An acidic heteropolysaccharide rich in galactose and arabinose derived from ginger: Structure and dynamics

多糖 阿拉伯糖 化学 半乳糖 单糖 丁酸 发酵 葡萄糖醛酸 鼠李糖 生物化学 醋酸 食品科学 戊酸 甘露糖 木糖
作者
Xiao-tong Lin,Bo-xian Xiao,Jun‐Ping Liu,Ming-yuan Cao,Zhiping Yang,Liyan Zhao,Guitang Chen
出处
期刊:Food bioscience [Elsevier]
卷期号:56: 103127-103127 被引量:7
标识
DOI:10.1016/j.fbio.2023.103127
摘要

Polysaccharide is one of the most important constituents of ginger, exhibiting extensive bioactivities. However, the structures of ginger polysaccharides are poorly understood and remain to be explored. In this study, a polysaccharide UGP1 was isolated from ginger and then a series of chemical, spectroscopic, chromatographic and thermal methods were applied to determine the properties and structure of it. In addition, the digestion and fecal fermentation processes of UGP1 were also investigated. Results showed that the saccharide content of UGP1 was 91.11% ± 0.42% and UGP1 was revealed to be an acidic heteropolysaccharide with helix structure comprised of six kinds of monosaccharide, including galactose, arabinose, rhamnose, glucose, mannose and glucuronic acid, among which galactose (29.32%) and arabinose (19.55%) accounted for the highest proportion. Specifically, in the backbone of UGP1 existed the →4)-α-D-GlcpA-(1→, →3)-α-L-Rhap-(1→, →4,6)-β-D-Galp-(1→, →6)-β-D-Galp-(1→, →3,6)-β-D-Manp-(1→ and →3)-β-D-Glcp-(1→ residues and in the branch chains of UGP1 located the α-L-Araf-(1→ and α-D-Glcp-(1→ residues. Besides, UGP1 was almost not digested by saliva and gastrointestinal tract but could be fermented by gut microbiota into short chain fatty acids (SCFA), containing acetic acid, propionic acid, n-valeric acid and a bit of i-butyric acid and n-butyric acid, which might mediate the interactions between gut microbiota and organisms and thus regulate the health of the human body. The current study reveals the structure of another ginger polysaccharide and helps understand its physiological process, lays the structural foundation of its activities and provides possibility for developing UGP1 into a novel prebiotic.
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