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滇黄精中的一种新型多糖:结构解析、体外抗炎活性及对肠道微生物群的调节作用

A novel polysaccharide in Polygonatum kingianum: structure elucidation, the activities of anti-inflammatory and the regulation of gut microbiota in vitro.

作者信息

Han Xiao, Ren Xin-Xiu, Zhang Dan-Yang, Guo Qin-Feng, Li Shi-Meng, Xiu Zhi-Long, Dong Yue-Sheng

机构信息

MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, 116024, Liaoning, China.

College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, China.

出版信息

Nat Prod Bioprospect. 2025 Sep 2;15(1):60. doi: 10.1007/s13659-025-00542-7.

DOI:10.1007/s13659-025-00542-7
PMID:40892304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12405078/
Abstract

Polysaccharides are the primary active constituents of Polygonatum kingianum Coll. et Hemsl. However, the comprehensive characterization of P. kingianum polysaccharides (PKP) remains scarce, impeding investigations into the structure-activity relationship. In this study, a novel polysaccharide, PKP1, was purified using Cellulose DE-52 and Sephadex G-50 column chromatography, and its complete structure was elucidated through monosaccharide composition analysis, methylation analysis, as well as 1D and 2D NMR analysis. The results revealed that PKP1 primarily comprised Fru and Glc, exhibiting a molecular weight of 5.3 × 10 Da and a polymer dispersity index of 1.20. The completed structure of PKP1 consisted of β-D-Fruf-(2 → , → 1,2)-β-D-Fruf-(6 → , → 1)-β-D-Fruf-(2 → and → 1)-α-D-Glcp-(6 → as the main chain sugar residues, with β-D-Fruf-(2 → and → 2)-β-D-Fruf-(6 → serving as the side chains sugar residues. The detailed structure of PKP1 suggested it is a novel Fru-dominated neutral polysaccharide. Biological assays indicated that PKP1 significantly reduced the levels of NO, IL-6, and TNF-α in RAW264.7 macrophages, while also exerting regulatory effects on the gut microbiota structure and its metabolites in vitro. Our findings enriched the understanding of the structural characteristics of P. kingianum polysaccharides and laid a solid foundation for considering P. kingianum as a potential functional food supplement.

摘要

多糖是滇黄精的主要活性成分。然而,滇黄精多糖(PKP)的全面表征仍然匮乏,这阻碍了对其构效关系的研究。在本研究中,通过纤维素DE - 52和葡聚糖凝胶G - 50柱色谱法纯化得到一种新型多糖PKP1,并通过单糖组成分析、甲基化分析以及一维和二维核磁共振分析阐明了其完整结构。结果表明,PKP1主要由果糖(Fru)和葡萄糖(Glc)组成,分子量为5.3×10 Da,聚合物分散指数为1.20。PKP1的完整结构由β - D - 果糖基 - (2→,→1,2)-β - D - 果糖基 - (6→,→1)-β - D - 果糖基 - (2→和→1)-α - D - 葡萄糖基 - (6→作为主链糖残基,β - D - 果糖基 - (2→和→2)-β - D - 果糖基 - (6→作为侧链糖残基。PKP1的详细结构表明它是一种新型的以果糖为主的中性多糖。生物学试验表明,PKP1显著降低了RAW264.7巨噬细胞中一氧化氮(NO)、白细胞介素 - 6(IL - 6)和肿瘤坏死因子 - α(TNF - α)的水平,同时在体外对肠道微生物群结构及其代谢产物也具有调节作用。我们的研究结果丰富了对滇黄精多糖结构特征的认识,为将滇黄精视为一种潜在的功能性食品补充剂奠定了坚实基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/1542df103d37/13659_2025_542_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/20f5c2f6504f/13659_2025_542_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/92f38fccf764/13659_2025_542_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/799deae035ab/13659_2025_542_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/08d5a51f4993/13659_2025_542_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/dfd4f0de797a/13659_2025_542_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/6fcf43300948/13659_2025_542_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/d03e2e8598d5/13659_2025_542_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/1542df103d37/13659_2025_542_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/20f5c2f6504f/13659_2025_542_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/92f38fccf764/13659_2025_542_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/799deae035ab/13659_2025_542_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/08d5a51f4993/13659_2025_542_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/dfd4f0de797a/13659_2025_542_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/6fcf43300948/13659_2025_542_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/d03e2e8598d5/13659_2025_542_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99ab/12405078/1542df103d37/13659_2025_542_Fig8_HTML.jpg

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