湖北农业科学 ›› 2026, Vol. 65 ›› Issue (6): 174-181.doi: 10.14088/j.cnki.issn0439-8114.2026.06.028

• 贮藏·加工 • 上一篇    下一篇

超声辅助酶法提取北沙参多糖工艺优化

李贝贝1, 安莹1,2, 周洪雷2, 吴子玄1, 于萍1, 赵贺1, 刘可春1, 张轩铭1, 夏青1   

  1. 1.齐鲁工业大学(山东省科学院)/山东省科学院生物研究所,济南 250103;
    2.山东中医药大学药学院,济南 250355
  • 收稿日期:2026-02-02 出版日期:2026-06-25 发布日期:2026-06-26
  • 通讯作者: 张轩铭(1982-),男,山东莱州人,副研究员,博士,主要从事天然活性产物的分析、制备、活性评价及功能产品研发等,(电子信箱)zhangmx@sdas.org;共同通信作者,夏青(1988-),男,山东宁阳人,副研究员,硕士生导师,博士,主要从事中药药效物质与作用机制研究,(电子信箱)sdxq1021@163.com。
  • 作者简介:李贝贝(2002-),女,山东滨州人,在读硕士研究生,研究方向为中药药效物质与作用机制,(电子信箱)libeibei0103@163.com。
  • 基金资助:
    国家自然科学基金联合基金项目(U23A20514); 齐鲁工业大学(山东省科学院)科教产融合试点工程重大创新专项(2025ZDZX14); 济南市“高校20条2025版”资助项目(202534030); 山东省中医药科技项目(M20242212); 外专双百项目(WSR2024032; WSP2024016); 山东生物健康食品高值开发利用技术创新中心重大创新任务(SDJSZX2025ZDRW03)

Optimization of ultrasound-assisted enzymatic extraction process for polysaccharides from Glehnia littoralis

LI Bei-bei1, AN Ying1,2, ZHOU Hong-lei2, WU Zi-xuan1, YU Ping1, ZHAO He1, LIU Ke-chun1, ZHANG Xuan-ming1, XIA Qing1   

  1. 1. Qilu University of Technology (Shandong Academy of Sciences)/Institute of Biology, Shandong Academy of Sciences, Jinan 250103,China;
    2. School of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355,China
  • Received:2026-02-02 Published:2026-06-25 Online:2026-06-26

摘要: 为优化北沙参多糖(GLP)的提取工艺,提高多糖提取率及其活性,利用超声辅助酶法提取GLP,系统评估了多种酶制剂对多糖提取效率、组分含量、体内抗炎活性及体外胃黏膜细胞保护活性的影响;通过单因素试验结合Box-Behnken响应面分析对提取参数进行系统优化;采用Sevage法对GLP进行纯化,并测定其中多糖及蛋白质的含量。结果表明,果胶酶提取物在CuSO4诱导的斑马鱼炎症模型、MNNG和乙醇诱导的人胃黏膜细胞(GES-1)损伤模型中分别表现出显著的抗炎和胃黏膜细胞保护活性,特别是在乙醇诱导的GES-1细胞损伤模型中的活性优于其他酶提取物。GLP的最优提取条件为果胶酶添加量0.44%,提取时间39 min,提取温度50 ℃,料液比1∶30(g∶mL)。该条件下多糖提取率达37.17%;经纯化后,GLP中多糖含量为60.8%,蛋白质残留量为0.243%。超声辅助果胶酶法不仅能高效制备GLP,而且所得多糖具有显著的抗炎与胃黏膜细胞保护活性,为其在功能性食品领域的开发提供了可靠的依据。

关键词: 北沙参多糖, 超声辅助酶法, 响应面法, 提取工艺, MNNG诱导损伤模型

Abstract: To optimize the extraction process of Glehnia littoralis polysaccharides (GLP) and improve both extraction yield and bioactivity, ultrasound-assisted enzymatic extraction was employed. The effects of different enzyme preparations on extraction efficiency, polysaccharide composition, in vivo anti-inflammatory activity, and in vitro gastric mucosal protective activity in gastric mucosal cells were systematically evaluated. Subsequently, single-factor experiments combined with Box-Behnken response surface methodology were used to optimize the extraction parameters. The GLP was further purified using the Sevag method, and the contents of polysaccharides and proteins were determined. The results showed that pectinase extract exerted significant anti-inflammatory activity in the CuSO4-induced zebrafish inflammation model, and obvious protective effects on human gastric mucosal GES-1 cells injured by MNNG and ethanol. In particular, its protective efficacy against ethanol-induced GES-1 cell damage was superior to other enzyme extracts. The optimal extraction condition for GLP was pectinase dosage of 0.44%, extraction time of 39 min, extraction temperature of 50 ℃, and solid-to-liquid ratio of 1∶30(g∶mL). Under this condition, the polysaccharide extraction yield reached 37.17%. After purification, the polysaccharide content of GLP was 60.8%, with a residual protein content of 0.243%. In conclusion, ultrasound-assisted pectinase extraction enabled efficient preparation of GLP, and the resulting polysaccharides exhibited pronounced anti-inflammatory and gastric mucosal protective activities, thereby providing a reliable basis for the development of GLP in the functional food industry.

Key words: Glehnia littoralis polysaccharides, ultrasound-assisted enzymatic method, response surface methodology, extraction process, MNNG-induced injury model

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