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1. (Article ID: 12626)
Ruuhola TM, Julkunen-Tiitto M-RK
Salicylates of intact Salix myrsinifolia plantlets do not undergo rapid metabolic turnover
Plant Physiology 122(3) (2000)
895-905
Salicylates, the main phenolic glucosides of northern willow (Salix spp.), play an important role in plant-herbivore interactions. Salicylates are labile metabolites that are thought to undergo metabolic turnover. Salicylates are synthesized from phenylalanine (Phe) via the shikimate pathway. 2-Aminoindan-2-phosphonic acid (AIP), a strong inhibitor of Phe ammonia-lyase (EC 4.3.1.5), was used to block the biosynthesis of salicylates. The aim of this study was to investigate long-term turnover of salicylates in intact micropropagated plantlets of Salix myrsinifolia Salisb. The biosynthesis of salicylates was inhibited efficiently but not completely by 30 microM 2-aminoindan-2-phosphonic acid. Inhibitor treatment, aside from leading to a high accumulation of Phe, also led to an increase in tyrosine and tryptophan, indicating that 2-aminoindan-2-phosphonic acid may also inhibit enzymes other than Phe ammonia-lyase. Salicylates were shown to be unexpectedly stable metabolites that did not undergo marked metabolic turnover in intact plants; in leaves no significant turnover occurred, and in the stems the five salicylates studied were turned over slowly, with half-lives of 11 to 25 d. The total amount of salicylate in mature shoots decreased only 0.6% per day.
salicylic acid, salicin, Salix myrsinifolia
NCBI PubMed ID: 10712554Publication DOI: 10.1104/pp.122.3.895Journal NLM ID: 0401224Publisher: American Society of Plant Biologists
Correspondence: ruuhola

cc.joensuu.fi
Institutions: Department of Biology, University of Joensuu, Joensuu, Finland
Methods: biological assays
The publication contains the following compound(s):
- Compound ID: 29194
|
b-D-Glcp-(1-2)-Subst
Subst = salicyl alcohol = SMILES O{2}C1=CC=CC=C1{7}CO |
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Structure type: monomer
Trivial name: salicin
Compound class: glycoside, phenolic glycoside
- Compound ID: 32698
|
b-D-Glcp-(1-7)-+
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b-D-Glcp-(1-2)-Subst
Subst = salicyl alcohol = SMILES O{2}C1=CC=CC=C1{7}CO |
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Structure type: oligomer
Trivial name: salicin diglucoside
Compound class: glycoside, phenolic glycoside
- Compound ID: 32699
|
b-D-Glcp2Ac-(1-2)-Subst
Subst = salicyl alcohol = SMILES O{2}C1=CC=CC=C1{7}CO |
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Structure type: monomer
Trivial name: 2'-O-acetylsalicin
Compound class: glycoside, phenolic glycoside
- Compound ID: 32700
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Subst1-(7-7)-+
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b-D-Glcp-(1-2)-Subst
Subst = salicyl alcohol = SMILES O{2}C1=CC=CC=C1{7}CO;
Subst1 = salicortin |
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Structure type: monomer
Trivial name: salicortin
Compound class: glycoside, phenolic glycoside
- Compound ID: 32701
|
Subst1-(7-7)-+
|
b-D-Glcp2Ac-(1-2)-Subst
Subst = salicyl alcohol = SMILES O{2}C1=CC=CC=C1{7}CO;
Subst1 = salicortin |
Show graphically |
Structure type: monomer
Trivial name: 2'-O-acetylsalicortin
Compound class: glycoside, phenolic glycoside
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