Saragliadis Athanasios, Klauser Benedikt, Hartig Jörg S
Department of Chemistry, University of Konstanz, Konstanz, Germany.
Methods Mol Biol. 2012;848:455-63. doi: 10.1007/978-1-61779-545-9_28.
The development of artificial switches of gene expression is of high importance for future applications in biotechnology and synthetic biology. We have developed a powerful RNA-based system which allows for the ligand-dependent and reprogrammable control of gene expression in Escherichia coli. Our system makes use of the hammerhead ribozyme (HHR) which acts as molecular scaffold for the sequestration of the ribosome binding site (RBS), mimicking expression platforms in naturally occurring riboswitches. Aptamer domains can be attached to the ribozyme as exchangeable ligand-sensing modules. Addition of ligands to the bacterial growth medium changes the activity of the ligand-dependent self-cleaving ribozyme which in turn switches gene expression. In this chapter, we describe the in vivo screening procedure allowing for reprogramming the ligand-specificity of our system.
基因表达人工开关的开发对于未来在生物技术和合成生物学中的应用至关重要。我们开发了一种强大的基于RNA的系统,该系统允许在大肠杆菌中对基因表达进行配体依赖性和可重新编程的控制。我们的系统利用锤头状核酶(HHR)作为分子支架来隔离核糖体结合位点(RBS),模仿天然存在的核糖开关中的表达平台。适体结构域可以作为可交换的配体传感模块连接到核酶上。向细菌生长培养基中添加配体会改变配体依赖性自我切割核酶的活性,进而切换基因表达。在本章中,我们描述了用于重新编程我们系统配体特异性的体内筛选程序。