SCI和EI收录∣中国化工学会会刊

Chin.J.Chem.Eng. ›› 2018, Vol. 26 ›› Issue (7): 1591-1597.DOI: 10.1016/j.cjche.2018.02.004

• Materials and Product Engineering • Previous Articles     Next Articles

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

Zhiguang Duan, Chenhui Zhu, Jingjing Shi, Daidi Fan, Jianjun Deng, Rongzhan Fu, Rong Huang, Cuiying Fan   

  1. Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China;Shanxi R & D Center of Biomaterials and Fermentation Engineering, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China
  • Received:2017-10-30 Revised:2018-01-22 Online:2018-08-16 Published:2018-07-28
  • Contact: Daidi Fan,E-mail address:fandaidi@nwu.edu.cn
  • Supported by:

    Supported by the National Natural Science Foundation of China (21476182, 21776227, 21776228); Shaanxi Key Laboratory of Degradable Biomedical Materials Program (2014SZS07-K04, 2014SZS07-P05, 15JS106, 2014SZS07-Z01, 2014SZS07-Z02, 2016SZSj-35, 2014SZS07-K03) and Shaanxi R&D Center of Biomaterials and Fermentation Engineering Program (2015HBGC-04).

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

Zhiguang Duan, Chenhui Zhu, Jingjing Shi, Daidi Fan, Jianjun Deng, Rongzhan Fu, Rong Huang, Cuiying Fan   

  1. Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China;Shanxi R & D Center of Biomaterials and Fermentation Engineering, School of Chemical Engineering, Northwest University, Taibai North Road 229, Xi'an 710069, China
  • 通讯作者: Daidi Fan,E-mail address:fandaidi@nwu.edu.cn
  • 基金资助:

    Supported by the National Natural Science Foundation of China (21476182, 21776227, 21776228); Shaanxi Key Laboratory of Degradable Biomedical Materials Program (2014SZS07-K04, 2014SZS07-P05, 15JS106, 2014SZS07-Z01, 2014SZS07-Z02, 2016SZSj-35, 2014SZS07-K03) and Shaanxi R&D Center of Biomaterials and Fermentation Engineering Program (2015HBGC-04).

Abstract: 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 and mild 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℃, ratio of snailase/substrate 0.21, and reaction time 48 h. On the basis of these parameters, the addition of 1.0 mmol·L-1 ferric ion was 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.

Key words: Ginsenoside Rb1, Ginsenoside Compound K, Snailase, Enzymolysis

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 and mild 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℃, ratio of snailase/substrate 0.21, and reaction time 48 h. On the basis of these parameters, the addition of 1.0 mmol·L-1 ferric ion was 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.

关键词: Ginsenoside Rb1, Ginsenoside Compound K, Snailase, Enzymolysis