Abstract

Metabolomics is facing a major challenge: the lack of knowledge about metabolites present in a given biological system. Thus, large-scale discovery of metabolites is considered an essential step toward a better understanding of plant metabolism. We show here that the application of a metabolomics approach generating structural information for the analysis of Arabidopsis (Arabidopsis thaliana) mutants allows the efficient cataloging of metabolites. Fifty-six percent of the features that showed significant differences in abundance between seeds of wild-type, transparent testa4, and transparent testa5 plants could be annotated. Seventy-five compounds were structurally characterized, 21 of which could be identified. About 40 compounds had not been known from Arabidopsis before. Also, the high-resolution analysis revealed an unanticipated expansion of metabolic conversions upstream of biosynthetic blocks. Deficiency in chalcone synthase results in the increased seed-specific biosynthesis of a range of phenolic choline esters. Similarly, a lack of chalcone isomerase activity leads to the accumulation of various naringenin chalcone derivatives. Furthermore, our data provide insight into the connection between p-coumaroyl-coenzyme A-dependent pathways. Lack of flavonoid biosynthesis results in elevated synthesis not only of p-coumarate-derived choline esters but also of sinapate-derived metabolites. However, sinapoylcholine is not the only accumulating end product. Instead, we observed specific and sophisticated changes in the complex pattern of sinapate derivatives.

Highlights

  • Metabolomics is facing a major challenge: the lack of knowledge about metabolites present in a given biological system

  • An essential first step toward a better comprehension of regulation and dynamics is the large-scale discovery of metabolites in Arabidopsis (Arabidopsis thaliana) and other model plants or crops and the cataloging of all of the metabolites that are synthesized in a system under investigation (Last et al, 2007)

  • Through profiling and structural elucidation via collision-induced dissociation (CID)-MS/MS and ESI-Fourier transform ion cyclotron resonance (FTICR)-MS analyses, we found a surprising diversification of compounds upstream of metabolic blocks

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Summary

Introduction

Metabolomics is facing a major challenge: the lack of knowledge about metabolites present in a given biological system. Large-scale discovery of metabolites is considered an essential step toward a better understanding of plant metabolism. We show here that the application of a metabolomics approach generating structural information for the analysis of Arabidopsis (Arabidopsis thaliana) mutants allows the efficient cataloging of metabolites. The strategy we are adopting to contribute to cataloging the Arabidopsis metabolome is the application of a powerful metabolite profiling approach that has the potential to generate structural information (von Roepenack-Lahaye et al, 2004; De Vos et al, 2007) for the analysis of mutants with defined blocks in metabolic pathways. Coupling to reversed-phase chromatography covers compounds in the medium polarity range, among them representatives of five of the six biosynthetic classes distinguished to date in Arabidopsis secondary metabolism: glucosinolates and their breakdown products (isothiocyanates, nitriles), N-containing compounds (indole derivatives), phenylpropanoids, flavonoids/polyketides, and fatty acid derivatives (D’Auria and Gershenzon, 2005). Flavonoids negatively regulate polar auxin transport (Brown et al, 2001; Buer and Muday, 2004; Besseau et al, 2007)

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