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响应面优化铁线蕨多糖脱蛋白工艺及生物活性研究

Optimization of Deproteinization Process and Biological Activity of Adiantum capillus-veneris Polysaccharide by Response Surface Methodology

  • 摘要: 以铁线蕨为试材,采用单因素试验和响应面试验相结合的优化方法,对铁线蕨多糖脱蛋白工艺进行优化,测定了脱蛋白前后的铁线蕨多糖对α-葡萄糖苷酶的抑制活性与对DPPH自由基的清除能力,以期为铁线蕨多糖的综合利用提供参考依据。结果表明:铁线蕨多糖的最佳脱蛋白工艺条件为多糖溶液与Sevage试剂的体积比为2∶1,脱蛋白时间为10 min,脱蛋白次数为5次,蛋白质脱除率可达73.41%,多糖损失率为25.92%;未脱蛋白的铁线蕨多糖对α-葡萄糖苷酶与对DPPH自由基的IC50值分别为0.31、0.81 mg·mL-1;脱蛋白后的铁线蕨多糖对α-葡萄糖苷酶与对DPPH自由基的IC50值分别为0.26、0.59 mg·mL-1,相较于未脱蛋白分别提高了0.05、0.22 mg·mL-1,表明Sevage法脱除蛋白质可以有效提高铁线蕨多糖抑制α-葡萄糖苷酶的能力与抗氧化能力。

     

    Abstract: Taking Adiantum capillus-veneris as test material,the optimization method of combining single factor experiments and response interviews was used to optimize the deproteinization process of polysaccharides from Adiantum capillus-veneris.The effects of polysaccharides from Adiantum capillus-veneris before and after deproteinization were measuredα-glucasidase inhibitory activity of glucosidase and its ability to scavenge DPPH free radicals were expected,in order to provide reference for the comprehensive utilization of polysaccharides from Adiantum capillus-veneris.The results showed that the optimal deproteinization process conditions of Adiantum capillus-veneris polysaccharides were as follows,the volume ratio between polysaccharide solution and Sevage reagent was 2∶1,the deproteinization time was 10minutes,the deproteinization time was 5times,the protein removal rate could reach 73.41%,and the polysaccharide loss was 25.92%.The IC50of undeproteinized Adiantum capillus-veneris polysaccharides forα-glucosidase and DPPH radicals were0.31,0.81mg·mL-1,respectively.The IC50of clematis Adiantum capillus-veneris polysaccharides forα-glucosidase and DPPH radicals were 0.26,0.59 mg·mL-1,respectively,which increased by0.05,0.22mg·mL-1 compared with undeproteinized proteins,respectively,which proved that the removal of protein by Sevage method could effectively improve the ability of Adiantum capillusveneris polysaccharides to inhibitα-glucosidase and antioxidant capacity.

     

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