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首页> 外文期刊>Microbiological Research >Agrobacterium tumefaciens mediated fused egfp-hph gene expression under the control of gpd promoter in Pleurotus ostreatus
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Agrobacterium tumefaciens mediated fused egfp-hph gene expression under the control of gpd promoter in Pleurotus ostreatus

机译:在平菇中gpd启动子控制下,根癌农杆菌介导的egfp-hph基因融合表达

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摘要

A transformation system for the basidiomycete Pleurotus ostreatus was established using agrobacterium-mediated infection. Following P ostreatus glyceraldehyde-3-phosphate dehydrogenase gene analysis, its promoter region including two introns was used as cis-regulatory element to drive expression of enhanced green fluorescent protein (eGFP). As a selection marker, the hygromycin phosphotransferase (hph) gene cassette was used in the binary vector pPEH. Mycelia without pretreatment were found to be the most efficient recipients in transformation experiments while fruiting body tissue or basidiospores showed lower transformation rates. A transformation efficiency of 75% was achieved. After subculturing, putative transformants were screened by PCR and Southern blot analysis showing the expected ectopic integration of the transforming DNA. At the same time, the promotor region was shown to drive expression of selection marker as well as eGFP that could be visualized, which will be helpful for future investigation using Agrobacterium tumefaciens mediated transformation for functional characterization of genes in the mushroom forming basidioymcete P ostreatus
机译:利用农杆菌介导的感染建立了平菇侧耳菌的转化系统。在P. ostreatus甘油醛-3-磷酸脱氢酶基因分析之后,其启动子区域(包括两个内含子)被用作顺式调节元件,以驱动增强型绿色荧光蛋白(eGFP)的表达。作为选择标记,潮霉素磷酸转移酶(hph)基因盒被用于二元载体pPEH中。发现未经预处理的菌丝体是转化实验中最有效的受体,而结实的人体组织或担子孢子则显示出较低的转化率。实现了75%的转化效率。继代培养后,通过PCR和Southern印迹分析筛选推定的转化体,显示预期的转化DNA的异位整合。同时,显示出启动子区域可驱动选择标记以及可以可视化的eGFP的表达,这将有助于进一步利用根癌农杆菌介导的转化研究蘑菇中形成芽孢杆菌的基因的功能表征。

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