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体细胞突变
突变率
质粒
DNA聚合酶
生物
DNA复制
DNA旋转酶
定向进化
计算生物学
转化(遗传学)
遗传学
DNA
大肠杆菌
突变体
B细胞
抗体
基因
细菌圆形染色体
作者
Christian S. Diercks,Philipp Sondermann,Cynthia Rong,Tammy Gillis,Yahui Ban,C. Joanne Wang,David A. Dik,Peter G. Schultz
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-08-07
卷期号:389 (6760): 618-622
被引量:21
标识
DOI:10.1126/science.adp9583
摘要
Systems that perform continuous hypermutation of designated genes without compromising the integrity of the host genome can substantially accelerate the evolution of new or enhanced protein functions. We describe an orthogonal DNA replication system in Escherichia coli based on the controlled expression of the replisome of bacteriophage T7 (T7-ORACLE). The system replicates circular plasmids that enable high transformation efficiencies and seamless integration into standard molecular biology workflows. Engineering of T7 DNA polymerase yielded variant proteins with mutation rates of 1.7 × 10 −5 substitutions per base in vivo—100,000-fold above the genomic mutation rate. We demonstrated continuous evolution using the T7 replisome by expanding the substrate scope of TEM-1 β-lactamase and increasing activity 5000-fold against clinically relevant monobactam and cephalosporin antibiotics in less than 1 week.
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