Improved stability of TMS derivatives for the robust quantification of plant polar metabolites by gas chromatography–mass spectrometry

• Published in: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2014-11, Vol.970, p.36-43
• Main Authors: Quéro, Anthony, Jousse, Cyril, Lequart-Pillon, Michelle, Gontier, Eric, Guillot, Xavier, Courtois, Bernard, Courtois, Josiane, Pau-Roblot, Corinne
• Format: Article
• Language: English
• Subjects: Amino acids; Amino Acids - analysis; Amino Acids - chemistry; Arabidopsis - metabolism; Carbohydrates - analysis; Carbohydrates - chemistry; Derivatives; Gas Chromatography-Mass Spectrometry - methods; GC–MS; Ionization; Life Sciences; Metabolite profiling; Metabolites; Metabolome - physiology; Metabolomics - methods; Quantitative analysis; Sampling; Searching; Seeds - chemistry; Stability; Temperature; TMS derivatives; Trimethylsilyl Compounds - analysis; Trimethylsilyl Compounds - chemistry; Vials
• ISSN: 1570-0232; 1873-376X
• DOI: 10.1016/j.jchromb.2014.08.040

•Problem for polar metabolites quantification with GC–MS due to low stability of some TMS derivatives.•TMS derivatives stability: importance of temperature storage before injection into GC–MS.•TMS derivatives stability: avoid multiple samplings from a unique vial.•Recommendations for robust quantification of plant polar metabolites by GC–MS. Plant metabolite profiling is commonly carried out by GC–MS of methoximated trimethylsilyl (TMS) derivatives. This technique is robust and enables a library search for spectra produced by electron ionization. However, recent articles have described problems associated with the low stability of some TMS derivatives. This limits the use of GC–MS for metabolomic studies that need large sets of qualitative and quantitative analyses. The aim of this work is to determine the experimental conditions in which the stability of TMS derivatives could be improved. This would facilitate the analysis of the large-scale experimental designs needed in the metabolomics approach. For good repeatability, the sampling conditions and the storage temperature of samples during analysis were investigated. Multiple injections of one sample from one vial led to high variations while injection of one sample from different vials improved the analysis. However, before injection, some amino acid TMS derivatives were degraded during the storage of vials in the autosampler. Only 10% of the initial quantity of glutamine 3 TMS and glutamate 3 TMS and 66% of α-alanine 2 TMS was detected 48h after derivatization. When stored at 4°C until injection, all TMS derivatives remained stable for 12h; at −20°C, they remained stable for 72h. From the integration of all these results, a detailed analytical procedure is thus proposed. It enables a robust quantification of polar metabolites, useful for further plant metabolomics studies using GC–MS.