• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Role of rec genes in SOS-induced inhibition of cell division in Escherichia coli.

作者信息

Knezević-Vukcević J, Vuković B, Simić D

机构信息

Botanical Institute and Garden, University of Belgrade, Yugoslavia.

出版信息

Mutat Res. 1987 Dec;192(4):247-52. doi: 10.1016/0165-7992(87)90064-9.

DOI:10.1016/0165-7992(87)90064-9
PMID:2446129
Abstract

The inhibition of cell division induced by bleomycin (BM) and UV irradiation in the set of rec mutants of E. coli K12 was studied. Data presented in this work indicate that BM treatment requires mainly the RecBC pathway for the induction of cell filamentation. In the recB21 mutant cell filamentation is delayed and reduced compared to the wild type. Cell filamentation is BM-induced with similar kinetics in strains with a proficient RecBC recombination pathway (rec+, recF143 and recN262), as well as in the strain with a fully expressed RecF pathway (recB21recC22sbcB15). Induction is completely abolished in the recB21recF143 double mutant. On the other hand cell filamentation was induced similarly by UV irradiation in all strains with a functional recF gene and in the strain with a fully operative RecF pathway, but it was delayed in the recF143 and recB21recF143 mutants.

摘要

相似文献

1
Role of rec genes in SOS-induced inhibition of cell division in Escherichia coli.
Mutat Res. 1987 Dec;192(4):247-52. doi: 10.1016/0165-7992(87)90064-9.
2
Participation of rec genes of Escherichia coli K 12 in W-reactivation of UV-irradiated phage lambda.
Mutat Res. 1990 Feb;243(2):159-64. doi: 10.1016/0165-7992(90)90039-m.
3
Constitutive and UV-mediated activation of RecA protein: combined effects of recA441 and recF143 mutations and of addition of nucleosides and adenine.RecA蛋白的组成型及紫外线介导的激活:recA441和recF143突变以及核苷和腺嘌呤添加的联合效应
J Bacteriol. 1991 Sep;173(18):5869-75. doi: 10.1128/jb.173.18.5869-5875.1991.
4
Influence of the recB21 mutation of Escherichia coli K12 on prophage lambda induction.
Mutat Res. 1985 Apr;142(4):159-62. doi: 10.1016/0165-7992(85)90016-8.
5
Activation of RecA protein in recombination-deficient strains of Escherichia coli following DNA-damaging treatments.DNA损伤处理后大肠杆菌重组缺陷菌株中RecA蛋白的激活。
Mutat Res. 1991 May;254(3):255-62. doi: 10.1016/0921-8777(91)90064-v.
6
RecBC promoted repair of bleomycin damage in Escherichia coli.RecBC促进了大肠杆菌中博来霉素损伤的修复。
Biochimie. 1991 Apr;73(4):497-500. doi: 10.1016/0300-9084(91)90118-k.
7
Regulatory role of recF in the SOS response of Escherichia coli: impaired induction of SOS genes by UV irradiation and nalidixic acid in a recF mutant.recF在大肠杆菌SOS应答中的调控作用:recF突变体中紫外线照射和萘啶酸对SOS基因诱导作用受损。
J Bacteriol. 1987 Apr;169(4):1731-6. doi: 10.1128/jb.169.4.1731-1736.1987.
8
Survival and induction of SOS in Escherichia coli treated with cisplatin, UV-irradiation, or mitomycin C are dependent on the function of the RecBC and RecFOR pathways of homologous recombination.用顺铂、紫外线照射或丝裂霉素C处理的大肠杆菌中,SOS的存活和诱导依赖于同源重组的RecBC和RecFOR途径的功能。
Mutat Res. 2001 Jun 5;486(1):21-9. doi: 10.1016/s0921-8777(01)00077-5.
9
Overlapping functions for recF and priA in cell viability and UV-inducible SOS expression are distinguished by dnaC809 in Escherichia coli K-12.在大肠杆菌K-12中,recF和priA在细胞活力和紫外线诱导的SOS表达中的重叠功能可通过dnaC809加以区分。
Mol Microbiol. 1996 Feb;19(4):871-80. doi: 10.1046/j.1365-2958.1996.429959.x.
10
A minor pathway of postreplication repair in Escherichia coli is independent of the recB, recC and recF genes.大肠杆菌中复制后修复的一条次要途径独立于recB、recC和recF基因。
Mutat Res. 1985 Sep;146(2):169-76. doi: 10.1016/0167-8817(85)90007-0.

引用本文的文献

1
Effect of host species on recG phenotypes in Helicobacter pylori and Escherichia coli.宿主物种对幽门螺杆菌和大肠杆菌recG表型的影响。
J Bacteriol. 2004 Nov;186(22):7704-13. doi: 10.1128/JB.186.22.7704-7713.2004.