Chem. J. Chinese Universities ›› 2020, Vol. 41 ›› Issue (5): 1010.doi: 10.7503/cjcu20190626

• Organic Chemistry • Previous Articles     Next Articles

Transformation of Ginsenoside Rb3 and C-Mx by Recombinant β-Xylosidase

ZHU Ling,WANG Yuchen,ZHAO Jiangyuan,WEN Mengliang,LI Minggang(),HAN Xiulin()   

  1. Yunnan Key Laboratory of Bioresource Conservation and Utilization,Key Laboratory of Microbial Diversity of Southwest China,Ministry of Education, Institute of Microbiology,College of Life Sciences, Yunnan University, Kunming 650091, China
  • Received:2019-12-04 Online:2020-05-10 Published:2020-01-13
  • Contact: Minggang LI,Xiulin HAN E-mail:mgli727@126.com;xlhan@ynu.edu.cn
  • Supported by:
    † Supported by the Excellent Young Talents Program of Yunnan University, China(XT412003);the Yunnan Provincial Education Department Research Fund Project, China(2019J0028)

Abstract:

The β-xylosidase gene anxyl which was amplified from Aspergillus niger NG1306 was cloned into pPICZαA to construct the recombinant expression vector(pPICZαA-anxyl). The recombinant protein(Anxyl) was further expressed in Pichia pastoris KM71H for ginsenoside Rb3, C-Mx biotransformation and catalytic kinetic study. The results showed that anxyl could convert ginsenosides Rb3 and C-Mx to Rd and C-K, respectively. The results of corresponding enzymatic properties showed that the optimum pH of Anxyl was 2.5, and the optimum reaction temperature was 35 ℃. It has good stability at pH of 2.0—5.0 and 20—30 ℃. Mg 2+ could improve the catalytic activity of Anxyl and had good tolerance for glucose and ethanol. The Kmvalues of p-nitrophenyl-β-D-xylopyranoside(pNPX), ginsenoside Rb3 and C-Mx were 3.1, 1.55 and 1.04 mmol/L, the Vmaxvalues of pNPX, Rb3 and C-Mx were 1.9 10 2, 0.8 103 and 8 103 mmol/min, and the Kcat values of pNPX, Rb3 and C-Mx were 5.55, 0.17 and 1.85 s -1, respectively. The results indicated that the recombinant Anxyl had a higher affinity for the natural substrates Rb3 and C-Mx.

Key words: Aspergillus niger, β-Xylosidase, Ginsenoside biotransformation, Enzyme kinetic

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