• 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

大肠杆菌trpE基因在大肠杆菌K12菌株中的表达:邻氨基苯甲酸合成酶产生的最大水平、速率及起始时间。

Expression of the Escherichia coli trpE gene in E. coli K12 bacteria: maximum level, rate and time of initiation of anthranilate synthetase production.

作者信息

Hessing H G, van Rotterdam C, Pouwels P H

机构信息

Medical Biological Laboratory TNO, Rijswijk, The Netherlands.

出版信息

Mol Gen Genet. 1987 Dec;210(2):256-61. doi: 10.1007/BF00325691.

DOI:10.1007/BF00325691
PMID:3325775
Abstract

We have investigated the effect of alterations in the structure of the plasmid-borne Escherichia coli tryptophan (trp) coding region and other regions of the same replicon on the level, rate and time of initiation of anthranilate synthetase component I (ASase) synthesis in E. coli K12. The maximum level of ASase produced corresponds to 60%-65% of the total cellular proteins. Adding sequences downstream of the trpE coding region decreases the level but does not affect the time of initiation and rate of trpE expression (ASase synthesis). The presence of additional protein coding sequences on the plasmid outside the trpE-A region causes ASase production to start earlier and decreases the rate of ASase synthesis. A second copy of the trpE coding sequences, if present within or outside the trpE-A coding region on the same replicon, doubles the rate of synthesis of ASase and slightly increases its final level of production. The initiation of ASase production occurs earlier when the two trpE copies are located within two distinct transcription units.

摘要

我们研究了质粒携带的大肠杆菌色氨酸(trp)编码区及同一复制子其他区域结构的改变对大肠杆菌K12中邻氨基苯甲酸合成酶组分I(ASase)合成的起始水平、速率和时间的影响。所产生的ASase的最大水平相当于细胞总蛋白的60% - 65%。在trpE编码区下游添加序列会降低水平,但不影响trpE表达(ASase合成)的起始时间和速率。trpE - A区域外的质粒上存在额外的蛋白质编码序列会使ASase产生更早开始,并降低ASase合成速率。如果trpE编码序列的第二个拷贝存在于同一复制子的trpE - A编码区内或区外,ASase的合成速率会加倍,并略微提高其最终产生水平。当两个trpE拷贝位于两个不同的转录单元中时,ASase产生的起始会更早发生。

相似文献

1
Expression of the Escherichia coli trpE gene in E. coli K12 bacteria: maximum level, rate and time of initiation of anthranilate synthetase production.大肠杆菌trpE基因在大肠杆菌K12菌株中的表达:邻氨基苯甲酸合成酶产生的最大水平、速率及起始时间。
Mol Gen Genet. 1987 Dec;210(2):256-61. doi: 10.1007/BF00325691.
2
Identification and characterization of genes for a second anthranilate synthase in Pseudomonas aeruginosa: interchangeability of the two anthranilate synthases and evolutionary implications.铜绿假单胞菌中第二种邻氨基苯甲酸合酶基因的鉴定与表征:两种邻氨基苯甲酸合酶的互换性及进化意义
J Bacteriol. 1990 Feb;172(2):884-900. doi: 10.1128/jb.172.2.884-900.1990.
3
Molecular cloning of the genes for anthranilate synthetase from Streptomyces venezuelae ISP 5230.委内瑞拉链霉菌ISP 5230邻氨基苯甲酸合成酶基因的分子克隆
FEMS Microbiol Lett. 1991 Mar 1;62(2-3):177-81. doi: 10.1016/0378-1097(91)90154-3.
4
Complementation of a trpE deletion in Escherichia coli by Spirochaeta aurantia DNA encoding anthranilate synthetase component I activity.编码邻氨基苯甲酸合成酶组分I活性的橙色螺旋体DNA对大肠杆菌色氨酸E缺失的互补作用。
J Bacteriol. 1987 Aug;169(8):3764-9. doi: 10.1128/jb.169.8.3764-3769.1987.
5
Nucleotide sequence of the Bacillus subtilis trpE and trpD genes.枯草芽孢杆菌色氨酸E和色氨酸D基因的核苷酸序列。
Gene. 1984 Jan;27(1):55-65. doi: 10.1016/0378-1119(84)90238-5.
6
Molecular characterization and expression analysis of the anthranilate synthase gene of Pseudomonas syringae subsp. savastanoi.丁香假单胞菌 savastanoi 亚种邻氨基苯甲酸合酶基因的分子特征及表达分析
J Bacteriol. 1991 Jan;173(2):463-71. doi: 10.1128/jb.173.2.463-471.1991.
7
In vitro synthesis of enzymes of the tryptophan operon of Escherichia coli.大肠杆菌色氨酸操纵子酶的体外合成
Mol Gen Genet. 1975;136(3):185-97. doi: 10.1007/BF00334014.
8
Studies on the involvement of the UGA readthrough process in the mechanism of attenuation of the tryptophan operon of Escherichia coli.关于UGA通读过程参与大肠杆菌色氨酸操纵子衰减机制的研究。
Mol Gen Genet. 1982;188(1):156-60. doi: 10.1007/BF00333011.
9
Naturally occurring sites within the Shigella dysenteriae tryptophan operon severely limit tryptophan biosynthesis.痢疾志贺氏菌色氨酸操纵子内的天然存在位点严重限制色氨酸的生物合成。
J Bacteriol. 1976 May;126(2):668-78. doi: 10.1128/jb.126.2.668-678.1976.
10
Sequence changes preceding a Shine-Dalgarno region influence trpE mRNA translation and decay.先于夏因-达尔加诺序列区域的序列变化会影响色氨酸合成酶E(trpE)信使核糖核酸(mRNA)的翻译及降解。
J Mol Biol. 1988 Nov 5;204(1):51-60. doi: 10.1016/0022-2836(88)90598-0.

引用本文的文献

1
synthesis of 1-phenethylisoquinoline in engineered .工程化中1-苯乙基异喹啉的合成
Synth Syst Biotechnol. 2024 Nov 9;10(1):271-280. doi: 10.1016/j.synbio.2024.10.007. eCollection 2025.
2
Functions of the gene products of Escherichia coli.大肠杆菌基因产物的功能。
Microbiol Rev. 1993 Dec;57(4):862-952. doi: 10.1128/mr.57.4.862-952.1993.

本文引用的文献

1
[Inhibition of the synthesis of the enzymes participating in the formation of tryptophan in Escherichia coli].[对大肠杆菌中参与色氨酸形成的酶的合成的抑制作用]
C R Hebd Seances Acad Sci. 1959 Jun 15;248(24):3490-2.
2
High-level expression of a chemically synthesized gene for human interferon-gamma using a prokaryotic expression vector.使用原核表达载体对化学合成的人γ干扰素基因进行高水平表达。
Proc Natl Acad Sci U S A. 1984 Apr;81(8):2290-4. doi: 10.1073/pnas.81.8.2290.
3
Identification of a sex-factor-affinity site in E. coli as gamma delta.
在大肠杆菌中鉴定出作为γδ的性别因子亲和位点。
Cold Spring Harb Symp Quant Biol. 1981;45 Pt 1:135-40. doi: 10.1101/sqb.1981.045.01.022.
4
Construction of new cloning vehicles with genes of the tryptophan operon of Escherichia coli as genetic markers.构建以大肠杆菌色氨酸操纵子基因作为遗传标记的新型克隆载体。
Gene. 1980 Apr;9(1-2):69-85. doi: 10.1016/0378-1119(80)90167-5.
5
Quantitation of proteins on Coomassie blue-stained polyacrylamide gels based on spectrophotometric determination of electroeluted dye.基于分光光度法测定电洗脱染料对考马斯亮蓝染色聚丙烯酰胺凝胶上蛋白质的定量分析。
Anal Biochem. 1984 Sep;141(2):503-9. doi: 10.1016/0003-2697(84)90078-2.
6
Cloning with tandem gene systems for high level gene expression.用于高水平基因表达的串联基因系统克隆
Nucleic Acids Res. 1984 Sep 11;12(17):6797-812. doi: 10.1093/nar/12.17.6797.
7
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.在噬菌体T4头部组装过程中结构蛋白的切割
Nature. 1970 Aug 15;227(5259):680-5. doi: 10.1038/227680a0.
8
Anthranilate synthetase, an enzyme specified by the tryptophan operon of Escherichia coli: purification and characterization of component I.邻氨基苯甲酸合成酶,一种由大肠杆菌色氨酸操纵子所编码的酶:组分I的纯化及特性分析
J Bacteriol. 1969 Feb;97(2):725-33. doi: 10.1128/jb.97.2.725-733.1969.
9
Mutants of Escherichia coli with an altered tryptophanyl-transfer ribonucleic acid synthetase.色氨酸转移核糖核酸合成酶发生改变的大肠杆菌突变体。
J Bacteriol. 1968 Apr;95(4):1283-94. doi: 10.1128/jb.95.4.1283-1294.1968.
10
Regulation of in vitro transcription of the tryptophan operon by purified RNA polymerase in the presence of partially purified repressor and tryptophan.在部分纯化的阻遏物和色氨酸存在的情况下,利用纯化的RNA聚合酶对色氨酸操纵子进行体外转录调控。
Nat New Biol. 1973 Oct 3;245(144):133-7. doi: 10.1038/newbio245133a0.