ライフサイエンスコーパス: campestris

1 marked and genotyped field crickets (Gryllus campestris).

2 olved in the regulation of heat stress in B. campestris.

3 (Pseudomonas) solanacearum, and Xanthomonas campestris.

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

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

6 a (Pseudomonas) solanacearum and Xanthomonas campestris.

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

8 terial pathogens P. syringae and Xanthomonas campestris.

9 glycopeptide processing by X. campestris pv. campestris.

10 significant homology to RpfF in Xanthomonas campestris.

11 o a virulent bacterial pathogen, Xanthomonas campestris.

12 gae, Pseudomonas aeruginosa, and Xanthomonas campestris.

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

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

15 ra43 (Abra43) and Xanthomonas campestris pv. campestris 8004 (Xcc8004), on the structure and function

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

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

18 Cuscuta campestris, a stem parasitic plant, has served as a valu

19 Ms of Pseudomonas aeruginosa and Xanthomonas campestris, albeit not in the enzymes from Pseudomonas f

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

21 Transformed C. campestris also produced flowers and viable transgenic s

22 2, conditions monogenic resistance to X. c.; campestris and was mapped to a 5.5 cM interval of chromo

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

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

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

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

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

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

29 campestris Class 2 OLD proteins at 2.24 angstrom and 1.8

30 Our results evidenced that X. campestris pv campestris CN08 tales are relevant for symptom developme

31 cted vegetables (Spinacia oleracea, Brassica campestris, Coriandrum sativum, and Mentha spicata) were

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

33 The parasitic plant Cuscuta campestris (dodder) produces many microRNAs that specifi

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

35 eported that, the Xanthomonas campestris pv. campestris effector XopP compromises AtExo70B1, while by

36 The velvet longhorned beetle, Trichoferus campestris (Faldermann) ("VLB"; Coleoptera: Cerambycidae

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

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

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

40 .9 (A. campestris) for gallic acid, 38.7 (A. campestris) for p-hydroxybenzoic acid and 7.08 (A. campe

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

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

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

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

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

46 regardless of host species and occurs in C. campestris haustoria produced in the absence of any host

47 A new study explores this in Xanthomonas campestris, highlighting its adaptation into a virulent

48 This promoter element distinguishes C. campestris IIM loci from other plant small RNAs.

49 Our data suggest that C. campestris IIMs are produced in a manner distinct from c

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

51 The loci-encoding C. campestris interface-induced microRNAs are distinguished

52 We found that induction of C. campestris interface-induced microRNAs is similar regard

53 tryptophan 2,3-dioxygenase from Xanthomonas campestris into a monooxygenase for oxidative cyclizatio

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

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

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

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

58 ality of flowering Chinese cabbage (Brassica campestris L. ssp. chinensis var. utilis Tsen et Lee).

59 All confirmed C. campestris microRNAs with documented trans-species activ

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

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

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

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

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

65 he Burkholderia pseudomallei and Xanthamonas campestris p.v.

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

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

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

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

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

71 e stably transformed and regenerated RUBY C. campestris plants produced haustoria, the signature orga

72 minants of the vascular pathogen Xanthomonas campestris pv campestris (Xcc) during infection of the c

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

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

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

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

77 Our results evidenced that X. campestris pv campestris CN08 tales are relevant for sym

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

93 onas oryzae pv. oryzae (Xoo) and Xanthomonas campestris pv. campestris (Xcc).

94 f apo Zur from the phytopathogen Xanthomonas campestris pv. campestris (XcZur), which reveals the mol

95 brassicicola Abra43 (Abra43) and Xanthomonas campestris pv. campestris 8004 (Xcc8004), on the structu

96 Xanthomonas campestris pv. campestris can express AvrXa21 activity i

97 We previously reported that, the Xanthomonas campestris pv. campestris effector XopP compromises AtEx

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

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

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

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

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

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

104 thomonas wilt disease, caused by Xanthomonas campestris pv. musacearum (Xcm), is a major threat to ba

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

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

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

108 Here, we provide evidence that Xanthomonas campestris pv. vesicatoria (Xcv) suppresses host autopha

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

110 outer protein S (XopS), a T3E of Xanthomonas campestris pv. vesicatoria (Xcv), interacts with and inh

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

130 he biotrophic bacterial pathogen Xanthomonas campestris pv. vesicatoria.

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

132 Thus, the protocol for transformation of C. campestris reported here overcomes a major obstacle to C

133 However, a major barrier to C. campestris research is that a method to generate stable

134 ntitative and broad-spectrum resistance to X campestris RKS1-dependent gene expression was shown to i

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

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

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

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

139 id assay using the CO promoter from Brassica campestris (syn.

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

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

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

143 riboswitch (SAM-I(Xcc)) from the Xanthomonas campestris that regulates methionine synthesis via the m

144 cholerae, and the plant pathogen Xanthomonas campestris The bioconjugated phanorods could selectively

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

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

147 Xanthomonas campestris, the causal agent of black rot disease of cru

148 In Xanthomonas campestris, the protein annotated as ornithine transcarb

149 sponse to the bacterial pathogen Xanthomonas campestris To tackle this challenge, we first performed

150 sight into the movement of molecules from C. campestris to the host during parasitism.

151 The Xanthomonas campestris transcription regulator OhrR contains a react

152 obust protocol for Agrobacterium-mediated C. campestris transformation.

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

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

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

156 nserved core-effector protein produced by X. campestris, which is essential for virulence.

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

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

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

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

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

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

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

164 vascular pathogen Xanthomonas campestris pv campestris (Xcc) during infection of the cauliflower hos

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

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

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

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

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

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

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

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

173 virulence of Xanthomonas campestris pathovar campestris (Xcc).

174 oryzae (Xoo) and Xanthomonas campestris pv. campestris (Xcc).

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

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

177 the phytopathogen Xanthomonas campestris pv. campestris (XcZur), which reveals the molecular mechanis

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

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