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

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