Structural characterization and Bacteroides proliferation promotion activity of a novel homogeneous arabinoglucuronoxylan from Commelina communis L.

IF 4.5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
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Abstract

Commelina communis L., a functional food and herbal plant in Asia, has been used against obesity, diabetes, and infections for centuries. A growing body of studies has demonstrated that indigestible polysaccharides are significant in obesity management. However, the structures and bioactivities of homogeneous polysaccharides from C. communis remain unclear. This study presented the structural characterization, simulated digestion, and human gut Bacteroides proliferation promotion activity of a novel homogeneous polysaccharide (CCB-3) from C. communis. The results showed that CCB-3 was an arabinoglucuronoxylan, primarily composed of arabinose, galactose, xylose, glucuronic acid (GlcA), and 4-O-methyl GlcA with a molecular weight (Mw) of 58.8 kDa. Following a 6-hour exposure to simulated gastrointestinal fluid, the Mw of CCB-3 remained unchanged, revealing that CCB-3 was an indigestible polysaccharide. Notably, CCB-3 could promote the proliferation of B. thetaiotaomicron, B. ovatus, and B. cellulosilyticus and produce short-chain fatty acids (SCFAs) and 1,2-propanediol. These findings might shed light on the discovery of polysaccharide-based leading compounds from C. communis against obesity.

Abstract Image

一种新型均质阿拉伯葡糖醛聚氧乙烯醚的结构特征和乳酸菌增殖促进活性
康乃馨(Commelina communis L.)是亚洲的一种功能性食品和草本植物,几个世纪以来一直被用于防治肥胖、糖尿病和感染。越来越多的研究表明,难以消化的多糖对肥胖症的治疗具有重要意义。然而,茜草多糖的结构和生物活性仍不清楚。本研究介绍了一种新型共生多糖(CCB-3)的结构特征、模拟消化和人体肠道乳杆菌增殖促进活性。结果表明,CCB-3 是一种阿拉伯葡萄糖醛酸聚糖,主要由阿拉伯糖、半乳糖、木糖、葡萄糖醛酸(GlcA)和 4-O-甲基 GlcA 组成,分子量(Mw)为 58.8 kDa。在模拟胃肠液中暴露 6 小时后,CCB-3 的分子量保持不变,这表明 CCB-3 是一种难消化多糖。值得注意的是,CCB-3 能促进大肠杆菌、卵形芽孢杆菌和纤维硅化性芽孢杆菌的增殖,并产生短链脂肪酸(SCFAs)和 1,2-丙二醇。这些发现可能会为从马齿苋中发现基于多糖的抗肥胖主导化合物提供启示。
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来源期刊
Bioorganic Chemistry
Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
9.70
自引率
3.90%
发文量
679
审稿时长
31 days
期刊介绍: Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry. For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature. The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.
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