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拓扑异构酶III可作为大肠杆菌中的细胞解连环酶。

Topoisomerase III can serve as the cellular decatenase in Escherichia coli.

作者信息

Nurse Pearl, Levine Cindy, Hassing Heide, Marians Kenneth J

机构信息

Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.

出版信息

J Biol Chem. 2003 Mar 7;278(10):8653-60. doi: 10.1074/jbc.M211211200. Epub 2002 Dec 31.

Abstract

topB, encoding topoisomerase III, was identified as a high copy suppressor of the temperature-sensitive parC1215 allele, encoding one of the subunits of topoisomerase IV. Overexpression of topoisomerase III at the nonpermissive temperature was shown subsequently to restore timely chromosome decatenation and suppress lethality in strains carrying either temperature-sensitive parE or parC alleles. By developing an assay in vitro for precatenane unlinking, we demonstrated directly that both topoisomerase III and topoisomerase IV were efficient at this task, whereas DNA gyrase was very inefficient at precatenane removal. These observations suggest that precatenane unlinking is sufficient to sustain decatenation of replicating daughter chromosomes in the cell.

摘要

编码拓扑异构酶III的topB被鉴定为温度敏感型parC1215等位基因的高拷贝抑制子,parC1215等位基因编码拓扑异构酶IV的一个亚基。随后表明,在非允许温度下拓扑异构酶III的过表达可恢复及时的染色体解连环,并抑制携带温度敏感型parE或parC等位基因的菌株中的致死性。通过开发一种体外前连环体解链测定法,我们直接证明拓扑异构酶III和拓扑异构酶IV在这项任务中都很有效,而DNA促旋酶在前连环体去除方面效率非常低。这些观察结果表明,前连环体解链足以维持细胞中复制子代染色体的解连环。

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