Carbon-13 Cross-Polarization Magic-Angle Spinning Nuclear Magnetic Resonance for Measuring Proanthocyanidin Content and Procyanidin to Prodelphinidin Ratio in Sainfoin (Onobrychis viciifolia) Tissues

被引:6
|
作者
Fryganas, Christos [1 ,5 ]
Drake, Christopher [1 ]
Ropiak, Honorata M. [1 ,6 ]
Mora-Ortiz, Marina [2 ]
Smith, Lydia M. J. [3 ]
Mueller-Harvey, Irene [1 ]
Kowalczyk, Radoslaw M. [4 ]
机构
[1] Univ Reading, Sch Agr Policy & Dev, POB 236,1 Earley Gate, Reading RG6 6AT, Berks, England
[2] Univ Reading, Dept Food & Nutr Sci, Whiteknights Campus,POB 226, Reading RG6 6AP, Berks, England
[3] Natl Inst Agr Bot, Huntingdon Rd, Cambridge CB3 OLE, England
[4] Univ Reading, Sch Chem Food & Pharm, Chem Anal Facil, POB 224,Whiteknights Campus, Reading RG6 6AD, Berks, England
[5] Wageningen Univ, Biobased Chem & Technol, POB 17,Bornse Weilanden 9, NL-6700 AA Wageningen, Netherlands
[6] Pirbright Inst, Ash Rd, Woking GU24 0NF, Surrey, England
关键词
condensed tannins; CPMAS NMR; thiolysis; HCl-butanol-acetone assay; extractable and nonextractable proanthocyanidins; sainfoin; CONDENSED TANNINS; NMR-SPECTROSCOPY; FORAGE LEGUMES; DEGRADATION; POLYPHENOLS; PLANTS; QUALITY; BARK;
D O I
10.1021/acs.jafc.8b01215
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
A procedure based on C-13 CPMAS NMR was developed to study procyanidins (PCs) and prodelphinidins (PDs) directly in milled sainfoin plant tissues. Blackcurrant and Tilia samples enabled reference spectra of purified proanthocyanidin (PA) fractions, crude extracts, and milled plant tissues, with characteristic resonances at 155, 144, and 132 ppm. PC/PD ratios were estimated from the I-132/I-155 intensity ratio and differed by 2.5 to 5.9% compared to thiolysis data. Normalization to the 155 ppm signal intensity from reference spectra enabled analysis of PA contents with an error of ca. 8 g PAs/100 g plant tissue. The procedure estimates the lignin contribution and allows for a correction of the PA content. In six sainfoin accessions, estimated PA contents were 1.6- to 20.8-fold higher than the thiolysis and 1.4- to 2.6-fold higher than the HCl-butanol-acetone results. Method differences may reflect the presence of unextractable, possibly high molecular weight PAs in sainfoin.
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页码:4073 / 4081
页数:9
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