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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.
16 A resolution crystal structure of PutA from Bradyrhizobium japonicum, along with data from small-ang
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
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
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
30 ition of chitin and lipo-chitin oligomers to Bradyrhizobium japonicum cultures resulted in a signific
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
38 arison of the structures of two forms of the Bradyrhizobium japonicum FixL heme domain, one in the "o
44 y diverse enolase superfamily encoded by the Bradyrhizobium japonicum genome (bll6730; GI:27381841).
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
54 s by the nitrogen-fixing symbiotic bacterium Bradyrhizobium japonicum is a complex process coordinate
55 e iron response regulator (Irr) protein from Bradyrhizobium japonicum is a conditionally stable prote
61 >3),beta-(1-->6)-D-glucan synthesis locus of Bradyrhizobium japonicum is composed of at least two gen
64 nfection of soybean roots by nitrogen-fixing Bradyrhizobium japonicum leads to expression of plant no
70 of an active cyt cbb3 oxidase, and unlike in Bradyrhizobium japonicum, no active CcoN-CcoO subcomplex
72 the effect of the inoculation of G. max with Bradyrhizobium japonicum on the metabolite profile and a
73 ivum) seed lectin (PSL) were inoculated with Bradyrhizobium japonicum or Rhizobium leguminosarum bv v
74 reas human, pea, Pseudomonas aeruginosa, and Bradyrhizobium japonicum PBGS are insensitive to inhibit
77 tagenesis was used to study the roles of two Bradyrhizobium japonicum proteins, HoxX and HoxA, in hyd
78 icroM to 2.4 mM for human, Escherichia coli, Bradyrhizobium japonicum, Pseudomonas aeruginosa, and pe
79 tion of the iron response regulator (Irr) in Bradyrhizobium japonicum raised the question of whether
80 responsive degradation of its counterpart in Bradyrhizobium japonicum, readily detectable levels of I
82 s (e.g. soybean) and rhizobia bacteria (e.g. Bradyrhizobium japonicum) results in root nodules where
83 l SWEET homologs with only 3-TM and that the Bradyrhizobium japonicum SemiSWEET1, like Arabidopsis SW
85 L. cv Merr.) seeds inoculated with a mutant Bradyrhizobium japonicum strain unable to catabolize Pro
88 We isolated a mutant strain of the bacterium Bradyrhizobium japonicum that, under iron limitation, ac
89 nt of a physical framework for the genome of Bradyrhizobium japonicum, the nitrogen-fixing symbiont o
91 l structure of ent-kaur-16-ene synthase from Bradyrhizobium japonicum, together with the results of a
94 o guanine deaminases from disparate sources (Bradyrhizobium japonicum USDA 110 and Homo sapiens) that
96 e report that BjaI from the soybean symbiont Bradyrhizobium japonicum USDA110 is closely related to R
98 ketoglutarate dehydrogenase, was cloned from Bradyrhizobium japonicum USDA110, and its nucleotide seq
99 hitin oligosaccharide Nod signal produced by Bradyrhizobium japonicum was also shown to be a competit
100 e nitrogen-fixing symbiotic (rhizo)bacterium Bradyrhizobium japonicum was found to carry adjacent gen
101 and directly downstream of the hypB gene of Bradyrhizobium japonicum was shown by mutational analysi
102 ere, we show that cytochrome c1 protein from Bradyrhizobium japonicum was strongly affected by the ir
103 soybean and its nitrogen-fixing endosymbiont Bradyrhizobium japonicum, we wanted to assess the role o
105 c L. corniculatus plant roots in response to Bradyrhizobium japonicum, which nodulates soybean and no
106 soybean and its nitrogen-fixing endosymbiont Bradyrhizobium japonicum, yet little is known about rhiz
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