Furukawa H, Kuroiwa T, Mizushima S
J Bacteriol. 1983 May;154(2):938-45. doi: 10.1128/jb.154.2.938-945.1983.
The process of phage T4 DNA injection into the host cell was studied under a fluorescent microscope, using 4',6-diamidino-2-phenylindole as a DNA-specific fluorochrome. The phage DNA injection was observed when spheroplasts were infected with the artificially contracted phage particles having a protruding core. The DNA injection was mediated by the interaction of the core tip with the cytoplasmic membrane of the spheroplast. A membrane potential was not required for the process of DNA injection. On the other hand, DNA injection upon infection by intact noncontracted phage of the intact host cell was inhibited by an energy poison. Based on these observations, together with results from previous work, a model for the T4 infection process is presented, and the role of the membrane potential in the infection process is discussed.
利用4',6-二脒基-2-苯基吲哚作为DNA特异性荧光染料,在荧光显微镜下研究了T4噬菌体DNA注入宿主细胞的过程。当原生质球用具有突出核心的人工收缩噬菌体颗粒感染时,观察到噬菌体DNA注入。DNA注入是由核心尖端与原生质球细胞质膜的相互作用介导的。DNA注入过程不需要膜电位。另一方面,完整宿主细胞被完整的未收缩噬菌体感染时的DNA注入受到能量毒物的抑制。基于这些观察结果,结合先前工作的结果,提出了T4感染过程的模型,并讨论了膜电位在感染过程中的作用。