Kolenbrander P E, Hemphill H E, Whiteley H R
J Virol. 1972 May;9(5):776-84. doi: 10.1128/JVI.9.5.776-784.1972.
The synthesis of host macromolecules was shut off very slowly and incompletely by bacteriophage SPO2c(1). No change in the rate of incorporation of radioactive precursors into protein and ribonucleic acid (RNA) could be detected after infection, and the rate of incorporation of thymidine was increased only slightly. The relative proportions of phage and host species of nucleic acids at various intervals in the latent period were determined by means of nucleic acid hybridization. Phage-specific RNA populations synthesized early were different from those synthesized late in the latent period. Host deoxyribonucleic acid (DNA) replication continued until 8 to 10 min after SPO2c(1) infection and then decreased markedly as phage-specific DNA synthesis was initiated. Host DNA was not degraded to trichloroacetic acid-soluble fragments, and its nucleotides were not found in either newly synthesized intracellular phage DNA or in progeny phage particles. The average burst size of SPO2c(1) was approximately 200 plaque-forming units per cell.
噬菌体SPO2c(1)能非常缓慢且不完全地阻断宿主大分子的合成。感染后,未检测到放射性前体掺入蛋白质和核糖核酸(RNA)的速率有变化,胸苷掺入速率仅略有增加。通过核酸杂交确定潜伏期不同时间间隔噬菌体和宿主核酸种类的相对比例。潜伏期早期合成的噬菌体特异性RNA群体与后期合成的不同。宿主脱氧核糖核酸(DNA)复制一直持续到SPO2c(1)感染后8至10分钟,然后随着噬菌体特异性DNA合成开始而显著下降。宿主DNA未降解为三氯乙酸可溶片段,其核苷酸也未出现在新合成的细胞内噬菌体DNA或子代噬菌体颗粒中。SPO2c(1)的平均裂解量约为每细胞200个噬菌斑形成单位。