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Systematic approach to Escherichia coli cell population control using a genetic lysis circuit

机译:使用遗传裂解电路控制大肠杆菌细胞群的系统方法

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Background Cell population control allows for the maintenance of a specific cell population density. In this study, we use lysis gene BBa_K117000 from the Registry of Standard Biological Parts, formed by MIT, to lyse Escherichia coli ( E. coli ). The lysis gene is regulated by a synthetic genetic lysis circuit, using an inducer-regulated promoter-RBS component. To make the design more easily, it is necessary to provide a systematic approach for a genetic lysis circuit to achieve control of cell population density. Results Firstly, the lytic ability of the constructed genetic lysis circuit is described by the relationship between the promoter-RBS components and inducer concentration in a steady state model. Then, three types of promoter-RBS libraries are established. Finally, according to design specifications, a systematic design approach is proposed to provide synthetic biologists with a prescribed I/O response by selecting proper promoter-RBS component set in combination with suitable inducer concentrations, within a feasible range. Conclusion This study provides an important systematic design method for the development of next-generation synthetic gene circuits, from component library construction to genetic circuit assembly. In future, when libraries are more complete, more precise cell density control can be achieved.
机译:背景细胞种群控制允许维持特定的细胞种群密度。在这项研究中,我们使用由麻省理工学院(MIT)成立的标准生物部分注册处的裂解基因BBa_K117000裂解大肠杆菌(E. coli)。使用诱导物调节的启动子-RBS成分,通过合成的基因裂解电路来调控裂解基因。为了使设计更容易,有必要为遗传裂解电路提供一种系统的方法,以实现对细胞种群密度的控制。结果首先,在稳态模型中,通过启动子-RBS成分与诱导剂浓度之间的关系描述了构建的基因裂解电路的裂解能力。然后,建立了三种类型的启动子-RBS文库。最后,根据设计规范,提出了一种系统化的设计方法,通过在可行范围内选择合适的启动子-RBS组分组合以及合适的诱导剂浓度,为合成生物学家提供指定的I / O响应。结论本研究为开发下一代合成基因电路提供了重要的系统设计方法,从元件库的构建到基因电路的组装。将来,当库更完整时,可以实现更精确的细胞密度控制。

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