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大肠杆菌K-12中限制活性的蛋白水解控制

The proteolytic control of restriction activity in Escherichia coli K-12.

作者信息

Doronina V A, Murray N E

机构信息

Institute of Cell and Molecular Biology, Kings Buildings, Mayfield Road, Edinburgh EH9 3JR, UK.

出版信息

Mol Microbiol. 2001 Jan;39(2):416-28. doi: 10.1046/j.1365-2958.2001.02232.x.

Abstract

The endonuclease activity of EcoKI is regulated by the ClpXP-dependent degradation of the subunit that is essential for restriction, but not modification. We monitored proteolysis in mutants blocked at different steps in the restriction pathway. Mutations that prevent DNA translocation render EcoKI refractory to proteolysis, whereas those that permit DNA translocation, but block endonuclease activity, do not. Although proteolysis alleviates restriction in a mutant that lacks modification activity, some restriction activity remains; our evidence indicates residual EcoKI associated with the membrane fraction. ClpXP protects the bacterial chromosome, but little effect was detected on unmodified foreign DNA within the cytoplasm of a restriction-proficient cell. The molecular basis for the distinction between unmodified resident and foreign DNA remains to be determined.

摘要

EcoKI的核酸内切酶活性受ClpXP依赖性降解的调控,该降解作用于限制(但不作用于修饰)所必需的亚基。我们监测了在限制途径不同步骤受阻的突变体中的蛋白水解情况。阻止DNA易位的突变使EcoKI对蛋白水解具有抗性,而那些允许DNA易位但阻断核酸内切酶活性的突变则不然。尽管蛋白水解减轻了缺乏修饰活性的突变体中的限制作用,但仍有一些限制活性存在;我们的证据表明,残余的EcoKI与膜部分相关。ClpXP保护细菌染色体,但在限制功能正常的细胞胞质内未修饰的外源DNA上几乎未检测到影响。未修饰的内源DNA和外源DNA之间差异的分子基础仍有待确定。

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