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1 aneous treatment with an ethylene precursor (1-aminocyclopropane-1-carboxylic acid).
2 vity to exogenous ethylene and its precursor 1-aminocyclopropane-1-carboxylic acid.
3 Phe, L-Trp, L-Ala, or the ethylene precursor 1-aminocyclopropane-1-carboxylic acid.
4 (IAA), axr1-24 had decreased sensitivity to 1-aminocyclopropane-1-carboxylic acid, 6-benzylamino-pur
6 -signaling pathways, whereas the addition of 1-aminocyclopropane-1-carboxylic acid, a direct precurso
7 nhibition can be reversed by the addition of 1-aminocyclopropane-1-carboxylic acid, a direct precurso
8 agellin peptide (flg22) and the ET precursor 1-aminocyclopropane-1-carboxylic acid (ACC) but is block
12 of transgenic seedlings treated with either 1-aminocyclopropane-1-carboxylic acid (ACC) or alpha-nap
15 nthesis in plants is catalyzed by the enzyme 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase (ACC
16 ne production correlated with an increase in 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase (ACO
17 lots show that the mutant's abundance of the 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase mRNA
19 f SIPK coincided with a dramatic increase in 1-aminocyclopropane-1-carboxylic acid (ACC) synthase (AC
20 d-type, etiolated seedlings through distinct 1-aminocyclopropane-1-carboxylic acid (ACC) synthase (AC
22 wever, expression analysis on members of the 1-aminocyclopropane-1-carboxylic acid (ACC) synthase eth
23 suppressed by the expression of an antisense 1-aminocyclopropane-1-carboxylic acid (ACC) synthase gen
24 cterized an Arabidopsis cDNA (ACS6) encoding 1-aminocyclopropane-1-carboxylic acid (ACC) synthase whi
25 1 fei2 roots was suppressed by inhibition of 1-aminocyclopropane-1-carboxylic acid (ACC) synthase, an
27 lene biosynthesis is directed by a family of 1-aminocyclopropane-1-carboxylic acid (ACC) synthases (A
28 y, the application of the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC) to pollinate
29 step in ethylene biosynthesis, oxidation of 1-aminocyclopropane-1-carboxylic acid (ACC) to yield eth
30 reas treatments with salicylic acid (SA) and 1-aminocyclopropane-1-carboxylic acid (ACC) were ineffec
31 three cyclic and three acyclic analogues of 1-aminocyclopropane-1-carboxylic acid (ACC) with ACC oxi
32 ), and coronamic acid (CMA), which resembles 1-aminocyclopropane-1-carboxylic acid (ACC), a precursor
33 er treatment of plants with the ET precursor 1-aminocyclopropane-1-carboxylic acid (ACC), activation
35 1-1 mutations, or through the application of 1-aminocyclopropane-1-carboxylic acid (ACC), negatively
36 low concentrations of the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC), promotes th
39 ymes that convert S-adenosyl-L-methionine to 1-aminocyclopropane-1-carboxylic acid (ACC)] and PsACO (
40 he hypocotyl under -DIF was restored by both 1-aminocyclopropane-1-carboxylic acid (ACC; ethylene pre
41 tween the previously observed stress-induced 1-aminocyclopropane-1-carboxylic acid accumulation and D
42 raphic and electrophysiological studies with 1-aminocyclopropane-1-carboxylic acid (ACPC), 1-aminocyc
43 f plants treated with the ethylene precursor 1-aminocyclopropane- 1-carboxylic acid and by examinatio
45 plants, ethylene is produced by oxidation of 1-aminocyclopropane-1-carboxylic acid, as catalyzed by 1
46 the ribosomal protein L29 and presequence of 1-aminocyclopropane-1-carboxylic acid deaminase 1) and N
47 to genotypes impaired in ethylene synthesis (1-aminocyclopropane-1-carboxylic acid deaminase) and per
50 auxin, cytokinin, or the ethylene precursor 1-aminocyclopropane-1-carboxylic acid, indicating that t
51 oid, salicylic acid), chemicals (clofibrate, 1-aminocyclopropane-1 carboxylic acid), or environmental
52 n of ethylene precursors, S-adenosyl-Met and 1-aminocyclopropane-1-carboxylic acid, or PA biosynthesi
53 in plant cells, suppressing the activity of 1-aminocyclopropane-1-carboxylic acid oxidase (ACO), the
56 haracterized, with one corresponding to ACC (1-aminocyclopropane-1-carboxylic acid) oxidase, three to
57 mechanisms for Cellulose synthase (CesA) and 1-Aminocyclopropane-1-carboxylic acid oxidase1 and 3 (AC
58 e plants treated with the ethylene precursor 1-aminocyclopropane-1-carboxylic acid showed a root-spec
60 thermore, we found that selected isoforms of 1-aminocyclopropane-1-carboxylic acid synthase (ACS), th
61 ACS9, respectively; these encode isozymes of 1-aminocyclopropane-1-carboxylic acid synthase (ACS), wh
62 ffect the post-transcriptional regulation of 1-aminocyclopropane-1-carboxylic acid synthase (ACS).
64 e plant showed only a moderate regulation of 1-aminocyclopropane-1-carboxylic acid synthase and Yang
65 ated by sequence alignment of genes encoding 1-aminocyclopropane-1-carboxylic acid synthase from both
66 bited the auxin induction of only one of two 1-aminocyclopropane-1-carboxylic acid synthase genes tha
68 o be mediated by increase in net activity of 1-aminocyclopropane-1-carboxylic acid synthase, it might
70 tromules were induced by treatment with ACC (1-aminocyclopropane-1-carboxylic acid), the first commit
71 nhibitor II gene in response to Botrytis and 1-aminocyclopropane-1-carboxylic acid, the natural precu
72 at BAP increases ABA levels in the shoot and 1-aminocyclopropane-1-carboxylic acid, the rate-limiting
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