2013
DOI: 10.1016/j.plaphy.2013.04.026
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Metabolites of Ammopiptanthus mongolicus induced by Orgyia ericae attack and mechanical wounding

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Cited by 6 publications
(11 citation statements)
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“…And there was no mark of TIAs in stems under RT group. It indicates that the responses of RT group to wounding take place at the site of injure, that is local responses, where the metabolites were directly used for mechanical defense (Sun et al 2013). By contrast, the major site of action of these significantly different metabolites was stems in LT group.…”
Section: Discussionmentioning
confidence: 92%
See 1 more Smart Citation
“…And there was no mark of TIAs in stems under RT group. It indicates that the responses of RT group to wounding take place at the site of injure, that is local responses, where the metabolites were directly used for mechanical defense (Sun et al 2013). By contrast, the major site of action of these significantly different metabolites was stems in LT group.…”
Section: Discussionmentioning
confidence: 92%
“…By contrast, the major site of action of these significantly different metabolites was stems in LT group. Systemic response adopted by LT group and need time to regulations (Sun et al 2013). Therefore, different responses style was adopted between RT group and LT group in terms of TIAs accumulation.…”
Section: Discussionmentioning
confidence: 99%
“…Metabolites in roots were identified according to our previous results [19] and literature data [18], [24], [25], 2D NMR spectra or pure compounds and the 1 H chemical shifts and coupling constants of identified signals were listed in table 1. Metabolites identified from leaves and roots included fatty acids, organic acids, amino acids, sugars, alcohols, aromatic compounds, alkaloids and isoflavones.…”
Section: Resultsmentioning
confidence: 99%
“…Leaves and roots were extracted according to the method used by Kim et al [18] with some modifications as in our previous study [19]. Plant materials were grinded with pestle and mortar under liquid nitrogen into fine powder, and then were freeze-dried for 24 h. After weighting dried samples, solvent containing 0.75 ml CD 3 OD and 0.75 ml KH 2 PO 4 buffer in D 2 O (pH 6.0) with 0.05% (wt/wt) TSP were added into each centrifuge tube containing dried powder of fifty milligram leaves or forty milligram roots.…”
Section: Methodsmentioning
confidence: 99%
“…76 This method can also distinguish compounds with identical masses, including those with different isotopomer distributions, 77 and compounds that exhibit similar elution behavior in conventional chromatography. For instance, the isomers 3-Oand 5-O-caffeoylquinic acid, which are challenging to Saccharides and glycosylic portion stachyose, 34,35 rhamnose in rutin, 36 pinitol, 37 rhamnose in flavonoid, 38 raffinose, 36 gentisic acid glucoside, 36 neochlorogenic acid (3-O-caffeoylquinic acid), 33,35,38,39,43,63,64 4-O-caffeoylquinic acid, 38,63 chlorogenic acid (5-O-caffeoylquinic acid), 33,35,36,38,41,43,56,57,63,65 trans-caffeoyl derivatives, 50 trans-feruloyl derivatives, 50 trans-caftaric acid, 50 trans-fertaric acid, 50 caffeoyl esters of polyhydroxy compounds, 54 p-coumaric acid, 58 5-O-feruloyl quinic acid, 35,43 trans-cinnamic acid 50 Furano lactones limonin, 59,66 limonin glucoside 59,66,67 Glucosinolates neoglucobrassicin, 28 progoitrin, 28,30 gluconapin, 48 sinigrin 51 Alkaloids synephrine, 59,66,67 nicotine, 38 vindoline, 57 …”
Section: Potentials Of 1 H Nmr In Plant Researchmentioning
confidence: 99%