Harnessing Single Cell Sorting to Identify Cell Division Genes and Regulators in Bacteria

被引:21
作者
Burke, Catherine [1 ]
Liu, Michael [1 ]
Britton, Warwick [2 ,3 ]
Triccas, James A. [2 ,3 ]
Thomas, Torsten [4 ,5 ]
Smith, Adrian L. [2 ,3 ]
Allen, Steven [2 ,3 ]
Salomon, Robert [2 ,3 ]
Harry, Elizabeth [1 ]
机构
[1] Univ Technol Sydney, Ithree Inst, Sydney, NSW 2007, Australia
[2] Univ Sydney, Centenary Inst Canc Med & Cell Biol, Sydney, NSW 2006, Australia
[3] Univ Sydney, Dept Infect Dis & Immunol, Sydney, NSW 2006, Australia
[4] Univ New S Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW, Australia
[5] Univ New S Wales, Ctr Marine Bioinnovat, Sydney, NSW, Australia
来源
PLOS ONE | 2013年 / 8卷 / 04期
基金
澳大利亚研究理事会;
关键词
ESCHERICHIA-COLI; CHROMOSOME SEGREGATION; ELEMENT E14; FTSZ; PROTEIN; FILAMENTATION; INHIBITION; EXPRESSION; PREDATION; SYSTEM;
D O I
10.1371/journal.pone.0060964
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
Cell division is an essential cellular process that requires an array of known and unknown proteins for its spatial and temporal regulation. Here we develop a novel, high-throughput screening method for the identification of bacterial cell division genes and regulators. The method combines the over-expression of a shotgun genomic expression library to perturb the cell division process with high-throughput flow cytometry sorting to screen many thousands of clones. Using this approach, we recovered clones with a filamentous morphology for the model bacterium, Escherichia coli. Genetic analysis revealed that our screen identified both known cell division genes, and genes that have not previously been identified to be involved in cell division. This novel screening strategy is applicable to a wide range of organisms, including pathogenic bacteria, where cell division genes and regulators are attractive drug targets for antibiotic development.
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页数:13
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