Withers H L, Bernander R
Department of Microbiology, Biomedical Centre, Uppsala University, Sweden.
J Bacteriol. 1998 Apr;180(7):1624-31. doi: 10.1128/JB.180.7.1624-1631.1998.
Escherichia coli strains containing thermosensitive dnaC alleles were studied by flow cytometry. Strains containing either the dnaC2 or dnaC28 allele were shifted between different temperatures, and DNA content distributions were gathered. Inhibition of initiation of chromosome replication at nonpermissive temperature, as well as reinitiation of replication at permissive temperature, were found to be affected by a number of parameters. These included the choice of permissive and nonpermissive temperatures, the length of the time of incubation at the nonpermissive temperature, the growth medium, the type of temperature shift used for reinitiation of replication (transient or nontransient), the genetic background of the host cell, and the cell concentration. Reinitiation of replication required neither transcription nor translation, whereas the elongation stage of replication was dependent upon ongoing protein synthesis in the mutants. Efficient use of dnaC mutants for cell cycle studies is discussed.
通过流式细胞术研究了含有温度敏感型dnaC等位基因的大肠杆菌菌株。含有dnaC2或dnaC28等位基因的菌株在不同温度之间转换,并收集DNA含量分布。发现在非允许温度下染色体复制起始的抑制以及在允许温度下复制的重新起始受到许多参数的影响。这些参数包括允许温度和非允许温度的选择、在非允许温度下的孵育时间长度、生长培养基、用于复制重新起始的温度转换类型(瞬时或非瞬时)、宿主细胞的遗传背景以及细胞浓度。复制的重新起始既不需要转录也不需要翻译,而复制的延伸阶段则依赖于突变体中正在进行的蛋白质合成。文中讨论了将dnaC突变体有效用于细胞周期研究的问题。