Polysaccharides from prunes: Gastroprotective activity and structural elucidation of bioactive pectins
Introduction
Prunes are the dried fruits from Prunus domestica L. which is originated from the Caucasus regions, bordering the Caspian Sea (Stacewicz-Sapuntzakis, Bowen, Hussain, Damayanti-Wood, & Farnsworth, 2011). This specie belongs to the genus Prunus (Rosaceae family), that comprises other plants that also produce edible fruits such as peach (Prunus persica), cherries (Prunus cerasus and Prunus avium) and apricot (Prunus insitia) (Stephen, 1983).
Prunes have a large economic impact especially in California, which is responsible for an average of 70% of the world’s prune supply, and was estimated to produce 120,000 tons of prunes in 2012 (Perez & Pollack, 2012). Thought the main usage of prunes is for direct consumption, there are several other applications for it in the culinary and industry, such as in the production of prune juice, prune puree, mixtures with cereal or even ground meat, and for the development of products that replace fat in baking (Stacewicz-Sapuntzakis et al., 2011).
Prunes are also used as a remedy for various diseases. Recent studies also showed clinical evidence of its activity in the treatment of constipation, osteoporosis, hypertension and dyslipidemia (Stacewicz-Sapuntzakis et al., 2011). It was also shown that fibres from prunes lowered plasma and liver lipids (Tinker, Davis, & Schneeman, 1994) and probably were the most important components responsible for satiety promoted by prunes consumption (Farajian, Katsagani, & Zampelas, 2010).
Carbohydrates are the main macronutrient in prunes, and consist 62.7% of their total weight (Stacewicz-Sapuntzakis et al., 2011). Despite this high content and their importance for some biological functions attributed to prunes, up to now, only the presence of a xyloglucan was reported in prunes (Ito & Kato, 2002). Thus, this paper reports the isolation, composition, and structural features of two rhamnogalacturonans with type I arabinogalactan side chains from prunes, as well as the anti-ulcer activity of both crude and a purified fractions. To our knowledge, neither the structure of these pectic polysaccharides isolated from prunes nor their gastroprotective activity has been reported yet.
Section snippets
Plant material
Pitted prunes (P. domestica) from cultivar d’Agen were purchased in a local market in Curitiba/PR (LA VIOLETERA®).
General analytical methods
Fractions were carboxy-reduced by the carbodiimide method (Taylor & Conrad, 1972) using NaBH4 as the reducing agent, giving products with the –COOH groups of its uronic acid residues reduced to –CH2OH.
The degree of acetylation (DA) was determined after spectrophotometric quantification of acetyl following the method of Hestrin (1949), employing galactose pentaacetate as a standard.
Extraction and purification of polysaccharides
Results and discussion
Polysaccharides were extracted from prunes with cold and hot water, giving fractions PWC (0.5% yield) and PWH (8.1% yield), respectively. Monosaccharide analysis of these fractions indicated Ara:Gal:Glc as neutral sugars in the 16:15:3 and 23:21:2 molar ratios, respectively. The content of uronic acids was determined spectrophotometrically and showed values of 66% and 54%, respectively.
A freeze-thaw treatment was applied in fractions PWC and PWH, however, no cold-water insoluble polysaccharides
Acknowledgements
This research was supported by Projeto Universal (Process 475747/2010-0) provided by CNPq foundation (Brazil) and by PRONEX-Carboidratos. C.H. Baggio is recipient of post-doctoral scholarship from the CNPq. The authors are grateful to Dr. Guilherme L. Sassaki and Arquimedes Santana-Filho for recording the NMR spectra.
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