Kozlov Iu I, Kalinina N A, Strongin A Ia, Gening I V, Rebentish B A
Mol Biol (Mosk). 1978 Jan-Feb;12(1):108-15.
In the paper a convenient procedure for the isolation of specific Eco RI-fragments of E. coli genome and their amplification on Km-resistance plasmid vector CKdelta11 is described. Plasmid CKdelta11 contains Col E1 replicon and has only one Eco RI site. The hybrid molecules were constructed in vitro using Eco RI-digestion followed by ligation. Then appropriated E. coli strain (polyauxotrophic strain E. coli K12 AB 2463) was transformed with ligated DNA mixture and hybrid plasmids, containing arg, leu, his and thr chromosomal markers were selected by molecular cloning and isolated from the obtained E. coli clones. The hybrid plasmids have two Eco RI sites and consist of one Eco RI-fragment of initial plasmid CKdelta11 and one Eco RI-fragment of El coli DNA. The method described allows to isolate and amplify on hybrid plasmids DNA fragments, containing any selectable genes or genes adjacent to the selectable ones.
本文描述了一种从大肠杆菌基因组中分离特定Eco RI片段并在卡那霉素抗性质粒载体CKdelta11上进行扩增的简便方法。质粒CKdelta11含有Col E1复制子,且只有一个Eco RI位点。通过Eco RI酶切后连接,在体外构建杂交分子。然后用连接后的DNA混合物转化合适的大肠杆菌菌株(多营养缺陷型大肠杆菌K12 AB 2463),通过分子克隆选择含有精氨酸、亮氨酸、组氨酸和苏氨酸染色体标记的杂交质粒,并从获得的大肠杆菌克隆中分离出来。这些杂交质粒有两个Eco RI位点,由初始质粒CKdelta11的一个Eco RI片段和大肠杆菌DNA的一个Eco RI片段组成。所述方法能够在杂交质粒上分离和扩增含有任何可选择基因或与可选择基因相邻的基因的DNA片段。