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1 t of the symbiotic nitrogen fixing bacterium Sinorhizobium meliloti.
2 nodulation (nod) genes in the soil bacterium Sinorhizobium meliloti.
3 o the sigma(54)-polymerase activator DctD of Sinorhizobium meliloti.
4 rsenic detoxification in the legume symbiont Sinorhizobium meliloti.
5 e symbiosis between alfalfa and its symbiont Sinorhizobium meliloti.
6 genome are similar to those of the symbiotic Sinorhizobium meliloti.
7 go truncatula plants grown in symbiosis with Sinorhizobium meliloti.
8  inducible within 3 h after inoculation with Sinorhizobium meliloti.
9 d factor from the alfalfa-nodulating strain, Sinorhizobium meliloti.
10 cteria, Propionibacterium freudenreichii and Sinorhizobium meliloti.
11 2308 by complementation of an exoB mutant of Sinorhizobium meliloti.
12 many strains of the nitrogen-fixing symbiont Sinorhizobium meliloti.
13 catula during the symbiotic interaction with Sinorhizobium meliloti.
14 eparate downstream responses to its symbiont Sinorhizobium meliloti.
15 ing of TraR in the closely related bacterium Sinorhizobium meliloti.
16 ut using the model root nodulating bacterium Sinorhizobium meliloti.
17 e-dimensional architecture of the biofilm of Sinorhizobium meliloti.
18 c interaction with the diazotropic bacterium Sinorhizobium meliloti.
19 l to form nodules following inoculation with Sinorhizobium meliloti.
20 ccinoglycan by the nitrogen-fixing bacterium Sinorhizobium meliloti 1021 is needed for an effective s
21  of 2-aminoethylphosphonate in the bacterium Sinorhizobium meliloti 1021 is proposed based on the ana
22 m (T4SS) of the plant intracellular symbiont Sinorhizobium meliloti 1021 is required for conjugal tra
23       The nitrogen-fixing rhizobial symbiont Sinorhizobium meliloti 1021 produces acidic symbiotic ex
24 r by tri-parental mating of these genes into Sinorhizobium meliloti 1021, a strain that lacks these p
25                      The gltA gene, encoding Sinorhizobium meliloti 104A14 citrate synthase, was isol
26 e of cyclic diguanylate (c-di-GMP) levels in Sinorhizobium meliloti 8530, a bacterium that does not c
27                                              Sinorhizobium meliloti, a gram-negative soil bacterium,
28                                              Sinorhizobium meliloti, a legume symbiont and Brucella a
29                                              Sinorhizobium meliloti, a legume symbiont, and Brucella
30 rovides protection against diverse phages in Sinorhizobium meliloti, a nitrogen-fixing alpha-proteoba
31                                           In Sinorhizobium meliloti (also known as Rhizobium meliloti
32                                          For Sinorhizobium meliloti (also known as Rhizobium meliloti
33 charide (LPS) plays in the symbiosis between Sinorhizobium meliloti and alfalfa has been studied for
34 e indeterminate symbiosis that forms between Sinorhizobium meliloti and alfalfa requires biosynthesis
35                     In the symbiosis between Sinorhizobium meliloti and alfalfa, mutations in GlnD, t
36  root systems that have been inoculated with Sinorhizobium meliloti and are developing root nodules.
37 n is essential for the long-term survival of Sinorhizobium meliloti and Brucella abortus within acidi
38             Two related alphaproteobacteria, Sinorhizobium meliloti and Caulobacter crescentus, serve
39 is presented here that two of these species, Sinorhizobium meliloti and Caulobacter crescentus, simpl
40                                 Membranes of Sinorhizobium meliloti and E. coli lack this activity.
41 proteobacteria Agrobacterium tumefaciens and Sinorhizobium meliloti and found that they are located a
42                                              Sinorhizobium meliloti and host legumes enter into a nit
43 and functional analyses of the SOE SorT from Sinorhizobium meliloti and its cognate electron acceptor
44  A successful symbiotic relationship between Sinorhizobium meliloti and its host Medicago sativa (alf
45  effective nitrogen-fixing symbiosis between Sinorhizobium meliloti and its legume host alfalfa (Medi
46        The nitrogen-fixing symbiosis between Sinorhizobium meliloti and its leguminous host plant Med
47 ages of symbiosis between the soil bacterium Sinorhizobium meliloti and its leguminous host plant, al
48        The nitrogen-fixing symbiosis between Sinorhizobium meliloti and Medicago sativa requires comp
49                                    Using the Sinorhizobium meliloti and Medicago truncatula symbiotic
50 LC) legumes, such as the interaction between Sinorhizobium meliloti and Medicago, bacteroid different
51  of 2 representative proteins, SMc02148 from Sinorhizobium meliloti and PA3455 from Pseudomonas aerug
52  There exist commonalities between symbiotic Sinorhizobium meliloti and pathogenic Brucella bacteria
53 h their counterparts in the che operons from Sinorhizobium meliloti and Rhodobacter sphaeroides, and
54                                              Sinorhizobium meliloti and Sinorhizobium medicae are two
55 ent chromosomes that have been classified as Sinorhizobium meliloti and Sinorhizobium medicae.
56 a, Vibrio cholerae, Shewanella putrefaciens, Sinorhizobium meliloti, and Caulobacter crescentus.
57 h of Medicago truncatula, its symbiosis with Sinorhizobium meliloti, and on soil microbial community
58 olonization by the nitrogen-fixing bacterium Sinorhizobium meliloti appeared to be normal in the npd1
59 mus intraradices and the rhizobial bacterium Sinorhizobium meliloti as well as with the pathogenic oo
60 em uses the closely related model bacterium, Sinorhizobium meliloti, as a heterologous host for expre
61 f the recent extension of the TspO system to Sinorhizobium meliloti, as described by Davey and de Bru
62 e were able to successfully predict sRNAs in Sinorhizobium meliloti, as well as in multiple and poorl
63                      The Medicago truncatula-Sinorhizobium meliloti association is an excellent model
64 iments involved three different diazotrophs (Sinorhizobium meliloti, Azotobacter vinelandii, and Rahn
65                                              Sinorhizobium meliloti bacA mutants are symbiotically de
66                                              Sinorhizobium meliloti bacteria produce a signal molecul
67  also occurs in the closely related bacteria Sinorhizobium meliloti, Brucella abortus, and Ochrobactr
68 Rhizobium leguminosarum, Rhizobium etli, and Sinorhizobium meliloti but not Escherichia coli.
69                           The AAA+ domain of Sinorhizobium meliloti C4-dicarboxylic acid transport pr
70                                              Sinorhizobium meliloti can live as a soil saprophyte and
71                                              Sinorhizobium meliloti can live as symbionts inside legu
72                            The Nod factor of Sinorhizobium meliloti carries O-sulphate, O-acetate and
73                                           In Sinorhizobium meliloti, catabolite repression is influen
74                                              Sinorhizobium meliloti cells store excess carbon as intr
75 but similar to that measured for the related Sinorhizobium meliloti CheA.
76 tion of the one HK-two RR motif found in the Sinorhizobium meliloti chemotaxis pathway and measuring
77 e constructed a strain of the soil bacterium Sinorhizobium meliloti containing a gfp gene fused to th
78 The symbiotic nitrogen-fixing soil bacterium Sinorhizobium meliloti contains three replicons: pSymA,
79 FixL/FixJ two-component regulatory system of Sinorhizobium meliloti controls the expression of nitrog
80                       In Rhizobium meliloti (Sinorhizobium meliloti) cultures, the endo-1, 3-1,4-beta
81                                           In Sinorhizobium meliloti, CuxR stimulates transcription of
82                                              Sinorhizobium meliloti dctA encodes a transport protein
83    In contrast to R. leguminosarum dctA, the Sinorhizobium meliloti dctA promoter region was found to
84  for the Mg2+-BeF3--bound receiver domain of Sinorhizobium meliloti DctD bearing amino acid substitut
85                                              Sinorhizobium meliloti DctD is an activator of sigma(54)
86 orms of the two-component receiver domain of Sinorhizobium meliloti DctD, a sigma(54)-dependent AAA+
87  this view by showing that, in the bacterium Sinorhizobium meliloti, deletion of the ribBA gene encod
88 sertion in a gene with similarity to exsH of Sinorhizobium meliloti did not nodulate the plant host P
89  the sigma(54)-dependent activator DctD from Sinorhizobium meliloti, displayed an altered DNase I foo
90 Rhizobium leguminosarum and the lpsB gene of Sinorhizobium meliloti encode protein orthologs that are
91      The soil-dwelling alpha-proteobacterium Sinorhizobium meliloti engages in a symbiosis with legum
92                                              Sinorhizobium meliloti enters into a symbiotic relations
93                    The alpha-proteobacterium Sinorhizobium meliloti establishes a chronic intracellul
94 er UV light, colonies of Rhizobium meliloti (Sinorhizobium meliloti) exoK mutants produce a fluoresce
95                        The production of the Sinorhizobium meliloti exopolysaccharide, succinoglycan,
96                                              Sinorhizobium meliloti ExoR regulates the production of
97                                          The Sinorhizobium meliloti ExoS/ChvI two-component signaling
98  in M. truncatula plants inoculated with the Sinorhizobium meliloti exoY mutant, and the M. truncatul
99 re we show that in the alpha-proteobacterium Sinorhizobium meliloti expression of the autoinducer syn
100     The symbiotic, nitrogen-fixing bacterium Sinorhizobium meliloti favors succinate and related dica
101                When tested for nodulation by Sinorhizobium meliloti, flavonoid-deficient roots had a
102 e sink" among the alpha-proteobacteria (e.g. Sinorhizobium meliloti), for dephosphorylating CheY-P.
103                                              Sinorhizobium meliloti forms symbiotic, nitrogen-fixing
104               Recently, we discovered that a Sinorhizobium meliloti gene, bluB, is necessary for DMB
105 sucrose uptake and hydrolysis, we screened a Sinorhizobium meliloti genomic library and discovered a
106 ion of nitric oxide in roots inoculated with Sinorhizobium meliloti greatly increased our understandi
107                                              Sinorhizobium meliloti growth inside infection threads w
108      The symbiotic nitrogen-fixing bacterium Sinorhizobium meliloti harbors a gene, SMc02396, which e
109 d RaxQ are similar to the bacterial symbiont Sinorhizobium meliloti host specificity proteins, NodP a
110 equence similarity with protein sequences of Sinorhizobium meliloti IdhA and MocA; Bacillus subtilis
111 hizobiales (e.g., Agrobacterium tumefaciens, Sinorhizobium meliloti), impairing PG crosslinkage and c
112  (nod) gene expression in the soil bacterium Sinorhizobium meliloti in response to the plant-secreted
113 nd cryo-electron microscopy structure of the Sinorhizobium meliloti-infecting T4 superfamily phage Ph
114 ent of plant flotillin-like genes (FLOTs) in Sinorhizobium meliloti infection of its host legume Medi
115 fection and cortical cell division following Sinorhizobium meliloti inoculation.
116 ediate the differentiation of the bacterium, Sinorhizobium meliloti into a nitrogen-fixing bacteroid
117  development of the symbiotic soil bacterium Sinorhizobium meliloti into nitrogen-fixing bacteroids,
118 l signal referred to as Nod factor, which in Sinorhizobium meliloti is a beta-(1,4)-linked tetramer o
119                                              Sinorhizobium meliloti is a free-living soil bacterium w
120                                              Sinorhizobium meliloti is a gram-negative soil bacterium
121                                              Sinorhizobium meliloti is a gram-negative soil bacterium
122                                              Sinorhizobium meliloti is a gram-negative soil bacterium
123                                              Sinorhizobium meliloti is a gram-negative soil bacterium
124                                              Sinorhizobium meliloti is a member of the Alphaproteobac
125                                              Sinorhizobium meliloti is a nitrogen-fixing bacterial sy
126                                              Sinorhizobium meliloti is a soil bacterium capable of in
127                                              Sinorhizobium meliloti is a soil bacterium that establis
128                                              Sinorhizobium meliloti is a soil bacterium which can est
129                                The bacterium Sinorhizobium meliloti is attracted to seed exudates of
130                           The soil bacterium Sinorhizobium meliloti is capable of entering into a nit
131                       We show that GroEL1 of Sinorhizobium meliloti is required for efficient infecti
132 (EPSs) by the nitrogen-fixing soil bacterium Sinorhizobium meliloti is required for efficient invasio
133              Exopolysaccharide production by Sinorhizobium meliloti is required for invasion of root
134 the gene coding for acetate kinase (ackA) in Sinorhizobium meliloti is up-regulated in response to ph
135 aying a central role during key steps of the Sinorhizobium meliloti-M. truncatula symbiotic interacti
136                         We show that, in the Sinorhizobium meliloti-Medicago truncatula interaction,
137                                          The Sinorhizobium meliloti megaplasmid pSymA has previously
138 gy with other dioxygenases and hydrolases in Sinorhizobium meliloti, Mesorhizobium loti, and Bradyrhi
139 mbiosis with the host plant Medicago sativa, Sinorhizobium meliloti must overcome an oxidative burst
140 oying a novel two-part screen, we identified Sinorhizobium meliloti mutants that were both sensitive
141 nt, heparin-stable complexes on heteroduplex Sinorhizobium meliloti nifH DNA mismatched next to the G
142 duction system ensures that a cascade of the Sinorhizobium meliloti nitrogen fixation genes is induce
143  is the key step in the hypoxic induction of Sinorhizobium meliloti nitrogen fixation genes.
144               We tested the ability of three Sinorhizobium meliloti nod gene products to modify Nod f
145 s involved in the synthesis of an inducer of Sinorhizobium meliloti nod genes, as well as a gene asso
146 prisingly, even sulfated fungal Myc-LCOs and Sinorhizobium meliloti Nod-LCOs, having very similar str
147                                              Sinorhizobium meliloti nodL and nodF mutations additivel
148                                              Sinorhizobium meliloti NRG247 has a Fix(+) phenotype on
149 ur analyses of lipopolysaccharide mutants of Sinorhizobium meliloti offer insights into how this bact
150 t of nitrogen-fixing root nodules induced by Sinorhizobium meliloti on the model plant Medicago trunc
151 eport here the first characterization of the Sinorhizobium meliloti open reading frame SMc01113.
152  R. leguminosarum and Rhizobium etli but not Sinorhizobium meliloti or E. coli.
153 y expressed in plants exposed for 24 h to WT Sinorhizobium meliloti or to the invasion defective S. m
154  established between Medicago truncatula and Sinorhizobium meliloti Our analysis revealed a poor corr
155                                              Sinorhizobium meliloti participates in a nitrogen-fixing
156                                        After Sinorhizobium meliloti penetrate the root nodules that t
157                          While screening for Sinorhizobium meliloti Pho regulatory mutants, a transpo
158 g system of the gram-negative soil bacterium Sinorhizobium meliloti plays an important role in the es
159                                              Sinorhizobium meliloti produces an exopolysaccharide cal
160 eed, eliminating SMc01113/YbeY expression in Sinorhizobium meliloti produces symbiotic and physiologi
161                   The symbiotic lifestyle of Sinorhizobium meliloti requires a drastic cellular diffe
162                                              Sinorhizobium meliloti requires exopolysaccharides in or
163                                              Sinorhizobium meliloti requires ExoS/ChvI two-component
164  interaction between Medicago truncatula and Sinorhizobium meliloti results in the formation of nitro
165 c capsular polysaccharide produced by strain Sinorhizobium meliloti Rm1021 contributes to symbiosis w
166                                          The Sinorhizobium meliloti Rm1021 Delta glnD-sm2 mutant, whi
167 homologous regions of A. tumefaciens C58 and Sinorhizobium meliloti Rm1021 genomes.
168           The production of succinoglycan by Sinorhizobium meliloti Rm1021 is required for successful
169 ows the greatest identity to SinI (71%) from Sinorhizobium meliloti Rm1021.
170                            As populations of Sinorhizobium meliloti Rm2011 were similar in bulk/disso
171 level incompatibility with the microsymbiont Sinorhizobium meliloti Rm41.
172                 The nitrogen-fixing symbiont Sinorhizobium meliloti senses and responds to constantly
173              Here we report evidence that in Sinorhizobium meliloti, sensing of AHLs with acyl chains
174 include: the nitrogen-fixing plant symbionts Sinorhizobium meliloti (SINME) and Mesorhizobium loti (M
175                   Proline utilization A from Sinorhizobium meliloti (SmPutA) is a 1233-residue bifunc
176 ventional X-ray crystallography of PutA from Sinorhizobium meliloti (SmPutA) were used to capture hig
177                                           In Sinorhizobium meliloti, specific NF modifications (nodL-
178                                              Sinorhizobium meliloti stores carbon and energy in poly-
179  bacterial symbiont of one of these species (Sinorhizobium meliloti strain Rm1021) and an opportunist
180                                              Sinorhizobium meliloti strains lacking BacA function are
181 n Network Analysis (WGCNA) for a panel of 20 Sinorhizobium meliloti strains that vary in symbiotic pa
182 mes of A. tumefaciens and the plant symbiont Sinorhizobium meliloti suggest a recent evolutionary div
183 g in the morphologically symmetric bacterium Sinorhizobium meliloti suggests that this type of cell c
184 cterial status in mutant nodules, we assayed Sinorhizobium meliloti symbiosis gene promoters (nodF, e
185                   In the Medicago truncatula-Sinorhizobium meliloti symbiosis, chemical signaling ini
186          However, in the Medicago truncatula-Sinorhizobium meliloti symbiosis, incompatibility betwee
187                   In the Medicago truncatula/Sinorhizobium meliloti symbiosis, the plant undergoes a
188 fixing nodules (Fix+) in Medicago truncatula-Sinorhizobium meliloti symbiosis.
189 cs in nodules, using the Medicago truncatula-Sinorhizobium meliloti symbiotic system.
190 scale metabolic model of the legume symbiont Sinorhizobium meliloti that is integrated with carbon ut
191 quenced three genes from Rhizobium meliloti (Sinorhizobium meliloti) that are involved in sulfate act
192 hm to a symbiotic nitrogen-fixing bacterium, Sinorhizobium meliloti The LDSS-P profiles that overlap
193  focused on the study of trehalose uptake by Sinorhizobium meliloti, the demonstrated approach is app
194 e and dynamics of Sma0114 from the bacterium Sinorhizobium meliloti, the first such characterization
195                          First discovered in Sinorhizobium meliloti, the main response regulator CheY
196                          Here we identify in Sinorhizobium meliloti, the Medicago symbiont, a cAMP-si
197                       Quorum sensing (QS) in Sinorhizobium meliloti, the N-fixing bacterial symbiont
198  in the presence of the compatible bacterium Sinorhizobium meliloti, the nip mutant showed nitrogen d
199                                              Sinorhizobium meliloti, the nitrogen-fixing symbiont of
200                        In the plant symbiont Sinorhizobium meliloti, the ortholog of VtlR, named LsrB
201 to the Rhizobiales order: the plant symbiont Sinorhizobium meliloti, the plant pathogen Agrobacterium
202                                           In Sinorhizobium meliloti, the production of exopolysacchar
203                            In particular, in Sinorhizobium meliloti there are four groESL operons and
204                                           In Sinorhizobium meliloti there are two rpoH genes, four gr
205                         This peptide affects Sinorhizobium meliloti transcription, translation, and c
206 y, we showed that a FadD-deficient mutant of Sinorhizobium meliloti, unable to convert free fatty aci
207 he nitro -fixing symbiosis with host plants, Sinorhizobium meliloti undergoes a profound cellular dif
208 n factors produced by the bacterial symbiont Sinorhizobium meliloti using a dual-dye ratiometric imag
209                     When they are available, Sinorhizobium meliloti utilizes C(4)-dicarboxylic acids
210 at catalyzes the synthesis of PC, and Pcs in Sinorhizobium meliloti was characterized.
211                The CbcX orthologue ChoX from Sinorhizobium meliloti was similar to CbcX in these bind
212 thogenic E. coli O127:H6, Achromobacter, and Sinorhizobium meliloti, where the outer domains dimerize
213 dicago truncatula and its rhizobial symbiont Sinorhizobium meliloti, which includes more than 23,000
214  The dicarboxylate transport (Dct) system of Sinorhizobium meliloti, which is essential for a functio
215 biosis between Medicago truncatula roots and Sinorhizobium meliloti would identify regulated plant ge
216  contrast to a previous report, we show that Sinorhizobium meliloti YbeY exhibits endoribonuclease ac

 
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