s: Adriana Garibay-Hern andez, Nikolas Kessler; Adriana Garibay-Hern andez and Hans-Peter Mock wrote the manuscript. All authors reviewed and approved the final manuscript. DATA AVAILABILITY STATEMENT The data supporting this study are openly available through the e!DAL electronic data archive library (Arend et al., 2014) at: https://doi.org/10.5447/ipk/2021/11 694 GARIBAY-HERN ANDEZ ET AL. Physiologia Plantarum 13993054, 2021, 3, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/ppl.13458, Wiley Online Library on [26/08/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are govern
Open resource ↗e!DAL · 10.5447/ipk/2021/11 · pdf-raw-page:15 lines:80-149Unverified paper record
Untargeted metabotyping to study phenylpropanoid diversity in crop plants.
Physiologia plantarum · 27 May 2021 · 10.1111/ppl.13458
Abstract
Plant genebanks constitute a key resource for breeding to ensure crop yield under changing environmental conditions. Because of their roles in a range of stress responses, phenylpropanoids are promising targets. Phenylpropanoids comprise a wide array of metabolites; however, studies regarding their diversity and the underlying genes are still limited for cereals. The assessment of barley diversity via genotyping-by-sequencing is in rapid progress. Exploring these resources by integrating genetic association studies to in-depth metabolomic profiling provides a valuable opportunity to study barley phenylpropanoid metabolism; but poses a challenge by demanding large-scale approaches. Here, we report an LC-PDA-MS workflow for barley high-throughput metabotyping. Without prior construction of a species-specific library, this method produced phenylpropanoid-enriched metabotypes with which the abundance of putative metabolic features was assessed across hundreds of samples in a single-processed data matrix. The robustness of the analytical performance was tested using a standard mix and extracts from two selected cultivars: Scarlett and Barke. The large-scale analysis of barley extracts showed (1) that barley flag leaf profiles were dominated by glycosylation derivatives of isovitexin, isoorientin, and isoscoparin; (2) proved the workflow's capability to discriminate within genotypes; (3) highlighted the role of glycosylation in barley phenylpropanoid diversity. Using the barley S42IL mapping population, the workflow proved useful for metabolic quantitative trait loci purposes. The protocol can be readily applied not only to explore the barley phenylpropanoid diversity represented in genebanks but also to study species whose profiles differ from those of cereals: the crop Helianthus annuus (sunflower) and the model plant Arabidopsis thaliana.
Plant phenotyping relevance
植物試料の代謝状態を大規模に抽出するLC-PDA-MSメタボタイピング・ワークフローが研究の中心で、分析性能の検証と遺伝型識別・代謝QTLへの適用まで示しているため、単なる生物学的測定ではない。
abstractHere, we report an LC-PDA-MS workflow for barley high-throughput metabotyping.
abstractThe robustness of the analytical performance was tested using a standard mix and extracts from two selected cultivars: Scarlett and Barke.
abstractThe protocol can be readily applied not only to explore the barley phenylpropanoid diversity represented in genebanks but also to study species whose profiles differ from those of cereals: the crop Helianthus annuus (sunflower) and the model plant Arabidopsis thaliana.
Code and data availability
The paper's LC–MS metabotyping data (barley, sunflower, Arabidopsis phenylpropanoid profiles) are openly deposited in the IPK e!DAL archive, per the Data Availability Statement. No author analysis code is described; MetaboScape is proprietary software.
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