Siegel P J, Schaechter M
J Virol. 1973 Mar;11(3):359-67. doi: 10.1128/JVI.11.3.359-367.1973.
We have presented a new approach to studying bacteriophage T4 head maturation. Using a modified M-band technique, we have shown that progeny deoxyribonucleic acid (DNA) was synthesized on the host cell membrane throughout infection. This DNA was released from the membrane later in infection as the result of formation of the phage head; detachment of the DNA required the action of gene products 20, 21, 22, 23, 24, 31, 16, 17 and 49, known to be necessary for normal head formation. Gene products 2, 4, 50, 64, 65, 13 and 14, also involved in head morphogenesis were not required to detach progeny DNA from the membrane; the presence of the phage tail and tail fibers also was not required. DNA was released in the form of immature heads and initially was sensitive to deoxyribonuclease (DNase). Conversion to DNase resistance followed rapidly. The amount of phage precursors present at the time of DNA synthesis determined the time of onset and detachment rate of DNA from the M band as well as the kinetics by which the detached DNA become DNase resistant.
我们提出了一种研究噬菌体T4头部成熟的新方法。利用改良的M带技术,我们发现子代脱氧核糖核酸(DNA)在整个感染过程中于宿主细胞膜上合成。在感染后期,由于噬菌体头部的形成,这种DNA从膜上释放出来;DNA的分离需要基因产物20、21、22、23、24、31、16、17和49的作用,已知这些基因产物是正常头部形成所必需的。参与头部形态发生的基因产物2、4、50、64、65、13和14对于从膜上分离子代DNA不是必需的;噬菌体尾部和尾丝的存在也不是必需的。DNA以未成熟头部的形式释放,最初对脱氧核糖核酸酶(DNase)敏感。随后迅速转变为对DNase有抗性。DNA合成时存在的噬菌体前体的量决定了DNA从M带开始释放的时间和分离速率,以及分离出的DNA变为对DNase有抗性的动力学过程。