Neubort S, Marmur J
J Virol. 1973 Nov;12(5):1078-84. doi: 10.1128/JVI.12.5.1078-1084.1973.
Cultures of Bacillus subtilis infected with phage SP-15 were examined to investigate the metabolic origin of two of the unique components of the phage DNA: the component responsible for the unusually high buoyant density in CsCl and the unusual pyrimidine, 5-(4', 5'-dihydroxypentyl) uracil (DHPU). Newly synthesized pulse-labeled DNA was light in buoyant density and shifted to the high density of mature phage DNA upon further incubation. Parental DNA was converted to a light-density intermediate form prior to replication. When labeled uracil, thymidine, or DHPU were added to infected cells, it was found that only uracil served as the precursor to DHPU and thymine in phage DNA. Analysis of the bases from hydrolyzed DNA of labeled phage or infected cells indicated that the uracil was incorporated into the DNA as such (presumably via deoxyuridine triphosphate) and later converted to DHPU and thymine at the macromolecular level. The sequence of events after phage infection appeared to be: (i) injection of parental DNA; (ii) conversion of parental DNA to a light form; (iii) DNA replication, yielding light DNA containing uracil; (iv) conversion of uracil to DHPU and thymine; and (v) addition of the heavy component.
对感染噬菌体SP - 15的枯草芽孢杆菌培养物进行了检测,以研究噬菌体DNA的两种独特成分的代谢起源:负责在CsCl中具有异常高浮力密度的成分和异常嘧啶5-(4', 5'-二羟基戊基)尿嘧啶(DHPU)。新合成的脉冲标记DNA浮力密度较轻,在进一步孵育后转变为成熟噬菌体DNA的高密度形式。亲代DNA在复制前转变为低密度中间形式。当将标记的尿嘧啶、胸腺嘧啶或DHPU添加到感染细胞中时,发现只有尿嘧啶作为噬菌体DNA中DHPU和胸腺嘧啶的前体。对标记噬菌体或感染细胞水解DNA的碱基分析表明,尿嘧啶原样掺入DNA(大概是通过脱氧尿苷三磷酸),随后在大分子水平上转化为DHPU和胸腺嘧啶。噬菌体感染后的事件顺序似乎是:(i) 亲代DNA的注入;(ii) 亲代DNA转变为轻形式;(iii) DNA复制,产生含尿嘧啶的轻DNA;(iv) 尿嘧啶转化为DHPU和胸腺嘧啶;以及(v) 重成分的添加。