Plasmids pRecAgfp and pUvrAgfp were constructed after DNA damage-inducible promoters of recA and uvrA from Escherichia coli were fused to the reporter gene gfpmut3a operon.
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释义
将报告基因绿色荧光蛋白基因(gfpmut3a)分别置于recA和uvrA启动子调控下;构建成质粒pRecAgfp和pUvrAgfp;并转化E.
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