Gustafsson P, Nordström K
J Bacteriol. 1980 Jan;141(1):106-10. doi: 10.1128/jb.141.1.106-110.1980.
Plasmid R1 replication was studied in shifts between two steady states of copy number. The copy number was varied in two ways. First, we utilized the fact that it decreases with increasing growth rate. To minimize the metabolic effects of changes in the growth rate, the downshifts were obtained by adding alpha-methylglucoside to cultures growing in glucose-minimal medium, and the upshifts were obtained by adding glucose to cultures growing in the presence of glucose plus alpha-methylglucoside. Second, we used a temperature-dependent copy mutant of plasmid R1 (pKN301). Plasmid pPK301 shows a threefold higher copy number at 40 than at 30 degrees C. In both types of shift, plasmid replication immediately adjusted to the postshift differential rate. The copy number asymptotically adjusted to the new steady state. Hence, the system that controls plasmid R1 replication sets the frequency of replication without measuring the actual copy number. It has been suggested that plasmid R1 replication is under negative control by an R1-mediated repressor protein. Among the replication control models that involve negative control, the Pritchard inhibitor dilution model, the Sompayrac-Maaløe autorepressor model, and the plasmid lambdadv system all predict gene dose-independent copy number control.
在质粒R1拷贝数的两个稳定状态之间的转换过程中,对其复制情况进行了研究。拷贝数通过两种方式进行改变。首先,我们利用了拷贝数随生长速率增加而降低这一事实。为了将生长速率变化的代谢影响降至最低,通过向在葡萄糖基本培养基中生长的培养物中添加α-甲基葡萄糖苷来实现向下转换,而通过向在葡萄糖加α-甲基葡萄糖苷存在下生长的培养物中添加葡萄糖来实现向上转换。其次,我们使用了质粒R1的温度依赖性拷贝突变体(pKN301)。质粒pPK301在40℃时的拷贝数比在30℃时高3倍。在这两种转换类型中,质粒复制都能立即根据转换后的差异速率进行调整。拷贝数渐近地调整到新的稳定状态。因此,控制质粒R1复制的系统在不测量实际拷贝数的情况下设定复制频率。有人提出质粒R1复制受R1介导的阻遏蛋白的负调控。在涉及负调控的复制控制模型中,普里查德抑制剂稀释模型、索姆派拉克-马勒自阻遏模型以及质粒λdv系统都预测了基因剂量独立的拷贝数控制。