Abstract

Methods to analyze lipidomes have considerably evolved, more and more based on mass spectrometry technics (LC-MS/MS). However, accurate quantifications using these methods require 13C-labeled standards for each lipid, which is not feasible because of the very large number of molecules. Thus, quantifications rely on standard molecules representative of a whole class of lipids, which might lead to false estimations of some molecular species. Here, we determined and compared glycerolipid distributions from three different types of cells, two microalgae (Phaeodactylum tricornutum, Nannochloropsis gaditana) and one higher plant (Arabidopsis thaliana), using either LC-MS/MS or Thin Layer Chromatography coupled with Gas Chromatography (TLC-GC), this last approach relying on the precise quantification of the fatty acids present in each glycerolipid class. Our results showed that the glycerolipid distribution was significantly different depending on the method used. How can one reconcile these two analytical methods? Here we propose that the possible bias with MS data can be circumvented by systematically running in tandem with the sample to be analyzed a lipid extract from a qualified control (QC) of each type of cells, previously analyzed by TLC-GC, and used as an external standard to quantify the MS results. As a case study, we applied this method to compare the impact of a nitrogen deficiency on the three types of cells.

Highlights

  • Understanding lipid metabolism is today an important field of research with potential applications in various domains such as health, food, biofuel, green chemistry and many others [1, 2]

  • We developed a Liquid chromatography (LC) protocol to separate in one run most of the glycerolipids, and we quantified these lipids by electrospray ionization (ESI)-mass spectrometry (MS)/MS

  • We compared these results with those obtained after separation of the lipids by thin layer chromatography (TLC) followed by the analyses of their fatty acids (FA) by GC-Flame ionization detector (FID)

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Summary

Introduction

Understanding lipid metabolism is today an important field of research with potential applications in various domains such as health, food, biofuel, green chemistry and many others [1, 2] In this context, the number of reports concerning the characterization of lipidomes from numerous varieties of plants and microalgae increased exponentially this past decade. DAG can originate from de novo synthesis or by the recycling of membrane lipids [9, 10] Another route to produce TAG involves a phospholipid:DAG acyltransferase (PDAT) activity [9], where the FA moiety added at the sn-3 position of the glycerol backbone originates from a membrane lipid (mostly phosphatidylcholine, PC), and not from the acyl-CoA pool [11]. Membrane and storage lipids are intimately connected, and it is required to have a good understanding of the metabolisms and regulations involved in TAG synthesis to have a complete overview of the glycerolipidome

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