McIntosh P K, Dunker R, Mulder C, Brown N C
J Virol. 1978 Dec;28(3):865-76. doi: 10.1128/JVI.28.3.865-876.1978.
The genome of Bacillus subtilis bacteriophage SPP1, a linear, 28.5-megadalton DNA duplex, was mapped by analysis with the restriction endonucleases endo R.Sal I, Sma I, Xba I, Bgl I, Bgl II, and EcoRI. The SPP1 genome, like that of the Salmonella typhimurium phage, P22, was found to be a terminally repetitious, circularly permuted molecule. 6-(p-Hydroxyphenylazo)uracil, a selective, reversible inhibitor of SPP1 DNA synthesis, was exploited to synchronize the initiation of genome replication and to selectively label the site of its initiation with radioactive thymidine. Restriction endonuclease analysis of the distribution of the label located the origin of replicative synthesis at an area approximately 0.2 genome length from one molecular terminus.
枯草芽孢杆菌噬菌体SPP1的基因组是一种线性的28.5兆道尔顿DNA双链体,通过用限制性内切酶R.Sal I、Sma I、Xba I、Bgl I、Bgl II和EcoRI进行分析来绘制图谱。发现SPP1基因组与鼠伤寒沙门氏菌噬菌体P22的基因组一样,是一种末端重复、环状排列的分子。6-(对羟基苯偶氮)尿嘧啶是一种选择性、可逆的SPP1 DNA合成抑制剂,被用于同步基因组复制的起始,并用地放射性胸苷选择性标记其起始位点。对标记分布的限制性内切酶分析将复制合成的起点定位在距一个分子末端约0.2基因组长度的区域。