首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Liquid chromatography-mass spectrometry coupled with multivariate analysis for the characterization and discrimination of extractable and nonextractable polyphenols and glucosinolates from red cabbage and Brussels sprout waste streams
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Liquid chromatography-mass spectrometry coupled with multivariate analysis for the characterization and discrimination of extractable and nonextractable polyphenols and glucosinolates from red cabbage and Brussels sprout waste streams

机译:液相色谱-质谱联用多变量分析对红甘蓝和布鲁塞尔芽菜废液中可萃取和不可萃取的多酚和芥子油苷进行表征和鉴别

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摘要

Nonextractable polyphenol (NEP) fractions are usually ignored because conventional extraction methods do not release them from the plant matrix. In this study, we optimized the conditions for sonicated alkaline hydrolysis to the residues left after conventional polyphenol extraction of Brussels sprouts top (80 degrees C, 4 M NaOH, 30 min) and stalks (60 degrees C, 4M NaOH, 30 min), and red cabbage waste streams (80 degrees C, 4 M NaOH, 45 min) to release and characterize the NEP fraction. The NEP fractions of Brussels sprouts top (4.8 +/- 1.2 mg gallic acid equivalents [GAE]/g dry waste) and stalks (3.3 +/- 0.2 mg GAE/g dry waste), and red cabbage (11.5 mg GAE/g dry waste) waste have significantly higher total polyphenol contents compared to their respective extractable polyphenol (EP) fractions (1.5 +/- 0.0, 2.0 +/- 0.0 and 3.7 +/- 0.0 mg GAE/g dry waste, respectively). An LC-MS method combined with principal components analysis (PCA) and orthogonal partial least squares discriminant analysis (OPLS-DA) was used to tentatively identify and discriminate the polyphenol and glucosinolate composition of the EP and NEP fractions. Results revealed that phenolic profiles of the EP and NEP fractions are different and some compounds are only found in either fraction in all of the plant matrices. This suggests the need to account both fractions when analyzing the polyphenol and glucosinolate profiles of plant matrices to attain a global view of their composition. This is the first report on the discrimination of the phenolic and glucosinolate profiles of the EP and NEP fractions using metabolomics techniques. (C) 2015 Elsevier B.V. All rights reserved.
机译:不可提取的多酚(NEP)馏分通常被忽略,因为常规提取方法不会将其从植物基质中释放出来。在这项研究中,我们优化了超声处理碱性水解条件的条件,以常规方式对布鲁塞尔豆芽顶部(80摄氏度,4 M NaOH,30分钟)和秸秆(60摄氏度,4M NaOH,30分钟)进行多酚萃取后残留的残留物,和红甘蓝废物流(80摄氏度,4 M NaOH,45分钟)释放并表征NEP馏分。布鲁塞尔芽菜的NEP分数最高(4.8 +/- 1.2 mg没食子酸当量[GAE] / g干垃圾)和茎(3.3 +/- 0.2 mg GAE / g干垃圾)和红甘蓝(11.5 mg GAE / g相较于其各自的可提取多酚(EP)馏分,干废弃物中的总多酚含量要高得多(分别为1.5 +/- 0.0、2.0 +/- 0.0和3.7 +/- 0.0 mg GAE / g干废弃物)。结合主成分分析(PCA)和正交偏最小二乘判别分析(OPLS-DA)的LC-MS方法用于初步鉴定和区分EP和NEP馏分的多酚和芥子油苷成分。结果表明,EP和NEP馏分的酚类特征不同,并且在所有植物基质的任一馏分中都发现了某些化合物。这表明在分析植物基质的多酚和芥子油苷分布时,需要考虑这两个部分,以全面了解其组成。这是关于使用代谢组学技术区分EP和NEP馏分的酚类和芥子油苷谱的首次报道。 (C)2015 Elsevier B.V.保留所有权利。

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