复制子
生物
基因
遗传学
突变
基因组
定向诱变
体细胞突变
大肠杆菌
突变
DNA
噬菌体
整合酶
计算生物学
质粒
DNA复制
DNA聚合酶
染色体外DNA
突变率
聚合酶
转化(遗传学)
基因复制
定向进化
基因盒
复制的起源
四环素
DNA错配修复
基因组工程
合成生物学
作者
Fabian B. H. Rehm,Kim C. Liu,Rongzhen Tian,Jason W. Chin
标识
DOI:10.1038/s41587-025-02944-x
摘要
Organisms that permit hypermutation of target genes without off-target mutagenesis of the host genome enable the accelerated, continuous evolution of genes for new or enhanced functions. We develop and optimize an orthogonal DNA replication system in Escherichia coli that uses components from bacteriophage Φ29. The minimal system requires just two Φ29 genes to maintain the replicon and replicons can be efficiently engineered in vivo. We generate a highly mutagenic Φ29 DNA polymerase that introduces mutations at a frequency approaching 10-4 per base per generation (one mutation in a 1-kb gene every ten generations). Our system is stable for hundreds of generations and enables the continuous, accelerated evolution of new gene functions. We demonstrate the rapid evolution of a tetracycline resistance gene to confer resistance to tigecycline at higher levels than achieved with previously reported systems. We further evolve a 1,000-fold increase in β-lactamase activity for a third-generation cephalosporin in just 3 days.
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