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中国精品科技期刊2020
秦宇,华宗,张敏,等. 响应面法优化日本蛇菰多糖脱色、脱蛋白工艺[J]. 华体会体育,2023,44(10):177−184. doi: 10.13386/j.issn1002-0306.2022070206.
引用本文: 秦宇,华宗,张敏,等. 响应面法优化日本蛇菰多糖脱色、脱蛋白工艺[J]. 华体会体育,2023,44(10):177−184. doi: 10.13386/j.issn1002-0306.2022070206.
QIN Yu, HUA Zong, ZHANG Min, et al. Optimization of Decolorization and Deproteinization of Balanophora japonica Makino Polysaccharide by Response Surface Methodology[J]. Science and Technology of Food Industry, 2023, 44(10): 177−184. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022070206.
Citation: QIN Yu, HUA Zong, ZHANG Min, et al. Optimization of Decolorization and Deproteinization of Balanophora japonica Makino Polysaccharide by Response Surface Methodology[J]. Science and Technology of Food Industry, 2023, 44(10): 177−184. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022070206.

响应面法优化日本蛇菰多糖脱色、脱蛋白工艺

Optimization of Decolorization and Deproteinization of Balanophora japonica Makino Polysaccharide by Response Surface Methodology

  • 摘要: 研究日本蛇菰多糖双氧水脱色、Sevag法脱蛋白的条件并对其进行工艺优化。在单因素的基础上,以多糖脱色率为指标,采用响应面法设计三因素三水平实验对蛇菰多糖的脱色条件进行优化;以蛋白质脱除率、多糖保留率为指标,选取Sevag试剂比例(氯仿:正丁醇)、样液:Sevag试剂、振荡时间为因素水平设计响应面试验,得到最佳工艺条件。结果表明,在pH为8的条件下双氧水脱色最佳工艺为:双氧水用量为20%、脱色时间为46 min、脱色温度为60 ℃,在此条件下蛇菰多糖的脱色率为84.21%。脱蛋白最佳工艺条件为:氯仿:正丁醇5:1、样液:Sevag试剂4:1、振荡时间15 min,在此条件下,多糖保留率为81.03%,蛋白质脱除率为40.44%。双氧水和Sevag法脱色脱蛋白工艺稳定,方法可行操作简单,适用于蛇菰多糖的脱色、脱蛋白。

     

    Abstract: To study the decolorization and deproteinization conditions of Balanophora japonica polysaccharide by hydrogen peroxide and Sevag method, and to optimize the process. Based on single factor experiments, the response surface methodology was used to design a three factor and three level experiments to optimize the decolorization conditions of Balanophora japonica polysaccharides using the decolorization rate of polysaccharides as an index. Using protein removal rate and polysaccharide retention rate as indicators, a response surface experiment was designed at the factor level of Sevag reagent ratio (chloroform:n-butanol), sample solution: Sevag reagent and oscillation time to obtain the optimal process conditions. Results showed that, under the condition of pH8, the optimal decolorization process was as follows: The dosage of hydrogen peroxide was 20%, the decolorization time was 46 min, and the decolorization temperature was 60 ℃. Under this condition, the decolorization rate of polysaccharides was 84.21%. The optimal deproteinization conditions were chloroform:n-butanol 5:1, sample solution:Sevag reagent 4:1, and shock time 15 min, under this condition, the polysaccharide retention rate was 81.03%, and the protein removal rate was 40.44%. The decolorization and deproteinization of Balanophora japonica polysaccharide by hydrogen peroxide and Sevag method was stable, feasible and simple, and would be suitable for decolorization and deproteinization of Balanophora japonica polysaccharide.

     

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