Molecular cloning and isolation of a recombinant alpha-Momorcharin in E. coli against Pyricularia oryzae

T. T. T. Nguyen, D. T. Dang
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Abstract

Introduction : Alpha-Momorcharin ( a -MMC) is a member of the ribosome-inactivating protein (RIP) family that has been widely used as an antitumor, antiviral and antifungal agent. Methods : In this study, the codons of DNA encoding a -MMC were optimized for expression in E. coli and cloned into the pET-28a(+) vector . The protein was then expressed in E. coli strain BL21 (DE3) and purified by nickel affinity chromatography. Results : Under IPTG induction, a -MMC was expressed at approximately 50% of the total protein, showing high-level recombinant protein expression in E. coli . A high amount of purified a -MMC (70 mg) was isolated from 1 L LB culture medium of E. coli BL21 (DE3) with approximately 95% purity. Interestingly, a -MMC inhibited the mycelial growth of Pyriculariaoryzae in a concentration-dependent manner. Conclusion: Using a microbial system for a -MMC expression provides a promising method for the design of a new agent against pathogens.
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大肠杆菌抗稻瘟病菌重组α -苦瓜素的克隆与分离
α - momorcharin (a -MMC)是核糖体失活蛋白(RIP)家族的一员,被广泛用作抗肿瘤、抗病毒和抗真菌药物。方法:优化编码a -MMC的DNA密码子在大肠杆菌中的表达,并将其克隆到pET-28a(+)载体中。该蛋白在大肠杆菌BL21 (DE3)中表达,经镍亲和层析纯化。结果:在IPTG诱导下,-MMC的表达量约为总蛋白的50%,在大肠杆菌中表现出高水平的重组蛋白表达。从1 L大肠杆菌BL21 (DE3) LB培养基中分离得到纯度约为95%的A -MMC,纯度为70 mg。有趣的是,a -MMC以浓度依赖的方式抑制pyricarioryzae的菌丝生长。结论:利用微生物系统表达-MMC为设计新的抗病原体药物提供了一种很有前途的方法。
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