TY - JOUR
T1 - Metabolomics for biomarker discovery
T2 - Key signatory metabolic profiles for the identification and discrimination of oat cultivars
AU - Pretorius, Chanel J.
AU - Tugizimana, Fidele
AU - Steenkamp, Paul A.
AU - Piater, Lizelle A.
AU - Dubery, Ian A.
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/3
Y1 - 2021/3
N2 - The first step in crop introduction—or breeding programmes—requires cultivar identification and characterisation. Rapid identification methods would therefore greatly improve registra-tion, breeding, seed, trade and inspection processes. Metabolomics has proven to be indispensable in interrogating cellular biochemistry and phenotyping. Furthermore, metabolic fingerprints are chemical maps that can provide detailed insights into the molecular composition of a biological system under consideration. Here, metabolomics was applied to unravel differential metabolic profiles of various oat (Avena sativa) cultivars (Magnifico, Dunnart, Pallinup, Overberg and SWK001) and to identify signatory biomarkers for cultivar identification. The respective cultivars were grown under controlled conditions up to the 3‐week maturity stage, and leaves and roots were harvested for each cultivar. Metabolites were extracted using 80% methanol, and extracts were analysed on an ultra‐high performance liquid chromatography (UHPLC) system coupled to a quadrupole time-of‐flight (qTOF) high‐definition mass spectrometer analytical platform. The generated data were processed and analysed using multivariate statistical methods. Principal component analysis (PCA) models were computed for both leaf and root data, with PCA score plots indicating cultivar‐related clustering of the samples and pointing to underlying differential metabolic profiles of these culti-vars. Further multivariate analyses were performed to profile differential signatory markers, which included carboxylic acids, amino acids, fatty acids, phenolic compounds (hydroxycinnamic and hy-droxybenzoic acids, and associated derivatives) and flavonoids, among the respective cultivars. Based on the key signatory metabolic markers, the cultivars were successfully distinguished from one another in profiles derived from both leaves and roots. The study demonstrates that metabo-lomics can be used as a rapid phenotyping tool for cultivar differentiation.
AB - The first step in crop introduction—or breeding programmes—requires cultivar identification and characterisation. Rapid identification methods would therefore greatly improve registra-tion, breeding, seed, trade and inspection processes. Metabolomics has proven to be indispensable in interrogating cellular biochemistry and phenotyping. Furthermore, metabolic fingerprints are chemical maps that can provide detailed insights into the molecular composition of a biological system under consideration. Here, metabolomics was applied to unravel differential metabolic profiles of various oat (Avena sativa) cultivars (Magnifico, Dunnart, Pallinup, Overberg and SWK001) and to identify signatory biomarkers for cultivar identification. The respective cultivars were grown under controlled conditions up to the 3‐week maturity stage, and leaves and roots were harvested for each cultivar. Metabolites were extracted using 80% methanol, and extracts were analysed on an ultra‐high performance liquid chromatography (UHPLC) system coupled to a quadrupole time-of‐flight (qTOF) high‐definition mass spectrometer analytical platform. The generated data were processed and analysed using multivariate statistical methods. Principal component analysis (PCA) models were computed for both leaf and root data, with PCA score plots indicating cultivar‐related clustering of the samples and pointing to underlying differential metabolic profiles of these culti-vars. Further multivariate analyses were performed to profile differential signatory markers, which included carboxylic acids, amino acids, fatty acids, phenolic compounds (hydroxycinnamic and hy-droxybenzoic acids, and associated derivatives) and flavonoids, among the respective cultivars. Based on the key signatory metabolic markers, the cultivars were successfully distinguished from one another in profiles derived from both leaves and roots. The study demonstrates that metabo-lomics can be used as a rapid phenotyping tool for cultivar differentiation.
KW - Avena sativa
KW - Cultivar distinction
KW - Liquid chromatography
KW - Mass spectrometry
KW - Metabo-lomics
KW - Multivariate data analysis
KW - Oat
KW - Secondary metabolites
UR - http://www.scopus.com/inward/record.url?scp=85103131475&partnerID=8YFLogxK
U2 - 10.3390/metabo11030165
DO - 10.3390/metabo11030165
M3 - Article
AN - SCOPUS:85103131475
SN - 2218-1989
VL - 11
JO - Metabolites
JF - Metabolites
IS - 3
M1 - 165
ER -