Site-directed insertion and deletion mutagenesis with cloned fragments in Escherichia coli

利用克隆片段在大肠杆菌中进行定点插入和缺失诱变

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Abstract

A mutation of a cloned gene that has been made by introducing a transposon or some other selectable genetic determinant can be crossed into the gene's original replicon by linearizing the cloned DNA and transforming a recB recC sbcB mutant. A number of applications of this method are described with genes of either chromosomal or plasmid origin.

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