Synchronization of Caulobacter Crescentus for Investigation of the Bacterial Cell Cycle

被引:32
作者
Schrader, Jared M. [1 ]
Shapiro, Lucy [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2015年 / 98期
关键词
Cellular Biology; Issue; 98; cell cycle; cell biology; systems biology; synchronization; Caulobacter; asymmetric cell division; STRINGENT RESPONSE; REPLICATION; PROTEIN;
D O I
10.3791/52633
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The cell cycle is important for growth, genome replication, and development in all cells. In bacteria, studies of the cell cycle have focused largely on unsynchronized cells making it difficult to order the temporal events required for cell cycle progression, genome replication, and division. Caulobacter crescentus provides an excellent model system for the bacterial cell cycle whereby cells can be rapidly synchronized in a G0 state by density centrifugation. Cell cycle synchronization experiments have been used to establish the molecular events governing chromosome replication and segregation, to map a genetic regulatory network controlling cell cycle progression, and to identify the establishment of polar signaling complexes required for asymmetric cell division. Here we provide a detailed protocol for the rapid synchronization of Caulobacter NA1000 cells. Synchronization can be performed in a large-scale format for gene expression profiling and western blot assays, as well as a small-scale format for microscopy or FACS assays. The rapid synchronizability and high cell yields of Caulobacter make this organism a powerful model system for studies of the bacterial cell cycle.
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页数:6
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