Autor: |
Zhang, Hui, Zhu, Hongxi, Luo, Xiuyuan, Deng, Yuanzhen, Zhang, Wei, Li, Shubo, Liang, Jingjuan, Pang, Zongwen |
Předmět: |
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Zdroj: |
World Journal of Microbiology & Biotechnology; Jan2023, Vol. 39 Issue 1, p1-10, 10p |
Abstrakt: |
Given the important pharmacological activity of ginsenoside Rd but its low content in plants, the production of Rd by enzymatic transformation is of interest. In this study, a β-xylosidase gene Ta-XylQS from Thermoascus aurantiacus was cloned and overexpressed in Komagataella phaffii. Purified recombinant Ta-XylQS specifically hydrolyzes substrates with xylosyl residues at the optimal pH of 3.5 and temperature of 60 °C. This study established a process for producing Rd by transforming ginsenoside Rb3 in the saponins of Panax notoginseng leaves via recombinant Ta-XylQS. After 60 h, 3 g L− 1 of Rb3 was transformed into 1.46 g L− 1 of Rd, and the maximum yield of Rd reached 4.31 g kg− 1 of Panax notoginseng leaves. This study is the first report of the biotransformation of ginsenoside Rb3 to Rd via a β-xylosidase, and the established process could potentially be adopted for the commercial production of Rd from Rb3. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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