对于大肠杆菌中染色体分离至关重要的新型拓酶
J Kato1, Y Nishimura, R Imamura
1Department of Bacteriology, National Institute of Health of Japan, Tokyo.
Cell
|October 19, 1990
概括
研究人员发现了两种新基因,parC和parE,对于大肠杆菌染色体分割至关重要. 这些基因编码了一种新型酶的子单元,topoisomerase IV,对细菌细胞分裂至关重要.
科学领域:
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
- 微生物学 微生物学
背景情况:
- 染色体分裂对于细菌细胞分裂至关重要.
- 在管理DNA拓上,DNA拓酶起着至关重要的作用.
- 大肠杆菌DNA旋转酶对于DNA复制和转录至关重要.
研究的目的:
- 识别和描述涉及大肠杆菌染色体分割的基因.
- 阐明新发现的基因与现有的拓酶的功能和关系.
主要方法:
- 在parC和parE基因的核酸测序.
- 氨基酸序列同质性分析.
- 对parE突变体的隔离和表型分析.
- 对细胞溶解物的酶活性测定.
- 基因补充研究与拓素酶I突变体.
主要成果:
- parC基因产物与旋转酶A子单元具有同质性.
- 发现了一种新型基因,parE,其产物与旋转酶B子单元相同.
- parE突变体表现出一个Par表型,表明其在分区中的作用.
- 过度产生的ParC和ParE增强了超的DNA的放松.
- 增加parC和parE的剂量可以弥补托皮索马酶I缺乏.
结论:
- parC和parE基因编码了一种新型DNA拓酶的子单元,称为拓酶IV.
- 拓聚酶IV对于大肠杆菌的染色体分离至关重要.
- 这一发现扩大了我们对DNA拓酶及其在细胞分裂中的作用的理解.
更多相关视频
相关概念视频
Replication in Prokaryotes
86.8K
Overview
86.8K
Mismatch Repair
38.2K
Overview
38.2K
DNA Topoisomerases
32.3K
Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
32.3K
Conservative Site-specific Recombination and Phase Variation
5.7K
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...
The recognition sites for Cre recombinase called LoxP...
5.7K
Mismatch Repair
5.4K
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...
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...
5.4K
Inhibitors of Bacterial DNA Synthesis
151
Bacterial pathogens depend on precise and efficient DNA replication to sustain infection. Two type II topoisomerases—DNA gyrase and topoisomerase IV—are critical to this process, as they resolve DNA supercoiling and unlink chromosomes during replication. Fluoroquinolones, synthetic derivatives of quinolones, exploit this mechanism by stabilizing the transient DNA–enzyme cleavage complex, preventing strand religation, and causing lethal double-strand breaks. These...
151


