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阿魏酸松柏苷到淫羊藿苷的高效生物转化由aspergillus nidulans 的糖苷酶完成。

Efficient bioconversion of epimedin C to icariin by a glycosidase from Aspergillus nidulans.

机构信息

National Engineering Laboratory for Cereal Fermentation Technology, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu 214122, China; Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu 214122, China; Jiangsu Provisional Research Center for Bioactive Product Processing Technology, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu 214122, China.

Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu 214122, China; The Key Laboratory of Carbohydrate Chemistry & Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi 214122, China.

出版信息

Bioresour Technol. 2019 Oct;289:121612. doi: 10.1016/j.biortech.2019.121612. Epub 2019 Jun 6.

Abstract

Herba Epimedii is a traditional Chinese herbal medicine that contains a mixture of bioactive flavonoid glycosides. Among them, icariin has the most outstanding bioactive functions, while epimedin C exhibits substantial toxicity. A recombinant α-L-rhamnosidase (AnRhaE) from Aspergillus nidulans was expressed in Escherichia coli to promote the efficient bioconversion of epimedin C to icariin. A hydrolase activity of 574.5 U L was acquired via optimized fed-batch fermentation in a 5-L bioreactor. The enzyme proved to be stable in an acidulous pH range below 55 °C with an optimal pH of 4.5 and optimal temperature of 55 °C. Epimedin C (1 g L) was 100% converted to icariin within 90 min using recombinant cells. The resting cells proved to be selective for epimedin C and 2″-O-rhamnosylicariside II in crude extracts of the epimedium plant. This work provides an original and efficient biocatalyst system that can be applied in industrialized production of icariin.

摘要

淫羊藿是一种传统的中药,含有多种生物活性的黄酮苷。其中,淫羊藿苷具有最突出的生物活性功能,而朝藿定 C 则表现出显著的毒性。通过在大肠杆菌中表达来自构巢曲霉的重组α-L-鼠李糖苷酶(AnRhaE),来促进淫羊藿苷向淫羊藿苷的高效生物转化。通过在 5 升生物反应器中进行优化的分批补料发酵,获得了 574.5 U/L 的水解酶活性。该酶在酸性 pH 值低于 55°C 的范围内稳定,最适 pH 值为 4.5,最适温度为 55°C。使用重组细胞,1g/L 的淫羊藿苷在 90 分钟内 100%转化为淫羊藿苷。固定化细胞对淫羊藿和粗提物中的 2″-O-鼠李糖苷淫羊藿苷 II 具有选择性。这项工作提供了一个原始而有效的生物催化剂系统,可应用于淫羊藿苷的工业化生产。

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