Ryder O A, Smith D W
Cell. 1975 Apr;4(4):337-45. doi: 10.1016/0092-8674(75)90154-3.
Analysis of folded chromosomes prepared from amino acid-starved E. coli cells of from a dnaC initiation mutant indicates that a unique structure is associated with completion or near completion of rounds of chromosome replication in E. coli. Chromosomes remain associated with portions of the bacterial cell envelope throughout the DNA replication cycle, but become more rapidly sedimenting as replication proceeds in the absence of reinitiation. Before reinitiation of chromosome replication occurs after restoring required amino acids to amino acid-starved cells or after lowering the temperature in a thermosensitive dnaC mutant, sedimentation velocities of the membrane-associated folded chromosomes decrease substantially. The decrease in sedimentation velocity does not depend on renewed DNA synthesis, but does require the activity of at least the dnaC gene product.
对由氨基酸饥饿的大肠杆菌细胞或dnaC起始突变体制备的折叠染色体的分析表明,一种独特的结构与大肠杆菌中染色体复制轮次的完成或接近完成相关。在整个DNA复制周期中,染色体始终与细菌细胞膜的部分区域相连,但在没有重新起始的情况下,随着复制的进行,它们的沉降速度会加快。在向氨基酸饥饿的细胞补充所需氨基酸后或在温度敏感的dnaC突变体中降低温度后,染色体复制重新起始之前,与膜相关的折叠染色体的沉降速度会大幅下降。沉降速度的下降不依赖于新的DNA合成,但确实需要至少dnaC基因产物的活性。