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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
22 r by tri-parental mating of these genes into Sinorhizobium meliloti 1021, a strain that lacks these p
24 e of cyclic diguanylate (c-di-GMP) levels in Sinorhizobium meliloti 8530, a bacterium that does not c
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
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
36 is presented here that two of these species, Sinorhizobium meliloti and Caulobacter crescentus, simpl
38 proteobacteria Agrobacterium tumefaciens and Sinorhizobium meliloti and found that they are located a
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
44 ages of symbiosis between the soil bacterium Sinorhizobium meliloti and its leguminous host plant, al
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
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
60 also occurs in the closely related bacteria Sinorhizobium meliloti, Brucella abortus, and Ochrobactr
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
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
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
86 er UV light, colonies of Rhizobium meliloti (Sinorhizobium meliloti) exoK mutants produce a fluoresce
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
93 e sink" among the alpha-proteobacteria (e.g. Sinorhizobium meliloti), for dephosphorylating CheY-P.
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
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
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
121 (EPSs) by the nitrogen-fixing soil bacterium Sinorhizobium meliloti is required for efficient invasio
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
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
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
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.
142 y expressed in plants exposed for 24 h to WT Sinorhizobium meliloti or to the invasion defective S. m
145 g system of the gram-negative soil bacterium Sinorhizobium meliloti plays an important role in the es
147 eed, eliminating SMc01113/YbeY expression in Sinorhizobium meliloti produces symbiotic and physiologi
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
161 include: the nitrogen-fixing plant symbionts Sinorhizobium meliloti (SINME) and Mesorhizobium loti (M
164 bacterial symbiont of one of these species (Sinorhizobium meliloti strain Rm1021) and an opportunist
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
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
180 in the presence of the compatible bacterium Sinorhizobium meliloti, the nip mutant showed nitrogen d
182 to the Rhizobiales order: the plant symbiont Sinorhizobium meliloti, the plant pathogen Agrobacterium
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
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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