G3 (Bethesda). 2011 Nov;1(6):417-26. doi: 10.1534/g3.111.001057. Epub 2011 Nov 1.
As nutrients are depleted and cell division ceases in batch cultures of bacteria, active processes are required to ensure that each cell has a complete copy of its genome. How chromosome number is manipulated and maintained in nondividing bacterial cells is not fully understood. Using flow cytometric analysis of cells from different growth phases, we show that the Holliday junction-processing enzymes RuvABC and RecG, as well as RecBCD, the enzyme complex that initiates DNA double-strand break repair, are required to establish the normal distribution of fluorescent peaks, which is commonly accepted to reflect the distribution of chromosome numbers. Our results reveal that these proteins are required for the proper processing of chromosomes in stationary phase.
当细菌的分批培养中营养物质耗尽且细胞分裂停止时,需要进行主动过程以确保每个细胞都具有其基因组的完整副本。在不分裂的细菌细胞中,染色体数目的操纵和维持方式尚未完全理解。通过对来自不同生长阶段的细胞进行流式细胞分析,我们表明 Holliday 连接处理酶 RuvABC 和 RecG 以及启动 DNA 双链断裂修复的酶复合物 RecBCD 都需要建立荧光峰的正常分布,这通常被认为反映了染色体数目的分布。我们的结果表明,这些蛋白质是在静止期正确处理染色体所必需的。