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渔业研究 ›› 2021, Vol. 43 ›› Issue (3): 275-281.DOI: 10.14012/j.cnki.fjsc.2021.03.006

• 论文与报告 • 上一篇    下一篇

红毛藻多糖的提取工艺优化及其抗氧化活性

吴云辉1,阎光宇1,余蕾1,张怡评2,3*,杨婷2,3,晋文慧2,3   

  1. 1. 厦门海洋职业技术学院,海洋生物学院
    2. 自然资源部第三海洋研究所,海洋生物资源开发利用工程技术创新中心
    3. 福建省海洋生物资源开发利用协同创新中心
  • 收稿日期:2021-02-24 修回日期:2021-04-12 出版日期:2021-06-25 发布日期:2021-06-25
  • 通讯作者: 吴云辉
  • 基金资助:
    福建省科技计划项目(2018N0014);自然资源部第三海洋研究所基本科研业务费专项资金资助项目;福建省高职院校海洋生物应用技术协同创新中心项目;福建省高职院校海洋生物应用技术协同创新中心项目

Optimization of extraction conditions and investigation of the antioxidant activity of polysaccharides from Bangia fusco-purpurea

  • Received:2021-02-24 Revised:2021-04-12 Online:2021-06-25 Published:2021-06-25

摘要: 本文以红毛藻为研究材料,对红毛藻多糖的提取工艺进行优化,并对其体外抗氧化活性进行研究。实验分别考察红毛藻的提取时间、提取温度、料液比对红毛藻多糖提取量的影响,并结合正交实验设计优选出最佳提取工艺,同时通过体外抗氧化活性评价研究其清除DPPH自由基和羟基自由基的能力。结果表明,以料液比1∶40(m/v)、在90℃下提取2.0 h为最佳提取工艺,在此工艺下红毛藻多糖提取量最高,达到(77.57±2.17)mg/g;体外抗氧化活性评价结果显示,红毛藻多糖对DPPH自由基和羟基自由基具有明显的清除效果,清除DPPH自由基的IC50值为0.36 mg/mL,清除羟基自由基的IC50值为0.65 mg/mL。本研究可为红毛藻多糖的进一步开发应用提供参考。

Abstract: In the present study, the extraction process of polysaccharide from Bangia fusco-purpurea was optimized and the antioxidant activity of polysaccharide was studied in vitro. The effects of the extraction time, extraction temperature and ratio of material to liquid on the extraction amount of polysaccharide from B. fusco-purpurea were investigated, respectively, and the optimum preparation conditions were selected with orthogonal design combined with multi-index test. Meanwhile, the antioxidant activity of polysaccharide from B. fusco-purpurea was evaluated by DPPH free radical and hydroxyl radical scavenging method. The results showed that the optimum extraction conditions were the ratio of solid to liquid was 1∶40 (m/v) at 90℃ for 2.0 h. Under the optimum extraction conditions, the maximum extraction yield of polysaccharide reached (77.57±2.17) mg/g. Additionally, the result of antioxidant activity in vitro showed that the polysaccharide form B. fusco-purpurea presented significant scavenging effects on DPPH free radical and hydroxyl free radical. The IC50 value of DPPH free radicals scavenging was 0.36 mg/mL, and the IC50 value of hydroxyl free radicals scavenging was 0.65 mg/mL. This study can be used for the further development and application of B. fusco-purpurea polysaccharide.

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