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通过DNA改组进行定向进化以改进和理解基因与启动子。

Directed evolution through DNA shuffling for the improvement and understanding of genes and promoters.

作者信息

Werkman Joshua R, Pattanaik Sitakanta, Yuan Ling

机构信息

Department of Plant and Soil Sciences, Kentucky Tobacco Research & Development Center, University of Kentucky, Lexington, KY, USA.

出版信息

Methods Mol Biol. 2011;754:325-42. doi: 10.1007/978-1-61779-154-3_19.

Abstract

Unlike rational protein engineering, directed evolution provides an a priori approach toward the engineering of improved proteins and novel promoters. This minimally recursive technique builds upon small improvements by selecting and combining the best changes. Protein-protein/DNA interactions, catalytic efficiency, or resilience to inhibitors can be improved by thousands of times. By working within a subspace of homologous sequences, DNA shuffling recombines that subspace. Individuals are screened for a particular trait or two and selected for when they meet a set threshold. Here we explain basic principles to follow and provide procedures for the preparation, fragmentation, efficient size fractionation, and purification of parental material, as well as for the reassembly and rescue polymerase chain reactions (PCRs).

摘要

与理性蛋白质工程不同,定向进化为改进蛋白质和新型启动子的工程提供了一种先验方法。这种最小递归技术通过选择和组合最佳变化,在小的改进基础上进行构建。蛋白质-蛋白质/DNA相互作用、催化效率或对抑制剂的抗性可提高数千倍。通过在同源序列的子空间内工作,DNA改组重组该子空间。针对一两个特定性状对个体进行筛选,当它们达到设定阈值时进行选择。在此,我们解释要遵循的基本原理,并提供亲本材料的制备、片段化、高效大小分级分离和纯化以及重组和拯救聚合酶链反应(PCR)的程序。

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