4.7 Article

Metabolite fingerprinting of pennycress (Thlaspi arvense L.) embryos to assess active pathways during oil synthesis

Journal

JOURNAL OF EXPERIMENTAL BOTANY
Volume 66, Issue 14, Pages 4267-4277

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jxb/erv020

Keywords

Alternative crop; erucic acid; GC-MS; jet fuel; LC-MS/MS; metabolomics; oilseed; pennycress; plant metabolism; Thlaspi arvense L.; triacylglycerols

Categories

Funding

  1. REU summer training grant [DBI-1062144]
  2. Center for Applied Plant Sciences (CAPS)
  3. Translational Plant Sciences Targeted Investment in Excellence (TIE)
  4. US Department of Energy, Office of Science [DE-FOA-0000995]
  5. US Department of Energy, Office of Basic Energy Sciences (BES) [DE-FOA-0000995]
  6. US Department of Energy, Office of Biological and Environmental Research (BER) [DE-FOA-0000995]
  7. Direct For Biological Sciences
  8. Div Of Molecular and Cellular Bioscience [1062144] Funding Source: National Science Foundation

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Pennycress (Thlaspi arvense L.), a plant naturalized to North America, accumulates high levels of erucic acid in its seeds, which makes it a promising biodiesel and industrial crop. The main carbon sinks in pennycress embryos were found to be proteins, fatty acids, and cell wall, which respectively represented 38.5, 33.2, and 27.0% of the biomass at 21 days after pollination. Erucic acid reached a maximum of 36% of the total fatty acids. Together these results indicate that total oil and erucic acid contents could be increased to boost the economic competitiveness of this crop. Understanding the biochemical basis of oil synthesis in pennycress embryos is therefore timely and relevant to guide future breeding and/or metabolic engineering efforts. For this purpose, a combination of metabolomics approaches was conducted to assess the active biochemical pathways during oil synthesis. First, gas chromatography-mass spectrometry (GC-MS) profiling of intracellular metabolites highlighted three main families of compounds: organic acids, amino acids, and sugars/sugar alcohols. Secondly, these intermediates were quantified in developing pennycress embryos by liquid chromatography-tandem mass spectrometry (LC-MS/MS) in multiple reaction monitoring mode. Finally, partitional clustering analysis grouped the intracellular metabolites that shared a similar pattern of accumulation over time into eight clusters. This study underlined that: (i) sucrose might be stored rather than cleaved into hexoses; (ii) glucose and glutamine would be the main sources of carbon and nitrogen, respectively; and (iii) glycolysis, the oxidative pentose phosphate pathway, the tricarboxylic acid cycle, and the Calvin cycle were active in developing pennycress embryos.

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