• 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

大肠杆菌生物素基因簇中启动子和操纵基因位点的定位。

Location of promoter and operator sites in the biotin gene cluster of Escherichia coli.

作者信息

Cleary P P, Campbell A, Chang R

出版信息

Proc Natl Acad Sci U S A. 1972 Aug;69(8):2219-23. doi: 10.1073/pnas.69.8.2219.

DOI:10.1073/pnas.69.8.2219
PMID:4559599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC426904/
Abstract

Biotin independence in E. coli requires five closely linked genes, bioA, bioB, bioF, bioC, and bioD. The residual gene activity of deletion mutants has been studied by complementation and enzyme assays. Deletion of the left end of the bioA gene does not impair expression of the remaining genes, but deletions from the left extending into bioB abolish all gene expression. Nonsense mutations in bioB reduce expression of bioC, bioF, and bioD. Therefore, the four genes, bioB, bioF, bioC, and bioD, are transcribed as a unit from left to right, from a promotor located between bioA and bioB. Expression of the bio genes is repressible by added biotin. Deletions removing the left end of bioA do not affect repressibility of bioD. Therefore the operator, as well as the promoter, lie to the right of bioA. One deletion that removes bioA, bioB, and bioF renders the bioD gene constitutive, presumably by fusion to an unknown operon. Therefore, the operator lies to the left of bioC.

摘要

大肠杆菌中生物素自主性需要五个紧密连锁的基因,即bioA、bioB、bioF、bioC和bioD。已通过互补和酶分析研究了缺失突变体的残余基因活性。bioA基因左端的缺失不会损害其余基因的表达,但从左端延伸至bioB的缺失会消除所有基因的表达。bioB中的无义突变会降低bioC、bioF和bioD的表达。因此,bioB、bioF、bioC和bioD这四个基因从位于bioA和bioB之间的启动子开始,作为一个单元从左向右转录。生物素基因的表达可被添加的生物素抑制。去除bioA左端的缺失不会影响bioD的可抑制性。因此,操纵基因以及启动子位于bioA的右侧。一个去除bioA、bioB和bioF的缺失使bioD基因组成型表达,推测是通过与一个未知操纵子融合。因此,操纵基因位于bioC的左侧。

相似文献

1
Location of promoter and operator sites in the biotin gene cluster of Escherichia coli.大肠杆菌生物素基因簇中启动子和操纵基因位点的定位。
Proc Natl Acad Sci U S A. 1972 Aug;69(8):2219-23. doi: 10.1073/pnas.69.8.2219.
2
Deletion and complementation analysis of biotin gene cluster of Escherichia coli.大肠杆菌生物素基因簇的缺失与互补分析
J Bacteriol. 1972 Nov;112(2):830-9. doi: 10.1128/jb.112.2.830-839.1972.
3
Complete sequence and organization of the Serratia marcescens biotin operon.粘质沙雷氏菌生物素操纵子的完整序列与组织
Microbiology (Reading). 1996 Nov;142 ( Pt 11):3295-303. doi: 10.1099/13500872-142-11-3295.
4
Genomic organization of the biotin biosynthetic genes of coryneform bacteria: cloning and sequencing of the bioA-bioD genes from Brevibacterium flavum.棒状杆菌生物素生物合成基因的基因组组织:来自黄色短杆菌的bioA-bioD基因的克隆与测序
DNA Seq. 1993;4(3):177-84. doi: 10.3109/10425179309015630.
5
A mutant of Escherichia coli that requires high concentrations of biotin.一种需要高浓度生物素的大肠杆菌突变体。
Proc Natl Acad Sci U S A. 1972 Mar;69(3):676-80. doi: 10.1073/pnas.69.3.676.
6
Cloning, sequencing, and characterization of the Bacillus subtilis biotin biosynthetic operon.枯草芽孢杆菌生物素生物合成操纵子的克隆、测序及特性分析。
J Bacteriol. 1996 Jul;178(14):4122-30. doi: 10.1128/jb.178.14.4122-4130.1996.
7
A deletion mutation placing the galactokinase gene of Escherichia coli under control of the biotin promoter.一种缺失突变,使大肠杆菌的半乳糖激酶基因受生物素启动子的控制。
Proc Natl Acad Sci U S A. 1974 Jul;71(7):2698-702. doi: 10.1073/pnas.71.7.2698.
8
Cloning and characterization of the Bacillus sphaericus genes controlling the bioconversion of pimelate into dethiobiotin.球形芽孢杆菌中控制庚二酸生物转化为去硫生物素的基因的克隆与特性分析
Gene. 1990 Mar 1;87(1):63-70. doi: 10.1016/0378-1119(90)90496-e.
9
The Escherichia coli biotin biosynthetic enzyme sequences predicted from the nucleotide sequence of the bio operon.
J Biol Chem. 1988 Dec 25;263(36):19577-85.
10
Genetic analysis of an incomplete bio operon in a biotin auxotrophic strain of Bacillus subtilis natto OK2.纳豆芽孢杆菌OK2生物素营养缺陷型菌株中一个不完整生物素操纵子的遗传分析。
Biosci Biotechnol Biochem. 2004 Mar;68(3):739-42. doi: 10.1271/bbb.68.739.

引用本文的文献

1
A bacterial methyltransferase that initiates biotin synthesis, an attractive anti-ESKAPE druggable pathway.一种启动生物素合成的细菌甲基转移酶,这是一条有吸引力的抗ESKAPE可成药途径。
Sci Adv. 2024 Dec 20;10(51):eadp3954. doi: 10.1126/sciadv.adp3954.
2
Advances and prospects in microbial production of biotin.生物素微生物生产的进展与展望。
Microb Cell Fact. 2024 May 12;23(1):135. doi: 10.1186/s12934-024-02413-1.
3
Construction of a Biotin-Overproducing Strain of Serratia marcescens.构建产生物素的粘质沙雷氏菌工程菌。
Appl Environ Microbiol. 1993 Sep;59(9):2857-63. doi: 10.1128/aem.59.9.2857-2863.1993.
4
Hypersensitivity of Escherichia coli Delta(uvrB-bio) mutants to 6-hydroxylaminopurine and other base analogs is due to a defect in molybdenum cofactor biosynthesis.大肠杆菌Delta(uvrB-bio)突变体对6-羟基氨基嘌呤和其他碱基类似物的超敏性是由于钼辅因子生物合成缺陷所致。
J Bacteriol. 2000 Jun;182(12):3361-7. doi: 10.1128/JB.182.12.3361-3367.2000.
5
Molecular breeding of a biotin-hyperproducing Serratia marcescens strain.一株生物素高产粘质沙雷氏菌菌株的分子育种
Appl Environ Microbiol. 1993 Oct;59(10):3225-32. doi: 10.1128/aem.59.10.3225-3232.1993.
6
Isolation of a cDNA encoding human holocarboxylase synthetase by functional complementation of a biotin auxotroph of Escherichia coli.通过大肠杆菌生物素营养缺陷型的功能互补分离编码人全羧化酶合成酶的cDNA。
Proc Natl Acad Sci U S A. 1995 May 9;92(10):4626-30. doi: 10.1073/pnas.92.10.4626.
7
Mutational specificity of UV light in Escherichia coli: indications for a role of DNA secondary structure.紫外线在大肠杆菌中的突变特异性:DNA二级结构作用的迹象
Proc Natl Acad Sci U S A. 1982 Jul;79(13):4123-7. doi: 10.1073/pnas.79.13.4123.
8
Base-pair substitution hotspots in GAG and GCG nucleotide sequences in Escherichia coli K-12 induced by cis-diamminedichloroplatinum (II).顺式二氯二氨合铂(II)诱导的大肠杆菌K-12中GAG和GCG核苷酸序列的碱基对替换热点。
Proc Natl Acad Sci U S A. 1981 Nov;78(11):7010-4. doi: 10.1073/pnas.78.11.7010.
9
Use of bio-lac fusion strains to study regulation of biotin biosynthesis in Escherichia coli.利用生物素-乳糖融合菌株研究大肠杆菌中生物素生物合成的调控。
J Bacteriol. 1980 Aug;143(2):789-800. doi: 10.1128/jb.143.2.789-800.1980.
10
The regulatory region of the divergent argECBH operon in Escherichia coli K-12.大肠杆菌K-12中反向排列的argECBH操纵子的调控区域。
Nucleic Acids Res. 1982 Dec 20;10(24):8031-48. doi: 10.1093/nar/10.24.8031.

本文引用的文献

1
An early intermediate in the biosynthesis of biotin: Incorporation studies with [1,7-C(2)]pimelic acid.生物素生物合成中的早期中间体:[1,7-C(2)]戊二酸的掺入研究。
Biochem J. 1966 Dec;101(3):601-6. doi: 10.1042/bj1010601.
2
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
3
THE BIOSYNTHESIS OF BIOTIN IN MICROORGANISMS. I. THE PHYSIOLOGY OF BIOTIN SYNTHESIS IN ESCHERICHIA COLI.微生物中生物素的生物合成。I. 大肠杆菌中生物素合成的生理学
Biochim Biophys Acta. 1965 Apr 12;100:28-35. doi: 10.1016/0304-4165(65)90423-x.
4
REGULATORY MECHANISMS IN THE BIOSYNTHESIS OF ISOLEUCINE AND VALINE. 3. MAP ORDER OF THE STRUCTURAL GENES AND OPERATOR GENES.异亮氨酸和缬氨酸生物合成中的调控机制。3. 结构基因和操纵基因的图谱顺序。
J Bacteriol. 1965 Mar;89(3):661-4. doi: 10.1128/jb.89.3.661-664.1965.
5
[THE PROMOTOR, A GENETIC ELEMENT NECESSARY TO THE EXPRESSION OF AN OPERON].[启动子,操纵子表达所必需的遗传元件]
C R Hebd Seances Acad Sci. 1964 Mar 16;258:3125-8.
6
CO-LINEARITY OF THE GENE WITH THE POLYPEPTIDE CHAIN.基因与多肽链的共线性
Nature. 1964 Jan 4;201:13-7. doi: 10.1038/201013a0.
7
The regulatory mechanism of enzyme synthesis in the tryptophan biosynthetic pathway of Escherichia coli K-12.大肠杆菌K-12色氨酸生物合成途径中酶合成的调控机制。
Biochem Biophys Res Commun. 1962 Oct 17;9:204-7. doi: 10.1016/0006-291x(62)90058-x.
8
Sensitive mutants of bacteriophage lambda.噬菌体λ的敏感突变体
Virology. 1961 May;14:22-32. doi: 10.1016/0042-6822(61)90128-3.
9
A strong suppressor specific for UGA.一种对UGA具有特异性的强抑制子。
Nature. 1967 Apr 29;214(5087):452-3. doi: 10.1038/214452a0.
10
Nonsense codons and polarity in the tryptophan operon.色氨酸操纵子中的无义密码子与极性
J Mol Biol. 1966 Nov 14;21(2):313-34. doi: 10.1016/0022-2836(66)90102-1.