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1
Characterization of the operator sites of the exu regulon in Escherichia coli K-12 by operator-constitutive mutations and repressor titration.通过操纵子组成型突变和阻遏物滴定法对大肠杆菌K-12中exu操纵子的操纵位点进行表征。
Genetics. 1983 Dec;105(4):829-42. doi: 10.1093/genetics/105.4.829.
2
Physical mapping of the exuT and uxaC operators by use of exu plasmids and generation of deletion mutants in vitro.利用exu质粒对exuT和uxaC操纵基因进行物理图谱分析并在体外构建缺失突变体。
J Bacteriol. 1983 Sep;155(3):973-82. doi: 10.1128/jb.155.3.973-982.1983.
3
Regulation of Escherichia coli K-12 hexuronate system genes: exu regulon.大肠杆菌K-12己糖醛酸系统基因的调控:exu操纵子
J Bacteriol. 1980 Sep;143(3):1095-107. doi: 10.1128/jb.143.3.1095-1107.1980.
4
Isolation of fusions between the lac genes and several genes of the exu regulon: analysis of their regulation, determination of the transcription direction of the uxaC-uxaA operon, in Escherichia coli K-12.lac基因与exu调节子几个基因之间融合体的分离:对其调控的分析、大肠杆菌K-12中uxaC-uxaA操纵子转录方向的确定
Mol Gen Genet. 1981;182(2):279-87. doi: 10.1007/BF00269671.
5
Determination of the transcription direction of the exuT gene in Escherichia coli K-12: divergent transcription of the exuT-uxaCA operons.大肠杆菌K-12中exuT基因转录方向的确定:exuT-uxaCA操纵子的双向转录
J Bacteriol. 1982 Jul;151(1):480-4. doi: 10.1128/jb.151.1.480-484.1982.
6
Physiological and genetic regulation of the aldohexuronate transport system in Escherichia coli.大肠杆菌中醛己糖醛酸转运系统的生理和遗传调控
J Bacteriol. 1976 Aug;127(2):706-18. doi: 10.1128/jb.127.2.706-718.1976.
7
Isolation of a functional exuR-repressor-beta-galactosidase hybrid protein by use of in vitro gene fusions.利用体外基因融合技术分离功能性exuR阻遏蛋白-β-半乳糖苷酶杂合蛋白。
Gene. 1983 Nov;25(1):9-20. doi: 10.1016/0378-1119(83)90162-2.
8
Interchangeability of repressors for the control of the uxu and uid operons in E. coli K12.大肠杆菌K12中阻遏物对uxu和uid操纵子控制的互换性。
Mol Gen Genet. 1983;191(2):263-70. doi: 10.1007/BF00334824.
9
Molecular cloning of Escherichia coli K-12 hexuronate system genes: exu region.大肠杆菌K-12己糖醛酸系统基因的分子克隆:exu区域
J Bacteriol. 1981 Jan;145(1):181-90. doi: 10.1128/jb.145.1.181-190.1981.
10
Construction of hybrid plasmids containing the Escherichia coli uxaB gene: analysis of its regulation and direction of transcription.含有大肠杆菌uxaB基因的杂种质粒的构建:其调控及转录方向分析
J Bacteriol. 1983 Feb;153(2):747-55. doi: 10.1128/jb.153.2.747-755.1983.

引用本文的文献

1
Differential Impact of Hexuronate Regulators ExuR and UxuR on the Proteome.Hexuronate 调节剂 ExuR 和 UxuR 对蛋白质组的差异影响。
Int J Mol Sci. 2022 Jul 29;23(15):8379. doi: 10.3390/ijms23158379.
2
Novel insights into E. coli's hexuronate metabolism: KduI facilitates the conversion of galacturonate and glucuronate under osmotic stress conditions.深入研究大肠杆菌的六碳糖醛酸盐代谢:在渗透胁迫条件下,KduI 有助于半乳糖醛酸盐和葡萄糖醛酸盐的转化。
PLoS One. 2013;8(2):e56906. doi: 10.1371/journal.pone.0056906. Epub 2013 Feb 21.
3
Escherichia coli strains that allow antibiotic-free plasmid selection and maintenance by repressor titration.通过阻遏物滴定实现无抗生素质粒选择和维持的大肠杆菌菌株。
Nucleic Acids Res. 2001 Mar 1;29(5):E26. doi: 10.1093/nar/29.5.e26.
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
Genetic analysis of uxuR and exuR genes: evidence for ExuR and UxuR monomer repressors interactions.uxuR和exuR基因的遗传分析:ExuR和UxuR单体阻遏物相互作用的证据
Mol Gen Genet. 1985;199(3):507-11. doi: 10.1007/BF00330766.
6
Linkage map of Escherichia coli K-12, edition 8.大肠杆菌K-12连锁图谱,第8版。
Microbiol Rev. 1990 Jun;54(2):130-97. doi: 10.1128/mr.54.2.130-197.1990.

本文引用的文献

1
Regulation of Escherichia coli K-12 hexuronate system genes: exu regulon.大肠杆菌K-12己糖醛酸系统基因的调控:exu操纵子
J Bacteriol. 1980 Sep;143(3):1095-107. doi: 10.1128/jb.143.3.1095-1107.1980.
2
How Escherichia coli sets different basal levels in SOS operons.大肠杆菌如何在SOS操纵子中设定不同的基础水平。
Biochimie. 1982 Aug-Sep;64(8-9):709-12. doi: 10.1016/s0300-9084(82)80115-6.
3
Isolation and characterization of an operator-constitutive mutation in the recA gene of E. coli K-12.大肠杆菌K-12 recA基因中一个操纵子组成型突变的分离与鉴定。
Mol Gen Genet. 1982;187(1):4-11. doi: 10.1007/BF00384376.
4
Sequence and properties of operator mutations in the bio operon of Escherichia coli.大肠杆菌生物操纵子中操纵基因突变的序列与特性
Gene. 1981 Jan-Feb;13(1):89-102. doi: 10.1016/0378-1119(81)90046-9.
5
A unitary account of the repression mechanism of arginine biosynthesis in Escherichia coli. I. The genetic evidence.大肠杆菌中精氨酸生物合成抑制机制的统一解释。I. 遗传学证据。
J Mol Biol. 1969 Jan 14;39(1):73-87. doi: 10.1016/0022-2836(69)90334-9.
6
lac Repressor-operator interaction. IX. The binding of lac repressor to operators containing Oc mutations.乳糖阻遏蛋白-操纵基因相互作用。IX. 乳糖阻遏蛋白与含Oc突变的操纵基因的结合。
J Mol Biol. 1974 May 15;85(2):231-48. doi: 10.1016/0022-2836(74)90362-3.
7
[Studies of mutations in the uronic isomerase and altronic oxidoreductase structural genes of Escherichia coli K 12 (author's transl)].大肠杆菌K12的糖醛异构酶和阿卓糖氧化还原酶结构基因中的突变研究(作者译)
Mol Gen Genet. 1974;128(4):301-19. doi: 10.1007/BF00268518.
8
General method for the isolation of plasmid deoxyribonucleic acid.质粒脱氧核糖核酸的分离通用方法。
J Bacteriol. 1973 Nov;116(2):1064-6. doi: 10.1128/jb.116.2.1064-1066.1973.
9
[2-Keto-3-deoxy-gluconate transport system in E. coli K 12: map location of a structural gene and of its operator].[大肠杆菌K12中的2-酮-3-脱氧葡萄糖酸盐转运系统:一个结构基因及其操纵基因的图谱定位]
Mol Gen Genet. 1973 Mar 1;121(2):163-80. doi: 10.1007/BF00277530.
10
Physiological and genetic regulation of the aldohexuronate transport system in Escherichia coli.大肠杆菌中醛己糖醛酸转运系统的生理和遗传调控
J Bacteriol. 1976 Aug;127(2):706-18. doi: 10.1128/jb.127.2.706-718.1976.

通过操纵子组成型突变和阻遏物滴定法对大肠杆菌K-12中exu操纵子的操纵位点进行表征。

Characterization of the operator sites of the exu regulon in Escherichia coli K-12 by operator-constitutive mutations and repressor titration.

作者信息

Mata-Gilsinger M, Ritzenthaler P, Blanco C

出版信息

Genetics. 1983 Dec;105(4):829-42. doi: 10.1093/genetics/105.4.829.

DOI:10.1093/genetics/105.4.829
PMID:6357945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1202228/
Abstract

In Escherichia coli, the exu regulon of the hexuronate system involves the three exuT, uxaCA and uxaB operons and is under the negative control of the exuR regulatory gene product. The technique developed by Casadaban, Chou and Cohen was employed to construct two plasmids containing operon fusions in which the lactose genes were fused to the uxaCA and exuT operons. These fusions were transferred into the chromosome by a reciprocal recombination event, and the resulting strains were used for isolation of mutants defective in repression. Two types of operator-constitutive mutants were obtained: one specific for the uxaCA operon expression and the other affecting the exuT gene expression. This genetic evidence confirms that these two operons which are divergently transcribed each possess their own operator site.--The derepressed expression of the two exuT-lac and uxaCA-lac operons and the uxaB gene was also examined upon introduction of plasmids bearing various operators of the exu regulon. The results of testing exuR repressor titration by multiple copies of the exu operators allowed us to show a gradation in the affinity degrees for the three exu operators: uxaBo has the strongest affinity for the exuR repressor and uxaCo the weakest, although that of exuTo seems to be just slightly greater. This gradation may play a role in the control of the exu regulon expression.

摘要

在大肠杆菌中,己糖醛酸系统的exu调节子涉及exuT、uxaCA和uxaB这三个操纵子,并受exuR调节基因产物的负调控。采用卡萨达班、周和科恩开发的技术构建了两个含有操纵子融合体的质粒,其中乳糖基因与uxaCA和exuT操纵子融合。这些融合体通过相互重组事件转移到染色体上,所得菌株用于分离阻遏缺陷型突变体。获得了两种类型的操纵子组成型突变体:一种对uxaCA操纵子表达具有特异性,另一种影响exuT基因表达。这一遗传学证据证实,这两个反向转录的操纵子各自拥有自己的操纵位点。——在导入携带exu调节子各种操纵子的质粒后,还检测了两个exuT-lac和uxaCA-lac操纵子以及uxaB基因的去阻遏表达。通过exu操纵子的多个拷贝对exuR阻遏物进行滴定测试的结果使我们能够显示出对三个exu操纵子的亲和程度存在梯度:uxaBo对exuR阻遏物的亲和力最强,uxaCo最弱,尽管exuTo的亲和力似乎略高一点。这种梯度可能在exu调节子表达的控制中起作用。