Vovis G F, Horiuchi K, Zinder N D
J Virol. 1975 Sep;16(3):674-84. doi: 10.1128/JVI.16.3.674-684.1975.
Replicative form DNA of bacteriophage f1 was found to be sensitive in vitro to restriction by endonuclease R-EcoRII if the DNA was isolated from an Escherichia coli strain deficient in cytosine methylase activity. A similar observation was previously made with DNA from the closely related bacteriophage fd (S. Schlagman, S. Hattman, M. S. May, and L. Berger, submitted for publication). The two DNA fragments produced by the endo R-EcoRII digestion of f1 DNA were localized on the f1 cleavage map and their genetic content was determined. The polypeptides synthesized in a "coupled" transcription-translation system under the direction of each RII fragment were examined. The results of such experiments allow the ordering of genes V and VII and indicate the location of a RNA promotor for gene VIII.
如果从缺乏胞嘧啶甲基化酶活性的大肠杆菌菌株中分离出噬菌体f1的复制型DNA,发现其在体外对核酸内切酶R-EcoRII的限制敏感。之前对密切相关的噬菌体fd的DNA也有类似观察结果(S. Schlagman、S. Hattman、M. S. May和L. Berger,已提交发表)。核酸内切酶R-EcoRII消化f1 DNA产生的两个DNA片段定位在f1切割图谱上,并确定了它们的遗传内容。检测了在每个RII片段指导下在“偶联”转录-翻译系统中合成的多肽。这些实验结果使基因V和VII得以排序,并表明了基因VIII的RNA启动子的位置。