antagonists/pathogens of root

25 family can form associations with rhizobial nitrogen-fixing bacteria, and this association is tightl

26 ent symbiosis between legumes (Fabaceae) and nitrogen-fixing bacteria, asking how labile is symbiosis

27 ixation, but in contrast to reports on other nitrogen-fixing bacteria, the expression of its alternat

28 etabolic integration of large populations of nitrogen-fixing bacteria.

29 s on their roots, called nodules, that house nitrogen-fixing bacteria.

30 bioses with beneficial mycorrhizal fungi and nitrogen-fixing bacteria.

31 plants, form root nodules in symbiosis with nitrogen-fixing bacteria.

32 lly-regulated incompatible interactions with nitrogen-fixing bacteria.

33 nce the ability of legumes to associate with nitrogen-fixing bacteria.

34 nodules that provide an ecological niche for nitrogen-fixing bacteria.

35 Sinorhizobium meliloti is a nitrogen-fixing bacterial symbiont of alfalfa and relate

36 gh our analysis of a mutant of the symbiotic nitrogen fixing bacterium Sinorhizobium meliloti.

37 we screened a library of nifH mutants in the nitrogen-fixing bacterium Azotobacter vinelandii for mut

38 we investigate the role of rnf genes in the nitrogen-fixing bacterium Azotobacter vinelandii.

39 f the exopolysaccharide succinoglycan by the nitrogen-fixing bacterium Sinorhizobium meliloti 1021 is

40 f nodule development and colonization by the nitrogen-fixing bacterium Sinorhizobium meliloti appeare

41 The symbiotic nitrogen-fixing bacterium Sinorhizobium meliloti harbors

42 se, we applied this algorithm to a symbiotic nitrogen-fixing bacterium, Sinorhizobium meliloti The LD

43 the bacterium, Sinorhizobium meliloti into a nitrogen-fixing bacteroid within the legume root nodules

44 69 in the differentiation and persistence of nitrogen fixing bacteroids in M. truncatula.

45 lopment of elongated polyploid noncultivable nitrogen fixing bacteroids that convert atmospheric dini

46 odules did not differentiate completely into nitrogen-fixing bacteroids and quickly degraded.

47 PN2 plays a primary role in iron delivery to nitrogen-fixing bacteroids in M. truncatula nodules.

48 ate physiologically and morphologically into nitrogen-fixing bacteroids inside legume host nodules.

49 trogen through a symbiotic relationship with nitrogen-fixing bacteroids that reside in root nodules.

50 fectors of endosymbionts' differentiation to nitrogen-fixing bacteroids, we demonstrate that specific

51 fferentiates into highly polyploid, enlarged nitrogen-fixing bacteroids.

52 gans: root nodules that host the bacteria as nitrogen-fixing bacteroids.

53 s and eventually form, albeit inefficiently, nitrogen-fixing bacteroids.

54 (IRLC) legumes, rhizobia differentiate into nitrogen-fixing bacteroids.

55 ia including sediment-dwelling pseudomonads, nitrogen-fixing bradyrhizobia and cyanobacteria, and myc

56 imilar biogeographic regions, acquisition of nitrogen-fixing capability via symbiosis islands, possib

57 ovel form of the heterocyst, the specialized nitrogen-fixing cell of the multicellular cyanobacterium

58 ion and maintenance of a periodic pattern of nitrogen-fixing cells called heterocysts by the filament

59 imately every 10th cell in the filament into nitrogen-fixing cells called heterocysts.

60 e indicated concentrations 10-fold higher in nitrogen-fixing cells than in switched-off and ammonium-

61 Differentiation of nitrogen-fixing cells, called heterocysts, by the cyanob

62 Root nodules formed by plants of the nitrogen-fixing clade (NFC) are symbiotic organs that fu

63 Also within the nitrogen-fixing clade are actinorhizal species that asso

64 nodulating and nonnodulating species in the nitrogen-fixing clade indicated that the nodulation trai

65 early complete genus-level time-tree for the nitrogen-fixing clade is a significant advance in unders

66 , including nonleguminous species within the nitrogen-fixing clade.

67 mon feature of nodulating species within the nitrogen-fixing clade.

68 Rosales, which are collectively known as the nitrogen-fixing clade.

69 -nodule symbioses are within a monophyletic 'nitrogen-fixing' clade and associated signalling process

70 owing photoheterotrophically on malate under nitrogen-fixing conditions compared to a mutant strain t

71 o nitrogenase-expressing strains grown under nitrogen-fixing conditions in Mo-containing medium.

72 on profiling of A. vinelandii cultured under nitrogen-fixing conditions under various metal amendment

73 se synthesis and assembly were induced under nitrogen-fixing conditions, depending on which nitrogena

74 are present in near equal proportions under nitrogen-fixing conditions, the 24 kDa form is predomina

75 sential for oxidative stress tolerance under nitrogen-fixing conditions.

76 ptake hydrogenase HupSL in heterocysts under nitrogen-fixing conditions.

77 es in the overall cellular FAD content under nitrogen-fixing conditions.

78 [4Fe-4S] clusters required for growth under nitrogen-fixing conditions.

79 the wild type, it evolved hydrogen gas under nitrogen-fixing conditions.

80 ng proceeds, of cool-adapted by warm-adapted nitrogen-fixing cyanobacteria (such as Scytonema) and a

81 Some functional groups such as nitrogen-fixing cyanobacteria and denitrifiers may be ne

82 uxinic sediments imply that the expansion of nitrogen-fixing cyanobacteria and diversification of euk

83 arance of both marine planktonic unicellular nitrogen-fixing cyanobacteria and non-nitrogen-fixing pi

84 abundant during the Cryogenian [7, 8], both nitrogen-fixing cyanobacteria and planktonic picocyanoba

85 s between adjacent cells in the filaments of nitrogen-fixing cyanobacteria have been known for decade

86 n fixation within the same cell, unicellular nitrogen-fixing cyanobacteria have to maintain a dynamic

87 in the biomass and productivity of symbiotic nitrogen-fixing cyanobacteria in association with diatom

88 Colonial nitrogen-fixing cyanobacteria in surface waters played a

89 Nitrogen-fixing cyanobacteria in the genus Trichodesmium

90 Current biotechnological interest in nitrogen-fixing cyanobacteria stems from their robust re

91 les of nitrogen fixation predict unicellular nitrogen-fixing cyanobacteria to function in a certain w

92 It is generally assumed that nitrogen-fixing cyanobacteria will dominate when nitroge

93 1734 are found only in two other filamentous nitrogen-fixing cyanobacteria, Anabaena variabilis and N

94 Compared with other nitrogen-fixing cyanobacteria, Cyanothece 51142 contains

95 In nitrogen-fixing cyanobacteria, hydrogen evolution is ass

96 of channels connecting cells in filamentous nitrogen-fixing cyanobacteria.

97 in low abundance microorganisms, such as the nitrogen-fixing cyanobacteria.

98 Our results are consistent with a nitrogen-fixing cyanobacterial ancestor, repeated loss o

99 ce, we discovered that the marine planktonic nitrogen-fixing cyanobacterial genus Crocosphaera has re

100 In most nitrogen-fixing cyanobacterial strains, there are one to

101 , a widely distributed planktonic uncultured nitrogen-fixing cyanobacterium (UCYN-A) was found to hav

102 The filamentous nitrogen-fixing cyanobacterium Anabaena sp. PCC 7120 dif

103 cyanobacteria-plant symbioses, the symbiotic nitrogen-fixing cyanobacterium has low photosynthetic ac

104 nsive study of transcriptional activity in a nitrogen-fixing cyanobacterium is necessary to understan

105 , from Clostridium acetobutylicum in the non-nitrogen-fixing cyanobacterium Synechococcus elongatus s

106 142 in a 4E-3 mutant strain of the model non-nitrogen-fixing cyanobacterium Synechocystis sp. PCC 680

107 is) raciborskii is an invasive, filamentous, nitrogen-fixing cyanobacterium that forms frequent bloom

108 nteractions among these factors, we grew the nitrogen-fixing cyanobacterium Trichodesmium for 1 year

109 lation to global transcription in the marine nitrogen-fixing cyanobacterium Trichodesmium.

110 The nitrogen-fixing cyanobacterium, Anabaena PCC7120 encodes

111 Nitrogen-fixing (diazotrophic) microorganisms regulate p

112 ium found either in free-living form or as a nitrogen-fixing endosymbiont of leguminous plants such a

113 ble for the 3-O-deacylation of lipid A among nitrogen-fixing endosymbionts has not been characterized

114 The role of 3-O-deacylated lipid A among nitrogen-fixing endosymbionts, plant endophytes, and pla

115 The evolution of the nitrogen-fixing enzyme nitrogenase, which reduces atmosp

116 In order to retain the functionality of the nitrogen-fixing enzyme, some of these are able to rapidl

117 Frankia sp. strains, the nitrogen-fixing facultative endosymbionts of actinorhiza

118 Here we show that a nitrogen-fixing Fe-N2 catalyst can be protonated to form

119 PCC 7120 is a nitrogen-fixing filamentous cyanobacterium.

120 Anabaena sp. PCC 7120 is a nitrogen-fixing filamentous cyanobacterium.

121 legume nodules, rhizobia differentiate into nitrogen-fixing forms called bacteroids, which are enclo

122 sociate with ectomycorrhizal (ECM) fungi and nitrogen-fixing Frankia bacteria and, although their ECM

123 ionships between bacteria and plants include nitrogen-fixing Gram-negative proteobacteria called rhiz

124 rogenases and expressed vnf and anf genes in nitrogen-fixing growth media that contained Mo and V at

125 ulatory iscR gene, improved the capacity for nitrogen-fixing growth of strains deficient in either Ni

126 psulatus is essential for diazotrophic (i.e. nitrogen-fixing) growth with the iron-only nitrogenase,

127 Anabaena sp. strain PCC 7120 differentiates nitrogen-fixing heterocyst cells in a periodic pattern.

128 Nitrogen-fixing heterocysts are arranged in a periodic p

129 s of filamentous cyanobacteria differentiate nitrogen-fixing heterocysts at regular intervals along u

130 bacterium Anabaena sp. strain PCC 7120 forms nitrogen-fixing heterocysts in a periodic pattern in res

131 the differentiation of vegetative cells into nitrogen-fixing heterocysts to establish and maintain a

132 strain PCC 7120 forms a periodic pattern of nitrogen-fixing heterocysts when grown in the absence of

133 ular cyanobacterium Nostoc PCC 7120 develops nitrogen-fixing heterocysts with a pattern of one hetero

134 it distinct morphologies: motile hormogonia, nitrogen-fixing heterocysts, and spore-like akinetes.

135 te into three mutually exclusive cell types: nitrogen-fixing heterocysts, spore-like akinetes, and mo

136 ately 10% of its cells to become specialized nitrogen-fixing heterocysts.

137 the photosynthetic vegetative cells and the nitrogen-fixing heterocysts.

138 stoc) sp. strain PCC 7120 differentiate into nitrogen-fixing heterocysts.

139 H, respectively) have been detected in a non-nitrogen-fixing hyperthermophilic methanogen, Methanocal

140 as europaea) were much more susceptible than nitrogen fixing (i.e., Azotobacter vinelandii, Rhizobium

141 The nitrogen-fixing legume kudzu (Pueraria montana) is a wid

142 erial signals essential for establishing the nitrogen-fixing legume-rhizobia symbiosis.

143 ertilisers or green manures from atmospheric nitrogen fixing legumes.

144 ressed is the increased input of nitrogen by nitrogen-fixing legumes.

145 the anoxic and microoxic, endosymbiotic, and nitrogen-fixing life styles of the alpha-proteobacterium

146 vents, we determined that seven actinorhizal nitrogen-fixing lineages originated during the Late Cret

147 been interpreted to reflect proliferation of nitrogen-fixing marine cyanobacteria.

148 ted FS406-22, was 99% similar to that of non-nitrogen fixing Methanocaldococcus jannaschii DSM 2661.

149 mulate in a NifZ-deficient background of the nitrogen-fixing microbe Azotobacter vinelandii These inc

150 2, associated with an increased abundance of nitrogen fixing microbes.

151 eficial organisms, including pollinators and nitrogen-fixing microbes.

152 rfering with the host and its nodulating and nitrogen-fixing microbes.

153 The marine nitrogen fixing microorganisms (diazotrophs) are a major

154 ike the regulatory mechanisms known in other nitrogen-fixing microorganisms, nitrogen-fixation gene r

155 gin of the symbiosis between angiosperms and nitrogen-fixing (N2) bacterial symbionts housed in nodul

156 putative surface anoxic niches, differential nitrogen fixing niches, and those coupled with methane m

157 ansport network to deliver essential iron to nitrogen-fixing nodule cells.

158 and morphology in addition to differences in nitrogen-fixing nodule structure.

159 Rhizobium nitrogen-fixing nodule symbiosis occurs in two taxonomic

160 and high expression persisted throughout the nitrogen-fixing nodule zone.

161 Nitrogen-fixing nodule-inducing bacteria provide nutriti

162 ycan, are necessary for the establishment of nitrogen-fixing nodules (Fix+) in Medicago truncatula-Si

163 ught resistance, maintenance of meristems in nitrogen-fixing nodules and photoperiod-dependent flower

164 temically induced in the presence of active, nitrogen-fixing nodules but not in that of noninfected o

165 The formation of nitrogen-fixing nodules in legumes is tightly controlled

166 ly exopolysaccharide biosynthetic steps form nitrogen-fixing nodules on L. japonicus Gifu after a del

167 The formation of nitrogen-fixing nodules on legume hosts is a finely tune

168 ects root hairs and induces the formation of nitrogen-fixing nodules on leguminous plants.

169 Among the rhizobia that establish nitrogen-fixing nodules on the roots of host plants, man

170 Sinorhizobium meliloti forms symbiotic, nitrogen-fixing nodules on the roots of Medicago truncat

171 the actinobacterium Micromonospora inhabits nitrogen-fixing nodules raised questions as to its poten

172 ecific genes are preferentially expressed in nitrogen-fixing nodules, indicating that evolution endow

173 ms, i.e. the primary root, lateral roots and nitrogen-fixing nodules.

174 ium etli, resulting in the formation of root nitrogen-fixing nodules.

175 interactions with rhizobial bacteria to form nitrogen-fixing nodules.

176 egulatory peptides force the bacteria into a nitrogen-fixing organelle-like state.

177 The nitrogen-fixing organism Azotobacter vinelandii contains

178 soil rhizobia culminates in the formation of nitrogen-fixing organs called nodules that support plant

179 he transition from the photosynthetic to the nitrogen-fixing phase is marked by the onset of various

180 trogen fixation, while the population of non-nitrogen-fixing phytoplankton decreases since a larger f

181 situation where Crocosphaera exists with non-nitrogen-fixing phytoplankton, the relative abundance of

182 llular nitrogen-fixing cyanobacteria and non-nitrogen-fixing picocyanobacteria (Synechococcus and Pro

183 polysaccharide in Rhizobium leguminosarum, a nitrogen-fixing plant endosymbiont, are strikingly diffe

184 many Rhizobium and Sinorhizobium strains are nitrogen-fixing plant mutualists, while many strains des

185 d, especially in marine bacterioplankton and nitrogen-fixing plant symbionts.

186 Parasponia andersonii is a nitrogen-fixing plant that expresses a symbiotic hemoglo

187 itrogen concentration per unit leaf mass for nitrogen-fixing plants (N2FP; mainly legumes plus some a

188 Symbiotic interactions between nitrogen-fixing prokaryotes and photosynthetic eukaryote

189 Growth of nitrogen-fixing prokaryotes or diazotrophs (Rhizobiales

190 y structure from mostly eukaryotes to mostly nitrogen-fixing prokaryotes.

191 H gene was enriched by a factor of 10 in the nitrogen-fixing reactors (compared to controls) attainin

192 oil bacterium capable of forming a symbiotic nitrogen-fixing relationship with its plant host, Medica

193 ork, we demonstrate the use of the efficient nitrogen-fixing rhizobacterium Pseudomonas protegens Pf-

194 flg22 treatment and the root symbioses with nitrogen-fixing rhizobia and arbuscular mycorrhiza were

195 fix atmospheric nitrogen via symbiosis with nitrogen-fixing rhizobia bacteria, in rotation with nonl

196 esult from interaction between the plant and nitrogen-fixing rhizobia bacteria.

197 Nitrogen-fixing rhizobia colonize legume roots via plant

198 c associations between leguminous plants and nitrogen-fixing rhizobia culminate in the formation of s

199 y enables the plant to exclude non-desirable nitrogen-fixing rhizobia in the root and pathogenic micr

200 In many legumes, root entry of symbiotic nitrogen-fixing rhizobia occurs via host-constructed tub

201 hment of binary symbiotic relationships with nitrogen-fixing rhizobia that trigger root nodule organo

202 ordinated interactions between the plant and nitrogen-fixing rhizobia.

203 have the ability to establish symbiosis with nitrogen-fixing rhizobia.

204 unique physiologies of C. crescentus and the nitrogen-fixing rhizobia.

205 n impaired root development and infection by nitrogen-fixing rhizobia.

206 tic plant cells host and harbor thousands of nitrogen-fixing rhizobia.

207 Genetic studies of legume symbiosis with nitrogen-fixing rhizobial bacteria have traditionally fo

208 Nitrogen-fixing rhizobial bacteria that associate with l

209 es to beneficial microbial partners--namely, nitrogen-fixing rhizobial bacteria that colonize roots o

210 phages that infect agriculturally important nitrogen-fixing rhizobial bacteria.

211 associations with mycorrhizal fungi and with nitrogen-fixing rhizobial bacteria.

212 corrhizal (AM) fungi and between legumes and nitrogen-fixing rhizobial bacteria.

213 Nitrogen-fixing rhizobial bacteroids import dicarboxylat

214 The nitrogen-fixing rhizobial symbiont Sinorhizobium melilot

215 Symbiotic nitrogen-fixing rhizobium bacteria and arbuscular mycorr

216 ommonalities with the evolutionarily younger nitrogen-fixing Rhizobium legume symbiosis (RLS)(8) or b

217 The nitrogen-fixing Rhizobium-legume partnership is presentl

218 Virtually since the discovery of nitrogen-fixing Rhizobium-legume symbioses, researchers

219 nic pseudomonads and in species of symbiotic nitrogen-fixing Rhizobium.

220 Nitrogen-fixing root nodulation in legumes challenged wi

221 umes improve their mineral nutrition through nitrogen-fixing root nodule symbioses with soil rhizobia

222 hizobial infection and nodulation during the nitrogen-fixing root nodule symbiosis in Medicago trunca

223 In contrast, the nitrogen-fixing root nodule symbiosis is almost complete

224 uiring arbuscular mycorrhiza (AM) as well as nitrogen-fixing root nodule symbiosis, but the mechanism

225 side living plant cells is restricted to the nitrogen-fixing root nodule symbiosis.

226 In addition, both promoters were active in nitrogen-fixing root nodules but not in ineffective nodu

227 itiation of symbiosis and the development of nitrogen-fixing root nodules depend on the activation of

228 The establishment of nitrogen-fixing root nodules in legume-rhizobia symbiosi

229 During the course of the development of nitrogen-fixing root nodules induced by Sinorhizobium me

230 The legume-rhizobium symbiosis results in nitrogen-fixing root nodules, and their formation involv

231 a Frankia spp. that lead to the formation of nitrogen-fixing root nodules.

232 GmN70 is expressed predominantly in mature nitrogen-fixing root nodules.

233 zobial bacteria, leading to the formation of nitrogen-fixing root nodules.

234 erential sensitivity of cyanobacterial taxa: nitrogen-fixing Scytonema spp. were the most sensitive,

235 ex symbiotic association between legumes and nitrogen-fixing soil bacteria called rhizobia culminates

236 a small number of phages of plant-symbiotic nitrogen-fixing soil bacteria have been studied at the m

237 ts can enter into root nodule symbioses with nitrogen-fixing soil bacteria known as rhizobia.

238 Legumes engage in root nodule symbioses with nitrogen-fixing soil bacteria known as rhizobia.

239 he symbiotic interaction between legumes and nitrogen-fixing soil bacteria results in a specialized p

240 f symbiotic root nodules in association with nitrogen-fixing soil rhizobia.

241 We found that actinorhizal nitrogen-fixing species are distributed in nine distinct

242 ilamentous cyanobacteria, in particular, the nitrogen-fixing species.

243 ty of certain semiaquatic species to develop nitrogen-fixing stem nodules.

244 Sinorhizobium meliloti, the nitrogen-fixing symbiont of alfalfa, has the ability to

245 The nitrogen-fixing symbiont Sinorhizobium meliloti senses a

246 In addition to a nitrogen-fixing symbiont, the plants harbored an endophy

247 ents that convert nonsymbiotic rhizobia into nitrogen-fixing symbionts of leguminous plants.

248 a to establish themselves within the host as nitrogen-fixing symbionts.

249 pothesis that multiple gains of actinorhizal nitrogen-fixing symbioses in angiosperms may have been a

250 r, the evolutionary patterns of actinorhizal nitrogen-fixing symbioses remain unclear to date.

251 arum is a Gram-negative bacterium that forms nitrogen-fixing symbioses with compatible leguminous pla

252 To form nitrogen-fixing symbioses, legume plants recognize a bac

253 In legume nitrogen-fixing symbioses, rhizobial nod genes are oblig

254 nogenesis and bacterial infection during the nitrogen fixing symbiosis established between common bea

255 on is an excellent model for dissecting this nitrogen-fixing symbiosis because of the availability of

256 The nitrogen-fixing symbiosis between legumes and rhizobia i

257 The nitrogen-fixing symbiosis between rhizobia and legume pl

258 pathway is required for the development of a nitrogen-fixing symbiosis between S. meliloti and its pl

259 The nitrogen-fixing symbiosis between Sinorhizobium meliloti

260 The establishment of an effective nitrogen-fixing symbiosis between Sinorhizobium meliloti

261 The establishment of the nitrogen-fixing symbiosis between soybean and Bradyrhizo

262 a transport protein needed for a successful nitrogen-fixing symbiosis between the bacteria and alfal

263 We found that the loss of nitrogen-fixing symbiosis dramatically alters community

264 l regulation of mRNAs at early stages of the nitrogen-fixing symbiosis established between Medicago t

265 mes suggests that the evolutionarily younger nitrogen-fixing symbiosis has recruited functions from t

266 agricultural importance, the legume-rhizobia nitrogen-fixing symbiosis is a powerful model for identi

267 ro-RNAs as regulators of the legume-rhizobia nitrogen-fixing symbiosis is emerging.

268 Establishment of nitrogen-fixing symbiosis requires the recognition of rh

269 , must have been coopted during evolution of nitrogen-fixing symbiosis to specifically mediate bacter

270 fair') bargaining power in a legume-rhizobia nitrogen-fixing symbiosis using measurements of carbon a

271 ve soil bacterium, capable of establishing a nitrogen-fixing symbiosis with its legume host, alfalfa

272 ChvI two-component signalling to establish a nitrogen-fixing symbiosis with legume hosts.

273 Sinorhizobium meliloti participates in a nitrogen-fixing symbiosis with legume plant host species

274 olysaccharides in order to form a successful nitrogen-fixing symbiosis with Medicago species.

275 ive as a soil saprophyte and can engage in a nitrogen-fixing symbiosis with plant roots.

276 e alpha-proteobacterium that can establish a nitrogen-fixing symbiosis within the roots of pea plants

277 In the legume-rhizobium nitrogen-fixing symbiosis, thousands of rhizobium micros

278 ways for the successful establishment of the nitrogen-fixing symbiosis.

279 o bacteroids and plays a crucial role in the nitrogen-fixing symbiosis.

280 f the root that combined are necessary for a nitrogen-fixing symbiosis.

281 called rhizobia have coevolved a facultative nitrogen-fixing symbiosis.

282 t nodules on Medicago sativa and establish a nitrogen-fixing symbiosis.

283 by rhizobia, soil bacteria that establish a nitrogen-fixing symbiosis.

284 Previously, the nitrogen-fixing symbiotic (rhizo)bacterium Bradyrhizobiu

285 n of soybean (Glycine max) root hairs by the nitrogen-fixing symbiotic bacterium Bradyrhizobium japon

286 to respond strongly to inoculation with the nitrogen-fixing symbiotic bacterium Bradyrhizobium japon

287 e Medicago truncatula model to regulate root nitrogen-fixing symbiotic nodulation.

288 The mechanisms of the few known molecular nitrogen-fixing systems, including nitrogenase enzymes,

289 rate is comparable to recent "breakthrough" nitrogen-fixing technologies and far higher than observe

290 ost benefits another aggressive invader, the nitrogen-fixing tree Morella faya.

291 The nitrogen-fixing tree Myrica faya doubled canopy nitrogen

292 A fifth invasive nitrogen-fixing tree, in combination with a midcanopy al

293 come can be restored by diversification with nitrogen-fixing trees and the cultivation of indigenous

294 Symbiotic nitrogen-fixing trees are thought to provide much of the

295 Nitrogen-fixing trees can supply vital quantities of the

296 theoretical model to suggest that symbiotic nitrogen-fixing trees could either mitigate (CO(2) seque

297 The model posits that nitrogen-fixing trees could exacerbate climate change gl

298 We estimate that including nitrogen-fixing trees in Neotropical reforestation proje

299 switching from commensal exploitation of the nitrogen-fixing Trichormus variabilis, for survival in n

300 a key determinant of belowground effects, as Nitrogen-fixing woody plants had higher soil fungal rich