食品研究与开发:2026,47(14):38-49
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茶多酚共价结合对阿拉伯木聚糖结构、抗氧化活性和肠道酵解特性的影响
周琬蕊1,2,马哲豪1,2,应阳杰1,2,周晋宇1,2,王静雯1,2,刘妍1,2 *,郭庆彬3
(1.浙江农林大学 森林食物资源挖掘与利用全国重点实验室,浙江 杭州 311300;2.浙江农林大学 食品与健康学院,浙江 杭州 311300;3.天津科技大学 食品科学与工程学院,天津 300457)
Effect of Covalent Binding with Tea Polyphenols on the Structure,Antioxidant Activity and Intestinal Characteristics of Arabinoxylan
ZHOU Wanrui1,2,MA Zhehao1,2,YING Yangjie1,2,ZHOU Jinyu1,2,WANG Jingwen1,2,LIU Yan1,2 *,GUO Qingbin3
(1. National Key Laboratory of Forest Food Resource Mining and Utilization,Zhejiang Agriculture and Forestry University,Hangzhou 311300,Zhejiang,China;2. College of Food and Health,Zhejiang Agriculture and Forestry University,Hangzhou 311300, Zhejiang,China;3. College of Food Science and Engineering,Tianjin University of Science and Technology,Tianjin 300457,China)
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投稿时间:2025-11-29    
中文摘要: 本研究旨在探究茶多酚(tea polyphenols,TP)与阿拉伯木聚糖(arabinoxylan,AX)共价结合后对AX结构与生物活性的影响,采用自由基催化法制备AX-TP共价复合物。结构方面,采用福林酚法和离心沉淀法分析TP取代度和AX溶解度变化,通过酸水解结合气相色谱-质谱联用(gas chromatography-mass spectrometry,GC-MS)法测定AX单糖组成变化,利用高效液相色谱联用多角度激光散射系统(high performance size exclusion chromatography multi-angle laser light scattering,HPSEC-MALLS)表征AX构象特征变化;生物活性方面,以秀丽隐杆线虫(Caenorhabditis elegans,C. elegans)为模型研究复合物抗氧化特性,并采用猪结肠消化物体外模拟发酵模型,比较复合物与TP、AX单体的结肠酵解特性。结果表明,自由基催化法可使TP在AX分子中的取代度达到(59.60±2.40)mg TP/g,但会显著降低AX溶解度(p<0.05)。结构分析显示,催化过程中不会破坏AX的单糖组成和构象特征,但会增加AX的分子量。生物活性分析表明,TP的共价结合会提高线虫抗氧化活性,使线虫体内超氧化物歧化酶和过氧化氢酶活性分别提升24.8%和19.0%,活性氧含量降低42.9%。此外,尽管TP的共价结合会部分弱化AX的肠道益生活性,复合物仍然具有促进肠道内有益菌乳酸菌属(Lactobacillus)、双歧杆菌属(Bifidobacterium)、土孢杆菌属(Terrisporobacter)等增殖,抑制有害菌大肠杆菌-志贺菌属(Escherichia-Shigella)、链球菌属(Streptococcus)等增殖的功效。综上所述,相比于TP和AX单体,AX-TP共价复合物显示出潜在的抗氧化和肠道益生功能。本研究阐明的AX与TP的共价结合机制及其对复合物结构与功能的调控规律,可为新型多糖-多酚复合物的精准制备提供理论依据,并为其在功能食品与保健品领域的应用提供实践指导。
Abstract:This study aimed to investigate the effects of covalent conjugation with tea polyphenols (TP) on the structure and bioactivity of arabinoxylan (AX). AX-TP covalent complexes were prepared using a free radicalinitiated method. Regarding structural characterization,the TP grafting rate and changes in AX solubility were analyzed using the Folin-Ciocalteu method and a centrifugation method,respectively. Monosaccharide composition changes were determined by acid hydrolysis coupled with GC-MS,and conformational characteristics were investigated using a high-performance size-exclusion chromatography system coupled with multi-angle laser light scattering (HPSEC-MALLS). For bioactivity assessment,the antioxidant properties of the complexes were studied in a Caenorhabditis elegans model,and an in vitro fermentation model using porcine colonic digesta was employed to compare the colonic fermentation characteristics of the complexes with those of TP and AX alone. The results showed that the free radical method achieved a TP grafting rate of (59.60±2.40) mg TP/g onto AX,although this significantly reduced the solubility of AX (P<0.05). Structural analysis revealed that the conjugation process did not alter the monosaccharide composition or conformational features of AX but did increase its molecular weight. Bioactivity assays demonstrated that covalent binding of TP enhanced the antioxidant capacity in C. elegans,increasing the activities of superoxide dismutase (SOD) and catalase (CAT) by 24.8% and 19.0%,respectively,while reducing reactive oxygen species (ROS) levels by 42.9%. Furthermore,although the covalent linkage of TP partially attenuated the prebiotic activity of AX,the complexes still effectively promoted the proliferation of beneficial bacteria,such as Lactobacillus, Bifidobacterium,and Terrisporobacter,and inhibited the growth of potentially harmful bacteria,such as Escherichia-Shigella and Streptococcus.In summary,compared to AX or TP alone,the AX-TP covalent complex exhibits potential antioxidant and prebiotic functions. This study elucidates the covalent binding mechanism between AX and TP and its regulatory effects on the structure and function of the resulting complex. These findings provide a theoretical basis for the precise preparation of novel polysaccharide-polyphenol complexes and offer practical guidance for their application in functional foods and nutraceuticals.
文章编号:202614005     中图分类号:    文献标志码:
基金项目:国家自然科学基金项目(C类)(22508364);浙江农林大学科研发展基金(2024LFR022);浙江省大学生科技创新活动计划(新苗人才计划)项目(2024R412A034)
Author NameAffiliation
ZHOU Wanrui 1. National Key Laboratory of Forest Food Resource Mining and Utilization,Zhejiang Agriculture and Forestry University,Hangzhou 311300,Zhejiang,China2. College of Food and Health,Zhejiang Agriculture and Forestry University,Hangzhou 311300, Zhejiang,China 
MA Zhehao 1. National Key Laboratory of Forest Food Resource Mining and Utilization,Zhejiang Agriculture and Forestry University,Hangzhou 311300,Zhejiang,China2. College of Food and Health,Zhejiang Agriculture and Forestry University,Hangzhou 311300, Zhejiang,China 
YING Yangjie 1. National Key Laboratory of Forest Food Resource Mining and Utilization,Zhejiang Agriculture and Forestry University,Hangzhou 311300,Zhejiang,China2. College of Food and Health,Zhejiang Agriculture and Forestry University,Hangzhou 311300, Zhejiang,China 
ZHOU Jinyu 1. National Key Laboratory of Forest Food Resource Mining and Utilization,Zhejiang Agriculture and Forestry University,Hangzhou 311300,Zhejiang,China2. College of Food and Health,Zhejiang Agriculture and Forestry University,Hangzhou 311300, Zhejiang,China 
WANG Jingwen 1. National Key Laboratory of Forest Food Resource Mining and Utilization,Zhejiang Agriculture and Forestry University,Hangzhou 311300,Zhejiang,China2. College of Food and Health,Zhejiang Agriculture and Forestry University,Hangzhou 311300, Zhejiang,China 
LIU Yan 1. National Key Laboratory of Forest Food Resource Mining and Utilization,Zhejiang Agriculture and Forestry University,Hangzhou 311300,Zhejiang,China2. College of Food and Health,Zhejiang Agriculture and Forestry University,Hangzhou 311300, Zhejiang,China 
GUO Qingbin 3. College of Food Science and Engineering,Tianjin University of Science and Technology,Tianjin 300457,China 
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