Cobbett C S, Pittard J
J Bacteriol. 1980 Dec;144(3):877-83. doi: 10.1128/jb.144.3.877-883.1980.
The transposon Tn10, coding for resistance to tetracycline, was inserted close to the tyrR+ gene at min 28 on the Escherichia coli chromosome. The homology between this transposon and a lambda (Tn10) phage was employed to direct integration of lambda close to tyrR+ with subsequent isolation of a lambda (Tn10) tyrR+ transducing phage. Results of restriction endonuclease analysis of the transducing phage are presented.
编码对四环素耐药性的转座子Tn10插入到大肠杆菌染色体上28分钟处的tyrR⁺基因附近。利用该转座子与λ(Tn10)噬菌体之间的同源性,将λ噬菌体定向整合到tyrR⁺基因附近,随后分离出λ(Tn10)tyrR⁺转导噬菌体。本文给出了转导噬菌体的限制性内切酶分析结果。