食品科学 ›› 2026, Vol. 47 ›› Issue (15): 165-178.doi: 10.7506/spkx1002-6630-20260105-023

• 营养卫生 • 上一篇    下一篇

黄大茶寡糖的酶解制备及其降糖降脂和肠道益生活性分析

王芯毅,吴晗,李依迪,李敏妮,许娜,葛慧芳,王一君,谢忠稳,李大祥,王红燕   

  1. (安徽农业大学食品与营养学院,茶树种质创新与资源利用国家重点实验室,大健康研究院食品营养健康联合研究中心,安徽?合肥 230036)
  • 出版日期:2026-08-15 发布日期:2026-08-24
  • 基金资助:
    大学生创新创业训练计划项目(202510364090;S202510364201); 国家自然科学基金青年科学基金项目(32302007);安徽农业大学引进和稳定人才科研资助项目(yj2020-64); 现代农业产业技术体系建设专项(CARS-18);大健康研究院食品营养健康联合研究中心专项(2023SJY02;2024SJY02)

Enzymatic Preparation of an Oligosaccharide from Large-leaf Yellow Tea and Evaluation of Its Hypoglycemic, Hypolipidemic, and Gut Microbiota-Modulating Activities

WANG Xinyi, WU Han, LI Yidi, LI Minni, XU Na, GE Huifang, WANG Yijun, XIE Zhongwen, LI Daxiang, WANG Hongyan   

  1. (National Key Laboratory of Tea Plant Germplasm Innovation and Resource Utilization, Joint Research Center for Food Nutrition and Health of IHM, School of Food and Nutrition, Anhui Agricultural University, Hefei 230036, China)
  • Online:2026-08-15 Published:2026-08-24

摘要: 为高效制备黄大茶寡糖并系统解析其结构特征与生物活性,本研究以黄大茶多糖为原料,采用纤维素酶-果胶酶复配体系进行定向酶解,结合单因素试验与Box-Behnken响应面试验对工艺参数进行优化。进一步通过高效凝胶渗透色谱、傅里叶变换红外光谱及原子力显微镜等技术对产物结构进行表征,并利用高脂饮食诱导的肥胖小鼠模型综合评价其降糖、降脂及肠道菌群调节活性。结果表明,黄大茶寡糖(ELYPW)的最优工艺为纤维素酶与果胶酶复配比1∶2、酶添加量0.8 mg/mL、pH 5.0、酶解温度40 ℃、酶解时间4 h。结构表征结果显示,ELYPW的分子质量为3.2×103 Da,主要由鼠李糖、半乳糖醛酸、葡萄糖、半乳糖、阿拉伯糖按物质的量比9.32∶39.17∶1.00∶23.11∶25.34组成,平均粒径为52.56 nm。体内实验表明,ELYPW可显著降低肥胖小鼠体质量、体脂率、空腹血糖及血清总胆固醇、甘油三酯、低密度脂蛋白胆固醇水平,提高高密度脂蛋白胆固醇水平,且能减轻肝脏脂肪堆积。肠道菌群分析表明,ELYPW可修复肥胖小鼠肠道菌群失衡,显著提高有益菌(Akkermansia、Bifidobacterium、Lachnospiraceae_NK4A136_group)丰度,降低有害菌(Romboutsia、unclassified_f__Atopobiaceae、Corynebacterium)丰度。本研究利用酶法制备的ELYPW在改善糖脂代谢紊乱和调节肠道菌群方面活性显著,可为茶源性功能性寡糖开发应用提供理论支撑,并为茶资源的高值化利用及针对代谢综合征的功能食品设计提供新思路。

关键词: 黄大茶寡糖;酶解工艺;结构表征;糖脂代谢;肠道菌群

Abstract: This study aimed to efficiently prepare oligosaccharides from large-leaf yellow tea and systematically elucidate their structural characteristics and biological activities. A mixture of cellulase and pectinase was used for targeted enzymatic hydrolysis of large-leaf yellow tea. The process parameters were optimized by the combined use of single-factor experiments and response surface methodology with Box-Behnken design. The obtained oligosaccharide (ELYPW) was structurally characterized by high performance gel permeation chromatography (HPGPC), Fourier transform infrared spectroscopy (FTIR), and atomic force microscopy (AFM). Its hypoglycemic, hypolipidemic, and gut microbiota-modulating effects were evaluated in a high-fat diet-induced obese mouse model. The results revealed that the optimal preparation conditions for ELYPW were as follows: a cellulose-to-pectinase ratio of 1:2, an enzyme concentration of 0.8 mg/mL, pH 5.0, hydrolysis temperature of 40 ℃, and a hydrolysis time of 4 h. Structural characterization indicated that ELYPW had a molecular mass of 3.2 × 103 Da; it was composed primarily of rhamnose, galacturonic acid, glucose, galactose, and arabinose at a molar ratio of 9.32:39.17:1.00:23.11:25.34, with an average particle size of 52.56 nm. In vivo experiments demonstrated that ELYPW significantly reduced body mass, fat mass, fasting blood glucose levels, and serum concentrations of total cholesterol, triglyceride, and low-density lipoprotein cholesterol in obese mice, while concurrently elevating serum high-density lipoprotein cholesterol levels and alleviating hepatic lipid accumulation. Furthermore, gut microbiota profiling showed that ELYPW ameliorated intestinal flora dysbiosis in obese mice, markedly increasing the abundances of beneficial bacterial taxa including Akkermansia, Bifidobacterium, and Lachnospiraceae_NK4A136_group, and decreasing the abundances of detrimental taxa such as Romboutsia, unclassified_f__Atopobiaceae, and Corynebacterium. Collectively, this study demonstrates that ELYPW exhibits prominent effects in ameliorating glycolipid metabolism disorders as well as regulating the gut microbiota. This finding provides theoretical support for the development and application of tea-derived functional oligosaccharides, and offers new insights for the high-value utilization of tea resources and the design of functional foods against metabolic syndrome.

Key words: large-leaf yellow tea oligosaccharides; enzymatic hydrolysis; structural characterization; glycolipid metabolism; gut microbiota

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