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Validated Method for Strigolactone Quantification by Ultra High‐Performance Liquid Chromatography – Electrospray Ionisation Tandem Mass Spectrometry Using Novel Deuterium Labelled Standards
Authors:Stéphanie Boutet‐Mercey  François Perreau  Amélie Roux  Guillaume Clavé  Jean‐Paul Pillot  Isabelle Schmitz‐Afonso  David Touboul  Grégory Mouille  Catherine Rameau  François‐Didier Boyer
Institution:1. Institut Jean‐Pierre Bourgin, INRA, AgroParisTech, CNRS, Université Paris‐Saclay, Versailles, France;2. Institut de Chimie des Substances Naturelles, CNRS UPR2301, Univ. Paris‐Sud, Université Paris‐Saclay, Gif‐sur‐Yvette, France;3. Normandie Univ, COBRA, UMR 6014 and Univ Rouen, INSA Rouen, CNRS, FR3038, IRCOF, France
Abstract:

Introduction

Strigolactones (SLs) are important plant hormones. They are difficult to analyse because they occur in very small concentrations especially in comparison with other plant hormones and other substances can interfere with their detection.

Objective

To develop a procedure for the extraction, purification and quantification of SLs from plant roots.

Methodology

Samples were prepared by extraction of plant root tissues with ethyl acetate. Then the extracts were further purified with silica column chromatography. The natural SLs in the final extracts were quantified using novel deuterium labelled SLs. The results of the methodology were compared with those of the procedure of Yoneyama and coworkers.

Results

This procedure required about 1‐g root samples to detect and quantify simultaneously the SLs (orobanchyl acetate and fabacyl acetate) concentration with high reliability.

Conclusion

A method was developed for determining endogenous fabacyl acetate and orobanchyl acetate in plant tissue based on novel deuterium labelled standards. A method of orobanchol quantification using a synthetic SL GR24 as internal standard was proposed. Copyright © 2017 John Wiley & Sons, Ltd.
Keywords:Strigolactones  plant hormones  deuterium‐labelled strigolactones  pea  UHPLC‐ESI‐MS/MS
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