Markewych O, Boghosian A, Dosmar M, Ende D, Witmer H
J Virol. 1977 Jan;21(1):84-95. doi: 10.1128/JVI.21.1.84-95.1977.
Bacillus subtilis W23 was infected with a clear-plaque variant of SP-10 phage, namely, SP-10c. Exogenous thymidine was not incorporated into phage DNA (even in the presence of deoxyadenosine), nor was there any transfer of thymidine nucleotides from bacterial to viral DNA. The lytic program was unaffected by concentrations of 5-fluorodeoxyuridine sufficient to reduce bacterial DNA synthesis by greater than 95%. Although these data are consistent with the interpretation that thymidine nucleotides are excluded from phage DNA, formic acid digests of SP-10c DNA contained what appeared to be the four conventional bases; however, adenine and thymine were not recovered in equimolar yields. DNA-RNA hybridization and hybridization competition experiments were done. Synthesis of host RNA started to wane moments postinfection and stopped completely by 36 min. SP-10c coded for discrete classes of early and late RNA. The possibility of discrete subclasses of early RNA exists. Replication of the bacterial genome appeared to terminate 12 min postinfection. Degradation of the host DNA to acid-soluble material started at 36 min and, by the end of the latent period, greater than 90% of the host chromosome was hydrolyzed. Four apparent phage-coded enzymes have been identified. A di- and triphosphatase degraded dUTP, dUDP, dTTP, and dTDP (and, to a lesser extent, dCDP and d CTP) to the corresponding monophosphates; the enzyme had no apparent activity on dATP and dGTP. SP10c also coded for a DNA-dependent DNA polymerase, lysozyme, and a nuclease that degrades native bacterial DNA. Judging from the dependence of enzyme synthesis on the time of addition of rifampin (an inhibitor of the initiation of RNA synthesis), messengers for the di- and triphosphatase, as well as the nuclease, are transcribed from promoters that start to function 6 min postinfection. Promoters for polymerase and lysozyme did not become functional until 8 and 16 min postinfection, respectively.
枯草芽孢杆菌W23被SP - 10噬菌体的一个清晰噬菌斑变体(即SP - 10c)感染。外源性胸苷未掺入噬菌体DNA(即使在脱氧腺苷存在的情况下),也没有胸苷核苷酸从细菌转移到病毒DNA。裂解程序不受足以使细菌DNA合成减少超过95%的5 - 氟脱氧尿苷浓度的影响。尽管这些数据与胸苷核苷酸被排除在噬菌体DNA之外的解释一致,但SP - 10c DNA的甲酸消化产物含有似乎是四种常规碱基的物质;然而,腺嘌呤和胸腺嘧啶的回收产量并不等摩尔。进行了DNA - RNA杂交和杂交竞争实验。感染后不久宿主RNA的合成开始减弱,并在36分钟时完全停止。SP - 10c编码了不同类别的早期和晚期RNA。早期RNA存在离散亚类的可能性。细菌基因组的复制似乎在感染后12分钟终止。宿主DNA降解为酸溶性物质在36分钟时开始,到潜伏期结束时,超过90%的宿主染色体被水解。已鉴定出四种明显由噬菌体编码的酶。一种二磷酸酶和三磷酸酶将dUTP、dUDP、dTTP和dTDP(以及在较小程度上的dCDP和dCTP)降解为相应的单磷酸盐;该酶对dATP和dGTP没有明显活性。SP10c还编码了一种依赖DNA的DNA聚合酶、溶菌酶和一种降解天然细菌DNA的核酸酶。从酶合成对利福平(一种RNA合成起始抑制剂)添加时间的依赖性判断,二磷酸酶和三磷酸酶以及核酸酶的信使RNA是从感染后6分钟开始起作用的启动子转录而来的。聚合酶和溶菌酶的启动子分别直到感染后8分钟和16分钟才开始起作用。