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1 elonged to Rubrivivax, Magnetospirillum, and Bradyrhizobium.
2 soil bacteria, belonging mainly to the genus Bradyrhizobium.
3 erall NAFLD patients had increased levels of Bradyrhizobium, Anaerococcus, Peptoniphilus, Propionibac
4                          Furthermore, genera Bradyrhizobium and Agromyces were significantly enriched
5 locus and closely linked nodulation genes of Bradyrhizobium (Arachis) sp. strain NC92 have been isola
6 stent with a model of nod gene expression in Bradyrhizobium (Arachis) sp. strain NC92 in which negati
7     TITAN suggested that Nitrosocosmicus and Bradyrhizobium, as the major nitrifier and denitrifier,
8 equences for isolates similar to Acidovorax, Bradyrhizobium, Brevibacillus, Caulobacter, Chryseobacte
9 s, 12 genera-Pseudomonas, Propionibacterium, Bradyrhizobium, Corynebacterium, Acinetobacter, Brevundi
10 e biochemical characterization of AAD-2 from Bradyrhizobium diazoefficiens USDA 110 as a catalyst to
11  symbiosis of Vigna radiata (mung bean) with Bradyrhizobium diazoefficiens USDA110 is determined by N
12                                              Bradyrhizobium diazoefficiens USDA110 is one of the most
13 ycine max) with its associated microsymbiont Bradyrhizobium diazoefficiens was developed and applied
14 that restricts nodulation by many strains of Bradyrhizobium elkanii.
15 d nolA genes of Bradyrhizobium japonicum and Bradyrhizobium elkanii.
16 discovered bacterium was provisionally named Bradyrhizobium enterica.
17 ss and prevent the extinction of ineffective Bradyrhizobium from natural populations.
18 ion between the fitness benefits provided by Bradyrhizobium genotypes and their local genotype freque
19                                 We uncovered Bradyrhizobium genotypes that provide negligible mutuali
20  of homology with genomes of bacteria in the bradyrhizobium genus.
21                             Some isolates of Bradyrhizobium have been shown to be non-symbiotic and d
22                       The slow-growing genus Bradyrhizobium is biologically important in soils, with
23                                        These Bradyrhizobium isolates are the first to be isolated and
24  Peanut plant root metabolites interact with Bradyrhizobium isolates contributing to initiate nodulat
25  European soil and are the first free-living Bradyrhizobium isolates, lacking both nodulation and nit
26 and gene annotations of two such free-living Bradyrhizobium isolates, named G22 and BF49, from soils
27 l isolates, and root nodulation by symbiotic Bradyrhizobium isolates.
28 study, we show that the affinity of Fur from Bradyrhizobium japonicum (BjFur) for its target DNA incr
29 A enzymes by examining the PutA protein from Bradyrhizobium japonicum (BjPutA).
30                                              Bradyrhizobium japonicum ALAD* is an engineered derivati
31  nodA, nodB, nodD1, nodD2, and nolA genes of Bradyrhizobium japonicum and Bradyrhizobium elkanii.
32 restrict nodulation with specific strains of Bradyrhizobium japonicum and Sinorhizobium fredii, respe
33                      The nodulation genes of Bradyrhizobium japonicum are essential for infection and
34 utative ferric siderophore receptor genes in Bradyrhizobium japonicum are positively controlled by th
35 entified mnoP in the Gram-negative bacterium Bradyrhizobium japonicum as a gene coregulated with the
36                                              Bradyrhizobium japonicum can use heme as an iron source,
37         Here, we show that aerobically grown Bradyrhizobium japonicum cells express a single catalase
38 ition of chitin and lipo-chitin oligomers to Bradyrhizobium japonicum cultures resulted in a signific
39                            Here we show that Bradyrhizobium japonicum cytochrome c550 polypeptide acc
40 Consistent with this, immunoblot analyses of Bradyrhizobium japonicum extracts with a polyclonal anti
41 ns, we replaced this residue with alanine in Bradyrhizobium japonicum FixL and examined the results o
42 ssessed the contributions of this residue in Bradyrhizobium japonicum FixL by determining the effects
43             Recent structural studies of the Bradyrhizobium japonicum FixL heme domain (BjFixLH) have
44                            Structures of the Bradyrhizobium japonicum FixL heme domain have been dete
45 arison of the structures of two forms of the Bradyrhizobium japonicum FixL heme domain, one in the "o
46                          Several recombinant Bradyrhizobium japonicum FixL heme domains (BjFixLH) hav
47                                              Bradyrhizobium japonicum FixL is a modular oxygen sensor
48 rebinding to two forms of the heme domain of Bradyrhizobium japonicum FixL.
49                          Here, we identified Bradyrhizobium japonicum frcB (bll3557) as a gene adjace
50                                              Bradyrhizobium japonicum Fur mediates manganese-responsi
51 y diverse enolase superfamily encoded by the Bradyrhizobium japonicum genome (bll6730; GI:27381841).
52               In this study, we identified a Bradyrhizobium japonicum genomic library clone that comp
53                       Microarray analysis of Bradyrhizobium japonicum grown under copper limitation u
54 of hydrogenase structural gene expression in Bradyrhizobium japonicum have been investigated.
55 he Brucella BhuQ protein is a homolog of the Bradyrhizobium japonicum heme oxygenases HmuD and HmuQ.
56 nodulation signal (nod signal) purified from Bradyrhizobium japonicum induced nodule primordia on soy
57 t changes in their expression in response to Bradyrhizobium japonicum infection and in representative
58     Utilization of heme as an iron source by Bradyrhizobium japonicum involves induction of the outer
59                                              Bradyrhizobium japonicum Irr is a conditionally stable t
60 s by the nitrogen-fixing symbiotic bacterium Bradyrhizobium japonicum is a complex process coordinate
61 itrogen-fixing symbiosis between soybean and Bradyrhizobium japonicum is a complex process.
62 e iron response regulator (Irr) protein from Bradyrhizobium japonicum is a conditionally stable prote
63                          The FixL protein of Bradyrhizobium japonicum is a dimeric oxygen sensor resp
64                                              Bradyrhizobium japonicum is a facultative chemoautotroph
65                        The HypB protein from Bradyrhizobium japonicum is a metal-binding GTPase requi
66                                              Bradyrhizobium japonicum is a nitrogen-fixing bacterium
67                                    FixL from Bradyrhizobium japonicum is a PAS sensor protein in whic
68                                              Bradyrhizobium japonicum is a symbiotic bacterium that n
69 >3),beta-(1-->6)-D-glucan synthesis locus of Bradyrhizobium japonicum is composed of at least two gen
70           The Irr protein from the bacterium Bradyrhizobium japonicum is expressed under iron limitat
71                            The irr gene from Bradyrhizobium japonicum is under the control of Fur.
72 nfection of soybean roots by nitrogen-fixing Bradyrhizobium japonicum leads to expression of plant no
73                           Here, we show that Bradyrhizobium japonicum MbfA (Blr7895) is an inner memb
74                                              Bradyrhizobium japonicum Mur and Escherichia coli Fur ar
75                                            A Bradyrhizobium japonicum mutant defective in the gene en
76                                            A Bradyrhizobium japonicum mutant defective in the high-af
77                                              Bradyrhizobium japonicum nod gene expression was previou
78 the effect of the inoculation of G. max with Bradyrhizobium japonicum on the metabolite profile and a
79 ivum) seed lectin (PSL) were inoculated with Bradyrhizobium japonicum or Rhizobium leguminosarum bv v
80 reas human, pea, Pseudomonas aeruginosa, and Bradyrhizobium japonicum PBGS are insensitive to inhibit
81                                              Bradyrhizobium japonicum porphobilinogen synthase (B. ja
82                                              Bradyrhizobium japonicum possessed lipid A species with
83 tagenesis was used to study the roles of two Bradyrhizobium japonicum proteins, HoxX and HoxA, in hyd
84 tion of the iron response regulator (Irr) in Bradyrhizobium japonicum raised the question of whether
85                                The PBGS from Bradyrhizobium japonicum requires Mg(II) in catalytic me
86 l SWEET homologs with only 3-TM and that the Bradyrhizobium japonicum SemiSWEET1, like Arabidopsis SW
87                         The Irr protein from Bradyrhizobium japonicum senses iron through the status
88  L. cv Merr.) seeds inoculated with a mutant Bradyrhizobium japonicum strain unable to catabolize Pro
89                                   However, a Bradyrhizobium japonicum sucA mutant that is missing alp
90                                              Bradyrhizobium japonicum synthesizes periplasmic cyclic
91 We isolated a mutant strain of the bacterium Bradyrhizobium japonicum that, under iron limitation, ac
92 mprehensive understanding of the response of Bradyrhizobium japonicum to drought.
93                                          The Bradyrhizobium japonicum transcriptional regulator Irr (
94                                              Bradyrhizobium japonicum transports oligopeptides and th
95 o guanine deaminases from disparate sources (Bradyrhizobium japonicum USDA 110 and Homo sapiens) that
96                                The bacterium Bradyrhizobium japonicum USDA110 does not synthesize sid
97 e report that BjaI from the soybean symbiont Bradyrhizobium japonicum USDA110 is closely related to R
98                           A mutant strain of Bradyrhizobium japonicum USDA110 lacking isocitrate dehy
99 ketoglutarate dehydrogenase, was cloned from Bradyrhizobium japonicum USDA110, and its nucleotide seq
100 hitin oligosaccharide Nod signal produced by Bradyrhizobium japonicum was also shown to be a competit
101 e nitrogen-fixing symbiotic (rhizo)bacterium Bradyrhizobium japonicum was found to carry adjacent gen
102  and directly downstream of the hypB gene of Bradyrhizobium japonicum was shown by mutational analysi
103 ere, we show that cytochrome c1 protein from Bradyrhizobium japonicum was strongly affected by the ir
104 oil bacteria (e.g. soybean [Glycine max] and Bradyrhizobium japonicum) initiated by the infection of
105 s (e.g. soybean) and rhizobia bacteria (e.g. Bradyrhizobium japonicum) results in root nodules where
106                                              Bradyrhizobium japonicum, a diazotropic symbiont of soyb
107                                              Bradyrhizobium japonicum, a symbiotic nitrogen-fixing ba
108  A resolution crystal structure of PutA from Bradyrhizobium japonicum, along with data from small-ang
109 is a global regulator of iron homeostasis in Bradyrhizobium japonicum, and a subset of genes within t
110      Here, we identify the mntH homologue of Bradyrhizobium japonicum, and demonstrate that it is ess
111 and microaerobic metabolism in the bacterium Bradyrhizobium japonicum, and evidence suggests that hem
112 bacteria Thermosynechococcus elongatus BP-1, Bradyrhizobium japonicum, and Zymomonas mobilis and clon
113                             In the bacterium Bradyrhizobium japonicum, expression of the gene encodin
114                                           In Bradyrhizobium japonicum, members of two global regulato
115 of an active cyt cbb3 oxidase, and unlike in Bradyrhizobium japonicum, no active CcoN-CcoO subcomplex
116 icroM to 2.4 mM for human, Escherichia coli, Bradyrhizobium japonicum, Pseudomonas aeruginosa, and pe
117 responsive degradation of its counterpart in Bradyrhizobium japonicum, readily detectable levels of I
118 nt of a physical framework for the genome of Bradyrhizobium japonicum, the nitrogen-fixing symbiont o
119 l structure of ent-kaur-16-ene synthase from Bradyrhizobium japonicum, together with the results of a
120 soybean and its nitrogen-fixing endosymbiont Bradyrhizobium japonicum, we wanted to assess the role o
121         Expression of PutA(Ec) and PutA from Bradyrhizobium japonicum, which exhibit low oxygen react
122 c L. corniculatus plant roots in response to Bradyrhizobium japonicum, which nodulates soybean and no
123 soybean and its nitrogen-fixing endosymbiont Bradyrhizobium japonicum, yet little is known about rhiz
124 iotic root nodules elicited by the bacterium Bradyrhizobium japonicum.
125 in the N(2)-fixing, H(2)-oxidizing bacterium Bradyrhizobium japonicum.
126 genase, was cloned from the soybean symbiont Bradyrhizobium japonicum.
127 ing life styles of the alpha-proteobacterium Bradyrhizobium japonicum.
128  10, 12, 16, and 20 d after inoculation with Bradyrhizobium japonicum.
129 t, between 12 and 96 h post inoculation with Bradyrhizobium japonicum.
130 with the nitrogen-fixing symbiotic bacterium Bradyrhizobium japonicum.
131  to inoculation with the symbiotic bacterium Bradyrhizobium japonicum.
132 ir ability to induce the nodulation genes of Bradyrhizobium japonicum.
133 orhizobium meliloti, Mesorhizobium loti, and Bradyrhizobium japonicum.
134          Merr.) and its compatible symbiont, Bradyrhizobium japonicum.
135 Escherichia coli and equivalent cyc genes of Bradyrhizobium japonicum.
136     Rhizobia (e.g. Rhizobium, Sinorhizobium, Bradyrhizobium, Mesorhizobium and Azorhizobium species)
137 teria currently classified within the genera Bradyrhizobium, Mesorhizobium and Sinorhizobium have a r
138 with plant growth-promoting bacteria such as Bradyrhizobium, Mycobacterium, and Actinoplanes.
139 enation and dehalogenation processes such as Bradyrhizobium or Pseudomonas.
140 ynthetic stem-nodulating member of the genus Bradyrhizobium produces a small molecule signal that eli
141 opolysaccharides (LPS) from three strains of Bradyrhizobium (slow-growing rhizobia) have been establi
142 , F487A, and PI262090 after inoculation with Bradyrhizobium sp.
143 bium leguminosarum A34 in peas and beans and Bradyrhizobium sp. 32H1 in peanuts and cowpeas.
144 royl-HSL is made by other bacteria including Bradyrhizobium sp. and Silicibacter pomeroyi.
145 de O-antigen of the nitrogen-fixing bacteria Bradyrhizobium sp. BTAi1 and sp. ORS278, has been achiev
146 obacteria of the order Rhizobiales including Bradyrhizobium sp. ORS 375, encoding a four-domain heme-
147 -nitroanthranilic acid (5NAA) degradation by Bradyrhizobium sp. strain JS329 is a hydrolytic deaminat
148 factors are not involved in the Aeschynomene-Bradyrhizobium spp. interaction suggests that alternativ
149 otyped to quantify strain occupancy, and the Bradyrhizobium strain genome sequences were analyzed to
150                          Our stem-nodulating Bradyrhizobium strain responds to picomolar concentratio
151    Here we demonstrate that a photosynthetic Bradyrhizobium strain, symbiont of Aeschynomene legumes,
152                                          The Bradyrhizobium strains displayed conserved growth effect
153                                 Furthermore, Bradyrhizobium strains having different effector sets we
154                                         Some Bradyrhizobium strains nodulate certain Aeschynomene spe
155 on strigosus from six populations with three Bradyrhizobium strains that vary in symbiotic effectiven
156                                      Diverse Bradyrhizobium strains varying in their capacity to fix
157 he phylogeny and denitrification capacity of Bradyrhizobium strains, most of them isolated from peanu
158 n in a metapopulation of root-nodule forming Bradyrhizobium symbionts in Acmispon hosts.
159       Among genera common to all ecosystems, Bradyrhizobium, the Acidobacteria genus RB41, and Strept
160                               The ability of Bradyrhizobium to produce and respond to cinnamoyl-HSL s
161 tion and no NH2Cl residual) was dominated by Bradyrhizobium (total cumulative distribution: 38%), whi
162 ching to host cells as in the interaction of Bradyrhizobium with plant root hairs (3) or the polar pi

 
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