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中国精品科技期刊2020
杨娟, 李尚勇, 马子宾, 刘均忠, 郝建华, 王跃军, 孙谧. 海洋金属蛋白酶MP仿生亲和材料纯化条件的优化[J]. 食品工业科技, 2017, (15): 146-152. DOI: 10.13386/j.issn1002-0306.2017.15.028
引用本文: 杨娟, 李尚勇, 马子宾, 刘均忠, 郝建华, 王跃军, 孙谧. 海洋金属蛋白酶MP仿生亲和材料纯化条件的优化[J]. 食品工业科技, 2017, (15): 146-152. DOI: 10.13386/j.issn1002-0306.2017.15.028
YANG Juan, LI Shang-yong, MA Zi-bin, LIU Jun-zhong, HAO Jian-hua, WANG Yue-jun, SUN Mi. Optimization of purification protocol of biomimetic affinity material for marine metalloprotease MP[J]. Science and Technology of Food Industry, 2017, (15): 146-152. DOI: 10.13386/j.issn1002-0306.2017.15.028
Citation: YANG Juan, LI Shang-yong, MA Zi-bin, LIU Jun-zhong, HAO Jian-hua, WANG Yue-jun, SUN Mi. Optimization of purification protocol of biomimetic affinity material for marine metalloprotease MP[J]. Science and Technology of Food Industry, 2017, (15): 146-152. DOI: 10.13386/j.issn1002-0306.2017.15.028

海洋金属蛋白酶MP仿生亲和材料纯化条件的优化

Optimization of purification protocol of biomimetic affinity material for marine metalloprotease MP

  • 摘要: 目的:建立一种高效的海洋金属蛋白酶MP仿生亲和纯化方法。方法:采用硼酸仿生亲和材料,利用单因素实验,Plackett-Burman实验设计、Box-Behnken实验等响应面优化法,对纯化条件进行优化,利用SDS-PAGE及HPLC分析纯化后样品纯度。结果:利用单因素法和响应面法对纯化条件进行优化和分析,获得硼酸琼脂糖凝胶亲和柱的最佳纯化条件为:粗酶液浓度在100 mg/m L,上样缓冲液为p H8.6的甘氨酸-氢氧化钠,上样速度1 m L/min,洗脱缓冲液为p H5.2的磷酸氢二钠-柠檬酸,洗脱速度2 m L/min,洗脱缓冲液加入75 mmol/L的甘露醇时纯化效果最好,纯化效率提高了11倍,纯化后的样品纯度达到98.8%。 

     

    Abstract: Objective: To establish an efficient method for biomimetic affinity purification of marine metalloprotease MP.Methods: Using the biomimetic affinity materials to optimize the purification conditions by response surface optimization method, such as the single factor experiment, Plackett-Burman experiment design, Box-Behnken experiment.And the purity of purified samples by SDS-PAGE and HPLC was analyzed. Results: The purification conditions were optimized by single factor experiment and the response surface design. The study indicated that the best purification conditions of the boronic acid gel were: When enzyme concentration was 100 mg/m L, the optimal loading buffer was glycine-sodium hydroxide of p H8.6 and the sample rate was 1 m L/min. The elution buffer was disodium hydrogen phosphate-citric acid of p H5.2, and elution rate was2 m L/min, the elution buffer added to mannitol of 75 mmol/L, the purification efficiency was enhanced 11 times and the purity above 98.8%.

     

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