4.7 Article

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

Journal

FOOD CHEMISTRY
Volume 115, Issue 2, Pages 609-614

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.foodchem.2008.12.082

Keywords

Longan; Polysaccharide; GC/MS; NMR; Methylation analysis

Funding

  1. National Natural Science Foundation of China [30425040, 30700557]
  2. International Foundation of Science [F/4451-1]
  3. Science Foundation of South China [200807]

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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.

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