Ditta G, Stanfield S, Corbin D, Helinski D R
Proc Natl Acad Sci U S A. 1980 Dec;77(12):7347-51. doi: 10.1073/pnas.77.12.7347.
A broad host range cloning vehicle that can be mobilized at high frequency into Gram-negative bacteria has been constructed from the naturally occurring antibiotic resistance plasmid RK2. The vehicle is 20 kilobase pairs in size, encodes tetracycline resistance, and contains two single restriction enzyme sites suitable for cloning. Mobilization is effected by a helper plasmid consisting of the RK2 transfer genes linked to a ColE1 replicon. By use of this plasmid vehicle, a gene bank of the DNA from a wild-type strain of Rhizobium meliloti has been constructed and established in Escherichia coli. One of the hybrid plasmids in the bank contains a DNA insert of approximately 26 kilobase pairs which has homology to the nitrogenase structural gene region of Klebsiella pneumoniae.
一种能以高频转移到革兰氏阴性菌中的广宿主范围克隆载体,是由天然存在的抗性质粒RK2构建而成。该载体大小为20千碱基对,编码四环素抗性,并含有两个适合克隆的单一限制性酶切位点。转移是由一个辅助质粒实现的,该辅助质粒由与ColE1复制子相连的RK2转移基因组成。利用这种质粒载体,构建了苜蓿根瘤菌野生型菌株DNA的基因文库,并在大肠杆菌中建立。文库中的一个杂交质粒含有一个约26千碱基对的DNA插入片段,它与肺炎克雷伯菌的固氮酶结构基因区域具有同源性。