• 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

利用表型芯片对大肠杆菌lysA插入靶向突变体进行表征。

Characterization of an Escherichia coli lysA insertion targeted mutant using phenotype arrays.

作者信息

Li X, Ricke S C

机构信息

Poultry Science Department, Texas A&M University, Kleberg Center, Room 101, College Station, TX 77843-2472, USA.

出版信息

Bioresour Technol. 2003 Sep;89(3):249-53. doi: 10.1016/s0960-8524(03)00072-5.

DOI:10.1016/s0960-8524(03)00072-5
PMID:12798115
Abstract

The objective of this study was to investigate the effect of a lysine biosynthesis insertion mutation on the growth response and phenotype of Escherichia coli. The lysA gene encodes the last enzyme in the lysine biosynthetic pathway in most bacteria. This E. coli insertion mutant exhibited altered growth physiology and phenotype of the recipient E. coli. The constructed mutant could grow in the absence of lysine supplementation although the extent of growth after 7 h incubation in the presence of most lysine concentration was significantly (p<0.05) decreased compared to that observed with the parent E. coli strain. The mutant was also less able to utilize carbon and nitrogen substrates than the parent E. coli strain as determined by using phenotype arrays. These results suggest that the carbon and nitrogen phenotype profiles of E. coli when measured on phenotype arrays are altered after targeted insertion mutagenesis in the lysA gene. Creation of altered phenotypes may have potential for pharmaceutical and biotechnological applications of lysine E. coli metabolism.

摘要

本研究的目的是调查赖氨酸生物合成插入突变对大肠杆菌生长反应和表型的影响。lysA基因编码大多数细菌中赖氨酸生物合成途径的最后一种酶。这种大肠杆菌插入突变体表现出受体大肠杆菌生长生理学和表型的改变。构建的突变体在不补充赖氨酸的情况下能够生长,尽管在大多数赖氨酸浓度下培养7小时后的生长程度与亲本大肠杆菌菌株相比显著(p<0.05)降低。通过使用表型阵列确定,该突变体利用碳和氮底物的能力也低于亲本大肠杆菌菌株。这些结果表明,在lysA基因中进行靶向插入诱变后,通过表型阵列测量的大肠杆菌碳和氮表型谱会发生改变。改变表型的产生可能对赖氨酸大肠杆菌代谢的制药和生物技术应用具有潜在意义。

相似文献

1
Characterization of an Escherichia coli lysA insertion targeted mutant using phenotype arrays.利用表型芯片对大肠杆菌lysA插入靶向突变体进行表征。
Bioresour Technol. 2003 Sep;89(3):249-53. doi: 10.1016/s0960-8524(03)00072-5.
2
Generation of an Escherichia coli lysA targeted deletion mutant by double cross-over recombination for potential use in a bacterial growth-based lysine assay.通过双交换重组产生靶向缺失突变的大肠杆菌lysA,用于基于细菌生长的赖氨酸测定的潜在用途。
Lett Appl Microbiol. 2003;37(6):458-62. doi: 10.1046/j.1472-765x.2003.01425.x.
3
Regulatory pattern of the Escherichia coli lysA gene: expression of chromosomal lysA-lacZ fusions.大肠杆菌lysA基因的调控模式:染色体lysA-lacZ融合体的表达
J Bacteriol. 1983 Dec;156(3):1198-203. doi: 10.1128/jb.156.3.1198-1203.1983.
4
Regulation of diaminopimelate decarboxylase synthesis in Escherichia coli. I. Identification of a lysR gene encoding an activator of the lysA gene.大肠杆菌中二氨基庚二酸脱羧酶合成的调控。I. 编码lysA基因激活剂的lysR基因的鉴定。
J Mol Biol. 1983 Aug 5;168(2):307-20. doi: 10.1016/s0022-2836(83)80020-5.
5
Heterologous expression and regulation of the lysA genes of Pseudomonas aeruginosa and Escherichia coli.铜绿假单胞菌和大肠杆菌lysA基因的异源表达与调控
Mol Gen Genet. 1986 Jun;203(3):430-4. doi: 10.1007/BF00422067.
6
[Cloning and regulation of the expression of the lysA gene from Bacillus subtilis].[枯草芽孢杆菌lysA基因的克隆及表达调控]
Genetika. 1992 May;28(5):5-10.
7
Construction of hybrid plasmids containing the lysA gene of Escherichia coli: studies of expression in Escherichia coli and Saccharomyces cerevisiae.含有大肠杆菌lysA基因的杂种质粒的构建:在大肠杆菌和酿酒酵母中的表达研究。
Mol Gen Genet. 1981;182(3):456-61. doi: 10.1007/BF00293935.
8
H-NS controls metabolism and stress tolerance in Escherichia coli O157:H7 that influence mouse passage.H-NS控制大肠杆菌O157:H7中的代谢和应激耐受性,这些因素会影响其在小鼠体内传代。
BMC Microbiol. 2006 Aug 15;6:72. doi: 10.1186/1471-2180-6-72.
9
Improved production of L-lysine by over-expression of Meso-diaminopimelate decarboxylase enzyme of Corynebacterium glutamicum in Escherichia coli.通过在大肠杆菌中过表达谷氨酸棒杆菌的中-二氨基庚二酸脱羧酶来提高L-赖氨酸的产量。
Pak J Biol Sci. 2010 May 15;13(10):504-8. doi: 10.3923/pjbs.2010.504.508.
10
Isolation and properties of a mutant of Escherichia coli with an insertional inactivation of the uspA gene, which encodes a universal stress protein.编码一种通用应激蛋白的uspA基因发生插入失活的大肠杆菌突变体的分离与特性
J Bacteriol. 1993 Jul;175(13):3949-56. doi: 10.1128/jb.175.13.3949-3956.1993.