Dawson P, Hohn B, Hohn T, Skalka A
J Virol. 1976 Feb;17(2):576-83. doi: 10.1128/JVI.17.2.576-583.1976.
This report described lambda phage morphogenesis in a mutant system in which the normal pathways for late phage DNA (concatemer) synthesis are blocked and early (monomeric circular) DNA replication products accumulate. As shown earlier (Dawson et al., 1975) under these conditions, late proteins are synthesized and assembled into headlike structures. These structures that accumulate in the mutant are empty, suggesting the monomeric circular DNA molecules cannot be encapsulated. The present results show that crude extracts of induced lysogens of the mutant contain the complementation activities of preheads (the empty precursors to DNA-filled heads), tails, and DNA terminigenerating protein(s). Sucrose gradients of these crude extracts yield fractions containing prehead activity in relative amounts expected from the concentration of late proteins and empty structures. Furthermore, the proteins present in these fractions coelectrophorese with the known capsid proteins of preheads, and empty structures that look like preheads are observed in electron microscope examination of samples from the fractions. Based on our biological, biochemical, and electron microscope analyses, we conclude that the empty structures that accumulate in the induced lysogen of the mutant are normal preheads, which could become filled phage heads if DNA of the appropriate structure (i.e., "late DNA") were available.
本报告描述了在一个突变系统中的λ噬菌体形态发生过程,在该系统中,晚期噬菌体DNA(多联体)合成的正常途径被阻断,早期(单体环状)DNA复制产物积累。如先前所示(Dawson等人,1975年),在这些条件下,晚期蛋白质被合成并组装成类似头部的结构。在突变体中积累的这些结构是空的,这表明单体环状DNA分子无法被包装。目前的结果表明,突变体诱导溶原菌的粗提物含有前头部(充满DNA的头部的空前体)、尾部和DNA末端生成蛋白的互补活性。这些粗提物的蔗糖梯度产生的组分含有前头部活性,其相对量与晚期蛋白质和空结构的浓度预期相符。此外,这些组分中存在的蛋白质与已知的前头部衣壳蛋白共电泳,并且在对这些组分的样品进行电子显微镜检查时观察到了看起来像前头部的空结构。基于我们的生物学、生物化学和电子显微镜分析,我们得出结论,在突变体诱导溶原菌中积累的空结构是正常的前头部,如果有合适结构的DNA(即“晚期DNA”),它们可以变成充满DNA的噬菌体头部。