生物
质粒
复制子
科尔1
根瘤菌
遗传学
基因
质体制备
大肠杆菌
分子克隆
限制性酶
多克隆站点
微生物学
克隆载体
PBR322电话
基因表达
表达式向量
重组DNA
作者
Gary S. Ditta,Samantha Stanfield,D. E. Cox,Donald R. Helinski
标识
DOI:10.1073/pnas.77.12.7347
摘要
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.
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