ライフサイエンスコーパス: Erwinia

1 in both blackleg and soft rotting species of Erwinia.

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

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

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

5 The fire blight pathogen, Erwinia amylovora (EA), causes significant economic loss

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

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

8 ved AvrE-family effectors, including DspE in Erwinia amylovora and AvrE in Pseudomonas syringae, have

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

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

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

12 and Bacillus subtilis and the apple pathogen Erwinia amylovora by direct detection on HPTLC plates an

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

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

15 ere, we report that the fire blight pathogen Erwinia amylovora enters apple leaves through naturally

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

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

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

19 The enterobacterium Erwinia amylovora is a devastating plant pathogen causin

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

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

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

23 Erwinia amylovora was shown to secrete DspE, a pathogeni

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

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

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

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

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

29 activity against Agrobacterium tumefaciens, Erwinia amylovora, and Pectobacterium atrosepticum by me

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

31 tive can recognize the AvrRpt2 effector from Erwinia amylovora, but the details of this recognition r

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

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

34 t, a devastating bacterial disease caused by Erwinia amylovora, is a priority for apple breeding prog

35 light, caused by the bacterial phytopathogen Erwinia amylovora, is an economically important and mech

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

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

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

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

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

41 Erwinia amylovora, the bacterium responsible for fire bl

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

43 Erwinia amylovora, the causative agent of fire blight di

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

45 onella enterica, Pseudomonas aeruginosa, and Erwinia amylovora, these phages are of interest for phag

46 nthetic operons of Klebsiella pneumoniae and Erwinia amylovora.

47 se of apple and pear caused by the bacterium Erwinia amylovora.

48 the transmission of the fire blight pathogen Erwinia amylovora.

49 inhibition of the plant-pathogenic bacterium Erwinia amylovora.

50 thogenic enterobacteria Dickeya dadantii and Erwinia amylovora.

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

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

53 different strains of the causative pathogen-Erwinia amylovora.

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

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

56 The Erwinia and Pantoea branches still contain the complete

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

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

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

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

61 n, patients were started with 20,000 IU/m(2) Erwinia asparaginase 3 times per week, and l-asparagine

62 Erwinia asparaginase administered with this schedule ach

63 ysanthemi [recombinant]-rywn), a recombinant Erwinia asparaginase derived from a novel expression pla

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

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

66 Switching to Erwinia asparaginase leads to effective asparaginase lev

67 uM in 96% and 67% of the PEGasparaginase and Erwinia asparaginase levels > 100 IU/L, respectively.

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

69 chia coli asparaginase (PEGasparaginase) and Erwinia asparaginase treatment of pediatric acute lympho

70 Erwinia asparaginase was used in case of clinical hypers

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

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

73 scribed PEG-ASNase doses versus switching to Erwinia but receiving all doses versus not receiving all

74 susceptibility to the necrotrophic bacteria Erwinia caratovora pv.

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

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

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

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

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

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

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

82 intestinal lumen, pathogenic strains such as Erwinia carotovora or Bacillus thuringiensis, are blocke

83 Erwinia carotovora produces the beta-lactam antibiotic,

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

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

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

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

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

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

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

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

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

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

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

95 Erwinia carotovora subsp. carotovora produces an array o

96 Erwinia carotovora subsp. carotovora produces extracellu

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

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

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

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

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

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

103 In Erwinia carotovora subspecies, N-acyl homoserine lactone

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

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

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

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

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

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

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

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

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

113 plant cell wall by the pathogenic bacterium Erwinia carotovora.

114 condary metabolites are regulated by rsmA in Erwinia carotovora.

115 ous observations on the homologous system in Erwinia carotovora.

116 onsible for production of this carbapenem in Erwinia carotovora.

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

118 ved co-crystal structures of the prokaryote (Erwinia) channel ELIC bound either to a positive or a ne

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

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

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

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

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

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

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

126 efficacy and safety of JZP458 (asparaginase erwinia chrysanthemi [recombinant]-rywn), a recombinant

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

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

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

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

131 The plant pathogens Erwinia chrysanthemi and Erwinia carotovora secrete extr

132 The plant pathogens Erwinia chrysanthemi and Erwinia carotovora secrete seve

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

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

135 Erwinia chrysanthemi ASNase (Erwinia) substitution was a

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

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

138 1,4-xylan hydrolase (xylanase A) produced by Erwinia chrysanthemi D1 isolated from corn was analyzed

139 The Erwinia chrysanthemi dsbC gene was identified in a previ

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

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

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

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

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

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

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

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

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

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

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

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

152 ly reported for the prokaryotic homolog, the Erwinia chrysanthemi ligand-gated ion channel (ELIC).

153 conserved in homomeric GABA(A)Rs and in the Erwinia chrysanthemi ligand-gated ion channel and may be

154 n suggested that the bacterial homolog ELIC (Erwinia chrysanthemi ligand-gated ion channel) has a sim

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

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

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

158 Erwinia chrysanthemi produces a battery of hydrolases an

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

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

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

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

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

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

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

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

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

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

169 ae, Burkholderia glumae, Xanthomonas oryzae, Erwinia chrysanthemi, Pseudomonas syringae, and Acidovor

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

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

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

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

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

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

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

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

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

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

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

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

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

183 rious biofilm forming plant pathogens of the Erwinia family.

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

185 Erwinia has, however, been intermittently unavailable be

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

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

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

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

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

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

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

193 In Erwinia herbicola, this plasmid brings about the accumul

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

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

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

197 rentially binds to and stabilizes the pLGIC, Erwinia ligand-gated ion channel (ELIC), and decreases E

198 pentameric ligand-gated ion channel (pLGIC), Erwinia ligand-gated ion channel (ELIC), in different na

199 ed charge reduction in the membrane protein, Erwinia ligand-gated ion channel (ELIC).

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

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

202 We demonstrate that the model pLGIC, ELIC (Erwinia ligand-gated ion channel), is positively modulat

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

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

205 Erwinia persicinus was first described in 1990 after bei

206 Here we show that Erwinia phage Asesino, one member of this PhuZ-less clad

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

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

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

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

211 esults illustrate the severe consequences of Erwinia shortages.

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

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

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

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

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

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

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

219 Xanthomonas spp., Ralstonia solanacearum and Erwinia species.

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

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

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

223 The impact of Erwinia substitution or complete ASNase discontinuation

224 Patients with Erwinia substitution who completed subsequent courses we

225 Erwinia chrysanthemi ASNase (Erwinia) substitution was approved in 2011 for allergic

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

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

228 Erwinia tracheiphila is a bacterial plant pathogen that

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

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

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