• 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

相似文献

1
The recA gene and cadmium toxicity in Escherichia coli K12.
Microbios. 1996;86(346):23-6.
2
The Escherichia coli RecA protein complements recombination defective phenotype of the Saccharomyces cerevisiae rad52 mutant cells.大肠杆菌RecA蛋白可弥补酿酒酵母rad52突变细胞的重组缺陷表型。
Yeast. 2003 Apr 15;20(5):389-96. doi: 10.1002/yea.971.
3
A homolog of Escherichia coli RecA in mitochondria of the cellular slime mold Dictyostelium discoideum.细胞黏菌盘基网柄菌线粒体中大肠杆菌RecA的同源物。
DNA Repair (Amst). 2004 May 4;3(5):515-25. doi: 10.1016/j.dnarep.2004.01.014.
4
[Operator-constitutive mutation in the recA gene enhances radiation resistance of Escherichia coli].[recA基因中的操纵子组成型突变增强大肠杆菌的辐射抗性]
Genetika. 2009 Aug;45(8):1048-54.
5
Role of RecA in DNA damage repair in Deinococcus radiodurans.RecA在耐辐射球菌DNA损伤修复中的作用。
FEMS Microbiol Lett. 2007 Sep;274(2):342-7. doi: 10.1111/j.1574-6968.2007.00862.x. Epub 2007 Jul 20.
6
recA mutants of E. coli K12: a personal turning point.大肠杆菌K12的recA突变体:一个个人的转折点。
Bioessays. 1996 Sep;18(9):767-72. doi: 10.1002/bies.950180912.
7
RecJ nuclease is required for SOS induction after introduction of a double-strand break in a RecA loading deficient recB mutant of Escherichia coli.在大肠杆菌RecA装载缺陷型recB突变体中引入双链断裂后,SOS诱导需要RecJ核酸酶。
Biochimie. 2008 Sep;90(9):1347-55. doi: 10.1016/j.biochi.2008.04.002. Epub 2008 Apr 10.
8
Molecular cloning and isolation of a cyanobacterial gene which increases the UV and methyl methanesulphonate survival of recA strains of Escherichia coli K12.一种能提高大肠杆菌K12的recA菌株对紫外线和甲磺酸甲酯耐受性的蓝细菌基因的分子克隆与分离。
J Gen Microbiol. 1987 Jan;133(1):119-26. doi: 10.1099/00221287-133-1-119.
9
Influence of RecA on in vivo virulence and Shiga toxin 2 production in Escherichia coli pathogens.RecA对大肠杆菌病原体体内毒力及志贺毒素2产生的影响。
Microb Pathog. 1999 Jul;27(1):13-23. doi: 10.1006/mpat.1999.0279.
10
The expression of Escherichia coli SOS genes recA and uvrA is inducible by polyamines.大肠杆菌SOS基因recA和uvrA的表达可被多胺诱导。
Biochem Biophys Res Commun. 1999 Oct 22;264(2):584-9. doi: 10.1006/bbrc.1999.1553.

引用本文的文献

1
Proteomics and bioinformatics analysis reveal potential roles of cadmium-binding proteins in cadmium tolerance and accumulation of .蛋白质组学和生物信息学分析揭示了镉结合蛋白在镉耐受性和镉积累中的潜在作用。
PeerJ. 2019 Sep 2;7:e6904. doi: 10.7717/peerj.6904. eCollection 2019.
2
Metal complexation by histidine-rich peptides confers protective roles against cadmium stress in as revealed by proteomics analysis.蛋白质组学分析表明,富含组氨酸的肽与金属络合赋予了对镉胁迫的保护作用。
PeerJ. 2018 Jul 26;6:e5245. doi: 10.7717/peerj.5245. eCollection 2018.
3
Pseudomonas aeruginosa KUCD1, a possible candidate for cadmium bioremediation.
铜绿假单胞菌 KUCD1,一种可能的镉生物修复候选菌。
Braz J Microbiol. 2009 Jul;40(3):655-62. doi: 10.1590/S1517-838220090003000030. Epub 2009 Sep 1.
4
Linkage map of Escherichia coli K-12, edition 10: the traditional map.大肠杆菌K-12连锁图谱,第10版:传统图谱。
Microbiol Mol Biol Rev. 1998 Sep;62(3):814-984. doi: 10.1128/MMBR.62.3.814-984.1998.
5
Cadmium removal by a new strain of Pseudomonas aeruginosa in aerobic culture.一株新的铜绿假单胞菌在需氧培养中对镉的去除
Appl Environ Microbiol. 1997 Oct;63(10):4075-8. doi: 10.1128/aem.63.10.4075-4078.1997.

The recA gene and cadmium toxicity in Escherichia coli K12.

作者信息

Shapiro N, Keasling J D

机构信息

Department of Chemical Engineering, University of California, Berkeley 94720-1462, USA.

出版信息

Microbios. 1996;86(346):23-6.

PMID:8771773
Abstract

The influence of the recA gene on cadmium toxicity was studied in Escherichia coli K12 strains. Those strains mutant in the recA gene showed a 1,000-fold loss of viability upon exposure to cadmium, but recovered and started growing approximately 16-20 h following the initial exposure to cadmium. In contrast to previous studies with E. coli B strains, the E. coli K12 strains carrying a functional recA gene showed little or no loss of viability upon exposure to cadmium. The cells also exhibited a significant lag period in which no net growth occurred and then began growing 16-20 h after initial exposure to cadmium. These results indicate the importance of the recA gene to cell survival during exposure to metals, and also support the hypothesis that cadmium causes DNA damage.

摘要