ライフサイエンスコーパス: elicitor

1 veral pathogen-associated molecules (general elicitors).

2 es of H. calycinum after the addition of the elicitor.

3 calcium signalling in response to cryptogein elicitor.

4 nzofuran-3-one) as a major response to yeast elicitor.

5 and cell death responses to cell wall glucan elicitor.

6 zae pv. oryzae strains producing the AvrXa21 elicitor.

7 g that virion structural proteins act as the elicitor.

8 d in OcXII RNAi plants subjected to a fungal elicitor.

9 the biosynthetic pathways switched on by the elicitor.

10 served after treatment with each the abiotic elicitor.

11 dants, which can be improved in plants using elicitors.

12 hich its expression was induced by microbial elicitors.

13 arkably little about the diversity of immune elicitors.

14 bon-based defence production and response to elicitors.

15 edlings were observed between MeJA and other elicitors.

16 patterns seen in the few well-characterized elicitors.

17 enous peptide elicitors and pathogen-derived elicitors.

18 rk that decreases gut permeability to immune elicitors.

19 t-insect interactions by triggering salivary elicitors.

20 molecular patterns and in plants are called elicitors.

21 line upon challenge with multiple microbial elicitors.

22 in animals) in response to one of three PCD elicitors.

23 e structurally distinct from natural defense elicitors.

24 onse (HR) to C. fulvum-derived race-specific elicitors.

25 ugh the manipulation of growth conditions by elicitors.

26 icotiana tabacum) leaves treated with fungal elicitors.

27 e structurally distinct from natural defense elicitors.

28 f prenylated stilbenoids upon treatment with elicitors.

29 e exogenous application of chemical inducers/elicitors.

30 activated when plant NLRs recognize non-self elicitors.

31 oids, respectively, in response to microbial elicitors.

32 ng silent gene clusters using small molecule elicitors.

33 The P. sojae cell wall glucan elicitor, a potent elicitor of 5-deoxyisoflavonoids, tri

34 Most studies indicate that microbial elicitors activate the PO cascade, which results in proc

35 ellin and elongation factor EF-Tu (and their elicitor-active epitopes flg22 and elf18), respectively.

36 P1 RECEPTOR1 (PEPR1) and PEPR2 recognize the elicitor-active Pep epitopes conserved in Arabidopsis EL

37 (Arabidopsis thaliana), the receptor for the elicitor-active peptide epitope of bacterial flagellin,

38 remain unknown, the unpredictable nature of elicitor activity between plant species supports the exi

39 Critical to their elicitor activity is their display by the pathogen.

40 Vu-In(DeltaV); +ICDINGVCVDV-) retaining full elicitor activity was found to accumulate in VBC OS.

41 o investigate the phylogenic distribution of elicitor activity, we tested representatives from three

42 trypsin cleavage site rapidly lost OS-based elicitor activity.

43 structure of these proteins abolishes their elicitor activity.

44 idea that protease activity is necessary for elicitor activity.

45 i [corrected] plants treated with the fungal elicitor alamethicin, showing that they are also formed

46 etic pathways that are inducible by a fungal elicitor, alamethicin.

47 Moreover, the application of the yeast elicitor also enhanced grape stilbene content.

48 The application of the tested elicitor also influenced the chemical composition of bas

49 s) MPK3 and MPK6 after treatment with AOS or elicitor and is necessary for at least two very differen

50 xpression of AtLYK3 is strongly repressed by elicitors and fungal infection and is induced by the hor

51 Many strains produce elicitors and induce resistance in plants through coloni

52 ore oral secretions and fatty acid conjugate elicitors and is accompanied by a rapid transcriptional

53 mers may be similarly biologically active as elicitors and may help to reinforce the perception of da

54 that is typical of other endogenous peptide elicitors and pathogen-derived elicitors.

55 tion proposes a new approach for identifying elicitors and pathogenic factors.

56 reactive oxygen species (ROS) in response to elicitors and pathogens.

57 s, and responded to a wide range of pathogen elicitors and phytohormones.

58 Proteomic analysis of ECB salivary elicitors and plant receptors/signaling mechanisms invol

59 ulates the expression of genes responding to elicitors and plays an important role in pathogen defenc

60 applications of such compounds as efficient elicitors and reporters of nucleotide exchange.

61 dase activity in the presence of a number of elicitors and retains structural and functional integrit

62 wild and cultivated hosts of CPB by chemical elicitors and their symbiotic bacteria.

63 and allows a comparison of symptom patterns, elicitors and treatment habits between referral centres

64 Occurrence, elicitors and treatment of severe allergic reactions are

65 lants induced an HR in the absence of fungal elicitors and were designated auto-activators.

66 the oxidative burst in response to a fungal elicitor, and cause enhanced susceptibility to a broad r

67 re strongly affected by concentration of the elicitor, and time and intervals of its application.

68 e overcome by salient environmental response elicitors, and extends this notion by showing that D1 re

69 Elicitor application constitutes an interesting field of

70 lity of lettuce caused by different chemical elicitors: arachidonic acid (AA), jasmonic acid (JA), an

71 Synthetic elicitors are drug-like compounds that are structurally

72 Synthetic elicitors are drug-like compounds that induce plant immu

73 The most prevalent elicitors are fatty acid amides consisting of 18-carbon

74 usters, but also reveal that the majority of elicitors are themselves antibiotics, most in common cli

75 ion an autoinhibited state in the absence of elicitor as well as for the subsequent elicitor-induced

76 PTI1-2 is activated by the same stresses/elicitors as OXI1 and additionally flagellin.

77 The effect of elicitors associated with host defence on betacyanin acc

78 All elicitors at medium and high concentrations reduced the

79 orphyrin IX, and the hypersensitive response elicitor AvrRpt2.

80 tudy, we used representative danger signals (elicitors) belonging to the classes of the damage- and p

81 ld be induced by application of the chemical elicitor beta-amino butyric acid, the non-pathogenic bac

82 In rice (Oryza sativa), the chitin elicitor binding protein (CEBiP) recognizes chitin oligo

83 e LysM-containing protein, CEBiP (for chitin elicitor-binding protein), was shown to be involved in c

84 athway gene transcripts in response to yeast elicitor, but not MJ, and differential induction by the

85 Sucrose, identified as the most effective elicitor by principal component analysis, induced a sign

86 f Eschscholzia californica react to a fungal elicitor by the overproduction of antimicrobial benzophe

87 y to insects may involve early perception of elicitors by cell surface-localized PRRs, leading to sub

88 We then validated selected candidate elicitors by showing that they induce Arabidopsis thalia

89 we partially purified a novel proteinaceous elicitor called sclerotinia culture filtrate elicitor1 (

90 (PTI), which is triggered by recognition of elicitors called microbe-associated molecular patterns (

91 mmunity (PTI) is triggered by recognition of elicitors called microbe-associated molecular patterns (

92 potential microbial pathogens by recognizing elicitors called PAMPs.

93 refore, we hypothesized that novel bacterial elicitors can be identified through these opposing force

94 sistance and non-host responses or following elicitor challenges.

95 shown to be induced by the fungal cell wall elicitor chitin.

96 al and guard cells in response to the fungal elicitor chitin.

97 families examined responded to at least one elicitor class with significant increases in E and JA pr

98 tested representatives from three different elicitor classes on the time course of defense-related p

99 Some of the elicitor concentrations used also caused an increase in

100 In 13 patients (10.5%), no elicitor could be identified.

101 Therefore, treatment with elicitors could be a useful tool for improving the healt

102 bility is that immune priming with microbial elicitors could stimulate immune protection against subs

103 The fungal elicitor cryptogein triggers a light-dependent hypersens

104 s syringae pv. tomato DC3000 and the general elicitor cryptogein-induced cell death.

105 ty was not sufficient because we found three elicitor-defective mutants in which there was a high lev

106 sis thaliana, AtSERK3/BAK1 rapidly enters an elicitor-dependent complex with FLAGELLIN SENSING 2 (FLS

107 ferent elicitors produced concentration- and elicitor-dependent specific changes in the content of al

108 ave been identified as peptides, but peptide elicitors derived from the plant itself that activate de

109 mpose strong positive selective pressure for elicitor diversification to avoid host recognition.

110 nt model for studying the action of numerous elicitors, E and JA exist as highly conserved and readil

111 on by anthocyanins was stimulated by abiotic elicitors, except for JA-sample.

112 0muM), JA (250muM) and MET (10mM) before the elicitor exogenous treatment.

113 e activation with Arabidopsis upon bacterial elicitor flagellin perception.

114 d to signal from perception of the bacterial elicitor flagellin to the activation of basal defence-re

115 Arabidopsis cells treated with the bacterial elicitor flagellin.

116 Furthermore, the elicitor food (adjusted OR = 0.29; 95% CI, 0.21-0.41, P

117 PS A1 motif was included to act as an MHCII elicitor for a T-cell-dependent immune response with inc

118 es are specific and activated in plants when elicitors, frequently found in the herbivores' oral secr

119 AtPep1 is a 23-aa endogenous peptide elicitor from Arabidopsis leaves that signals the activa

120 Moreover, if the wall glucan elicitor from Phytophthora sojae was present during lact

121 nding or treatment with the cell wall glucan elicitor from Phytophthora sojae.

122 In rowan cell cultures treated with elicitor from the scab fungus, transient increases in th

123 Conversely, pSMV-G7d gained the elicitor function of Rsv1-mediated LSHR by a single amin

124 (V to M) and 953 (K to E) abolished pSMV-G7 elicitor function, provoking Rsv1-mediated SHR.

125 meras containing only P3 of SMV-G7d lost the elicitor function, while the reciprocal chimera of pSMV-

126 15 did not influence the loss or gain of the elicitor function.

127 (pSMV-G7) and SMV-G7d (pSMV-G7d), and their elicitor functions were assessed on PI 96983 (Rsv1).

128 ed by the perception of herbivore associated elicitors (HAE) that includes transient accumulations of

129 The hypersensitive response elicitor harpin (HrpN) of soft rot pathogen Erwinia chry

130 Some plant pathogen-derived elicitors have been identified as peptides, but peptide

131 Caeliferins are nonlepidopteran elicitors identified in insect herbivores.

132 The presence of an elicitor in S. sclerotiorum evoking MAMP-triggered immun

133 e hypothesis with the recognition of general elicitors in a single model.

134 The application of elicitors in bean seed during sprouting enhances their n

135 ioassay methods to determine the role of ECB elicitors in modulating defenses in both tomato and maiz

136 ere used to examine the role of the salivary elicitors in modulating gene expression.

137 Cow's milk and hen's egg were prevalent elicitors in the first 2 years, hazelnut and cashew in p

138 In response to elicitors in the oral secretions of caterpillars, plants

139 IR-NB-ARC portion is sufficient to induce an elicitor-independent cell death.

140 induced by certain phytohormones and fungal elicitors, indicating the involvement of a complex trans

141 Aphid-derived elicitors induce expression of PHYTOALEXIN DEFICIENT3 (P

142 licylic acid, hydrogen peroxide and a fungal elicitor induced PICBP expression in bean.

143 In contrast, both elicitors induced genes encoding enzymes for conversion

144 ce of elicitor as well as for the subsequent elicitor-induced activation.

145 The fungal elicitor-induced ELI12 gene from parsley has been previo

146 fferential tissue-specific and infection- or elicitor-induced expression, but not always in parallel

147 ugh its interaction with the LRR, translates elicitor-induced modulations of the C terminus into a si

148 Notably, ANPs are also required for both the elicitor-induced oxidative burst and the transduction of

149 te the genetic and biochemical regulation of elicitor-induced p-coumaraldehyde accumulation in plants

150 Elicitor-induced plant volatiles can function as attract

151 Treatment with herbivore or jasmonate elicitors induces emission of (E)-alpha-bergamotene in w

152 ouble knockdown of CYP76M7 and -8 suppresses elicitor inducible phytocassane production, indicating a

153 uced by non-host flagellins and the oomycete elicitor INF1.

154 that the EcNHX1 antiporter functions in the elicitor-initiated expression of alkaloid biosynthetic g

155 the activation of defenses by converting an elicitor into an antagonist effector and identify an ami

156 tection in maize and that the functional Sm1 elicitor is required for this activity.

157 The present study indicates that age, the elicitor itself and the presence of atopic diseases have

158 essing the mechanism of induction by the two elicitors led to the identification of a pathway-specifi

159 terns (DAMPs) was proposed to describe plant elicitors like oligogalacturonides (OGs), which can be d

160 terial pathogen-associated molecular pattern elicitor lipopolysaccharide activates a CNGC Ca(2+) curr

161 Elicitor-mediated folate enhancement also imparted reduc

162 BAK1 is required for GPA elicitor-mediated induction of reactive oxygen species a

163 ulated herbivory with the well-known defense elicitor methyl jasmonate (MeJA) to young leaves of Arab

164 e was to optimize the treatment doses of the elicitors: methyl jasmonate (MeJA), jasmonic acid (JA) a

165 present experiment, chitosan was used as an elicitor molecule to improve the phytochemical content o

166 luated the role of European corn borer (ECB) elicitors (molecules secreted by herbivores) that either

167 n vitro biosynthesis of the fatty acid amide elicitor, N-linolenoyl-l-glutamine, by microsomal fracti

168 d inhibition of seedling growth by the flg22 elicitor occurred normally in the Y610F-directed mutant.

169 athways induced by systemin, oligosaccharide elicitors (OEs), and ultraviolet (UV)-B radiation share

170 P. sojae cell wall glucan elicitor, a potent elicitor of 5-deoxyisoflavonoids, triggered a cell death

171 agweed (Ambrosia artemisiifolia) is a strong elicitor of allergic airway inflammation with worldwide

172 most important allergen sources and a major elicitor of allergic asthma.

173 hylaxis Registry confirmed food as the major elicitor of anaphylaxis in children, specifically hen's

174 abaci, or flg22 (a flagellin-derived peptide elicitor of basal resistance).

175 show here that the response to flagellin, an elicitor of basal resistance, is unaltered in srfr1-1.

176 lthough the amino acid glutamine is a potent elicitor of GLP-1 secretion, the responsible mechanism r

177 of Gram-negative peptidoglycan, is a potent elicitor of innate immune responses in Drosophila.

178 that human cytomegalovirus (CMV) is a potent elicitor of interferon-stimulated gene (ISG) expression.

179 Acute ozone is a model abiotic elicitor of oxidative stress and a useful tool for under

180 lg22 flagellin peptide, a well-characterized elicitor of plant basal immunity, did not induce closure

181 nase (Eix) of Trichoderma viride is a potent elicitor of plant defense responses in specific cultivar

182 hito-octamer is an important oligosaccharide elicitor of plant defenses.

183 treated with methyl jasmonate, a well-known elicitor of plant specialized metabolism.

184 mies: LA is a key component of volicitin, an elicitor of plant-volatile-signaling defenses.

185 To identify the elicitor of Rsv1-mediated LSHR, chimeras were constructe

186 uggest that strain-specific P3 of SMV is the elicitor of Rsv1-mediated LSHR.

187 ate (MeJA) treatment, which is considered an elicitor of secondary metabolites, and identified 388 ca

188 Fish is a frequent elicitor of severe IgE-mediated allergic reactions.

189 itively establishes TCT as the long-distance elicitor of systemic immune responses to intestinal bact

190 uced by an invading pathogen could act as an elicitor of the broad physiological and transcriptional

191 tification of the CMV 2a gene product as the elicitor of the necrosis response.

192 nclusion a protease (NIaPro) from PVY is the elicitor of the Ry-mediated resistance and that integrit

193 osophila antibacterial response, is also the elicitor of this behavioral change.

194 ccharides of attacking pathogens and release elicitors of additional plant defenses.

195 ed that subtle reciprocal cues remain potent elicitors of altruism, whereas a fourth study with presc

196 Elicitors of anaphylactic reactions are any sources of p

197 mologous in structure and described as major elicitors of anaphylactic reactions to peanut (allergens

198 sphingolipids, and lipid-binding proteins as elicitors of defense response.

199 The elicitors of immune responses in the nematode Caenorhabd

200 Administration of LPS or CpG, known elicitors of innate immune defense, reduced the loads of

201 g triggered by cryptogein and flagellin, two elicitors of plant defense reactions.

202 primary contributions involved race-specific elicitors of plant defenses and bacterial pectic enzymes

203 adds a category of insect herbivore-produced elicitors of plant responses, providing further evidence

204 ot MJ, and differential induction by the two elicitors of sets of genes encoding transcription factor

205 ur data show that food products are frequent elicitors of severe allergic reactions in the general po

206 pproach ("HiTES") to discover small molecule elicitors of silent biosynthetic gene clusters.

207 ther when the nucleotides are added with the elicitor oligogalacturonic acid.

208 effect of the application of three different elicitors on both grape and wine phenolic content.

209 the effects of benzothiadiazole and chitosan elicitors on content of sterols in grapes and their leve

210 However, research about the effect of elicitors on grape amino acid content is scarce.

211 phytoalexin medicarpin in response to yeast elicitor or methyl jasmonate (MJ), accompanied by decrea

212 ither directly by perception of pest-derived elicitors or indirectly through resistance protein recog

213 pathogen secretory proteins are known to be elicitors or pathogenic factors,which play an important

214 mediated by the tobacco mosaic virus defense elicitor p50.

215 f active fragments from a general resistance elicitor (pathogen-associated molecular pattern) is nece

216 that a member of the maize (Zea mays) plant elicitor peptide (Pep) family, ZmPep3, regulates respons

217 gene, which encodes the precursor protein of elicitor peptide 1 (AtPep1).

218 s MPK3 and MPK6 in response to the flagellin elicitor peptide flg22.

219 active Pep epitopes conserved in Arabidopsis ELICITOR PEPTIDE PRECURSORs (PROPEPs).

220 The Arabidopsis thaliana endogenous elicitor peptides (AtPeps) are released into the apoplas

221 work focuses on the Arabidopsis DAMPs plant elicitor peptides (Peps) and their receptors, PEPR1 and

222 Endogenous plant elicitor peptides (Peps) can act to facilitate immune si

223 ple plant receptors of fungal-derived chitin elicitors, phosphorylation of membrane-associated signal

224 Elicitors present in herbivore oral secretions are belie

225 The exposure to different elicitors produced concentration- and elicitor-dependent

226 The interaction of elicitor protein with the receptor protein activates a s

227 ion and characterization of an extracellular elicitor protein, designated AsES, produced by an avirul

228 ect evidence for the physical interaction of elicitor proteins and receptor proteins in several cases

229 with these, receptor kinases such as chitin elicitor receptor kinase (HvCERK1) and protein kinases s

230 Rice receptor kinase CHITIN ELICITOR RECEPTOR KINASE 1 (CERK1) and alpha/beta-fold h

231 aling mediated by the chitin receptor CHITIN ELICITOR RECEPTOR KINASE 1 (CERK1).

232 NG2 (FLS2), EF-TU RECEPTOR (EFR), and CHITIN ELICITOR RECEPTOR KINASE1 (CERK1) recognize microbe-asso

233 ucing the formation of a complex with CHITIN ELICITOR RECEPTOR KINASE1 (CERK1).

234 ive putative LYKs; among them, AtLYK1/CHITIN ELICITOR RECEPTOR KINASE1 is required for response to ch

235 LysM-containing receptor-like kinase1/chitin elicitor receptor kinase1) was shown to be essential for

236 er, little is known about the specificity of elicitor recognition in plants.

237 metabolite analysis revealed its role as an elicitor recognition receptor that triggered downstream

238 this activity can lead to multiple rounds of elicitor recognition, providing a means of signal amplif

239 The diversity of elicitors recognized by plants seems to support this hyp

240 Interferon elicitors recruited the transcription factor IRF3 to the

241 otein in N. attenuata (NaHER1; for herbivore elicitor regulated) and show that it is an indispensable

242 Furthermore, silencing of the elicitor-releasing endoglucanase (PR-2) led to a loss of

243 EGaseA, the major elicitor-releasing isozyme, is a high-affinity ligand fo

244 anisms involved in recognizing different ECB elicitors remains to be determined.

245 transferase, linalool synthase, peroxidases, elicitor responsive proteins, linamarase, nerolidol lina

246 o synthetic promoters 4D and 2S2D harbouring elicitor-responsive cis-elements.

247 Many of the elicitor-responsive cis-sequences also drive reporter ge

248 significantly increases the number of known elicitor-responsive cis-sequences and demonstrates the s

249 with an internal transformation control, 25 elicitor-responsive cis-sequences from 10 different moti

250 ioinformatics and synthetic promoters, novel elicitor-responsive cis-sequences were discovered in pro

251 e and adjacent nucleotides are essential for elicitor-responsive gene expression in a parsley protopl

252 In both plants, an elicitor-responsive phospholipase A2 (PLA2) at the plasm

253 Strongly elicitor-responsive phosphorylation sites may reflect di

254 n of a plant NB-LRR protein with its cognate elicitor results in an antiviral response that inhibits

255 The detection of microbial elicitors results in the up-regulation of defense-relate

256 The data presented suggest that the elicitor's aggregation may control the Trichoderma-plant

257 s of hydroponically grown plants to chemical elicitors selectively and reproducibly induced the produ

258 r kinase CERK1, which is critical for chitin elicitor signaling and resistance to fungal pathogens, p

259 cretes the highly effective hydrophobin-like elicitor Sm1 that induces systemic disease resistance in

260 some similarities to responses to well-known elicitors such as chitooligomers and OGs.

261 ion, with different concentrations of biotic elicitors such as chitosan and jasmonic acid also signif

262 Hormonal elicitors, such as jasmonates, trigger a complex signali

263 r work demonstrates the feasibility of using elicitors, such as plant stress hormones, by priming and

264 of damage by perceiving herbivore-associated elicitors, such as the fatty acid-amino acid conjugates

265 ted by fatty acid-amino acid conjugate (FAC) elicitors, such as volicitin [N-(17-hydroxylinolenoyl)-L

266 ed the influence of treatment with different elicitors (sucrose, mannitol, NaCl, 1-aminocyclopropane-

267 omal lipopeptides such as the plant immunity elicitor surfactin or the highly fungitoxic iturins and

268 terize severe allergic reactions in terms of elicitors, symptoms, emergency treatment, and long-term

269 -regulation of Sm1, the Trichoderma-secreted elicitor that systemically activates the defense mechani

270 ning, we previously identified 114 synthetic elicitors that activate expression of the pathogen-respo

271 ning, we previously identified 114 synthetic elicitors that activate the expression of a pathogen-res

272 ghput screening system for synthetic defense elicitors that can be used to trigger defined subsets of

273 phytopathogens and identifying 56 candidate elicitors that have an excess of positively selected res

274 Upon recognition of pathogen-derived elicitors, these NB-LRR proteins are thought to initiate

275 allergists reveal a different rank order of elicitors, this study suggests that food-allergic adult

276 influences plant responses to insect-derived elicitors through changes in E sensitivity and E-indepen

277 that express a narrow array of antigens and elicitors, thus favoring haploid parasites over diploid

278 upon environmental stress may function as an elicitor to activate plant defense responses.

279 ttention has been paid to the application of elicitors to vineyard.

280 ne that had been exposed to bacterial immune elicitors, to live E. coli infections or to no challenge

281 d to assess experimental wines obtained from elicitor-treated grapes.

282 lyses to discover prenyltransferase genes in elicitor-treated peanut hairy root cultures.

283 The biotic elicitor treatment could thus prove to be an important s

284 after pathogen-associated molecular pattern elicitor treatment, as well as enhanced resistance to bo

285 wounded leaves within 15 min, but upon Avr9 elicitor treatment, this upregulation is enhanced and ma

286 phytoalexin, hyperxanthone E, in response to elicitor treatment.

287 efense signaling in response to wounding and elicitor treatment.

288 signaling platform formation in response to elicitor treatment.

289 iple mutants show that ANPs are required for elicitor-triggered defense responses and protection agai

290 dependent efflux of vacuolar protons and (2) elicitor-triggered overproduction of alkaloids.

291 s we challenged aphids with bacterial immune elicitors twenty-four hours prior to live bacterial path

292 s content was significantly increased by all elicitors used in this study; however, no increase was o

293 The most common elicitor was drugs (41.1%) followed by venom (27.4%) and

294 In short, both the elicitors were able to increase the shelf life of fruits

295 The most common elicitors were food products (32.2%), drugs (29.2%) and

296 y fatty acid from grasshoppers, was the only elicitor with demonstrable activity in Arabidopsis thali

297 revealed similar concentrations of the three elicitors with 80% of the potential inceptin-related pep

298 Symptom patterns differed by elicitor, with the skin being affected most often (84.1%

299 we found that, in addition to PA, the fungal elicitor xylanase activated PDK1, suggesting that PDK1 h

300 cell suspension cultures responding to yeast elicitor (YE) or methyl jasmonate (MeJA).