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Journal of the American Oil Chemists' Society, 2019-03, Vol.96 (3), p.303-317
2019
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Autor(en) / Beteiligte
Titel
Primary Metabolites and Polyphenols in Rapeseed (Brassica napus L.) Cultivars in China
Ist Teil von
  • Journal of the American Oil Chemists' Society, 2019-03, Vol.96 (3), p.303-317
Ort / Verlag
Hoboken, USA: John Wiley & Sons, Inc
Erscheinungsjahr
2019
Quelle
Access via Wiley Online Library
Beschreibungen/Notizen
  • Defatted meals of 10 rapeseed (Brassica napus L.) varieties were investigated for their total phenolic, phenolic acid (free, esterified, and insoluble‐bound forms), and tannin contents. The antioxidant capacities (AC) of methanol extracts from samples were assessed using the 2,2′‐diphenyl‐1‐picrylhydrazyl radical (DPPH•), Folin–Ciocalteu method and ferric reducing antioxidant power (FRAP), and β‐carotene–linoleic acid tests. In the fraction of free phenolic acids, sinapic, caffeic, ferulic, syringic, gallic, and p‐coumaric acids were identified. In the fraction of esterified phenolic acids, sinapine, sinapoyl glucoside, and disinapoyl gentiobiose were identified. After basic hydrolysis, sinapic, ferulic, cinnamic, and 4‐hydroxybenzoic acids were identified, and sinapic acid (SA) constituted 98.3% to 99.6% of the total esterified phenolic acids. Eleven components (sinapic, protocatechuic, p‐coumaric, syringic, vanillic, gallic, caffeic, ferulic, salicylic, cinnamic, and 4‐hydroxybenzoic acids) in the fraction of insoluble‐bound phenolic acids were identified. The AC of the samples correlated with the total phenolic content. Overall, the total phenolics showed a better correlation with AC than the individual phenolic compounds. Moreover, SA, sinapoyl glucoside, and disinapoyl gentiobiose showed a highly significant and strong positive correlation with the AC of rapeseed meals, and the derivatives of cinnamic acid showed a higher correlation with AC than the derivatives of benzoic acid. The change in the canolol content in rapeseeds under microwave irradiation is discussed. The correlation of the canolol formed with SA and its derivatives is discussed.
Sprache
Englisch
Identifikatoren
ISSN: 0003-021X
eISSN: 1558-9331
DOI: 10.1002/aocs.12179
Titel-ID: cdi_crossref_primary_10_1002_aocs_12179

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