Fujisawa H, Hayashi M
J Virol. 1977 Oct;24(1):303-13. doi: 10.1128/JVI.24.1.303-313.1977.
A capsomeric structure sedimenting with an S value of 108 in sucrose gradients was isolated from Escherichia coli infected with bacteriophage phi X174. The 108S material contained viral proteins F, G, H, and D, and the relative amounts of these proteins in the 108S material were similar to those in the infectious 132S particle, which has previously been described as a possible intermediate in the assembly of 114S phage particles. Electron micrographs indicated that the size and shape of the 108S material resemble those of the 132S particle. The 108S material contained no DNA, and its formation occurred independently of DNA synthesis. The 108S material accumulated in infected cells when viral DNA replication was prevented either by mutation in phage genes A or C or by removal of thymidine from a culture infected with wild-type phage or with a lysis gene E mutant. Upon restoration of thymidine to cells infected with the lysis gene E mutant and then starved of thymidine, the accumulated 108S material was converted to 132S particles and to 114S phage particles, implying that the 108S material is a precursor of phage particles. A model that proposes possible functions for the products of phi X174 genes A, B, C, D, F, and G during viral replication and phage maturation is described.
从感染噬菌体φX174的大肠杆菌中分离出一种在蔗糖梯度中沉降系数为108S的衣壳结构。108S物质包含病毒蛋白F、G、H和D,这些蛋白在108S物质中的相对含量与感染性132S颗粒中的相似,132S颗粒先前被描述为114S噬菌体颗粒组装过程中可能的中间体。电子显微镜照片显示,108S物质的大小和形状与132S颗粒相似。108S物质不含DNA,其形成独立于DNA合成。当通过噬菌体基因A或C的突变,或从感染野生型噬菌体或裂解基因E突变体的培养物中去除胸苷来阻止病毒DNA复制时,108S物质在感染细胞中积累。在用裂解基因E突变体感染然后缺乏胸苷的细胞中恢复胸苷后,积累的108S物质转化为132S颗粒和114S噬菌体颗粒,这意味着108S物质是噬菌体颗粒的前体。描述了一个关于φX174基因A、B、C、D、F和G的产物在病毒复制和噬菌体成熟过程中可能功能的模型。