Comparison of three different thermophilic beta-glucosidases for baicalin transformation.
10.19540/j.cnki.cjcmm.20180201.002
- Author:
Tao WU
1
;
Shan-Shan ZHANG
2
;
Jian-Jun PEI
2
;
Wei XIAO
3
;
Zhen-Zhong WANG
3
;
Lin-Guo ZHAO
1
Author Information
1. Co-innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University， Nanjing 210037, China.
2. College of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, China.
3. Jiangsu Kanion Pharmaceutical Co., Ltd., Lianyungang 222001, China.
- Publication Type:Journal Article
- Keywords:
baicalein;
baicalin;
beta-glucosidase;
catalytic conversion
- From:
China Journal of Chinese Materia Medica
2018;43(8):1602-1609
- CountryChina
- Language:Chinese
-
Abstract:
Three different beta-glycosidase sequences of Ttebgl3, Tpebgl1 and Tpengl3 from Thermotoga thermarum DSM 5069 and Thermotoga petrophila RKU-1 were analyzed. Also, the influence of temperature, pH, concentration of DMSO, metal ions and kinetic constant on catalytic conversion of baicalin had been compared. The results indicated that the optimal pH and optimum temperature for transformation of baicalin was 4.5 85 °C, 5.0 80 °C and 5.5 80 °C, respectively. The family GH3 beta-glycosidase Ttebgl3 and Tpebgl3 had the better DMSO tolerance. The activation effect of the metal ions on the catalytic conversion of baicalin was not obvious, and the inhibition of the GH3 family beta glucosidase was significantly stronger than that of the GH1 family. The kinetic constants of three different beta-glucosidases catalyzed baicalin were significantly different. The Km and Vmax values of Tpebgl1, Tpebgl3 and Ttebgl3 were 0.029 2 mmol·L⁻¹ 4.85 U·mg⁻¹, 0.268 6 mmol·L⁻¹ 121.04 U·mg⁻¹ and 0.391 8 mmol·L⁻¹ 308.90 U·mg⁻¹, respectively. Family GH3 beta-glycosidase converted more baicalin than family GH1 with the optimal conditions, 0.02 g baicalin, and the conversion rate was 68%, 97.3%, 97.31% respectively. The results of the study provided a guarantee for the transformation of baicalin.
