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S-adenosyl-L-methionine + 9,10-dihydrojasmonic acid
S-adenosyl-L-homocysteine + ?
poor substrate
-
-
?
S-adenosyl-L-methionine + benzoate
S-adenosyl-L-homocysteine + methyl benzoate
22% activity compared to jasmonate
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
additional information
?
-
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
expression of the gene is induced both locally and systematically by wounding or methyl jasmonate treatement. The jasmonic acid carboxyl methyltransferase is a key enzyme for jasmonate-regulated plant responses. Activation of JMT expression leads to production of methyl jasmonate that could act as an intracellular regulator, a diffusible intercellular transducer, and an airborne signal mediating intra- and interplant communications
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
methyl jasmonate modulates diverse developmental processes and defense responses in plants, acting as an important cellular regulator
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
methyljasmonate formation is a key control point for jasmonate-responsive gene expression in plants, overview
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
additional information
?
-
the enzyme does not convert 12-oxo-phytodienoic acid, a precursor of jasmonic acid, salicylic acid, benzoic acid, linolenic acid or cinnamic acid into their corresponding methyl esters
-
-
?
additional information
?
-
-
the enzyme does not convert 12-oxo-phytodienoic acid, a precursor of jasmonic acid, salicylic acid, benzoic acid, linolenic acid or cinnamic acid into their corresponding methyl esters
-
-
?
additional information
?
-
-
the enzyme activity with benzoate and salicylate as substrates is less than 1.5% of that with jasmonate
-
-
?
additional information
?
-
-
the enzyme activity with benzoate and salicylate as substrates is less than 1.5% of that with jasmonate
-
-
?
additional information
?
-
-
the isozymes are specific for jasmonate, no or poor activities with indole-3-acetic acid, gibberellic acid 3, or salicylic acid
-
-
-
additional information
?
-
no activity with salicylic acid, indole-3-acetic acid, and gibberellic acid
-
-
?
additional information
?
-
-
no activity with salicylic acid, indole-3-acetic acid, and gibberellic acid
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
expression of the gene is induced both locally and systematically by wounding or methyl jasmonate treatement. The jasmonic acid carboxyl methyltransferase is a key enzyme for jasmonate-regulated plant responses. Activation of JMT expression leads to production of methyl jasmonate that could act as an intracellular regulator, a diffusible intercellular transducer, and an airborne signal mediating intra- and interplant communications
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
methyl jasmonate modulates diverse developmental processes and defense responses in plants, acting as an important cellular regulator
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
methyljasmonate formation is a key control point for jasmonate-responsive gene expression in plants, overview
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
?
S-adenosyl-L-methionine + jasmonate
S-adenosyl-L-homocysteine + methyl jasmonate
-
-
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
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evolution
-
the enzyme belongs to the protein family of SABATH methyltransferases, ten genes encode isozymes PaSABATH1-10. Five of the PaSABATH isozymes (PaSABATH3, PaSABATH6, PaSABATH7, PaSABATH8, and PaSABATH9) do not show activity with any of the four substrates, i.e. indole-3-acetic acid, jasmonic acid, giberellic acid A3, and salicylic acid, the other five of the PaSABATHs each show activity with one or more of the four substrates. PaSABATH1 has the highest level of specific activity with indole-3-acetic acid and is renamed as PaIAMT (EC 2.1.1.278). PaSABATH2 has the highest level of specific activity with salicylic acid and is designated as PaSAMT (EC 2.1.1.274). For comparison, PaSAMT is also assayed with two compounds of similar structure benzoic acid and anthranilic acid (cf. EC 2.1.1.273). While PaSAMT has no activity with anthranilic acid, its activity with benzoic acid is approximately 8% of that with salicylic acid. PaSABATH4, PaSABATH5 and PaSABATH10 show the highest level of specific activity with jasmonic acid and are renamed PaJAMT1, PaJAMT2, and PaJAMT3, respectively (EC 2.1.1.141). Their products are confirmed to be methyljasmonate
metabolism
overexpression of enzyme in the Glycine max seeds results in decreased amounts of tryptophan, palmitic acid, linolenic acid, and stachyose, but increased levels of gadoleic acid and genistein. In particular, seeds contain 120.0-130.5% more genistein and 60.5-82.1% less stachyose than the wild type
additional information
-
structural modeling of isozymes PaJAMT1 and PaJAMT3, docking structures with Indole-3-acetic acid (IAA) suggest that the active-site residues (e.g. V339 and F343 from PaJAMT1 and M347 and F351 from PaJAMT3) interfere with IAA binding for the methyl transfer, and this is consistent with the relatively low activities of these two enzymes toward IAA.When jasmonate (JA) is docked into the active sites of PaJAMT1 and PaJAMT3, the steric clashes with the active site residues are not observed, and this observation structurally validates that they are jasmonate methyltransferases, JAMTs
physiological function
the enzyme plays a role in plant defense against biotic stresses
physiological function
the enzyme plays a role in regulating plant development as well as herbivore-induced defense responses in rice
physiological function
-
ectopic expression of JMT in tomato does not increase the methyl jasmonate content, while the expression levels of endogenous methyl jasmonate biosynthesis genes are influenced, especially in the wound treatment
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
JMT_BRARP
392
0
43816
Swiss-Prot
other Location (Reliability: 2)
JMT1_THECC
373
0
41465
Swiss-Prot
other Location (Reliability: 3)
JMT2_THECC
373
0
41388
Swiss-Prot
other Location (Reliability: 2)
JMT_ARATH
389
0
43443
Swiss-Prot
other Location (Reliability: 3)
A0A5B7BIE8_DAVIN
170
0
19000
TrEMBL
other Location (Reliability: 3)
A0A0B2RN67_GLYSO
327
0
36917
TrEMBL
Secretory Pathway (Reliability: 5)
A0A7C8YUH2_OPUST
248
0
28107
TrEMBL
Secretory Pathway (Reliability: 3)
A0A7C8Z0M1_OPUST
117
0
12985
TrEMBL
other Location (Reliability: 3)
B9T2Q9_RICCO
330
0
37143
TrEMBL
other Location (Reliability: 3)
A0A2G9I2T0_9LAMI
175
0
19437
TrEMBL
other Location (Reliability: 3)
A0A7C9ER34_OPUST
399
0
45148
TrEMBL
Mitochondrion (Reliability: 4)
B9T7V8_RICCO
375
0
42315
TrEMBL
other Location (Reliability: 2)
A0A088Q2I5_ARTAN
366
0
40785
TrEMBL
other Location (Reliability: 2)
A0A5B6YH75_DAVIN
371
0
41905
TrEMBL
other Location (Reliability: 2)
A0A2P6PYT8_ROSCH
150
0
17056
TrEMBL
other Location (Reliability: 3)
A0A0B2Q6J3_GLYSO
346
0
39589
TrEMBL
other Location (Reliability: 3)
B9S6C3_RICCO
366
0
40958
TrEMBL
other Location (Reliability: 2)
A0A2I0AXP3_9ASPA
405
0
46314
TrEMBL
other Location (Reliability: 5)
A0A7C9EMJ4_OPUST
342
0
38425
TrEMBL
other Location (Reliability: 3)
A0A7C8YU87_OPUST
110
0
12174
TrEMBL
other Location (Reliability: 3)
A0A2I0A4M8_9ASPA
105
0
11935
TrEMBL
other Location (Reliability: 3)
A0A7C9A3Z8_OPUST
243
0
27452
TrEMBL
other Location (Reliability: 3)
A0A7C9CUC7_OPUST
229
0
25648
TrEMBL
other Location (Reliability: 3)
B9S6C1_RICCO
366
0
40748
TrEMBL
other Location (Reliability: 2)
A0A2P6R3D0_ROSCH
406
0
45602
TrEMBL
other Location (Reliability: 4)
A0A0B2QMV6_GLYSO
370
0
41592
TrEMBL
other Location (Reliability: 4)
A0A2I0AXR3_9ASPA
191
0
22044
TrEMBL
other Location (Reliability: 4)
A0A7C8ZN32_OPUST
145
0
16635
TrEMBL
other Location (Reliability: 3)
B9SYY5_RICCO
386
0
42525
TrEMBL
other Location (Reliability: 5)
A0A396JLG5_MEDTR
148
0
17084
TrEMBL
other Location (Reliability: 2)
A0A7C9A303_OPUST
109
0
12254
TrEMBL
other Location (Reliability: 3)
A0A7C9A3H5_OPUST
132
0
15018
TrEMBL
other Location (Reliability: 2)
A0A7C8YT27_OPUST
110
0
12298
TrEMBL
other Location (Reliability: 3)
I0DHG9_CYMEN
374
0
42024
TrEMBL
other Location (Reliability: 3)
A0A7C9A4J6_OPUST
178
0
19965
TrEMBL
other Location (Reliability: 3)
A0A7C9ECR0_OPUST
344
0
39087
TrEMBL
Mitochondrion (Reliability: 5)
A0A7C8YMU2_OPUST
233
0
26590
TrEMBL
Mitochondrion (Reliability: 5)
A0A0B2REV3_GLYSO
383
0
42069
TrEMBL
other Location (Reliability: 1)
B9STB4_RICCO
337
0
38204
TrEMBL
other Location (Reliability: 2)
A0A2P6PYS3_ROSCH
392
0
43903
TrEMBL
other Location (Reliability: 2)
A0A7C8YSM2_OPUST
372
0
41560
TrEMBL
other Location (Reliability: 2)
B9STC2_RICCO
364
0
41654
TrEMBL
other Location (Reliability: 2)
A0A0B2QRQ3_GLYSO
370
0
41584
TrEMBL
other Location (Reliability: 4)
A0A7G7R865_CAMSI
358
0
40103
TrEMBL
Chloroplast (Reliability: 5)
A0A7C9EEU0_OPUST
317
0
35891
TrEMBL
Mitochondrion (Reliability: 4)
A0A151TRY7_CAJCA
362
0
41431
TrEMBL
other Location (Reliability: 2)
B9SJ35_RICCO
377
0
42569
TrEMBL
other Location (Reliability: 2)
A0A2P6PYS6_ROSCH
270
0
30582
TrEMBL
other Location (Reliability: 1)
A0A5B7B816_DAVIN
368
0
41217
TrEMBL
other Location (Reliability: 3)
A0A0B2QW75_GLYSO
391
0
43172
TrEMBL
other Location (Reliability: 4)
A0A5B6YHD4_DAVIN
350
0
39668
TrEMBL
other Location (Reliability: 3)
A0A0B2QT01_GLYSO
341
0
38119
TrEMBL
other Location (Reliability: 4)
A0A7C9A3B5_OPUST
100
0
11320
TrEMBL
other Location (Reliability: 4)
A0A7C9DW93_OPUST
285
0
32464
TrEMBL
other Location (Reliability: 2)
A0A7C8ZAP4_OPUST
150
0
16863
TrEMBL
Secretory Pathway (Reliability: 5)
A0A7C8YU91_OPUST
169
0
18712
TrEMBL
other Location (Reliability: 3)
A0A7C9A1B7_OPUST
112
0
12631
TrEMBL
other Location (Reliability: 3)
A0A7C9DEB4_OPUST
115
0
12956
TrEMBL
Secretory Pathway (Reliability: 4)
A0A151SXK4_CAJCA
387
0
42698
TrEMBL
other Location (Reliability: 3)
A0A5B7BQ48_DAVIN
370
0
42124
TrEMBL
other Location (Reliability: 3)
A0A0B2QSJ4_GLYSO
370
0
41530
TrEMBL
other Location (Reliability: 4)
A0A0B2PDN6_GLYSO
364
0
41832
TrEMBL
other Location (Reliability: 2)
A0A2I0A4L4_9ASPA
200
0
22896
TrEMBL
other Location (Reliability: 4)
A0A7C9EKL7_OPUST
349
0
39238
TrEMBL
other Location (Reliability: 5)
A0A7C9DJA7_OPUST
351
0
39799
TrEMBL
other Location (Reliability: 2)
A0A7C8ZKZ2_OPUST
245
0
27164
TrEMBL
other Location (Reliability: 3)
A0A5B7B8V2_DAVIN
364
0
40762
TrEMBL
other Location (Reliability: 2)
U3M7S7_LONJA
365
0
42056
TrEMBL
Secretory Pathway (Reliability: 5)
A0A0B2QRP9_GLYSO
363
0
41232
TrEMBL
other Location (Reliability: 2)
B9RH75_RICCO
328
0
36876
TrEMBL
other Location (Reliability: 3)
A0A5B6YH69_DAVIN
349
0
39567
TrEMBL
other Location (Reliability: 3)
A0A0B2QN03_GLYSO
370
0
41530
TrEMBL
other Location (Reliability: 4)
A0A396JJI2_MEDTR
198
0
22221
TrEMBL
other Location (Reliability: 2)
A0A7C9DKQ2_OPUST
383
0
43437
TrEMBL
other Location (Reliability: 2)
A0A7C9CWQ4_OPUST
154
0
17374
TrEMBL
other Location (Reliability: 3)
B9STB2_RICCO
363
0
41306
TrEMBL
other Location (Reliability: 2)
B9S844_RICCO
363
0
40724
TrEMBL
other Location (Reliability: 1)
A0A2I0A1A8_9ASPA
111
0
13016
TrEMBL
other Location (Reliability: 2)
A0A7C8ZMX8_OPUST
245
0
27192
TrEMBL
other Location (Reliability: 3)
A0A7C9EV50_OPUST
281
0
31688
TrEMBL
other Location (Reliability: 5)
A0A7C8YUL5_OPUST
318
0
35727
TrEMBL
other Location (Reliability: 3)
B9R7Y1_RICCO
372
0
41804
TrEMBL
other Location (Reliability: 3)
B9SUG7_RICCO
369
0
40873
TrEMBL
other Location (Reliability: 3)
A0A5B7APP7_DAVIN
366
0
41299
TrEMBL
other Location (Reliability: 3)
A0A7C9DHX4_OPUST
222
0
24956
TrEMBL
other Location (Reliability: 2)
A0A7C9CTC8_OPUST
254
0
28774
TrEMBL
other Location (Reliability: 2)
A0A7C8ZE83_OPUST
132
0
14921
TrEMBL
other Location (Reliability: 3)
B9T7Z3_RICCO
310
0
34956
TrEMBL
other Location (Reliability: 2)
A0A396JMF6_MEDTR
217
0
24857
TrEMBL
other Location (Reliability: 2)
A0A396JGX7_MEDTR
125
0
14733
TrEMBL
other Location (Reliability: 2)
A0A7C9A2B9_OPUST
112
0
12861
TrEMBL
other Location (Reliability: 5)
A0A7C9A3B1_OPUST
113
0
12897
TrEMBL
other Location (Reliability: 2)
A0A7C8ZMJ3_OPUST
386
0
43224
TrEMBL
other Location (Reliability: 3)
A0A7C9ELE9_OPUST
372
0
41688
TrEMBL
other Location (Reliability: 5)
A0A7C8Z0Y9_OPUST
106
0
11961
TrEMBL
other Location (Reliability: 5)
B9H4E1_POPTR
369
0
41175
TrEMBL
-
Q9FW31_ORYSJ
373
0
41001
TrEMBL
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
agriculture
expression of the enzyme in transgenic Chinese cabbage plants provides high levels of field resistance against Erwinia carotovora
N361S
the mutation leads to higher specific activity with benzoate than with jasmonate
S153Y
the mutation leads to strongly reduced activity with benzoate or jasmonate
S153Y/N361S
the mutation leads to strongly reduced activity with benzoate or jasmonate
L245DEL
-
the deletion mutant is inactive
L245DEL
-
the deletion mutant is inactive
additional information
transcript profile of transgenic Arabidopsis thaliana plants constitutively producing methyl jasmonate by microarray analysis, the recombinant overexpression influences several parameters of the plant metabolism, leading to e.g. upregulation of the defense and oxidative stress response, or senescence, and downregulation of photosynthesis involved enzymes and cold/drought stress involved enzymes, overview
additional information
-
overexpressing Arabidopsis thaliana jasmonic acid JMT results in stimulation of root growth and ginsenoside heterogeneity in Panax ginseng, phenotypes, overview
additional information
-
overexpression of gene JMT in Solanum tuberosum increases tuber yield and size of the transgenic plants, phenotypes, overview
additional information
construction of enzyme overexpressing Glycine max plants showing significant differences in leaf and root growth patterns compared to the wild-type plants, the leaves of the transgenic plants are slightly elongated in length but dramatically narrowed in width compared to wild-type plants. In addition, elongation of primary root is inhibited in the overexpressed transgenic soybean plantlets, whereas the development of lateral root is stimulated relative to the nontransformed plants. The leaves of the transgenic plants show 2-2.5-fold higher levels of methyljasmonate than the control plants, phenotype, overview
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Seo, H.S.; Song, J.T.; Cheong, J.J.; Lee, Y.H.; Lee, Y.W.; Hwang, I.; Lee, J.S.; Choi, Y.D.
Jasmonic acid carboxyl methyltransferase: A key enzyme for jasmonate-regulated plant responses
Proc. Natl. Acad. Sci. USA
98
4788-4793
2001
Arabidopsis thaliana (Q9AR07), Arabidopsis thaliana
brenda
Seo, H.S.; Song, J.T.; Koo, Y.J.; Jung, C.; Yeu, S.Y.; Kim, M.; Song, S.I.; Lee, J.S.; Hwang, I.; Cheong, J.J.; Choi, Y.D.
Floral nectary-specific gene NTR1 encodes a jasmonic acid carboxyl methyltransferase
Agric. Chem. Biotechnol.
44
119-124
2001
Brassica rapa subsp. oleifera
-
brenda
Jung, C.; Lyou, S.H.; Koo, Y.J.; Song, J.T.; Choi, Y.D.; Cheong, J.J.
Constitutive expression of defense genes in transgenic Arabidopsis overproducing methyl jasmonate
Agric. Chem. Biotechnol.
46
52-57
2003
Arabidopsis thaliana
-
brenda
Afitlhile, M.M.; Fukushige, H.; Hildebrand, D.
Labeling of major plant lipids and jasmonic acid using [1-14C] lauric acid
Phytochemistry
65
2679-2684
2004
Artemisia tridentata
brenda
Song, M.S.; Kim, D.G.; Lee, S.H.
Isolation and characterization of a jasmonic acid carboxyl methyltransferase gene from hot pepper (Capsicum annuum L.)
J. Plant Biol.
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2005
Capsicum annuum
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brenda
Barkman, T.J.
A role of evolutionary predictions in gene isolation and characterization studies
J. Plant Biol.
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331-335
2006
Capsicum annuum
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brenda
Xue, R.; Zhang, B.
Increased endogenous methyl jasmonate altered leaf and root development in transgenic soybean plants
J. Genet. Genomics
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339-346
2007
Brassica rapa subsp. oleifera (Q9SBK6)
brenda
Jung, C.; Yeu, S.Y.; Koo, Y.J.; Kim, M.; Choi, Y.D.; Cheong, J.
Transcript profile of transgenic Arabidopsis constitutively producing methyl jasmonate
J. Plant Biol.
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2007
Arabidopsis thaliana (Q9AR07)
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brenda
Sohn, H.; Lee, H.; Seo, J.; Jung, C.; Jeon, J.; Kim, J.; Lee, Y.; Lee, J.; Cheong, J.; Choi, Y.
Overexpression of jasmonic acid carboxyl methyltransferase increases tuber yield and size in transgenic potato
Plant Biotechnol. Rep.
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27-34
2011
Arabidopsis thaliana
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brenda
Kim, Y.; Han, J.; Lim, S.; Kim, H.; Lee, M.; Choi, Y.
Overexpressing Arabidopsis jasmonic acid carboxyl methyltransferase (AtJMT) results in stimulation of root growth and ginsenoside heterogeneity in Panax ginseng
Plant OMICS
5
28-32
2012
Arabidopsis thaliana
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brenda
Nam, K.; Kim, D.; Pack, I.; Park, J.; Seo, J.; Choi, Y.; Cheong, J.; Kim, C.; Kim, C.
Comparative analysis of chemical compositions between non-transgenic soybean seeds and those from plants over-expressing AtJMT, the gene for jasmonic acid carboxyl methyltransferase
Food Chem.
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2016
Arabidopsis thaliana (Q9AR07)
brenda
Qi, J.; Li, J.; Han, X.; Li, R.; Wu, J.; Yu, H.; Hu, L.; Xiao, Y.; Lu, J.; Lou, Y.
Jasmonic acid carboxyl methyltransferase regulates development and herbivory-induced defense response in rice
J. Integr. Plant Biol.
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564-576
2015
Oryza sativa (Q9FW31), Oryza sativa
brenda
Cho, W.; Min, B.
Bacterial pathogen protection in transgenic chinese cabbage by expression of jasmonic acid carboxyl methyltransferase gene
J. Plant Biotechnol.
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99-105
2012
Arabidopsis thaliana (Q9AR07)
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brenda
Preuss, A.; Augustin, C.; Figueroa, C.R.; Hoffmann, T.; Valpuesta, V.; Sevilla, J.F.; Schwab, W.
Expression of a functional jasmonic acid carboxyl methyltransferase is negatively correlated with strawberry fruit development
J. Plant Physiol.
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Fragaria x ananassa, Fragaria vesca
brenda
Scalschi, L.; Vicedo, B.; Camanes, G.; Fernandez-Crespo, E.; Lapena, L.; Gonzalez-Bosch, C.; Garcia-Agustin, P.
Hexanoic acid is a resistance inducer that protects tomato plants against Pseudomonas syringae by priming the jasmonic acid and salicylic acid pathways
Mol. Plant Pathol.
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342-355
2013
Solanum lycopersicum
brenda
Zhao, N.; Yao, J.; Chaiprasongsuk, M.; Li, G.; Guan, J.; Tschaplinski, T.J.; Guo, H.; Chen, F.
Molecular and biochemical characterization of the jasmonic acid methyltransferase gene from black cottonwood (Populus trichocarpa)
Phytochemistry
94
74-81
2013
Populus trichocarpa (B9H4E1), Populus trichocarpa
brenda
Xu, Q.; Wang, S.; Hong, H.; Zhou, Y.
Transcriptomic profiling of the flower scent biosynthesis pathway of Cymbidium faberi Rolfe and functional characterization of its jasmonic acid carboxyl methyltransferase gene
BMC Genomics
20
125
2019
Cymbidium faberi
brenda
Chaiprasongsuk, M.; Zhang, C.; Qian, P.; Chen, X.; Li, G.; Trigiano, R.N.; Guo, H.; Chen, F.
Biochemical characterization in Norway spruce (Picea abies) of SABATH methyltransferases that methylate phytohormones
Phytochemistry
149
146-154
2018
Picea abies
brenda
Bai, H.; Lu, G.; Lu, J.; Guan, L.; Tang, X.; Zhang, T.
Cloning and expression analysis of jasmonic acid carboxyl methyltransferase gene from Perilla frutescens
Sci. Agric. Sin.
52
1657-1666
2019
Perilla frutescens
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brenda