Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Replication in Prokaryotes02:35

Replication in Prokaryotes

99.9K
Overview
99.9K
Replication in Prokaryotes01:32

Replication in Prokaryotes

28.4K
DNA replication has three main steps: initiation, elongation, and termination. Replication in prokaryotes begins when initiator proteins bind to the single origin of replication (ori) on the cell's circular chromosome. Replication then proceeds around the entire circle of the chromosome in each direction from the two replication forks, resulting in two DNA molecules.
Many Proteins Work Together to Replicate the Chromosome
Replication is coordinated and carried out by a host of specialized...
28.4K
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

6.9K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
6.9K
Mutations in Microorganisms01:18

Mutations in Microorganisms

868
Mutations are heritable changes in an organism’s genome involving alterations in the base sequence of DNA or RNA. These changes can influence cellular processes and phenotypic traits, potentially transforming the unaltered wild type into a mutant form. Such changes, termed forward mutations, are pivotal in shaping the genetic diversity of organisms.RNA viruses exhibit the highest mutation rates due to the absence of robust proofreading mechanisms during genome replication. In contrast,...
868
Mismatch Repair01:20

Mismatch Repair

6.8K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
6.8K
DNA Bacteriophages01:26

DNA Bacteriophages

1.2K
Bacteriophages, or phages, are viruses that specifically infect bacteria, utilizing their genetic material to hijack host cellular machinery for replication. DNA bacteriophages employ single-stranded DNA (ssDNA) or double-stranded DNA (dsDNA) genomes. These phages exhibit diverse replication strategies and host interactions, influencing their ecological roles and applications in biotechnology and medicine.ssDNA BacteriophagesssDNA phages, with their small genomes, utilize unique strategies to...
1.2K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Rational Design of Plant-Derived Protein Ligases with Altered Substrate Specificity.

Biochemistry·2026
Same author

High-fidelity human chromosome transfer and elimination.

Science (New York, N.Y.)·2025
Same author

<i>Escherichia coli</i> with a 57-codon genetic code.

Science (New York, N.Y.)·2025
Same author

Genetic Code-Locking Confers Stable Virus Resistance to a Recoded Organism.

Biochemistry·2025
Same author

Asparaginyl Ligases with Engineered Substrate Specificity for Controlled, Sequential Transpeptidation Reactions.

Journal of the American Chemical Society·2025
Same author

An evolved, orthogonal ssDNA generator for targeted hypermutation of multiple genomic loci.

Nucleic acids research·2025
Same journal

Mapping and engineering the human cell-cell interactome.

Nature biotechnology·2026
Same journal

Efficient generation of epitope-targeted antibodies with Germinal.

Nature biotechnology·2026
Same journal

Affordable centimeter-scale 3D microscopy with submicrometer resolution.

Nature biotechnology·2026
Same journal

Optimized R2 retroelement complexes for DNA insertion into plant genomes.

Nature biotechnology·2026
Same journal

Efficient site-specific gene addition using R2 retrotransposons in tobacco and rice.

Nature biotechnology·2026
Same journal

Publisher Correction: Lung and liver editing by lipid nanoparticle delivery of a stable CRISPR-Cas9 ribonucleoprotein.

Nature biotechnology·2026
查看所有相关文章
  1. 首页
  2. 在大肠杆菌中使用基于 Φ29 的直角复制系统的高致变异性连续进化.
  1. 首页
  2. 在大肠杆菌中使用基于 Φ29 的直角复制系统的高致变异性连续进化.

相关实验视频

Mutagenesis and Functional Selection Protocols for Directed Evolution of Proteins in E. coli
09:01

Mutagenesis and Functional Selection Protocols for Directed Evolution of Proteins in E. coli

Published on: March 16, 2011

31.2K

在大肠杆菌中使用基于 Φ29 的直角复制系统的高致变异性连续进化.

Fabian B H Rehm1, Kim C Liu2, Rongzhen Tian2

  • 1Medical Research Council Laboratory of Molecular Biology, Cambridge, UK. frehm@mrc-lmb.cam.ac.uk.

Nature biotechnology
|February 24, 2026

在PubMed 上查看摘要

概括
此摘要是机器生成的。

我们在大肠杆菌中设计了一个稳定的DNA复制系统,使用菌体F29组件加速基因进化. 这个系统有效地引入突变,使新的基因功能能够迅速发展.

更多相关视频

Quantification of Plasmid-Mediated Antibiotic Resistance in an Experimental Evolution Approach
12:32

Quantification of Plasmid-Mediated Antibiotic Resistance in an Experimental Evolution Approach

Published on: December 14, 2019

14.7K
In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity
09:16

In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity

Published on: March 25, 2020

7.8K

相关实验视频

Mutagenesis and Functional Selection Protocols for Directed Evolution of Proteins in E. coli
09:01

Mutagenesis and Functional Selection Protocols for Directed Evolution of Proteins in E. coli

Published on: March 16, 2011

31.2K
Quantification of Plasmid-Mediated Antibiotic Resistance in an Experimental Evolution Approach
12:32

Quantification of Plasmid-Mediated Antibiotic Resistance in an Experimental Evolution Approach

Published on: December 14, 2019

14.7K
In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity
09:16

In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity

Published on: March 25, 2020

7.8K

科学领域:

  • 分子生物学分子生物学
  • 合成生物学 合成生物学
  • 遗传学 遗传学 是一个

背景情况:

  • 加快基因进化需要精确的超变异,而不会产生异常效应.
  • 现有的基因进化系统在效率和稳定性方面存在局限性.

研究的目的:

  • 开发和优化一个直角DNA复制系统,以加速大肠杆菌的基因进化.
  • 为了设计一种高度突变的DNA聚合酶,用于向基因修饰.

主要方法:

  • 利用菌体 Φ29 的组件来创建一个最小的正交直角 DNA 复制系统.
  • 在体内设计复制品,并开发出一种高度致变性的 Φ29 DNA 聚合酶.
  • 在数百代人中保持了系统的稳定性.

主要成果:

  • 实现的突变频率接近每基数每代10^-4.
  • 证明了对tigecycline耐药性的四环素的快速演变.
  • 在3天内,第三代头素的β-乳糖酶活性增加了1000倍.

结论:

  • 开发的基于 Φ29 的系统使基因功能能够稳定,连续和加速进化.
  • 该系统显著提高了工程新或改进的基因特征的速度和有效性.
  • 为合成生物学和蛋白质工程应用提供了强大的工具.