Skogman G S, Björk G R
J Gen Virol. 1976 Apr;31(1):9-20. doi: 10.1099/0022-1317-31-1-9.
Growth of phages phi W and T7 was restricted in Escherichia coli lysogenic for phage P1. Only a fraction of the infected cells gave burst of phages. Cells permitting phage growth gave normal burst size. Host strains carrying P1 mutants with defective endonuclease gave no restriction of phages T7 and phi 3, the latter a host-range mutant of phi W. Degradation but not modification of parental phage DNA could be demonstrated. Although no DNA, RNA or protein was synthesized in phi W infected P1 lysogenic cells, the parental phage DNA was found in increasingly larger complexes during the course of infection. At early times after infection, parental phage DNA was found to sediment about twice as fast as mature phage DNA. At later times during the infection the parental phage DNA was recovered as a very rapidly sedimenting material. Such material was also found in alkaline sucrose gradient centrifugation after treatment of the cell extract with sodium dodecyl sulphate, pronase digestion and phenol extractions.
噬菌体φW和T7在溶源性大肠杆菌P1中的生长受到限制。只有一小部分被感染的细胞产生噬菌体爆发。允许噬菌体生长的细胞产生正常的爆发量。携带具有缺陷核酸内切酶的P1突变体的宿主菌株对噬菌体T7和φ3没有限制作用,后者是φW的宿主范围突变体。可以证明亲代噬菌体DNA发生了降解但未发生修饰。尽管在感染φW的P1溶源性细胞中没有合成DNA、RNA或蛋白质,但在感染过程中发现亲代噬菌体DNA存在于越来越大的复合物中。感染后早期,发现亲代噬菌体DNA的沉降速度约为成熟噬菌体DNA的两倍。在感染后期,亲代噬菌体DNA以一种沉降速度非常快的物质形式回收。在用十二烷基硫酸钠处理细胞提取物、蛋白酶消化和苯酚提取后,在碱性蔗糖梯度离心中也发现了这种物质。