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首页> 外文期刊>Biochemistry and molecular biology education >Laboratory Exercise Continuous In Vitro Evolution of a Ribozyme Ligase: A Model Experiment for the Evolution of a Biomolecule
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Laboratory Exercise Continuous In Vitro Evolution of a Ribozyme Ligase: A Model Experiment for the Evolution of a Biomolecule

机译:核糖核酸连接酶的实验室运动连续体外进化:一种生物分子进化的模型实验

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Evolution is a defining criterion Of life and is central to understanding biological systems. However, the timescale of evolutionary shifts in phenotype limits most classroom evolution experiments to simple probability simulations. In vitro directed evolution (IVDE) frequently serves as a model system for the study of Darwinian evolution but produces noticeable phenotypic shifts in a matter of hours. An IVDE demonstration lab would serve to both directly demonstrate how Darwinian selection can act on a pool of variants and introduce students to an essential method of modern molecular biology. To produce an IVDE demonstration lab, continuous IVDE of a T500 ribozyme ligase population has been paired with a fluorescent strand displacement reporter system to visualize the selection of improved catalytic function. A ribozyme population iS taken through rounds of isothermal amplification dependent on the self-ligation of a T7 promoter. As the population is selectively enriched with better ligase activity, the strand displacement system allows for the monitoring of the population's ligation rate. The strand displacement reporter system permits the detection of ligated ribozyme. Once ligated with the T7 promoter, the 5' end of the ribozyme displaces paired fluorophore-quencher oligonucleotides, in turn, generating visible signal upon UV light excitation. As the ligation rate pf the population increases, due to the selection for faster ligating species, the fluorescent signal develops more rapidly. The pairing of the continuous isothermal system with the fluorescent reporting scheme allows any user, provided with minimal materials, to model the continuous directed evolution of a biomolecule. ?2013 by The International Union of Biochemistry and Molecular Biology, 41(6):433-442, 2013
机译:进化是生命的决定性标准,对于理解生物系统至关重要。但是,表型进化变化的时间尺度将大多数课堂进化实验限制为简单的概率模拟。体外定向进化(IVDE)通常充当研究达尔文进化的模型系统,但在数小时内产生明显的表型变化。 IVDE示范实验室不仅可以直接证明达尔文式选择如何作用于多种变异,还可以向学生介绍现代分子生物学的基本方法。为了建立IVDE示范实验室,已将T500核酶连接酶群体的连续IVDE与荧光链置换报告系统配对,以可视化选择改进的催化功能。通过几轮等温扩增获得的核酶群体取决于T7启动子的自连接。随着群体选择性地富集更好的连接酶活性,链置换系统允许监测群体的连接率。链位移报告系统允许检测结扎的核酶。一旦与T7启动子连接,核酶的5'末端就会取代成对的荧光团猝灭剂寡核苷酸,进而在紫外线激发下产生可见信号。随着连接速率pf的增加,由于选择了更快的连接物种,荧光信号发展得更快。连续等温系统与荧光报告方案的配对,使使用最少材料的任何用户都可以对生物分子的连续定向进化进行建模。国际生物化学与分子生物学联合会的《 2013年》,2013年41(6):433-442

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