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1          Merr.) and its compatible symbiont, Bradyrhizobium japonicum.
2 ing life styles of the alpha-proteobacterium Bradyrhizobium japonicum.
3  10, 12, 16, and 20 d after inoculation with Bradyrhizobium japonicum.
4 t, between 12 and 96 h post inoculation with Bradyrhizobium japonicum.
5 with the nitrogen-fixing symbiotic bacterium Bradyrhizobium japonicum.
6  to inoculation with the symbiotic bacterium Bradyrhizobium japonicum.
7 ir ability to induce the nodulation genes of Bradyrhizobium japonicum.
8 orhizobium meliloti, Mesorhizobium loti, and Bradyrhizobium japonicum.
9 Escherichia coli and equivalent cyc genes of Bradyrhizobium japonicum.
10 iotic root nodules elicited by the bacterium Bradyrhizobium japonicum.
11 in the N(2)-fixing, H(2)-oxidizing bacterium Bradyrhizobium japonicum.
12 genase, was cloned from the soybean symbiont Bradyrhizobium japonicum.
13                                              Bradyrhizobium japonicum, a diazotropic symbiont of soyb
14                                              Bradyrhizobium japonicum, a symbiotic nitrogen-fixing ba
15                                              Bradyrhizobium japonicum ALAD* is an engineered derivati
16  A resolution crystal structure of PutA from Bradyrhizobium japonicum, along with data from small-ang
17  nodA, nodB, nodD1, nodD2, and nolA genes of Bradyrhizobium japonicum and Bradyrhizobium elkanii.
18 restrict nodulation with specific strains of Bradyrhizobium japonicum and Sinorhizobium fredii, respe
19 is a global regulator of iron homeostasis in Bradyrhizobium japonicum, and a subset of genes within t
20      Here, we identify the mntH homologue of Bradyrhizobium japonicum, and demonstrate that it is ess
21 and microaerobic metabolism in the bacterium Bradyrhizobium japonicum, and evidence suggests that hem
22 bacteria Thermosynechococcus elongatus BP-1, Bradyrhizobium japonicum, and Zymomonas mobilis and clon
23                      The nodulation genes of Bradyrhizobium japonicum are essential for infection and
24 utative ferric siderophore receptor genes in Bradyrhizobium japonicum are positively controlled by th
25 entified mnoP in the Gram-negative bacterium Bradyrhizobium japonicum as a gene coregulated with the
26 study, we show that the affinity of Fur from Bradyrhizobium japonicum (BjFur) for its target DNA incr
27 A enzymes by examining the PutA protein from Bradyrhizobium japonicum (BjPutA).
28                                              Bradyrhizobium japonicum can use heme as an iron source,
29         Here, we show that aerobically grown Bradyrhizobium japonicum cells express a single catalase
30 ition of chitin and lipo-chitin oligomers to Bradyrhizobium japonicum cultures resulted in a signific
31                            Here we show that Bradyrhizobium japonicum cytochrome c550 polypeptide acc
32                             In the bacterium Bradyrhizobium japonicum, expression of the gene encodin
33 Consistent with this, immunoblot analyses of Bradyrhizobium japonicum extracts with a polyclonal anti
34 ns, we replaced this residue with alanine in Bradyrhizobium japonicum FixL and examined the results o
35 ssessed the contributions of this residue in Bradyrhizobium japonicum FixL by determining the effects
36             Recent structural studies of the Bradyrhizobium japonicum FixL heme domain (BjFixLH) have
37                            Structures of the Bradyrhizobium japonicum FixL heme domain have been dete
38 arison of the structures of two forms of the Bradyrhizobium japonicum FixL heme domain, one in the "o
39                          Several recombinant Bradyrhizobium japonicum FixL heme domains (BjFixLH) hav
40                                              Bradyrhizobium japonicum FixL is a modular oxygen sensor
41 rebinding to two forms of the heme domain of Bradyrhizobium japonicum FixL.
42                          Here, we identified Bradyrhizobium japonicum frcB (bll3557) as a gene adjace
43                                              Bradyrhizobium japonicum Fur mediates manganese-responsi
44 y diverse enolase superfamily encoded by the Bradyrhizobium japonicum genome (bll6730; GI:27381841).
45               In this study, we identified a Bradyrhizobium japonicum genomic library clone that comp
46                       Microarray analysis of Bradyrhizobium japonicum grown under copper limitation u
47 of hydrogenase structural gene expression in Bradyrhizobium japonicum have been investigated.
48 he Brucella BhuQ protein is a homolog of the Bradyrhizobium japonicum heme oxygenases HmuD and HmuQ.
49 nodulation signal (nod signal) purified from Bradyrhizobium japonicum induced nodule primordia on soy
50 t changes in their expression in response to Bradyrhizobium japonicum infection and in representative
51 oil bacteria (e.g. soybean [Glycine max] and Bradyrhizobium japonicum) initiated by the infection of
52     Utilization of heme as an iron source by Bradyrhizobium japonicum involves induction of the outer
53                                              Bradyrhizobium japonicum Irr is a conditionally stable t
54 s by the nitrogen-fixing symbiotic bacterium Bradyrhizobium japonicum is a complex process coordinate
55 itrogen-fixing symbiosis between soybean and Bradyrhizobium japonicum is a complex process.
56 e iron response regulator (Irr) protein from Bradyrhizobium japonicum is a conditionally stable prote
57                          The FixL protein of Bradyrhizobium japonicum is a dimeric oxygen sensor resp
58                                              Bradyrhizobium japonicum is a facultative chemoautotroph
59                        The HypB protein from Bradyrhizobium japonicum is a metal-binding GTPase requi
60                                              Bradyrhizobium japonicum is a nitrogen-fixing bacterium
61                                    FixL from Bradyrhizobium japonicum is a PAS sensor protein in whic
62                                              Bradyrhizobium japonicum is a symbiotic bacterium that n
63 >3),beta-(1-->6)-D-glucan synthesis locus of Bradyrhizobium japonicum is composed of at least two gen
64           The Irr protein from the bacterium Bradyrhizobium japonicum is expressed under iron limitat
65                            The irr gene from Bradyrhizobium japonicum is under the control of Fur.
66 nfection of soybean roots by nitrogen-fixing Bradyrhizobium japonicum leads to expression of plant no
67                           Here, we show that Bradyrhizobium japonicum MbfA (Blr7895) is an inner memb
68                                           In Bradyrhizobium japonicum, members of two global regulato
69                                              Bradyrhizobium japonicum Mur and Escherichia coli Fur ar
70                                            A Bradyrhizobium japonicum mutant defective in the gene en
71                                            A Bradyrhizobium japonicum mutant defective in the high-af
72 of an active cyt cbb3 oxidase, and unlike in Bradyrhizobium japonicum, no active CcoN-CcoO subcomplex
73                                              Bradyrhizobium japonicum nod gene expression was previou
74 the effect of the inoculation of G. max with Bradyrhizobium japonicum on the metabolite profile and a
75 ivum) seed lectin (PSL) were inoculated with Bradyrhizobium japonicum or Rhizobium leguminosarum bv v
76 reas human, pea, Pseudomonas aeruginosa, and Bradyrhizobium japonicum PBGS are insensitive to inhibit
77                                              Bradyrhizobium japonicum porphobilinogen synthase (B. ja
78                                              Bradyrhizobium japonicum possessed lipid A species with
79 tagenesis was used to study the roles of two Bradyrhizobium japonicum proteins, HoxX and HoxA, in hyd
80 icroM to 2.4 mM for human, Escherichia coli, Bradyrhizobium japonicum, Pseudomonas aeruginosa, and pe
81 tion of the iron response regulator (Irr) in Bradyrhizobium japonicum raised the question of whether
82 responsive degradation of its counterpart in Bradyrhizobium japonicum, readily detectable levels of I
83                                The PBGS from Bradyrhizobium japonicum requires Mg(II) in catalytic me
84 s (e.g. soybean) and rhizobia bacteria (e.g. Bradyrhizobium japonicum) results in root nodules where
85 l SWEET homologs with only 3-TM and that the Bradyrhizobium japonicum SemiSWEET1, like Arabidopsis SW
86                         The Irr protein from Bradyrhizobium japonicum senses iron through the status
87  L. cv Merr.) seeds inoculated with a mutant Bradyrhizobium japonicum strain unable to catabolize Pro
88                                   However, a Bradyrhizobium japonicum sucA mutant that is missing alp
89                                              Bradyrhizobium japonicum synthesizes periplasmic cyclic
90 We isolated a mutant strain of the bacterium Bradyrhizobium japonicum that, under iron limitation, ac
91 nt of a physical framework for the genome of Bradyrhizobium japonicum, the nitrogen-fixing symbiont o
92 mprehensive understanding of the response of Bradyrhizobium japonicum to drought.
93 l structure of ent-kaur-16-ene synthase from Bradyrhizobium japonicum, together with the results of a
94                                          The Bradyrhizobium japonicum transcriptional regulator Irr (
95                                              Bradyrhizobium japonicum transports oligopeptides and th
96 o guanine deaminases from disparate sources (Bradyrhizobium japonicum USDA 110 and Homo sapiens) that
97                                The bacterium Bradyrhizobium japonicum USDA110 does not synthesize sid
98 e report that BjaI from the soybean symbiont Bradyrhizobium japonicum USDA110 is closely related to R
99                           A mutant strain of Bradyrhizobium japonicum USDA110 lacking isocitrate dehy
100 ketoglutarate dehydrogenase, was cloned from Bradyrhizobium japonicum USDA110, and its nucleotide seq
101 hitin oligosaccharide Nod signal produced by Bradyrhizobium japonicum was also shown to be a competit
102 e nitrogen-fixing symbiotic (rhizo)bacterium Bradyrhizobium japonicum was found to carry adjacent gen
103  and directly downstream of the hypB gene of Bradyrhizobium japonicum was shown by mutational analysi
104 ere, we show that cytochrome c1 protein from Bradyrhizobium japonicum was strongly affected by the ir
105 soybean and its nitrogen-fixing endosymbiont Bradyrhizobium japonicum, we wanted to assess the role o
106         Expression of PutA(Ec) and PutA from Bradyrhizobium japonicum, which exhibit low oxygen react
107 c L. corniculatus plant roots in response to Bradyrhizobium japonicum, which nodulates soybean and no
108 soybean and its nitrogen-fixing endosymbiont Bradyrhizobium japonicum, yet little is known about rhiz

 
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