Burton A J
J Virol. 1970 Oct;6(4):455-62. doi: 10.1128/JVI.6.4.455-462.1970.
When Escherichia coli is infected with bacteriophage phiR, parental deoxyribonucleic acid (the single- or double-stranded DNA containing the isotopic label of the infecting phage) becomes firmly attached to a cellular structure and can be isolated as a rapidly sedimenting component as described earlier for phiX174. If this component is centrifuged to equilibrium, two peaks of infective DNA are observed at densities of 1.30 and 1.15 g/ml. At low multiplicities of infection, (32)P-labeled parental DNA is found associated with only the cellular components in the dense band; as the multiplicities of infection are increased, the dense band becomes saturated and parental DNA molecules are then found at the light density as well. Actively replicating host DNA is found only in the dense band, whereas progeny DNA, which does not replicate semiconservatively, can become associated with cellular components in the light band. This fractionation of cellular components on the basis of their buoyant density separates primary sites of DNA replication associated with the dense band from nonfunctional binding sites in the light band.
当大肠杆菌被噬菌体phiR感染时,亲代脱氧核糖核酸(含有感染噬菌体同位素标记的单链或双链DNA)会牢固地附着在细胞结构上,并可作为一种快速沉降的成分分离出来,如同之前对phiX174的描述那样。如果将该成分进行平衡离心,会在密度为1.30和1.15 g/ml处观察到两个感染性DNA峰。在低感染复数时,(32)P标记的亲代DNA仅与致密带中的细胞成分相关联;随着感染复数的增加,致密带饱和,此时也能在低密度处发现亲代DNA分子。活跃复制的宿主DNA仅存在于致密带中,而不以半保留方式复制的子代DNA则可与低密度带中的细胞成分相关联。这种基于浮力密度对细胞成分的分级分离,将与致密带相关的DNA复制主要位点与低密度带中的无功能结合位点区分开来。