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Agrobacterium tumefaciens-mediated transformation of the plant pathogenic fungus Rosellinia necatrix

机译:根癌农杆菌介导的植物病原真菌玫瑰茄的转化

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Rosellinia necatrix is a soil-borne root pathogen affecting a wide range of commercially important plant species. The mycelium of R. necatrix was transformed to hygromycin B resistance by an Agrobacterium tumefaciens-mediated transformation system using a binary plasmid vector containing the hygromycin B phosphotransferase (hph) gene controlled by the heterologous fungal Aspergillus nidulans P-gpd (glyceraldehyde 3-phosphate dehydrogenase) promoter and the trpC terminator. Co-cultivation of R. necatrix strain W1015 and A. tumefaciens strain AGL-1 at 25°C using the binary vector pAN26-CB1300, which contained the hygromycin B resistance cassette based on pAN26 and pCAMBIA1300, resulted in high frequencies of transformation. The presence of the hph gene in the transformants was detected by PCR, and single-copy integration of the marker gene was demonstrated by Southern b lot analy s is. This report of an Agrobacterium-mediated transformation method should allow the development of T-DNA tagging as a system for insertional mutagenesis in R. necatrix and provide a simple and reliable method for genetic manipulation.
机译:玫瑰色玫瑰(Nestrine necatrix)是一种土壤传播的根系病原体,会影响多种重要的商业植物。根癌农杆菌介导的转化系统使用含有由潮霉素尼杜兰霉P-gpd(甘油醛3-磷酸脱氢酶)控制的潮霉素B磷酸转移酶(hph)基因的二元质粒载体,通过根癌农杆菌介导的转化系统将中叶R. necatrix的菌丝体转化为潮霉素B抗性。 )启动子和trpC终止子。使用包含基于pAN26和pCAMBIA1300的潮霉素B抗性盒的二元载体pAN26-CB1300,在25°C下共培养R. necatrix菌株W1015和A. tumefaciens菌株AGL-1,导致了高频率的转化。通过PCR检测hph基因在转化体中的存在,并且通过Southern blot分析证明标记基因的单拷贝整合。农杆菌介导的转化方法的这一报告应允许开发T-DNA标签作为在R. necatrix中进行插入诱变的系统,并提供一种简单可靠的基因操作方法。

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