Andrésson O S, Davies J E
Mol Gen Genet. 1980;179(1):211-6. doi: 10.1007/BF00268465.
Small multicopy plasmids carrying the Escherichia coli genes ksgA and pdxA were constructed by ligation in vitro of an EcoRI restriction fragment from lambda ksg10 (Andrésson and Davies, 1980a) into the EcoRI sites of the ColE1 plasmids RSF2124 and pVH51. Cleavage maps of the plasmids were determined for 21 different restriction enzymes. The ksgA gene was located in a 750 basepairs (bp) region 1,450 bp clockwise of the EcoRI site in folA: pdxA is in a 2,040 bp region immediately clockwise of ksgA.
通过将来自λksg10的EcoRI限制片段(Andrésson和Davies,1980a)体外连接到ColE1质粒RSF2124和pVH51的EcoRI位点,构建了携带大肠杆菌基因ksgA和pdxA的小型多拷贝质粒。测定了21种不同限制酶对这些质粒的切割图谱。ksgA基因位于folA中EcoRI位点顺时针方向1450 bp处的一个750碱基对(bp)区域:pdxA位于ksgA紧邻的顺时针方向一个2040 bp区域。