Grossman N, Ron E Z
J Bacteriol. 1980 Jul;143(1):100-4. doi: 10.1128/jb.143.1.100-104.1980.
In Escherichia coli growing at different rates, the ratio of cell mass to the number of chromosome origins tended to be constant at the time of the initiation of deoxyribonucleic acid (DNA) replication. This observation led to the assumption that the initiation event is controlled in some way by cell mass, e.g., by a growth-dependent synthesis of an initiator or dilution of a repressor. We have now found that the initiation of DNA synthesis can be uncoupled from cell mass. We used a synchronous culture of newly divided cells of E. coli B which was obtained by the membrane elution technique (C.E. Helmstetter, J. Mol. Biol. 24: 417-427, 1967) and was starved for an amino acid. Upon restoration of the amino acid, the cells not only divided at a size that was smaller than normal, but also initiated DNA replication long before they could increase their masses to reach the expected ratio of mass/DNA presumably required for initiation.
在以不同速率生长的大肠杆菌中,在脱氧核糖核酸(DNA)复制起始时,细胞质量与染色体起始点数量的比值往往保持恒定。这一观察结果导致人们假定起始事件在某种程度上受细胞质量控制,例如,通过起始因子的生长依赖性合成或阻遏物的稀释来实现。我们现在发现,DNA合成的起始可以与细胞质量解偶联。我们使用了通过膜洗脱技术(C.E. 赫尔姆斯泰特,《分子生物学杂志》24: 417 - 427, 1967)获得的大肠杆菌B新分裂细胞的同步培养物,并使其缺乏一种氨基酸。当恢复该氨基酸时,细胞不仅以小于正常大小的尺寸进行分裂,而且在它们能够增加质量以达到推测的起始所需的质量/DNA预期比值之前很久就开始了DNA复制。