{"title":"Molecular cloning and isolation of a recombinant alpha-Momorcharin in E. coli against Pyricularia oryzae","authors":"T. T. T. Nguyen, D. T. Dang","doi":"10.32508/stdj.v26i1.4023","DOIUrl":null,"url":null,"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.","PeriodicalId":285953,"journal":{"name":"Science and Technology Development Journal","volume":"150 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science and Technology Development Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32508/stdj.v26i1.4023","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.