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1 e functional analog of jasmonoyl-isoleucine, coronatine.
2 p-regulated by ABA, bacterial infection, and coronatine.
3 uced sensitivity to the bacterial phytotoxin coronatine.
4 educed sensitivity to the bacterial effector coronatine.
5 rB in DC3000, suggesting that AvrB may mimic coronatine.
6 ds, 12-oxo-phytodienoic acid, and phytotoxin coronatine.
7 ae pv. tomato DC3000 produces the phytotoxin coronatine, a major determinant of the leaf chlorosis as
8                Pseudomonas syringae produces coronatine, a toxin that mimics the plant hormone jasmon
9 s the polyketide component of the phytotoxin coronatine, a virulence factor of the plant pathogen Pse
10 gest that P. syringae type III effectors and coronatine act by augmenting a COI1-dependent pathway to
11  coronatine-mediated virulence and show that coronatine activates three homologous NAC transcription
12 e hypotheses that the P. syringae phytotoxin coronatine acts to promote virulence by inhibiting host
13 s essential for production of the phytotoxin coronatine and for expression of the structural genes en
14          These results not only suggest that coronatine and JA-Ile target the physical interaction be
15                                              Coronatine and related bacterial phytotoxins are mimics
16  a combination of the bacterial JA-Ile mimic coronatine and type III virulence-associated effectors.
17  with PtCOI1 in the presence of the JA mimic coronatine, and PtJAZ6 is degraded in plant tissues afte
18 type III secretion system and the phytotoxin coronatine are required for RAP2.6 induction.
19 all other sequenced P. syringae strains with coronatine biosynthesis genes.
20  restore coronatine production, showing that coronatine biosynthesis requires factors other than hrpL
21 f Cfa1, suggesting that FabD plays a role in coronatine biosynthesis.
22  virulence genes, including hrp/hrc, avr and coronatine biosynthetic genes.
23                            Here we show that coronatine, but not its two biosynthetic precursors, als
24           Thus, a signaling cascade by which coronatine confers its multiple virulence activities has
25 to the plant host cell, while the phytotoxin coronatine (COR) contributes to virulence and disease sy
26                                              Coronatine (COR) facilitates entry of bacteria into the
27                                              Coronatine (COR) is a phytotoxin produced by several pat
28                                              Coronatine (COR) is a plasmid-encoded phytotoxin synthes
29                               The phytotoxin coronatine (COR) promotes various aspects of Pseudomonas
30                      The jasmonate-mimicking coronatine (COR) toxin produced by Pseudomonas syringae
31 solution was achieved through treatment with coronatine (COR), a high-affinity agonist of the JA rece
32 udomonas syringae pv. tomato DC3000 produces coronatine (COR), a jasmonic acid (JA) mimic.
33 Arabidopsis (Arabidopsis thaliana), produces coronatine (COR), a non-host-specific phytotoxin.
34 -elicited SIS is caused by the production of coronatine (COR), a pathogen-derived functional and stru
35 ic acid (CFA) is the polyketide component of coronatine (COR), a phytotoxin produced by the plant pat
36 ic acid (CFA) is the polyketide component of coronatine (COR), a phytotoxin produced by the plant pat
37 ic acid (CFA) is the polyketide component of coronatine (COR), a phytotoxin produced by the plant-pat
38 t tvrR mutant strains are able to synthesize coronatine (COR), a phytotoxin required for virulence of
39  phytohormone mimics, such as the phytotoxin coronatine (COR), have not been directly quantified in p
40  (flg22), and a pathogen-derived phytotoxin, coronatine (COR), induced a shoot-to-root signal regulat
41  effectors, as well as a JA-mimicking toxin, coronatine (COR), to activate JA signaling as a mechanis
42 smonate, JA-Ile, and its functional homolog, coronatine (COR), we demonstrate that (1) JA-Ile/COR-bas
43  Pseudomonas syringae produce the phytotoxin coronatine (COR), which contains an unusual amino acid,
44                         The virulence factor coronatine (COR), which is produced by plant pathogenic
45  proteins into host cells and the phytotoxin coronatine (COR), which is thought to mimic the action o
46 A-Ile) and the bacterial-produced phytotoxin coronatine (COR).
47 to P syringae pathovar tomato strain DC3118 (coronatine deficit)-induced stomatal closure.
48  Jas domain were identified as essential for coronatine-dependent COI1-JAZ interactions.
49 main of JAZ proteins, is critical for JA-Ile/coronatine-dependent interaction with COI1.
50 ds in the Jas domain in mediating the JA-Ile/coronatine-dependent JAZ interaction with COI1.
51 ic acid, and the bacterial virulence factor, coronatine, during progression of P. syringae infection
52                 Although the biosynthesis of coronatine has been investigated previously, the nature
53    The main genetic and metabolic targets of coronatine in Arabidopsis (Arabidopsis thaliana) remain
54                   Interestingly, the role of coronatine in RAP2.6 induction can be partially substitu
55                                              Coronatine-induced stomatal opening was initiated slowly
56  mutants demonstrates that these TFs mediate coronatine-induced stomatal reopening and bacterial prop
57 re, analysis of bacterial supernatants under coronatine-inducing conditions revealed that mutants lac
58                            The F-box protein Coronatine Insensitive (COI) is a receptor for the jasmo
59 C. roseus JA signaling components, including CORONATINE INSENSITIVE 1 (COI1) and JASMONATE ZIM domain
60                            The F-box protein CORONATINE INSENSITIVE 1 (COI1) mediates jasmonate signa
61 esponse to jasmonates (JAs), the JA receptor Coronatine Insensitive 1 (COI1) recruits JA-zinc-finger
62 ene response factor (ERF) gene, RAP2.6, in a coronatine insensitive 1 (COI1)-dependent manner.
63 biquitin ligase complex containing the F-box CORONATINE INSENSITIVE 1 (COI1).
64 A) promotes AAL toxin induced PCD in a COI1 (coronatine insensitive 1, JA receptor)-dependent manner
65 nic acid-isoleucine (JA-Ile), in contrast to CORONATINE INSENSITIVE 1, which sends JAZs for degradati
66                      Blocked JA signaling in coronatine-insensitive (coi1) and enhanced expression of
67 le), stimulates binding of the F-box protein coronatine-insensitive 1 (COI1) to, and subsequent ubiqu
68                          A new allele of the coronatine-insensitive locus (COI1) was isolated in a sc
69 f LBD20 expression in roots was abolished in coronatine insensitive1 (coi1) and myc2 (allelic to jasm
70 stablished pathway requiring the JA receptor CORONATINE INSENSITIVE1 (COI1) and the JA-regulated tran
71 eption of bioactive JAs by the F-box protein CORONATINE INSENSITIVE1 (COI1) causes degradation of JAZ
72 monoyl-L-isoleucine (JA-Ile) to the F-box of CORONATINE INSENSITIVE1 (COI1) is required for many JA-d
73 ated by constitutive expression of ERF1 in a coronatine insensitive1 (coi1) mutant background (35S::E
74  cells of wild-type (Col-0) Arabidopsis, the CORONATINE INSENSITIVE1 (COI1) mutant coi1-1 and the PM
75 a co-receptor complex with the F-box protein coronatine insensitive1 (COI1) that recognizes both jasm
76 gatively regulated by the jasmonate receptor Coronatine Insensitive1 (COI1), as loss of functional CO
77 AZ repressor proteins with the F-box protein CORONATINE INSENSITIVE1 (COI1), part of an S-phase kinas
78 main (JAZ) repressors with the F-box protein CORONATINE INSENSITIVE1 (COI1), which results in JAZ deg
79 that JA rapidly induces RGL3 expression in a CORONATINE INSENSITIVE1 (COI1)- and JASMONATE INSENSITIV
80 he plant defense hormone jasmonic acid (JA), CORONATINE INSENSITIVE1 (COI1).
81 ontrolling the transcriptional repression of CORONATINE INSENSITIVE1 in an evening-phase-specific man
82  the tomato ortholog of the ubiquitin ligase CORONATINE INSENSITIVE1 in Arabidopsis (Arabidopsis thal
83  that are deficient in jasmonate perception (coronatine insensitive1) or in the biogenesis of small i
84 ion, allene oxide synthase and coi1-16B (for coronatine insensitive1), respectively.
85                   Double mutants of ago1 and coronatine insensitive1, the jasmonate receptor, showed
86 inding to the F-box-containing JA coreceptor CORONATINE INSENSITIVE1.
87 tionally high JA levels and was dependent on CORONATINE INSENSITIVE1.
88          Moreover, elp2 is as susceptible as coronatine-insensitive1 (coi1) and ethylene-insensitive2
89 he loss of function of the tomato homolog of CORONATINE-INSENSITIVE1 (COI1), an F-box protein that is
90    Wound-induced expression of JAZ and other CORONATINE-INSENSITIVE1 (COI1)-dependent genes was not i
91 sis-like phenotype upon COR application in a Coronatine-Insensitive1 (COI1)-dependent manner.
92  acid fragment of the pseudomonal phytotoxin coronatine involves construction of the cyclopropane rin
93                                              Coronatine is a toxin produced by the bacterial pathogen
94                                              Coronatine is an important virulence factor produced by
95                                              Coronatine is produced by the ligation of two moieties,
96                             The structure of coronatine is similar to that of a class of plant hormon
97 IVE 1, which sends JAZs for degradation in a coronatine/JA-Ile dependent manner.
98 for proteasomal degradation independently of coronatine/jasmonic acid-isoleucine (JA-Ile), in contras
99                                              Coronatine-like phytotoxins disrupt these essential path
100        We examined the mechanisms underlying coronatine-mediated virulence and show that coronatine a
101 onsive to pathogen virulence factors such as coronatine (phytotoxin produced by the bacterium Pseudom
102                         The bacterial toxin, coronatine, produced by several pathogenic strains of Ps
103 showed the same virulence toward nrt2 as the coronatine-producing strain.
104 CmaL identifies a critical missing factor in coronatine production and provides a foundation for furt
105 idenced by the fact that wild-type levels of coronatine production are restored to a DeltacmaL mutant
106 f hrpL in ES4326 rpoN::Km(r) did not restore coronatine production, showing that coronatine biosynthe
107 (IaaL), and a subsidiary regulon controlling coronatine production.
108 ma operon or cmaL accumulate CFA rather than coronatine, supporting a role for CmaL in the regulation
109  addition, a P. syringae strain defective in coronatine synthesis showed the same virulence toward nr
110 clopropane), a constituent of the phytotoxin coronatine synthesized by the phytopathogenic bacterium
111 ants can be triggered by the bacterial toxin coronatine through a light-dependent process.
112  pv. tomato DC3000 uses the virulence factor coronatine to actively open stomata.
113                                              Coronatine-triggered and spontaneous lesion spreading in
114 0) responds by secreting a virulence factor, coronatine, which blocks the functioning of guard cells
115 nse was mediated by the bacterial phytotoxin coronatine, which exerts its virulence effects by co-opt
116 on system and a polyketide phytotoxin called coronatine, which structurally mimics the plant hormone

 
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