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基于细菌群体感应构建分子开关

[Construct a molecular switch based on bacterial quorum sensing].

作者信息

Zhang Zhiwei, Wu Sheng

机构信息

State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China

出版信息

Sheng Wu Gong Cheng Xue Bao. 2013 Sep;29(9):1301-12.

Abstract

Engineering the existing or manual assembling biosynthetic pathways involves two important issues: the activity and expression level of key enzymes in the pathway. Concerning the enzyme expression study, the conventional approach is to use strong promoter to initiate the overexpression of the target protein. The excessive expression of the target protein usually result in the intracellular accumulation of a large number of inactive inclusion bodies, thereby seriously affect the physiological state of the cell and the effective functioning of the relevant biological pathways. To solve this problem, we would like to design a molecular switch to precisely manipulate the expression level of key enzymes in the biosynthetic process, which has important practical value for the study of metabolic rhythm of the biosynthetic pathway and to promote the efficiency of the biosynthetic pathway. Based on the basic principles of quorum sensing existing in the bacterial community and combining the dynamic characteristics of the enzymatic catalysis, we first established cell-cell communication mechanisms mediated by signal molecule homoserine lactone (AHL) in the E. coli community and target protein EGFP was expressed under the control of the promoter P(lux1). In the process of cell growth, AHL accumulated to a certain concentration to start the expression of target gene egfp. At the different cell growth stages, AHL-degrading enzyme AiiA was induced and resulted in the degradation of AHL molecule in a controlled environment, thereby controlling the transcription efficiency of target gene egfp and ultimately achieve the precise control of the level of expression of the target protein EGFP. The detection of cell growth state, the mRNA level and protein expression level of the target gene showed the artificially designed molecular switch can control the level of expression of a target gene in a convenient and efficient manner with a spatial and temporal regulation of rigor. The molecular switch is expected to be widely used in the field of metabolic engineering and synthetic biology research areas.

摘要

构建现有的或手动组装的生物合成途径涉及两个重要问题

途径中关键酶的活性和表达水平。关于酶表达研究,传统方法是使用强启动子来启动目标蛋白的过表达。目标蛋白的过度表达通常会导致大量无活性包涵体在细胞内积累,从而严重影响细胞的生理状态和相关生物途径的有效运作。为了解决这个问题,我们希望设计一种分子开关来精确调控生物合成过程中关键酶的表达水平,这对于研究生物合成途径的代谢节律以及提高生物合成途径的效率具有重要的实际价值。基于细菌群体中存在的群体感应基本原理,并结合酶催化的动态特性,我们首先在大肠杆菌群体中建立了由信号分子高丝氨酸内酯(AHL)介导的细胞间通讯机制,目标蛋白EGFP在启动子P(lux1)的控制下表达。在细胞生长过程中,AHL积累到一定浓度以启动目标基因egfp的表达。在不同的细胞生长阶段,诱导AHL降解酶AiiA并在可控环境中导致AHL分子的降解,从而控制目标基因egfp的转录效率,最终实现对目标蛋白EGFP表达水平的精确控制。对细胞生长状态、目标基因的mRNA水平和蛋白质表达水平的检测表明,人工设计的分子开关能够以严谨的时空调控方式方便高效地控制目标基因的表达水平。该分子开关有望在代谢工程和合成生物学研究领域得到广泛应用。

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