A water-soluble arabinoxylan from Chinese liquor distillers' grains: Structural characterization and anti-colitic properties

被引:1
|
作者
Cui, Hao [1 ]
Li, Xia [1 ]
Que, Jiayi [1 ]
Li, Shuyue [1 ]
Shi, Xiaodan [2 ]
Yuan, Tao [1 ,2 ]
机构
[1] Jiangxi Normal Univ, Coll Life Sci, Natl Res Ctr Carbohydrate Synth, Nanchang 330022, Peoples R China
[2] Jiangxi Normal Univ, Sch Hlth, Nanchang 330022, Peoples R China
基金
中国国家自然科学基金;
关键词
Arabinoxylan; Chinese liquor distillers' grain; Inflammatory bowel disease; CHAIN FATTY-ACIDS; CROSS-LINKED ARABINOXYLANS; IN-VITRO FERMENTATION; ULCERATIVE-COLITIS; KAPPA-B; SIGNALING PATHWAY; CELLS; APOPTOSIS; ARABINAN; HEALTH;
D O I
10.1016/j.ijbiomac.2024.131186
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chinese liquor distillers' grain (CLDG) is a valuable and abundant by-product from traditional Chinese baijiu production, containing a diverse array of bioactive components that have attracted significant interest. Herein, a water-soluble polysaccharide, DGPS-2B, with a weight -average molecular weight of 37.3 kDa, was isolated from the alkali -extract fraction of CLDG. Methylation and NMR analysis identified that the primary constituents of DGPS-2B are arabinoxylans, with an arabinose-to-xylose ratio of 0.66. In an animal model of colitis, DGPS-2B treatment significantly altered the gut microbiota composition by increasing the SCFA-producing bacteria ( e. g. , Butyricicoccus ) and reducing the mucin-degrading bacteria such as Muribaculaceae . This microbial shift resulted in elevated production of butyrate, acetate, and propionate, which subsequently suppressed NF-xB signaling, decreased the levels of IL -18, IL -6, and TNF alpha, and potentially inactivated Notch signaling. These multifaceted effects stimulated mucin 2 production, reduced inflammation and apoptosis in the gut epithelium, and ultimately alleviated colitis symptoms. Collectively, this study not only elucidates the purification and characterization of DGPS-2B from CLDG but also illuminates its anti-colitic properties and the underlying molecular mechanisms. These findings underscore the potential of DGPS-2B as a therapeutic intervention for managing inflammatory bowel disease and emphasize CLDG as a promising source for developing value-added products.
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页数:15
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