ライフサイエンスコーパス: Xanthomonas campestris

1 rotein shows significant homology to RpfF in Xanthomonas campestris.

2 resistance to a virulent bacterial pathogen, Xanthomonas campestris.

3 omonas syringae, Pseudomonas aeruginosa, and Xanthomonas campestris.

4 a, Ralstonia (Pseudomonas) solanacearum, and Xanthomonas campestris.

5 of Ralstonia (Pseudomonas) solanacearum and Xanthomonas campestris.

6 h foliar bacterial pathogens P. syringae and Xanthomonas campestris.

7 We have identified in Xanthomonas campestris a novel N-acetylornithine transca

8 acterized PMMs of Pseudomonas aeruginosa and Xanthomonas campestris, albeit not in the enzymes from P

9 acterial pathogens, Pseudomonas syringae and Xanthomonas campestris, and an oomycete, Peronospora par

10 Recently, it was shown that the Xanthomonas campestris AvrBs2 protein can be delivered d

11 to few pathovars of Pseudomonas syringae and Xanthomonas campestris, but also enhanced the growth of

12 While phenotypes of a DeltarpfF strain in Xanthomonas campestris could be complemented by its own

13 The OleA from Xanthomonas campestris has been crystallized and its str

14 of Erwinia amylovora, Pseudomonas spp., and Xanthomonas campestris has impeded the control of severa

15 A new study explores this in Xanthomonas campestris, highlighting its adaptation into

16 transformed tryptophan 2,3-dioxygenase from Xanthomonas campestris into a monooxygenase for oxidativ

17 Tryptophan 2,3-dioxygenase (TDO) from Xanthomonas campestris is a highly specific heme-contain

18 The bacterium Xanthomonas campestris is an economically important path

19 lus subtilis OhrR) and 2-Cys (represented by Xanthomonas campestris OhrR).

20 , mutagenesis of the active site cysteine in Xanthomonas campestris OleA (Cys(143)) enabled trapping

21 function of two B. subtilis homologs of the Xanthomonas campestris organic hydroperoxide resistance

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

23 XopN is a virulence factor from Xanthomonas campestris pathovar vesicatoria (Xcv) that i

24 onstrate that XopD, a type III effector from Xanthomonas campestris pathovar vesicatoria (Xcv), suppr

25 itness determinants of the vascular pathogen Xanthomonas campestris pv campestris (Xcc) during infect

26 dependent hypersensitive response (HR) after Xanthomonas campestris pv campestris (Xcc) infection.

27 Xanthomonas campestris pv campestris (Xcc) is a plant pa

28 fense-eliciting activity of flagellins among Xanthomonas campestris pv campestris (Xcc) strains.

29 e adapted vascular phytopathogenic bacterium Xanthomonas campestris pv campestris (Xcc), the causal a

30 aliana accession Landsberg erecta (Ler) with Xanthomonas campestris pv campestris isolate 2D520 resul

31 om cold-treated, heat-treated, and pathogen (Xanthomonas campestris pv campestris)-infected plants, c

32 resistance gene are resistant to strains of Xanthomonas campestris pv vesicatoria (Xcv) expressing t

33 tion of tomato (Lycopersicon esculentum) and Xanthomonas campestris pv vesicatoria (Xcv), to examine

34 omato (Lycopersicon esculentum) and virulent Xanthomonas campestris pv vesicatoria (Xcv).

35 e 35S::Pto lines also were more resistant to Xanthomonas campestris pv vesicatoria and Cladosporium f

36 s of both genotypes with virulent bacterial (Xanthomonas campestris pv vesicatoria and Pseudomonas sy

37 AvrBsT is a type III effector from Xanthomonas campestris pv vesicatoria that is translocat

38 YopJ family effector from the plant pathogen Xanthomonas campestris pv vesicatoria, interacts with th

39 eviously identified 25.4-kbp pig region from Xanthomonas campestris pv. campestris (strain B-24).

40 p between the two signals in the Arabidopsis-Xanthomonas campestris pv. campestris (Xcc) compatible i

41 es and extracellular polysaccharide (EPS) in Xanthomonas campestris pv. campestris (Xcc) is regulated

42 ty acid signal DSF controls the virulence of Xanthomonas campestris pv. campestris (Xcc) to plants.

43 In Xanthomonas campestris pv. campestris (Xcc), the protein

44 d by Xanthomonas oryzae pv. oryzae (Xoo) and Xanthomonas campestris pv. campestris (Xcc).

45 structure of apo Zur from the phytopathogen Xanthomonas campestris pv. campestris (XcZur), which rev

46 Alternaria brassicicola Abra43 (Abra43) and Xanthomonas campestris pv. campestris 8004 (Xcc8004), on

47 Xanthomonas campestris pv. campestris can express AvrXa2

48 We previously reported that, the Xanthomonas campestris pv. campestris effector XopP comp

49 ) subgroup of the superfamily encoded by the Xanthomonas campestris pv. campestris str. ATCC 33913 ge

50 Xanthomonas campestris pv. campestris, the causal agent

51 resistance to the bacterial blight pathogen, Xanthomonas campestris pv. malvacearum (Xcm).

52 Banana Xanthomonas wilt disease, caused by Xanthomonas campestris pv. musacearum (Xcm), is a major

53 Whole-genome sequences of Xanthomonas campestris pv. raphani strain 756C and X. or

54 Strains of Xanthomonas campestris pv. vesicatoria (Xcv) carrying av

55 of the pepper Bs2 gene confers resistance to Xanthomonas campestris pv. vesicatoria (Xcv) pathogenic

56 Here, we provide evidence that Xanthomonas campestris pv. vesicatoria (Xcv) suppresses

57 The bacterial pathogen Xanthomonas campestris pv. vesicatoria (Xcv) uses a type

58 Xanthomonas outer protein S (XopS), a T3E of Xanthomonas campestris pv. vesicatoria (Xcv), interacts

59 with the disease-causing bacterial pathogen, Xanthomonas campestris pv. vesicatoria (Xcv).

60 igh titer inoculum of the non-host pathogen, Xanthomonas campestris pv. vesicatoria (Xcv).

61 he region was most similar to hrp genes from Xanthomonas campestris pv. vesicatoria and Ralstonia sol

62 ar characterization of the avrBs2 locus from Xanthomonas campestris pv. vesicatoria has revealed that

63 lene-insensitive tomato plants infected with Xanthomonas campestris pv. vesicatoria have greatly redu

64 esponse to virulent and avirulent strains of Xanthomonas campestris pv. vesicatoria in tomato (Lycope

65 , we show that infection of pepper plants by Xanthomonas campestris pv. vesicatoria strains expressin

66 ognizes and confers resistance to strains of Xanthomonas campestris pv. vesicatoria that contain the

67 rulence gene of the bacterial plant pathogen Xanthomonas campestris pv. vesicatoria triggers disease

68 Xanthomonas campestris pv. vesicatoria, causal agent of

69 rotein D), a type III secreted effector from Xanthomonas campestris pv. vesicatoria, is a desumoylati

70 inerea and the biotrophic bacterial pathogen Xanthomonas campestris pv. vesicatoria.

71 ity with a putative translocator, HrpF, from Xanthomonas campestris pv. vesicatoria.

72 shows homology to HrpF of the plant pathogen Xanthomonas campestris pv. vesicatoria.

73 uberculosis and AvrRxv of the plant pathogen Xanthomonas campestris pv. vesicatoria.

74 Previous work on Xanthomonas campestris showed that the RpfC/RpfG two-com

75 ve structural and biochemical studies of the Xanthomonas campestris TDO and a related protein SO4414

76 ize a SAM-I riboswitch (SAM-I(Xcc)) from the Xanthomonas campestris that regulates methionine synthes

77 and Vibrio cholerae, and the plant pathogen Xanthomonas campestris The bioconjugated phanorods could

78 Xanthomonas campestris, the causal agent of black rot di

79 In Xanthomonas campestris, the protein annotated as ornithi

80 aliana in response to the bacterial pathogen Xanthomonas campestris To tackle this challenge, we firs

81 The Xanthomonas campestris transcription regulator OhrR cont

82 enic bacteria, like Pseudomonas syringae and Xanthomonas campestris, use the type III secretion syste

83 In this study, OleA from Xanthomonas campestris was expressed in Escherichia coli

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

85 HfsA has sequence similarity to GumC from Xanthomonas campestris, which is involved in exopolysacc

86 such as Rhizobium meliloti (succinoglycan), Xanthomonas campestris (xanthan gum), and Salmonella ent

87 cterium carotovorum, Ralstonia solanacearum, Xanthomonas campestris, Xanthomonas oryzae, and Xylella

88 , several crystal structures of AOTCase from Xanthomonas campestris (xc) have been determined.

89 A genetic screen in the plant pathogen Xanthomonas campestris (Xcc) identified that XC_0250, wh

90 AGS-K) while it destabilized the NAGS-K from Xanthomonas campestris (XcNAGS-K).

91 idensis (sIDO) indoleamine 2,3-dioxygenases, Xanthomonas campestris (XcTDO) tryptophan 2,3-dioxygenas

92 , Erwinia chrysanthemi and carotovora (out), Xanthomonas campestris (xps), Pseudomonas aeruginosa (xc

93 nomeric tetratricopeptide repeat domain from Xanthomonas campestris YbgF, which is also able to trime