Rapid profiling of intact glucosinolates in Arabidopsis leaves by UHPLC-QTOFMS using a charged surface hybrid column.

Détails

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Etat: Public
Version: Author's accepted manuscript
ID Serval
serval:BIB_484BAC961282
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Rapid profiling of intact glucosinolates in Arabidopsis leaves by UHPLC-QTOFMS using a charged surface hybrid column.
Périodique
Phytochemical Analysis
Auteur⸱e⸱s
Glauser G., Schweizer F., Turlings T.C., Reymond P.
ISSN
1099-1565 (Electronic)
ISSN-L
0958-0344
Statut éditorial
Publié
Date de publication
2012
Volume
23
Numéro
5
Pages
520-528
Langue
anglais
Résumé
INTRODUCTION: The analysis of glucosinolates (GS) is traditionally performed by reverse-phase liquid chromatography coupled to ultraviolet detection after a time-consuming desulphation step, which is required for increased retention. Simpler and more efficient alternative methods that can shorten both sample preparation and analysis are much needed.
OBJECTIVE: To evaluate the feasibility of using ultrahigh-pressure liquid chromatography coupled to quadrupole time-of-flight mass spectrometry (UHPLC-QTOFMS) for the rapid profiling of intact GS.
METHODOLOGY: A simple and short extraction of GS from Arabidopsis thaliana leaves was developed. Four sub-2 µm reverse-phase columns were tested for the rapid separation of these polar compounds using formic acid as the chromatographic additive. High-resolution QTOFMS was used to detect and identify GS.
RESULTS: A novel charged surface hybrid (CSH) column was found to provide excellent retention and separation of GS within a total running time of 11 min. Twenty-one GS could be identified based on their accurate mass as well as isotopic and fragmentation patterns. The method was applied to determine the changes in GS content that occur after herbivory in Arabidopsis. In addition, we evaluated its applicability to the profiling of other Brassicaceae species.
CONCLUSION: The method developed can profile the full range of GS, including the most polar ones, in a shorter time than previous methods, and is highly compatible with mass spectrometric detection.
Mots-clé
Arabidopsis/chemistry, Brassica/chemistry, Chemical Fractionation/instrumentation, Chemical Fractionation/methods, Chromatography, High Pressure Liquid/instrumentation, Chromatography, High Pressure Liquid/methods, Chromatography, Reverse-Phase/instrumentation, Chromatography, Reverse-Phase/methods, Glucose/analogs & derivatives, Glucose/chemistry, Glucosinolates/analysis, Glucosinolates/chemistry, Imidoesters/chemistry, Imidoesters/isolation & purification, Inflorescence/chemistry, Mass Spectrometry/instrumentation, Mass Spectrometry/methods, Plant Extracts/chemistry, Plant Leaves/chemistry, Seeds/chemistry
Pubmed
Web of science
Open Access
Oui
Création de la notice
18/12/2012 18:17
Dernière modification de la notice
20/08/2019 14:55
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