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Single live-bacterial cell assay of promoter activity and regulation

机译:启动子活性和调控的单活细菌细胞测定

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Laboratory cultures of a single species of bacteria harboring the same genetic background include heterogeneous cell populations, each differing in apparent morphology and physiology, as found in natural environments. To get insights into difference in the genome expression between individual cells, we constructed various types of the cell chip for monitoring the growth and fate of individual bacterial cells. Immobilization of portions of Escherichia coli culture within these cell chips was established after raising the local temperature in the presence of poly-(N-isopropylacrylamide) (PNIPAAm). The newly developed cell-chip system allows the investigation of activity and regulation of green fluorescent protein (GFP)-fused promoter in single live-bacterial cells for prolonged time under controlled culture conditions. Using this single-cell observation system, we succeeded, for the first time, the real-time single-cell assay of promoter activity of the E. coli gcl gene encoding glyoxylate carboligase as a model system, and the kinetics of gcl induction by an effector glyoxylate. Marked heterogeneity was found in the expression level of the gcl promoter. The heterogeneity in gcl promoter activity was, however, confirmed by Flow cytometry of suspension cultures. Our success provides an experimental system for the increased demand of single-cell biology in bacterial studies.
机译:具有相同遗传背景的单个细菌的实验室培养物包括异种细胞群体,每种细胞群体在自然环境中均具有明显的形态学和生理学差异。为了深入了解单个细胞之间基因组表达的差异,我们构建了各种类型的细胞芯片来监控单个细菌细胞的生长和命运。在存在聚-(N-异丙基丙烯酰胺)(PNIPAAm)的情况下升高局部温度后,将部分大肠杆菌培养物固定在这些细胞芯片中。新开发的细胞芯片系统允许在受控培养条件下长时间研究单个活细菌细胞中绿色荧光蛋白(GFP)融合启动子的活性和调控。使用该单细胞观察系统,我们首次成功地实时编码了编码乙醛酸羧化酶的大肠杆菌gcl基因启动子活性的单细胞实时分析,并成功地通过DNA诱导了gcl的动力学。乙醛酸酯。在gcl启动子的表达水平中发现明显的异质性。然而,通过悬浮培养物的流式细胞术证实了gcl启动子活性的异质性。我们的成功为细菌研究中单细胞生物学需求的增长提供了一个实验系统。

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