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High efficiency production of ginsenoside compound K by catalyzing ginsenoside Rb1 using snailase

机译:通过使用Snailase催化人参皂苷Rb1高效生产人参皂苷K

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摘要

The rare ginsenoside Compound K (C-K) is attracting more attention because of its good physiological activity and urgent need. There are many pathways to obtain ginsenoside C-K, including chemical and biological methods. Among these, the conversion of PPD-type ginsenosides by enzymatic hydrolysis is a trend due to its high efficiency andmild conditions. For effectively extracting from the other panaxadiol saponins, the conversion process for ginsenoside C-K was investigated using snailases in this study. The univariate experimental design and response surface methodology were used to determine the optimal hydrolysis conditions for the conversion of ginsenoside Rb1 into ginsenoside C-K by snailases. The optimum conditions were as follows: pH 5.12, temperature 51 °C, ratio of snailase/substrate 0.21, and reaction time 48 h. On the basis of these parameters, the addition of 1.0mmol·L-1 ferric ionwas found to significantly improve the enzymolysis of snailases for the first time. With the above conditions, the maximum conversion rate reached 89.7%, suggesting that the process can obviously increase the yield of ginsenoside C-K. The bioassay tests indicated that the ginsenoside C-K showed anti-tumor activity in a series of tumor cell lines. Based on these results,we can conclude that the process of rare ginsenoside CK production by enzymolysis with snailase is feasible, efficient, and suitable for the industrial production and application.
机译:稀有的人参皂苷化合物K(C-K)由于其良好的生理活性和迫切需要而引起了更多关注。人参皂苷C-K的获得途径很多,包括化学方法和生物学方法。其中,由于其高效和温和的条件,通过酶促水解将PPD型人参皂苷转化为一种趋势。为了有效地从其他人参二醇皂苷中提取,在此研究中使用蜗牛酶研究了人参皂苷C-K的转化过程。使用单变量实验设计和响应面方法确定通过蜗牛酶将人参皂苷Rb1转化为人参皂苷C-K的最佳水解条件。最佳条件如下:pH 5.12,温度51°C,蜗牛酶/底物之比0.21,反应时间48 h。在这些参数的基础上,首次发现添加1.0mmol·L-1铁离子可显着改善蜗牛酶的酶解。在上述条件下,最大转化率达到了89.7%,说明该工艺可以明显提高人参皂苷C-K的收率。生物测定测试表明,人参皂苷C-K在一系列肿瘤细胞系中均显示出抗肿瘤活性。根据这些结果,我们可以得出结论,利用蜗牛酶酶解法生产人参皂苷CK的方法是可行,高效的,适合工业化生产和应用。

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  • 来源
    《中国化学工程学报(英文版)》 |2018年第7期|1591-1597|共7页
  • 作者单位

    Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China;

    Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China;

    Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China;

    Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China;

    Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China;

    Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China;

    Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China;

    Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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