Characterization of Epidermal Bladder Cells in Chenopodium quinoa
AuthorsOtterbach, Sophie L.
Kwan, Kim H.
Natera, Siria H. A.
Allen, Nathaniel M.
Jarvis, David E.
Schmoeckel, Sandra Manuela
KAUST Grant NumberNoha O. Saber
Embargo End Date2022-09-12
Permanent link to this recordhttp://hdl.handle.net/10754/669252
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AbstractChenopodium quinoa (quinoa) is considered a superfood with its favourable nutrient composition and being gluten free. Quinoa has high tolerance to abiotic stresses, such as salinity, water deficit (drought) and cold. The tolerance mechanisms are yet to be elucidated. Quinoa has Epidermal Bladder Cells (EBCs) that densely cover the shoot surface, particularly the younger parts of the plant. Here, we report on the EBC's primary and secondary metabolomes, as well as the lipidome in control conditions and in response to abiotic stresses. EBCs were isolated from plants after cold, heat, high-light, water deficit and salt treatments. We used untargeted Gas Chromatography-Mass Spectrometry (GC-MS) to analyse metabolites and untargeted and targeted Liquid Chromatography-MS (LC-MS) for lipids and secondary metabolite analyses. We identified 64 primary metabolites, including sugars, organic acids and amino acids, 19 secondary metabolites, including phenolic compounds, betanin and saponins and 240 lipids categorized in five groups including glycerolipids and phospholipids. We found only few changes in the metabolic composition of EBCs in response to abiotic stresses, these were metabolites related with heat, cold and high-light treatments, but not salt stress. Na+ concentrations were low in EBCs with all treatments, and approximately two orders of magnitude lower than K+ concentrations.
CitationOtterbach, S. L., Khoury, H., Rupasinghe, T., Mendis, H., Kwan, K. H., Lui, V., … Schmöckel, S. M. (2021). Characterization of Epidermal Bladder Cells in Chenopodium quinoa. Plant, Cell & Environment. doi:10.1111/pce.14181
SponsorsHK was supported by King Abdullah University of Science and Technology (VSRP funding). SMS received funding from the Ministry for Science, Research and Art of Baden-Wuerttemberg, Germany (Az: 75533-30-20/1). Lipid and primary metabolite analyses were performed at Metabolomics Australia at University of Melbourne, which is a National Collaborative Research Infrastructure Strategy initiative under Bioplatforms Australia Pty Ltd (http://www.bioplatforms.com/). We thank Noha O. Saber (KAUST, Saudi Arabia) for technical assistance, Alexa Wangler und Pascal Wendel (BSc, UHOH, Germany) for help with EBC collections. All authors declare no conflict of interest.
JournalPlant, Cell & Environment