REILLY B E, SPIZIZEN J
J Bacteriol. 1965 Mar;89(3):782-90. doi: 10.1128/jb.89.3.782-790.1965.
Reilly, Bernard E. (Western Reserve University, Cleveland, Ohio), and John Spizizen. Bacteriophage deoxyribonucleate infection of competent Bacillus subtilis. J. Bacteriol. 89:782-790. 1964.-Phenol extracts of the Bacillus subtilis bacteriophages phi1, phi25, and phi29 contained infectious deoxyribonucleic acid. The infectivity was destroyed by catalytic amounts of deoxyribonuclease but not by specific phage antiserum, ribonuclease, or trypsin. An infectivity of >10(6) infectious centers formed per mug of deoxyribonucleic acid (DNA) added was obtained. The stability of the infectious centers permitted an examination of a single cycle of phage replication in cells unable to adsorb the mature virus. A typical cycle was observed, although the latent period was increased and the burst size slightly reduced after DNA infection. The development of competence for bacterial transformation was strongly correlated with susceptibility to viral DNA infection. Both appeared and disappeared at the same phase of growth in the cell population. More than 4% of the viable cells in the competent population were infected by viral DNA. The kinetics of the transition of phi29 DNA infection to deoxyribonuclease insensitivity, and the relationship of infectivity to DNA dilution, were similar to the results obtained for bacterial transformation of a single marker. The doseresponse curve of phi1 and phi25 DNA was characteristic of that obtained in multiple transformation of unlinked genetic markers. Because of the low efficiency of infection, about 10(-4) per phage equivalent of DNA added, it was not possible to prove that DNA alone was sufficient to initiate infection.
赖利,伯纳德·E.(俄亥俄州克利夫兰市西储大学),以及约翰·斯皮齐曾。噬菌体脱氧核糖核酸对感受态枯草芽孢杆菌的感染。《细菌学杂志》89:782 - 790。1964年。——枯草芽孢杆菌噬菌体phi1、phi25和phi29的酚提取物含有感染性脱氧核糖核酸。催化量的脱氧核糖核酸酶可破坏其感染性,但特异性噬菌体抗血清、核糖核酸酶或胰蛋白酶则不能。每微克添加的脱氧核糖核酸(DNA)可形成>10⁶个感染中心的感染性。感染中心的稳定性使得能够在无法吸附成熟病毒的细胞中研究噬菌体复制的单个周期。观察到了典型的周期,尽管DNA感染后潜伏期延长且裂解量略有减少。细菌转化感受态的发展与对病毒DNA感染的敏感性密切相关。两者在细胞群体生长的同一阶段出现和消失。感受态群体中超过4%的活细胞被病毒DNA感染。phi29 DNA感染向脱氧核糖核酸酶不敏感性转变的动力学以及感染性与DNA稀释的关系,与单个标记细菌转化所获得的结果相似。phi1和phi25 DNA的剂量反应曲线具有在不连锁遗传标记的多重转化中所获得的特征。由于感染效率低,每添加一个噬菌体当量的DNA约为10⁻⁴,因此无法证明仅DNA就足以引发感染。