ライフサイエンスコーパス: Erwinia

1 robacter, and species of the plant pathogen, Erwinia.

2 in both blackleg and soft rotting species of Erwinia.

3 e 'missing link' between QS and virulence in Erwinia.

4 encoded by a gene with homology to hexA from Erwinia.

5 eudomonas syringae (the Delta CEL mutation), Erwinia amylovora (the dspA/E mutation), and Pantoea ste

6 ved between the E. coli cps promoter and the Erwinia amylovora ams promoter and previously shown to b

7 nce/avirulence proteins, including harpin of Erwinia amylovora and harpinPss of Pseudomonas syringae.

8 ocalization of type III effector proteins of Erwinia amylovora and Pseudomonas syringae pv. tomato al

9 nt pathogenic bacteria Pantoea stewartii and Erwinia amylovora are virulence factors in the cause of

10 The enterobacterial phytopathogen Erwinia amylovora causes fire blight, an invasive diseas

11 an 11.5-kb region of the hrp gene cluster of Erwinia amylovora containing hrpI, a previously characte

12 ogen and causal agent of fire blight disease Erwinia amylovora has not been studied previously.

13 to complementation groups II and III of the Erwinia amylovora hrp gene cluster was analyzed.

14 to the virulence of the fire blight pathogen Erwinia amylovora in host plants like apple (Malus x dom

15 The enterobacterium Erwinia amylovora is a devastating plant pathogen causin

16 (dsp) region next to the hrp gene cluster of Erwinia amylovora is required for pathogenicity but not

17 n antagonist to the bacterial plant pathogen Erwinia amylovora that causes fire blight, a devastating

18 The non-host HR to Erwinia amylovora was accompanied by a transient increas

19 Erwinia amylovora was shown to secrete DspE, a pathogeni

20 ertain phytopathogens (e.g., P. syringae and Erwinia amylovora) and are less well understood.

21 genus Erwinia (including the plant pathogen Erwinia amylovora) encode only the CobB(L) isoform.

22 pin (a protein from the pathogenic bacterium Erwinia amylovora).

23 nderstand the role of an orphan gene amyR in Erwinia amylovora, a functionally conserved ortholog of

24 e have identified and characterized TCSTs in Erwinia amylovora, a severe plant enterobacterial pathog

25 Harpins, such as HrpN of Erwinia amylovora, are extracellular glycine-rich protei

26 Harpin, the product of the hrpN gene of Erwinia amylovora, elicits the hypersensitive response a

27 Fire blight, caused by the bacterium Erwinia amylovora, is a devastating disease of apple (Ma

28 terica, Bacillus subtilis, Escherichia coli, Erwinia amylovora, Mycobacterium tuberculosis, and Geoba

29 om infection to occur, the causal bacterium, Erwinia amylovora, needs to increase its population size

30 ng plant pathogens include Dickeya dadantii, Erwinia amylovora, Pectobacterium carotovorum, Ralstonia

31 ergence of streptomycin-resistant strains of Erwinia amylovora, Pseudomonas spp., and Xanthomonas cam

32 ens Pseudomonas syringae pathovar tomato and Erwinia amylovora, respectively, and were more sensitive

33 Erwinia amylovora, the bacterium responsible for fire bl

34 d reduces the susceptibility of the scion to Erwinia amylovora, the causal agent of fire blight disea

35 determinants in the bacterial phytopathogen Erwinia amylovora, the cause of devastating fire blight

36 thogenic enterobacteria Dickeya dadantii and Erwinia amylovora.

37 nthetic operons of Klebsiella pneumoniae and Erwinia amylovora.

38 inhibition of the plant-pathogenic bacterium Erwinia amylovora.

39 or in the Gram-negative fire blight pathogen Erwinia amylovora.

40 plants caused by the Gram-negative bacterium Erwinia amylovora.

41 tacle can be overcome by the floral pathogen Erwinia amylovora.

42 s low with 8 genera identified, dominated by Erwinia and Paenibacillus.

43 The Erwinia and Pantoea branches still contain the complete

44 rtant plant pathogens in the genera Pantoea, Erwinia, and Pseudomonas.

45 o or silent inactivation of PEGasparaginase, Erwinia asparaginase (20 000 IU/m(2) 2-3 times weekly) w

46 AALL07P2 evaluated whether substitution of Erwinia asparaginase 25000 IU/m(2) for 6 doses given int

47 Following allergy to pegaspargase, Erwinia asparaginase 25000 IU/m(2) x 6 intramuscularly M

48 Erwinia asparaginase administered with this schedule ach

49 evel was not always completely depleted with Erwinia asparaginase in contrast to PEGasparaginase.

50 chia coli asparaginase (PEGasparaginase) and Erwinia asparaginase in pediatric acute lymphoblastic le

51 Switching to Erwinia asparaginase leads to effective asparaginase lev

52 Fifty-nine patients were included in the Erwinia asparaginase study; 2 (3%) developed an allergy

53 Erwinia asparaginase was used in case of clinical hypers

54 easured), 36 (72.0%) were subsequently given Erwinia asparaginase; seven (19.4%) reacted to this prep

55 mic placement of the enteric plant pathogens Erwinia, Brenneria, Pectobacterium, and Pantoea.

56 susceptibility to the necrotrophic bacteria Erwinia caratovora pv.

57 tic genes to ensure 'self-resistance' in the Erwinia carbapenem producer.

58 The Erwinia carotorova carA, carB, and carC gene products ar

59 AHL controls exoprotein production in Erwinia carotovora and consequently the virulence for pl

60 applied to the study of interactions between Erwinia carotovora and different generations of dendrigr

61 t SgrS homologs from Salmonella typhimurium, Erwinia carotovora and Klebsiella pneumoniae rescue E. c

62 coli yaeT to enable Stx phage adsorption to Erwinia carotovora and the phage adsorption patterns of

63 cal genes, and genes potentially encoding an Erwinia carotovora carotovoricin Er-like bacteriocin.

64 Erwinia carotovora produces the beta-lactam antibiotic,

65 The plant pathogens Erwinia chrysanthemi and Erwinia carotovora secrete extra-cellular pectate lyases

66 The plant pathogens Erwinia chrysanthemi and Erwinia carotovora secrete several isozymes of pectate l

67 In the Gram-negative phytopathogen, Erwinia carotovora ssp. atroseptica (Eca) virulence depe

68 rotovora (Ecc) and virulence and motility in Erwinia carotovora ssp. atroseptica (Eca).

69 lence factor synthesis in the plant pathogen Erwinia carotovora ssp. carotovora (Ecc) and virulence a

70 rratia sp. ATCC 39006 and the plant pathogen Erwinia carotovora ssp. carotovora (Ecc), the biosynthes

71 The enterobacterium Erwinia carotovora ssp. carotovora strain 71 (hereafter

72 The production of pectin lyase (Pnl) in Erwinia carotovora ssp. carotovora strain 71 is induced

73 re of the 40-kDa endo-polygalacturonase from Erwinia carotovora ssp. carotovora was solved by multipl

74 e include important plant pathogens, such as Erwinia carotovora subsp. atroseptica (Eca), the first p

75 (the elicitor of hypersensitive reaction) in Erwinia carotovora subsp. carotovora is regulated by Rsm

76 Erwinia carotovora subsp. carotovora produces an array o

77 Erwinia carotovora subsp. carotovora produces extracellu

78 , disease severity by the bacterial pathogen Erwinia carotovora subsp. carotovora was significantly r

79 ular protein production and pathogenicity in Erwinia carotovora subsp. carotovora.

80 uction and pathogenicity in soft rot-causing Erwinia carotovora subsp. carotovora.

81 nzymes, rsmB RNA, motility, and virulence of Erwinia carotovora subsp. carotovora.

82 virulence determinants in the phytopathogen, Erwinia carotovora subspecies carotovora.

83 acyl homoserine lactone (AHL) is required by Erwinia carotovora subspecies for the expression of vari

84 In Erwinia carotovora subspecies, N-acyl homoserine lactone

85 family 5 glycosyl hydrolases from Bacillus, Erwinia carotovora, and C. acetobutylicum species.

86 Klebsiella pneumoniae, Serratia marcescens, Erwinia carotovora, and Proteus vulgaris but not in seve

87 Klebsiella pneumoniae, Serratia marcescens, Erwinia carotovora, and Proteus vulgaris, strongly sugge

88 cteria, including Pseudomonas aeruginosa and Erwinia carotovora, both significant pathogens.

89 sis of the pigment in the heterologous host, Erwinia carotovora, demonstrating, for the first time, t

90 s similar to Pels from Nectria haematococca, Erwinia carotovora, Erwinia chrysanthemi, and Bacillus s

91 In the gamma-proteobacterium Erwinia carotovora, genes common to phosphonate biosynth

92 Strain GS101 of the bacterial phytopathogen, Erwinia carotovora, makes the simple beta-lactam antibio

93 grobacterium tumefaciens, Pantoea stewartii, Erwinia carotovora, Ralstonia solanacearum, Pseudomonas

94 plant cell wall by the pathogenic bacterium Erwinia carotovora.

95 condary metabolites are regulated by rsmA in Erwinia carotovora.

96 ous observations on the homologous system in Erwinia carotovora.

97 onsible for production of this carbapenem in Erwinia carotovora.

98 aft poly-L-lysines on Micrococcus luteus and Erwinia carotovora.

99 member ELIC, a cysteamine-gated channel from Erwinia chrisanthemi, a structural model of the protein

100 Removal of these genes from the Erwinia chromosome results in a carbapenem-sensitive phe

101 n of exoenzymes), is a close relative of the Erwinia chrysanthemi (Echr) gene pecT and encodes a memb

102 rystal structure of a bacterial homolog from Erwinia chrysanthemi (ELIC) agrees with previous structu

103 The ligand-gated ion channel from Erwinia chrysanthemi (ELIC) is a prokaryotic homolog of

104 annels from Gloeobacter violaceus (GLIC) and Erwinia chrysanthemi (ELIC), whose crystal structures ar

105 Both the Escherichia coli (EcAII) and Erwinia chrysanthemi (ErAII) type II ASNases currently u

106 ously reported homologous enzyme, XynA, from Erwinia chrysanthemi and analyzes the ligand binding sit

107 s a similar structural topology as Pels from Erwinia chrysanthemi and Bacillus subtilis.

108 pe II systems from Klebsiella oxytoca (pul), Erwinia chrysanthemi and carotovora (out), Xanthomonas c

109 PelC is secreted by the plant pathogen Erwinia chrysanthemi and degrades the pectate component

110 The plant pathogens Erwinia chrysanthemi and Erwinia carotovora secrete extr

111 The plant pathogens Erwinia chrysanthemi and Erwinia carotovora secrete seve

112 to genes encoding protease export systems in Erwinia chrysanthemi and Pseudomonas aeruginosa.

113 sequence showed 40% identity with PelE from Erwinia chrysanthemi and the pectate lyase from Glomerel

114 ally homologous to the C terminus of PelB of Erwinia chrysanthemi belonging to family 1 of pectate ly

115 We report that the type III machinery of Erwinia chrysanthemi cloned in Escherichia coli recogniz

116 1,4-xylan hydrolase (xylanase A) produced by Erwinia chrysanthemi D1 isolated from corn was analyzed

117 The Erwinia chrysanthemi dsbC gene was identified in a previ

118 ations were introduced into the pelC gene of Erwinia chrysanthemi EC16 that directed single or double

119 erichia coli B, Klebsiella oxytoca M5A1, and Erwinia chrysanthemi EC16.

120 ng gene tolC in the bacterial plant pathogen Erwinia chrysanthemi EC16.

121 The structure of the Erwinia chrysanthemi enzyme was solved by multiple isomo

122 specificity and the processive action of the Erwinia chrysanthemi enzyme.

123 C 3.2.1.8) from the bacterial plant pathogen Erwinia chrysanthemi expressed in Escherichia coli, a 45

124 Genes homologous to Escherichia coli and Erwinia chrysanthemi glucuronate and galacturonate metab

125 mensional structure of shikimate kinase from Erwinia chrysanthemi has been determined by multiple iso

126 ted our recently described structures of the Erwinia chrysanthemi l-asparaginase (ErA) to inform the

127 ution crystal structures of the complexes of Erwinia chrysanthemi L-asparaginase (ErA) with the produ

128 we report the x-ray crystal structure of the Erwinia chrysanthemi ligand-gated ion channel (ELIC) in

129 ptors, ion channels from prokaryote homologs-Erwinia chrysanthemi ligand-gated ion channel (ELIC), Gl

130 By comparison with the structure of Erwinia chrysanthemi pectate lyase C (PelC), the primary

131 Ca(2+) is essential for in vitro activity of Erwinia chrysanthemi pectate lyase C (PelC).

132 The structure and function of Erwinia chrysanthemi pectate lysase C, a plant virulence

133 Erwinia chrysanthemi produces a battery of hydrolases an

134 w that l-ases from both Escherichia coli and Erwinia chrysanthemi profoundly inhibit mTORC1 and prote

135 (typified by Escherichia coli HlyBD/TolC or Erwinia chrysanthemi PrtDEF) that utilize C-terminal sec

136 al structure of MtSK (this work) and that of Erwinia chrysanthemi SK suggest a concerted conformation

137 te in a community annotation project for the Erwinia chrysanthemi strain 3937 genome.

138 elicitor harpin (HrpN) of soft rot pathogen Erwinia chrysanthemi strains 3937 and EC16 is secreted v

139 carried on cosmid pCPP2156, was cloned from Erwinia chrysanthemi, a pathogen that differs from P. sy

140 trates in the enzymatic activity of PME from Erwinia chrysanthemi, a processive enzyme that catalyzes

141 om Nectria haematococca, Erwinia carotovora, Erwinia chrysanthemi, and Bacillus subtilis, and a purif

142 We found that ELIC, a pLGIC from Erwinia chrysanthemi, can be functionally inhibited by i

143 the pentameric ligand-gated ion channel from Erwinia chrysanthemi, is a prototype for Cys-loop recept

144 When modeled based on pectate lyase C of Erwinia chrysanthemi, the RHbetaH of AlgG has a long sha

145 Here, we demonstrate that Erwinia chrysanthemi, which does not carry curli genes,

146 resembles that of pehX, an exo-PG gene from Erwinia chrysanthemi, with 47.2% identity at the amino a

147 mophilus influenzae, Pseudomonas aeruginosa, Erwinia chrysanthemi, Yersinia pseudotuberculosis, Vibri

148 rticular the cbr locus of the plant pathogen Erwinia chrysanthemi.

149 se produced by Escherichia coli (ASNase) and Erwinia chrysanthemi.

150 the GH 5 endoxylanase secreted by strains of Erwinia chrysanthemi.

151 m, and negatively regulated by HexA (PecT in Erwinia chrysanthemi; LrhA [LysR homolog A] in Escherich

152 some proteins, such as the tetrameric enzyme Erwinia chrysanthemil-asparaginase (ErA), in which case

153 SirA orthologs in Pseudomonas, Vibrio, and Erwinia control the expression of distinct virulence gen

154 ion of four desaturations to lycopene by the Erwinia CrtI appears to require the absence of CrtC and,

155 ed DGC genes in E. amylovora (edc genes, for Erwinia diguanylate cyclase), edcA, edcC, and edcE, are

156 of Salmonella as well as within Citrobacter, Erwinia, Escherichia, Photorhabdus, and Yersinia species

157 We have mapped and sequenced the Erwinia genes encoding carbapenem production and have cl

158 id containing the carotenoid gene cluster in Erwinia herbicola and cloned into an Escherichia coli ex

159 Both E. coli and Erwinia herbicola possess ATCase holoenzymes which are d

160 Strains of the bacteria Erwinia herbicola produce antibiotics that effectively c

161 esaturase (CrtI) with the 4-step enzyme from Erwinia herbicola results in significant flux down the s

162 dependent: the effect was more pronounced in Erwinia herbicola than in Escherichia coli.

163 nvolved in indoleacetic acid biosynthesis in Erwinia herbicola, among individual cells on plants to g

164 eria Escherichia coli, Enterobacter cloacae, Erwinia herbicola, and Salmonella typhimurium.

165 In Erwinia herbicola, this plasmid brings about the accumul

166 The Erwinia hoeEr (homologue of rap) and the Yersinia horYe

167 Enterobacteriaceae, but species of the genus Erwinia (including the plant pathogen Erwinia amylovora)

168 which are similar to GSP genes of Aeromonas, Erwinia, Klebsiella, Pseudomonas, and Xanthomonas spp.

169 eterminants of chlorpromazine binding in the Erwinia ligand-gated ion channel (ELIC).

170 of two prokaryotic homologs, Gloebacter and Erwinia ligand-gated ion channel (GLIC and ELIC, respect

171 to, two proteins exported by the recombinant Erwinia machine, can also be secreted by the Yersinia ty

172 In the Gram-negative enterobacterium Erwinia (Pectobacterium) and Serratia sp. ATCC 39006, in

173 Erwinia persicinus was first described in 1990 after bei

174 e, we report that Lyz(103), the endolysin of Erwinia phage ERA103, is also a SAR endolysin.

175 nera of Gram-negative bacteria, Serratia and Erwinia, produce a beta-lactam antibiotic, 1-carbapen-2-

176 n signal molecules of Vibrio, Agrobacterium, Erwinia, Pseudomonas, and Burkholderia spp.

177 of E. persicinus is most similar to those of Erwinia rhapontici, Pantoea agglomerans, and Enterobacte

178 nd rsmB expression in these plant pathogenic Erwinia species is controlled by RsmC or a functional ho

179 component of the Csr system is CsrB (AepH in Erwinia species), a non-coding RNA molecule that forms a

180 dicated that hrpW is conserved among several Erwinia species, and hrpW, provided in trans, enhanced t

181 n referred to as CsrA or, in phytopathogenic Erwinia species, RsmA (repressor of stationary phase met

182 ent here that plant pathogenic and epiphytic Erwinia species, such as E. amylovora; E. carotovora sub

183 omologs of rsmB(Ecc) in non-soft-rot-causing Erwinia species, we cloned the rsmB genes of E. amylovor

184 nition factors in the Out systems of the two Erwinia species.

185 Xanthomonas spp., Ralstonia solanacearum and Erwinia species.

186 enesis factors in Pseudomonas aeruginosa and Erwinia spp., as well as T1 plasmid conjugal transfer in

187 d phytoene synthase, from the soil bacterium Erwinia stewartii, and the two carotene desaturases phyt

188 (T), phenobarbital, and bacterial pathogens (Erwinia stuartii, Acidovorax avenae), we have analyzed t

189 e regulator) family, which has been shown in Erwinia to regulate the expression of virulence genes.

190 at the beetle-transmitted bacterial pathogen Erwinia tracheiphila - which causes a fatal wilt disease

191 introducing this psy in combination with the Erwinia uredovora carotene desaturase (crtI) used to gen

192 reus and the C40 carotene synthase CrtB from Erwinia uredovora were swapped into their respective for

193 closely related plant pathogens of the genus Erwinia, which expressed CheAL and CheZ but not CheAs.