Structural characterisation of polysaccharides purified from longan (Dimocarpus longan Lour.) fruit pericarp

被引:114
作者
Yang, Bao [1 ]
Jiang, Yueming [1 ]
Zhao, Mouming [2 ]
Chen, Feng [3 ]
Wang, Rui [1 ]
Chen, Yulong [1 ]
Zhang, Dandan [1 ]
机构
[1] Chinese Acad Sci, S China Bot Garden, Guangzhou 510650, Guangdong, Peoples R China
[2] S China Univ Technol, Coll Light Ind & Food Sci, Guangzhou 510650, Guangdong, Peoples R China
[3] Clemson Univ, Dept Food Sci & Human Nutr, Clemson, SC 29634 USA
基金
中国国家自然科学基金;
关键词
Longan; Polysaccharide; GC/MS; NMR; Methylation analysis; EXTRACELLULAR POLYSACCHARIDES; ADVANCED GLYCATION; FT-IR; SPECTROSCOPY; ANTIOXIDANT; EXTRACTS;
D O I
10.1016/j.foodchem.2008.12.082
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this work, crude polysaccharides were extracted from longan fruit pericarp by hot water. After removal of proteins and purification by Sephadex G-100 gel filtration column, polysaccharicles of longan fruit pericarp (PLFP) were subjected to structural identification. Gas chromatography analysis indicated PLFP comprised of L-arabinofuranose (32.8%), D-glucopyranose (17.6%), D-galactopyranose (33.7%) and D-galacturonic acid (15.9%). The glycosidic linkages were determined by methylation analysis and gas chromatography/mass spectrometry (GC/MS). The results showed that the backbone consisted of -> 5)-L-Araf-(1 ->, -> 6)-D-GIcp-(1 ->, -> 3)-D-Galp-(1 ->, -> 3)-D-GalpA-(1 -> and -> 6)-D-Galp-(1 -> with a molar proportion of 2:1:1:1:1. The infrared spectra and nuclear magnetic resonance (NMR) spectra further confirmed that the configuration of L-arabinofuranose was of alpha-form, while D-glucopyranose, D-galactopyranose and D-galacturonic acid were of beta-form. The molecular weight of PLFP was measured to be 420 kDa by gel permeation chromatography. By determination of the anti-glycated activity, PLFP showed a good potential in inhibiting the glycation reaction in vitro. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:609 / 614
页数:6
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