研究报告

基于超支化β-葡聚糖的新型补锌剂制备与表征

  • 李萃 ,
  • 温嘉怡 ,
  • 徐萌萌 ,
  • 石贵阳 ,
  • 陈磊 ,
  • 丁重阳
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  • 1(江南大学 生物工程学院,糖化学与生物技术教育部重点实验室,江苏 无锡,214122)
    2(江南大学,粮食发酵与食品生物制造国家工程研究中心,江苏 无锡,214122)
第一作者:硕士研究生(丁重阳教授和陈磊副教授为共同通信作者,E-mail:bioding@163.com;leichen@jiangnan.edu.cn)

收稿日期: 2025-02-19

  修回日期: 2025-04-17

  网络出版日期: 2025-12-25

Preparation and characterization of a novel zinc supplement based on hyperbranched β-glucan

  • LI Cui ,
  • WEN Jiayi ,
  • XU Mengmeng ,
  • SHI Guiyang ,
  • CHEN Lei ,
  • DING Zhongyang
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  • 1(Key Laboratory of Carbohydrate Chemistry and Biotechnology of Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi 214122, China)
    2(National Engineering Research Center of Cereal Fermentation and Food Biomanufacturing, Jiangnan University, Wuxi 214122, China)

Received date: 2025-02-19

  Revised date: 2025-04-17

  Online published: 2025-12-25

摘要

为开发具有高消化特性的新型补锌剂,该研究设计并构建了虎奶菇超支化β-葡聚糖-锌螯合体系(Pleurotus tuber-regium hyperbranched β-glucane-Zn,PTR-HBG-Zn),系统优化其制备工艺并评估其生物利用特性。通过单因素试验明确了关键工艺参数的影响规律:在pH 6.0、50 ℃及0.35 mol/L ZnSO4初始浓度条件下持续反应2 h,获得最高锌结合量为(47.06±1.85)mg/g的产物。采用傅里叶变换红外光谱、X-射线衍射等确认成功制备螯合物,揭示了锌配位诱导多糖分子链构象的转变。研究发现,锌离子的配位作用显著改变了体系流变特性,黏弹性模量数据及冷场发射扫描电子显微镜图像证实体系转化为典型凝胶态。体外模拟胃肠代谢研究表明,相较于无机锌(ZnSO4)和二代有机锌(葡萄糖酸锌),PTR-HBG-Zn在肠道环境下的锌溶解率显著提升(P<0.05)。因此,PTR-HBG-Zn螯合物具有更好的生物利用率和稳定性,为开发新型多糖补锌剂提供了理论依据和数据支持。

本文引用格式

李萃 , 温嘉怡 , 徐萌萌 , 石贵阳 , 陈磊 , 丁重阳 . 基于超支化β-葡聚糖的新型补锌剂制备与表征[J]. 食品与发酵工业, 2025 , 51(23) : 219 -226 . DOI: 10.13995/j.cnki.11-1802/ts.042425

Abstract

To develop a novel zinc-fortifying agent with enhanced digestibility and absorption, this study designed a hyperbranched polysaccharide-zinc chelate (PTR-HBG-Zn) using Pleurotus tuber-regium hyperbranched β-glucan (PTR-HBG) as the ligand.The preparation process was systematically optimized through single-factor experiments.The optimal conditions, including pH 6.0, 50 ℃, and 0.35 mol/L initial zinc sulfate concentration with 2 h reaction duration, yielded a chelate with a zinc content of (47.06±1.85) mg/g.Multidimensional characterization techniques including FTIR and XRD confirmed successful chelation and revealed conformational transitions in the polysaccharide chain conformation upon zinc binding.Rheological analysis and FESEM observations further demonstrated that zinc coordination induced gelation.In vitro simulated gastrointestinal digestion revealed that PTR-HBG-Zn exhibited significantly higher zinc dissolution rates (P<0.05) in the intestinal phase compared to zinc sulfate and zinc gluconate.These findings highlight the superior bioavailability and stability of PTR-HBG-Zn, providing both theoretical foundations and experimental evidence for developing advanced polysaccharide-based zinc supplements.

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