Bourguignon G J, Sweeney T K, Delius H
J Virol. 1976 Apr;18(1):245-59. doi: 10.1128/JVI.18.1.245-259.1976.
Replicating T5 phage DNA was gently isolated using NaI density gradient centrifugation and examined by electron microscopy. At the beginning of phage DNA synthesis, linear unit-length T5 DNA molecules containing from one to four replicating "eye-loops" were consistently observed. Replication in these molecules was found to proceed bidirectionally from multiple, internal origins. A primary origin of replication is located near the center of the T5 genome, which does not coincide with the location of any of the nicks (single-strand breaks) found in mature T5 DNA. The initiation of replication at the various origins within an individual molecule does not appear to follow any definite temporal sequence. At later times in the infection, we have observed a significant number of circular T5 DNA molecules-both replicating and nonreplicating-whose average circumference is approximately the length of mature T5 DNA minus the terminal redundancy. The replicating circular molecules appear to be either in a theta configuration, a sigma configuration with the tails all being less than the length of the circle, or a combination of theta and sigma forms.
利用碘化钠密度梯度离心法轻柔地分离出正在复制的T5噬菌体DNA,并通过电子显微镜进行观察。在噬菌体DNA合成开始时,始终能观察到含有一到四个正在复制的“眼环”的线性单位长度T5 DNA分子。发现这些分子中的复制从多个内部起始点双向进行。一个主要的复制起始点位于T5基因组的中心附近,这与成熟T5 DNA中发现的任何切口(单链断裂)的位置都不一致。单个分子内各个起始点的复制起始似乎没有遵循任何确定的时间顺序。在感染后期,我们观察到大量的环状T5 DNA分子——既有正在复制的,也有未复制的——其平均周长约为成熟T5 DNA的长度减去末端冗余。正在复制的环状分子似乎要么呈θ构型,要么呈尾巴长度均小于环长的σ构型,要么是θ和σ形式的组合。