ライフサイエンスコーパス: Bradyrhizobium

1 soil bacteria, belonging mainly to the genus Bradyrhizobium.

2 erall NAFLD patients had increased levels of Bradyrhizobium, Anaerococcus, Peptoniphilus, Propionibac

3 locus and closely linked nodulation genes of Bradyrhizobium (Arachis) sp. strain NC92 have been isola

4 stent with a model of nod gene expression in Bradyrhizobium (Arachis) sp. strain NC92 in which negati

5 equences for isolates similar to Acidovorax, Bradyrhizobium, Brevibacillus, Caulobacter, Chryseobacte

6 s, 12 genera-Pseudomonas, Propionibacterium, Bradyrhizobium, Corynebacterium, Acinetobacter, Brevundi

7 d nolA genes of Bradyrhizobium japonicum and Bradyrhizobium elkanii.

8 that restricts nodulation by many strains of Bradyrhizobium elkanii.

9 discovered bacterium was provisionally named Bradyrhizobium enterica.

10 of homology with genomes of bacteria in the bradyrhizobium genus.

11 Some isolates of Bradyrhizobium have been shown to be non-symbiotic and d

12 The slow-growing genus Bradyrhizobium is biologically important in soils, with

13 These Bradyrhizobium isolates are the first to be isolated and

14 European soil and are the first free-living Bradyrhizobium isolates, lacking both nodulation and nit

15 and gene annotations of two such free-living Bradyrhizobium isolates, named G22 and BF49, from soils

16 study, we show that the affinity of Fur from Bradyrhizobium japonicum (BjFur) for its target DNA incr

17 A enzymes by examining the PutA protein from Bradyrhizobium japonicum (BjPutA).

18 Bradyrhizobium japonicum ALAD* is an engineered derivati

19 nodA, nodB, nodD1, nodD2, and nolA genes of Bradyrhizobium japonicum and Bradyrhizobium elkanii.

20 restrict nodulation with specific strains of Bradyrhizobium japonicum and Sinorhizobium fredii, respe

21 The nodulation genes of Bradyrhizobium japonicum are essential for infection and

22 utative ferric siderophore receptor genes in Bradyrhizobium japonicum are positively controlled by th

23 entified mnoP in the Gram-negative bacterium Bradyrhizobium japonicum as a gene coregulated with the

24 Bradyrhizobium japonicum can use heme as an iron source,

25 Here, we show that aerobically grown Bradyrhizobium japonicum cells express a single catalase

26 ition of chitin and lipo-chitin oligomers to Bradyrhizobium japonicum cultures resulted in a signific

27 Here we show that Bradyrhizobium japonicum cytochrome c550 polypeptide acc

28 Consistent with this, immunoblot analyses of Bradyrhizobium japonicum extracts with a polyclonal anti

29 ns, we replaced this residue with alanine in Bradyrhizobium japonicum FixL and examined the results o

30 ssessed the contributions of this residue in Bradyrhizobium japonicum FixL by determining the effects

31 Recent structural studies of the Bradyrhizobium japonicum FixL heme domain (BjFixLH) have

32 Structures of the Bradyrhizobium japonicum FixL heme domain have been dete

33 arison of the structures of two forms of the Bradyrhizobium japonicum FixL heme domain, one in the "o

34 Several recombinant Bradyrhizobium japonicum FixL heme domains (BjFixLH) hav

35 Bradyrhizobium japonicum FixL is a modular oxygen sensor

36 rebinding to two forms of the heme domain of Bradyrhizobium japonicum FixL.

37 Here, we identified Bradyrhizobium japonicum frcB (bll3557) as a gene adjace

38 Bradyrhizobium japonicum Fur mediates manganese-responsi

39 y diverse enolase superfamily encoded by the Bradyrhizobium japonicum genome (bll6730; GI:27381841).

40 In this study, we identified a Bradyrhizobium japonicum genomic library clone that comp

41 Microarray analysis of Bradyrhizobium japonicum grown under copper limitation u

42 of hydrogenase structural gene expression in Bradyrhizobium japonicum have been investigated.

43 he Brucella BhuQ protein is a homolog of the Bradyrhizobium japonicum heme oxygenases HmuD and HmuQ.

44 nodulation signal (nod signal) purified from Bradyrhizobium japonicum induced nodule primordia on soy

45 t changes in their expression in response to Bradyrhizobium japonicum infection and in representative

46 Utilization of heme as an iron source by Bradyrhizobium japonicum involves induction of the outer

47 Bradyrhizobium japonicum Irr is a conditionally stable t

48 s by the nitrogen-fixing symbiotic bacterium Bradyrhizobium japonicum is a complex process coordinate

49 e iron response regulator (Irr) protein from Bradyrhizobium japonicum is a conditionally stable prote

50 The FixL protein of Bradyrhizobium japonicum is a dimeric oxygen sensor resp

51 Bradyrhizobium japonicum is a facultative chemoautotroph

52 The HypB protein from Bradyrhizobium japonicum is a metal-binding GTPase requi

53 FixL from Bradyrhizobium japonicum is a PAS sensor protein in whic

54 Bradyrhizobium japonicum is a symbiotic bacterium that n

55 >3),beta-(1-->6)-D-glucan synthesis locus of Bradyrhizobium japonicum is composed of at least two gen

56 The Irr protein from the bacterium Bradyrhizobium japonicum is expressed under iron limitat

57 The irr gene from Bradyrhizobium japonicum is under the control of Fur.

58 nfection of soybean roots by nitrogen-fixing Bradyrhizobium japonicum leads to expression of plant no

59 Here, we show that Bradyrhizobium japonicum MbfA (Blr7895) is an inner memb

60 Bradyrhizobium japonicum Mur and Escherichia coli Fur ar

61 A Bradyrhizobium japonicum mutant defective in the gene en

62 A Bradyrhizobium japonicum mutant defective in the high-af

63 Bradyrhizobium japonicum nod gene expression was previou

64 the effect of the inoculation of G. max with Bradyrhizobium japonicum on the metabolite profile and a

65 ivum) seed lectin (PSL) were inoculated with Bradyrhizobium japonicum or Rhizobium leguminosarum bv v

66 reas human, pea, Pseudomonas aeruginosa, and Bradyrhizobium japonicum PBGS are insensitive to inhibit

67 Bradyrhizobium japonicum porphobilinogen synthase (B. ja

68 Bradyrhizobium japonicum possessed lipid A species with

69 tagenesis was used to study the roles of two Bradyrhizobium japonicum proteins, HoxX and HoxA, in hyd

70 tion of the iron response regulator (Irr) in Bradyrhizobium japonicum raised the question of whether

71 The PBGS from Bradyrhizobium japonicum requires Mg(II) in catalytic me

72 l SWEET homologs with only 3-TM and that the Bradyrhizobium japonicum SemiSWEET1, like Arabidopsis SW

73 The Irr protein from Bradyrhizobium japonicum senses iron through the status

74 L. cv Merr.) seeds inoculated with a mutant Bradyrhizobium japonicum strain unable to catabolize Pro

75 However, a Bradyrhizobium japonicum sucA mutant that is missing alp

76 Bradyrhizobium japonicum synthesizes periplasmic cyclic

77 We isolated a mutant strain of the bacterium Bradyrhizobium japonicum that, under iron limitation, ac

78 mprehensive understanding of the response of Bradyrhizobium japonicum to drought.

79 The Bradyrhizobium japonicum transcriptional regulator Irr (

80 Bradyrhizobium japonicum transports oligopeptides and th

81 o guanine deaminases from disparate sources (Bradyrhizobium japonicum USDA 110 and Homo sapiens) that

82 The bacterium Bradyrhizobium japonicum USDA110 does not synthesize sid

83 e report that BjaI from the soybean symbiont Bradyrhizobium japonicum USDA110 is closely related to R

84 A mutant strain of Bradyrhizobium japonicum USDA110 lacking isocitrate dehy

85 ketoglutarate dehydrogenase, was cloned from Bradyrhizobium japonicum USDA110, and its nucleotide seq

86 hitin oligosaccharide Nod signal produced by Bradyrhizobium japonicum was also shown to be a competit

87 e nitrogen-fixing symbiotic (rhizo)bacterium Bradyrhizobium japonicum was found to carry adjacent gen

88 and directly downstream of the hypB gene of Bradyrhizobium japonicum was shown by mutational analysi

89 ere, we show that cytochrome c1 protein from Bradyrhizobium japonicum was strongly affected by the ir

90 oil bacteria (e.g. soybean [Glycine max] and Bradyrhizobium japonicum) initiated by the infection of

91 s (e.g. soybean) and rhizobia bacteria (e.g. Bradyrhizobium japonicum) results in root nodules where

92 Bradyrhizobium japonicum, a diazotropic symbiont of soyb

93 Bradyrhizobium japonicum, a symbiotic nitrogen-fixing ba

94 A resolution crystal structure of PutA from Bradyrhizobium japonicum, along with data from small-ang

95 is a global regulator of iron homeostasis in Bradyrhizobium japonicum, and a subset of genes within t

96 Here, we identify the mntH homologue of Bradyrhizobium japonicum, and demonstrate that it is ess

97 and microaerobic metabolism in the bacterium Bradyrhizobium japonicum, and evidence suggests that hem

98 bacteria Thermosynechococcus elongatus BP-1, Bradyrhizobium japonicum, and Zymomonas mobilis and clon

99 In the bacterium Bradyrhizobium japonicum, expression of the gene encodin

100 In Bradyrhizobium japonicum, members of two global regulato

101 of an active cyt cbb3 oxidase, and unlike in Bradyrhizobium japonicum, no active CcoN-CcoO subcomplex

102 icroM to 2.4 mM for human, Escherichia coli, Bradyrhizobium japonicum, Pseudomonas aeruginosa, and pe

103 responsive degradation of its counterpart in Bradyrhizobium japonicum, readily detectable levels of I

104 nt of a physical framework for the genome of Bradyrhizobium japonicum, the nitrogen-fixing symbiont o

105 l structure of ent-kaur-16-ene synthase from Bradyrhizobium japonicum, together with the results of a

106 soybean and its nitrogen-fixing endosymbiont Bradyrhizobium japonicum, we wanted to assess the role o

107 Expression of PutA(Ec) and PutA from Bradyrhizobium japonicum, which exhibit low oxygen react

108 c L. corniculatus plant roots in response to Bradyrhizobium japonicum, which nodulates soybean and no

109 soybean and its nitrogen-fixing endosymbiont Bradyrhizobium japonicum, yet little is known about rhiz

110 Merr.) and its compatible symbiont, Bradyrhizobium japonicum.

111 in the N(2)-fixing, H(2)-oxidizing bacterium Bradyrhizobium japonicum.

112 genase, was cloned from the soybean symbiont Bradyrhizobium japonicum.

113 ing life styles of the alpha-proteobacterium Bradyrhizobium japonicum.

114 10, 12, 16, and 20 d after inoculation with Bradyrhizobium japonicum.

115 t, between 12 and 96 h post inoculation with Bradyrhizobium japonicum.

116 with the nitrogen-fixing symbiotic bacterium Bradyrhizobium japonicum.

117 to inoculation with the symbiotic bacterium Bradyrhizobium japonicum.

118 ir ability to induce the nodulation genes of Bradyrhizobium japonicum.

119 orhizobium meliloti, Mesorhizobium loti, and Bradyrhizobium japonicum.

120 Escherichia coli and equivalent cyc genes of Bradyrhizobium japonicum.

121 iotic root nodules elicited by the bacterium Bradyrhizobium japonicum.

122 Rhizobia (e.g. Rhizobium, Sinorhizobium, Bradyrhizobium, Mesorhizobium and Azorhizobium species)

123 teria currently classified within the genera Bradyrhizobium, Mesorhizobium and Sinorhizobium have a r

124 enation and dehalogenation processes such as Bradyrhizobium or Pseudomonas.

125 ynthetic stem-nodulating member of the genus Bradyrhizobium produces a small molecule signal that eli

126 opolysaccharides (LPS) from three strains of Bradyrhizobium (slow-growing rhizobia) have been establi

127 , F487A, and PI262090 after inoculation with Bradyrhizobium sp.

128 bium leguminosarum A34 in peas and beans and Bradyrhizobium sp. 32H1 in peanuts and cowpeas.

129 royl-HSL is made by other bacteria including Bradyrhizobium sp. and Silicibacter pomeroyi.

130 -nitroanthranilic acid (5NAA) degradation by Bradyrhizobium sp. strain JS329 is a hydrolytic deaminat

131 factors are not involved in the Aeschynomene-Bradyrhizobium spp. interaction suggests that alternativ

132 Our stem-nodulating Bradyrhizobium strain responds to picomolar concentratio

133 Here we demonstrate that a photosynthetic Bradyrhizobium strain, symbiont of Aeschynomene legumes,

134 The ability of Bradyrhizobium to produce and respond to cinnamoyl-HSL s

135 tion and no NH2Cl residual) was dominated by Bradyrhizobium (total cumulative distribution: 38%), whi

136 ching to host cells as in the interaction of Bradyrhizobium with plant root hairs (3) or the polar pi