Inhibition of the gyrA promoter by transcription-coupled DNA supercoiling in Escherichia coli

被引:12
|
作者
Dages, Samantha [1 ,2 ]
Dages, Kelley [1 ,2 ]
Zhi, Xiaoduo [1 ,2 ]
Leng, Fenfei [1 ,2 ]
机构
[1] Florida Int Univ, Biomol Sci Inst, 11200 SW 8th St, Miami, FL 33199 USA
[2] Florida Int Univ, Dept Chem & Biochem, 11200 SW 8th St, Miami, FL 33199 USA
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
基金
美国国家卫生研究院;
关键词
LEU-500; PROMOTER; GENE-EXPRESSION; TOPOISOMERASE-I; HOMEOSTATIC REGULATION; PLASMID DNA; SUPPRESSION; DEFICIENT; MUTATION; SENSITIVITY; ACTIVATION;
D O I
10.1038/s41598-018-33089-4
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 E. coli gyrA promoter (P-gyrA) is a DNA supercoiling sensitive promoter, stimulated by relaxation of DNA templates, and inhibited by (-) DNA supercoiling in bacteria. However, whether P-gyrA can be inhibited by transient and localized transcription-coupled DNA supercoiling (TCDS) has not been fully examined. In this paper, using different DNA templates including the E. coli chromosome, we show that transient and localized TCDS strongly inhibits P-gyrA in E. coli. This result can be explained by a twin-supercoiled domain model of transcription in which (+) and (-) supercoiled domains are generated around the transcribing RNA polymerase. We also find that fluoroquinolones, such as ciprofloxacin, can substantially increase the expression of the firefly luciferase under the control of the P-gyrA coupled to a divergent IPTG-inducible promoter in the presence of IPTG. This stimulation of P-gyrA by fluoroquinolones can be also explained by the twin-supercoiled domain model of transcription. This unique property of TCDS may be configured into a high throughput-screening (HTS) assay to identify antimicrobial compounds targeting bacterial DNA gyrase.
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页数:9
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