ライフサイエンスコーパス: campestris

1 marked and genotyped field crickets (Gryllus campestris).

2 (Pseudomonas) solanacearum, and Xanthomonas campestris.

3 ith RXC4 confers digenic resistance to X. c. campestris.

4 s RXC1, a gene conferring tolerance to X. c. campestris.

5 a (Pseudomonas) solanacearum and Xanthomonas campestris.

6 from the Brassica pathogen X. campestris pv. campestris.

7 significant homology to RpfF in Xanthomonas campestris.

8 o a virulent bacterial pathogen, Xanthomonas campestris.

9 gae, Pseudomonas aeruginosa, and Xanthomonas campestris.

10 glycopeptide processing by X. campestris pv. campestris.

11 In contrast, the X. campestris 2-Cys OhrR is inactivated when the initially

12 nuclear genes condition resistance to X. c. campestris 2D520.

13 We have identified in Xanthomonas campestris a novel N-acetylornithine transcarbamylase th

14 In X. campestris, a regulatory system mediated by the signal m

15 To correlate well with activities, A. campestris also exhibited greater total phenolics and to

16 2, conditions monogenic resistance to X. c.; campestris and was mapped to a 5.5 cM interval of chromo

17 hogens, Pseudomonas syringae and Xanthomonas campestris, and an oomycete, Peronospora parasitica.

18 E. coli and plant pathogens X. oryzae and X. campestris, as well as against human fungal pathogens C.

19 Recently, it was shown that the Xanthomonas campestris AvrBs2 protein can be delivered directly into

20 ound in Allium cepa, Beta vulgaris, Brassica campestris, Brassica oleracea, Pennisetum glaucum, Pinus

21 vars of Pseudomonas syringae and Xanthomonas campestris, but also enhanced the growth of the host pat

22 Xanthomonas campestris pv. campestris can express AvrXa21 activity if raxST, encodi

23 notypes of a DeltarpfF strain in Xanthomonas campestris could be complemented by its own DSF, the DSF

24 bution of each gene to the induction of a X. campestris DSF-dependent gene was assessed.

25 . microcarpus) for p-coumaric acid, 20.3 (A. campestris) for ferulic acid, 561.9 (A. campestris) for

26 (A. campestris) for ferulic acid, 561.9 (A. campestris) for gallic acid, 38.7 (A. campestris) for p-

27 tris) for p-hydroxybenzoic acid and 7.08 (A. campestris) for myricetin.

28 .9 (A. campestris) for gallic acid, 38.7 (A. campestris) for p-hydroxybenzoic acid and 7.08 (A. campe

29 B. campestris, for its simplicity of possessing only the AA

30 We cloned and overexpressed this X. campestris gene in Escherichia coli and show that it cat

31 Results showed that A. campestris had the greatest antioxidant activity in all

32 The OleA from Xanthomonas campestris has been crystallized and its structure deter

33 amylovora, Pseudomonas spp., and Xanthomonas campestris has impeded the control of several important

34 ted, and pathogen (Xanthomonas campestris pv campestris)-infected plants, callus, roots, and young se

35 ophan 2,3-dioxygenase (TDO) from Xanthomonas campestris is a highly specific heme-containing enzyme f

36 The bacterium Xanthomonas campestris is an economically important pathogen of many

37 odis pv. vesicatoria or to X. campestris pv. campestris is associated with increased synthesis of the

38 erecta (Ler) with Xanthomonas campestris pv campestris isolate 2D520 results in extensive necrosis a

39 ility to activate mouse NAGS, and inhibit X. campestris NAGS-K.

40 Like the X. campestris OhrR protein, these mutants (G120C and Q124C)

41 OhrR) and 2-Cys (represented by Xanthomonas campestris OhrR).

42 s of the active site cysteine in Xanthomonas campestris OleA (Cys(143)) enabled trapping of two catal

43 two B. subtilis homologs of the Xanthomonas campestris organic hydroperoxide resistance (ohr) gene.

44 enzymes and reduced virulence of Xanthomonas campestris pathovar campestris (Xcc).

45 XopN is a virulence factor from Xanthomonas campestris pathovar vesicatoria (Xcv) that is translocat

46 t XopD, a type III effector from Xanthomonas campestris pathovar vesicatoria (Xcv), suppresses sympto

47 thogen fitness and its prevalence in many X. campestris pathovars suggests that the Bs2 gene may be d

48 omparative mapping approach between Brassica campestris plants homozygous for the S8 haplotype and Ar

49 persensitive response (HR) after Xanthomonas campestris pv campestris (Xcc) infection.

50 Xanthomonas campestris pv campestris (Xcc) is a plant pathogenic bac

51 ing activity of flagellins among Xanthomonas campestris pv campestris (Xcc) strains.

52 scular phytopathogenic bacterium Xanthomonas campestris pv campestris (Xcc), the causal agent of blac

53 sion Landsberg erecta (Ler) with Xanthomonas campestris pv campestris isolate 2D520 results in extens

54 ted, heat-treated, and pathogen (Xanthomonas campestris pv campestris)-infected plants, callus, roots

55 gene are resistant to strains of Xanthomonas campestris pv vesicatoria (Xcv) expressing the bacterial

56 to (Lycopersicon esculentum) and Xanthomonas campestris pv vesicatoria (Xcv), to examine the interact

57 ersicon esculentum) and virulent Xanthomonas campestris pv vesicatoria (Xcv).

58 ines also were more resistant to Xanthomonas campestris pv vesicatoria and Cladosporium fulvum.

59 notypes with virulent bacterial (Xanthomonas campestris pv vesicatoria and Pseudomonas syringae pv to

60 rBsT is a type III effector from Xanthomonas campestris pv vesicatoria that is translocated into plan

61 effector from the plant pathogen Xanthomonas campestris pv vesicatoria, interacts with the proteasoma

62 ntified 25.4-kbp pig region from Xanthomonas campestris pv. campestris (strain B-24).

63 from the Xcv library were conjugated into X. campestris pv. campestris (Xcc) and exconjugants were sc

64 e two signals in the Arabidopsis-Xanthomonas campestris pv. campestris (Xcc) compatible interaction.

65 cellular polysaccharide (EPS) in Xanthomonas campestris pv. campestris (Xcc) is regulated by a cluste

66 al DSF controls the virulence of Xanthomonas campestris pv. campestris (Xcc) to plants.

67 In Xanthomonas campestris pv. campestris (Xcc), the proteins encoded by

68 Xanthomonas campestris pv. campestris can express AvrXa21 activity i

69 thomonas axonopodis pv. vesicatoria or to X. campestris pv. campestris is associated with increased s

70 f the superfamily encoded by the Xanthomonas campestris pv. campestris str. ATCC 33913 genome (GI:212

71 Xanthomonas campestris pv. campestris, the causal agent of black rot

72 log was cloned from the Brassica pathogen X. campestris pv. campestris.

73 e a model of N-glycopeptide processing by X. campestris pv. campestris.

74 o the bacterial blight pathogen, Xanthomonas campestris pv. malvacearum (Xcm).

75 Whole-genome sequences of Xanthomonas campestris pv. raphani strain 756C and X. oryzae pv. ory

76 Strains of Xanthomonas campestris pv. vesicatoria (Xcv) carrying avrBs2 are spe

77 r Bs2 gene confers resistance to Xanthomonas campestris pv. vesicatoria (Xcv) pathogenic strains whic

78 The bacterial pathogen Xanthomonas campestris pv. vesicatoria (Xcv) uses a type III secreti

79 ease-causing bacterial pathogen, Xanthomonas campestris pv. vesicatoria (Xcv).

80 oculum of the non-host pathogen, Xanthomonas campestris pv. vesicatoria (Xcv).

81 ose to the tomato bacterial spot pathogen X. campestris pv. vesicatoria 85-10, with a completely diff

82 s most similar to hrp genes from Xanthomonas campestris pv. vesicatoria and Ralstonia solanacearum.

83 g the molecular basis for virulence of 20 X. campestris pv. vesicatoria field strains that were isola

84 ization of the avrBs2 locus from Xanthomonas campestris pv. vesicatoria has revealed that expression

85 tive tomato plants infected with Xanthomonas campestris pv. vesicatoria have greatly reduced disease

86 irulent and avirulent strains of Xanthomonas campestris pv. vesicatoria in tomato (Lycopersicon escul

87 o to those of X. axonopodis pv. citri and X. campestris pv. vesicatoria provides valuable insights in

88 We generated isogenic X. campestris pv. vesicatoria strains by chromosomal avrBs2

89 at infection of pepper plants by Xanthomonas campestris pv. vesicatoria strains expressing the AvrBs2

90 confers resistance to strains of Xanthomonas campestris pv. vesicatoria that contain the correspondin

91 of the bacterial plant pathogen Xanthomonas campestris pv. vesicatoria triggers disease resistance i

92 Xanthomonas campestris pv. vesicatoria, causal agent of bacterial sp

93 resistance to B. cinerea infection and to X. campestris pv. vesicatoria, correlated with cuticle perm

94 type III secreted effector from Xanthomonas campestris pv. vesicatoria, is a desumoylating enzyme wi

95 -type NR cDNA were infected with virulent X. campestris pv. vesicatoria.

96 and AvrRxv of the plant pathogen Xanthomonas campestris pv. vesicatoria.

97 he biotrophic bacterial pathogen Xanthomonas campestris pv. vesicatoria.

98 utative translocator, HrpF, from Xanthomonas campestris pv. vesicatoria.

99 gy to HrpF of the plant pathogen Xanthomonas campestris pv. vesicatoria.

100 ore conserved between B. oleracea S13 and B. campestris S8, two haplotypes that have been proposed to

101 Previous work on Xanthomonas campestris showed that the RpfC/RpfG two-component syste

102 ly encoded by the Xanthomonas campestris pv. campestris str. ATCC 33913 genome (GI:21233491).

103 p pig region from Xanthomonas campestris pv. campestris (strain B-24).

104 L. edodes) and five wild (L. sulphureus, A. campestris, T. clypeatus, T. microcarpus and T. letestui

105 l and biochemical studies of the Xanthomonas campestris TDO and a related protein SO4414 from Shewane

106 e in A. hydrophila is more similar to the X. campestris than A. hydrophila genes.

107 defense responses against P. syringae and X. campestris The P. syringae T3SE HopZ1a is an acetyltrans

108 Xanthomonas campestris pv. campestris, the causal agent of black rot disease of Bra

109 In Xanthomonas campestris, the protein annotated as ornithine transcarb

110 The Xanthomonas campestris transcription regulator OhrR contains a react

111 a, like Pseudomonas syringae and Xanthomonas campestris, use the type III secretion system as a molec

112 In this study, OleA from Xanthomonas campestris was expressed in Escherichia coli and purifie

113 To test this conjecture, rpfC and rpfF of X. campestris were replaced by those of X. fastidiosa, and

114 mate synthase-kinase (NAGS-K) of Xanthomonas campestris, which is inhibited by arginine.

115 sequence similarity to GumC from Xanthomonas campestris, which is involved in exopolysaccharide expor

116 zobium meliloti (succinoglycan), Xanthomonas campestris (xanthan gum), and Salmonella enterica (O ant

117 tovorum, Ralstonia solanacearum, Xanthomonas campestris, Xanthomonas oryzae, and Xylella fastidiosa T

118 ystal structures of AOTCase from Xanthomonas campestris (xc) have been determined.

119 brary were conjugated into X. campestris pv. campestris (Xcc) and exconjugants were scored for an alt

120 n the Arabidopsis-Xanthomonas campestris pv. campestris (Xcc) compatible interaction.

121 tic screen in the plant pathogen Xanthomonas campestris (Xcc) identified that XC_0250, which encodes

122 esponse (HR) after Xanthomonas campestris pv campestris (Xcc) infection.

123 Xanthomonas campestris pv campestris (Xcc) is a plant pathogenic bacterium that co

124 ccharide (EPS) in Xanthomonas campestris pv. campestris (Xcc) is regulated by a cluster of genes call

125 f flagellins among Xanthomonas campestris pv campestris (Xcc) strains.

126 the virulence of Xanthomonas campestris pv. campestris (Xcc) to plants.

127 thogenic bacterium Xanthomonas campestris pv campestris (Xcc), the causal agent of black rot disease

128 In Xanthomonas campestris pv. campestris (Xcc), the proteins encoded by the rpf (regul

129 virulence of Xanthomonas campestris pathovar campestris (Xcc).

130 it destabilized the NAGS-K from Xanthomonas campestris (XcNAGS-K).

131 O) indoleamine 2,3-dioxygenases, Xanthomonas campestris (XcTDO) tryptophan 2,3-dioxygenase, and the H

132 rysanthemi and carotovora (out), Xanthomonas campestris (xps), Pseudomonas aeruginosa (xcp), Aeromona

133 atricopeptide repeat domain from Xanthomonas campestris YbgF, which is also able to trimerize.