Lawhorne L, Kleber I, Mitchell C, Benzinger R
J Virol. 1973 Oct;12(4):733-40. doi: 10.1128/JVI.12.4.733-740.1973.
The change of infectivity of phage DNAs after heat and alkali denaturation (and renaturation) was measured. T7 phage DNA infectivity increased 4- to 20-fold after denaturation and decreased to the native level after renaturation. Both the heavy and the light single strand of T7 phage DNA were about five times as infective as native T7 DNA. T4 and P22 phage DNA infectivity increased 4- to 20-fold after denaturation and increased another 10- to 20-fold after renaturation. These data, combined with other authors' results on the relative infectivity of various forms of phiX174 and lambda DNAs give the following consistent pattern of relative infectivity. Covalently closed circular double-stranded DNA, nicked circular double-stranded DNA, and double-stranded DNA with cohesive ends are all equally infective and also most highly infectious for Escherichia coli lysozyme-EDTA spheroplasts; linear or circular single-stranded DNAs are about 1/5 to 1/20 as infective; double-stranded DNAs are only 1/100 as infective. Two exceptions to this pattern were noted: lambda phage DNA lost more than 99% of its infectivity after alkaline denaturation; this infectivity could be fully recovered after renaturation. This behavior can be explained by the special role of the cohesive ends of the phage DNA. T5 phage DNA sometimes showed a transient increase in infectivity at temperatures below the completion of the hyperchròmic shift; at higher temperatures, the infectivity was completely destroyed. T5 DNA denatured in alkali lost more than 99.9% of its infectivity; upon renaturation, infectivity was sometimes recovered. This behavior is interpreted in terms of the model of T5 phage DNA structure proposed by Bujard (1969). The results of the denaturation and renaturation experiments show higher efficiencies of transfection for the following phage DNAs (free of single-strand breaks): T4 renatured DNA at 10(-3) instead of 10(-5) for native DNA; renatured P22 DNA at 3 x 10(-7) instead of 3 x 10(-9) for native DNA; and denatured T7 DNA at 3 x 10(-6) instead of 3 x 10(-7) for native DNA.
测定了噬菌体DNA经热和碱变性(及复性)后感染性的变化。T7噬菌体DNA变性后感染性增加4至20倍,复性后降至天然水平。T7噬菌体DNA的重链和轻链单链的感染性均约为天然T7 DNA的五倍。T4和P22噬菌体DNA变性后感染性增加4至20倍,复性后又增加10至20倍。这些数据与其他作者关于各种形式的phiX174和λ DNA相对感染性的结果相结合,得出了以下相对感染性的一致模式。共价闭合环状双链DNA、带切口的环状双链DNA和具有粘性末端的双链DNA对大肠杆菌溶菌酶 - EDTA原生质球的感染性相同且都是最高的;线性或环状单链DNA的感染性约为其1/5至1/20;双链DNA的感染性仅为其1/100。注意到该模式有两个例外:λ噬菌体DNA经碱变性后其感染性丧失超过99%;复性后这种感染性可完全恢复。这种行为可通过噬菌体DNA粘性末端的特殊作用来解释。T5噬菌体DNA有时在增色效应完成之前的温度下感染性会短暂增加;在较高温度下,感染性完全被破坏。在碱中变性的T5 DNA丧失其感染性的99.9%以上;复性后,感染性有时会恢复。这种行为根据Bujard(1969)提出的T5噬菌体DNA结构模型来解释。变性和复性实验结果表明,对于以下无单链断裂的噬菌体DNA,转染效率更高:T4复性DNA为10^(-3),而天然DNA为10^(-5);P22复性DNA为3×10^(-7),而天然DNA为3×10^(-9);变性T7 DNA为3×10^(-6),而天然DNA为3×10^(-7)。