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通过体内连续进化增强细胞和酶的特性。

Enhancing Cellular and Enzymatic Properties Through In Vivo Continuous Evolution.

作者信息

Chu Weiran, Guo Yaxin, Wu Yaokang, Lv Xueqin, Li Jianghua, Liu Long, Du Guocheng, Chen Jian, Liu Yanfeng

机构信息

School of Biotechnology and Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, China.

Science Center for Future Foods, Jiangnan University, Wuxi, 214122, China.

出版信息

Chembiochem. 2024 Dec 16;25(24):e202400564. doi: 10.1002/cbic.202400564. Epub 2024 Oct 29.

DOI:10.1002/cbic.202400564
PMID:39248206
Abstract

Directed evolution seeks to evolve target genes at a rate far exceeding the natural mutation rate, thereby endowing cellular and enzymatic properties with desired traits. In vivo continuous directed evolution achieves these purposes by generating libraries within living cells, enabling a continuous cycle of mutant generation and selection, enhancing the exploration of gene variants. Continuous evolution has become powerful tools for unraveling evolution mechanism and improving cellular and enzymatic properties. This review categorizes current continuous evolution into three distinct classes: non-targeted chromosomal, targeted chromosomal, and extra-chromosomal hypermutation approaches. It also compares various continuous evolution strategies based on different principles, providing a reference for selecting suitable methods for specific evolutionary goals. Furthermore, this review discusses the two primary limitations for further widespread application of in vivo continuous evolution, which are lack of general applicability and insufficient mutagenic capability. We envision that developing generally applicable mutagenic components and methods to enhance mutation rates for in vivo continuous evolution are promising future directions for wide range applications of continuous evolution.

摘要

定向进化旨在以远超自然突变率的速度进化目标基因,从而赋予细胞和酶的特性以所需的性状。体内连续定向进化通过在活细胞内生成文库来实现这些目的,实现突变产生和选择的连续循环,增强对基因变体的探索。连续进化已成为揭示进化机制和改善细胞及酶特性的有力工具。本综述将当前的连续进化分为三类不同的方法:非靶向染色体、靶向染色体和染色体外超突变方法。它还比较了基于不同原理的各种连续进化策略,为针对特定进化目标选择合适的方法提供参考。此外,本综述讨论了体内连续进化进一步广泛应用的两个主要限制,即缺乏普遍适用性和诱变能力不足。我们设想,开发普遍适用的诱变元件和方法以提高体内连续进化的突变率是连续进化广泛应用的有前景的未来方向。

相似文献

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Chembiochem. 2024 Dec 16;25(24):e202400564. doi: 10.1002/cbic.202400564. Epub 2024 Oct 29.
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Growth-coupled continuous directed evolution by MutaT7 enables efficient and automated enzyme engineering.通过MutaT7进行的生长偶联连续定向进化可实现高效且自动化的酶工程。
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An evolved, orthogonal ssDNA generator for targeted hypermutation of multiple genomic loci.一种经过改进的、用于多个基因组位点靶向超突变的正交单链DNA生成器。
Nucleic Acids Res. 2025 Jan 24;53(3). doi: 10.1093/nar/gkaf051.