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1
Complex glnA-glnL-glnG operon of Escherichia coli.大肠杆菌的复杂谷氨酰胺合成酶基因-谷氨酰胺基因-谷氨酰胺调节基因操纵子
J Bacteriol. 1982 Apr;150(1):202-13. doi: 10.1128/jb.150.1.202-213.1982.
2
Polarity in the glnA operon: suppression of the reg- phenotype by rho mutations.谷氨酰胺合成酶操纵子中的极性:rho突变对reg-表型的抑制作用。
J Bacteriol. 1982 Jun;150(3):1314-21. doi: 10.1128/jb.150.3.1314-1321.1982.
3
Effects of glnL and other regulatory loci on regulation of transcription of glnA-lacZ fusions in Klebsiella aerogenes.谷氨酰胺合成酶基因L及其他调控位点对产气克雷伯菌中谷氨酰胺合成酶基因A-乳糖操纵子融合转录调控的影响。
J Bacteriol. 1982 Apr;150(1):231-8. doi: 10.1128/jb.150.1.231-238.1982.
4
Role of glnA-linked genes in regulation of glutamine synthetase and histidase formation in Klebsiella aerogenes.谷氨酰胺合成酶连接基因在产气克雷伯菌中对谷氨酰胺合成酶和组氨酸酶形成的调控作用。
J Bacteriol. 1982 Apr;150(1):221-30. doi: 10.1128/jb.150.1.221-230.1982.
5
Fine-structure deletion map and complementation analysis of the glnA-glnL-glnG region in Escherichia coli.大肠杆菌中谷氨酰胺合成酶基因(glnA)-谷氨酰胺转运蛋白基因(glnL)-谷氨酰胺基因激活蛋白基因(glnG)区域的精细结构缺失图谱及互补分析
J Bacteriol. 1982 Jun;150(3):1302-13. doi: 10.1128/jb.150.3.1302-1313.1982.
6
Role of glnB and glnD gene products in regulation of the glnALG operon of Escherichia coli.谷氨酰胺B和谷氨酰胺D基因产物在大肠杆菌谷氨酰胺合成酶操纵子调节中的作用。
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Physical and genetic characterization of the glnA--glnG region of the Escherichia coli chromosome.大肠杆菌染色体谷氨酰胺合成酶基因(glnA)-谷氨酰胺合成酶基因激活蛋白基因(glnG)区域的物理和遗传特征分析
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Characterization of a gene, glnL, the product of which is involved in the regulation of nitrogen utilization in Escherichia coli.一个基因(glnL)的特性,其产物参与大肠杆菌氮利用的调控。
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Expression of glnA in Escherichia coli is regulated at tandem promoters.大肠杆菌中谷氨酰胺合成酶基因(glnA)的表达受串联启动子调控。
Proc Natl Acad Sci U S A. 1985 Apr;82(7):1979-83. doi: 10.1073/pnas.82.7.1979.
10
Regulation of transcription of glnA, the structural gene encoding glutamine synthetase, in glnA::Mu d1 (ApR, lac) fusion strains of Salmonella typhimurium.鼠伤寒沙门氏菌glnA::Mu d1(ApR,lac)融合菌株中谷氨酰胺合成酶编码结构基因glnA的转录调控。
Mol Gen Genet. 1983;192(1-2):187-97. doi: 10.1007/BF00327665.

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本文引用的文献

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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.
2
Linkage map of Escherichia coli K-12, edition 6.大肠杆菌K-12连锁图谱,第6版。
Microbiol Rev. 1980 Mar;44(1):1-56. doi: 10.1128/mr.44.1.1-56.1980.
3
Analysis of gene control signals by DNA fusion and cloning in Escherichia coli.通过在大肠杆菌中进行DNA融合和克隆分析基因控制信号。
J Mol Biol. 1980 Apr;138(2):179-207. doi: 10.1016/0022-2836(80)90283-1.
4
Physical and genetic characterization of the glnA--glnG region of the Escherichia coli chromosome.大肠杆菌染色体谷氨酰胺合成酶基因(glnA)-谷氨酰胺合成酶基因激活蛋白基因(glnG)区域的物理和遗传特征分析
Proc Natl Acad Sci U S A. 1981 Jun;78(6):3743-7. doi: 10.1073/pnas.78.6.3743.
5
Nitrogen regulatory locus "glnR" of enteric bacteria is composed of cistrons ntrB and ntrC: identification of their protein products.肠道细菌的氮调节基因座“glnR”由顺反子ntrB和ntrC组成:其蛋白质产物的鉴定。
Proc Natl Acad Sci U S A. 1981 Apr;78(4):2135-9. doi: 10.1073/pnas.78.4.2135.
6
Regulation of expression from the glnA promoter of Escherichia coli in the absence of glutamine synthetase.在缺乏谷氨酰胺合成酶的情况下,大肠杆菌谷氨酰胺合成酶基因(glnA)启动子的表达调控
Proc Natl Acad Sci U S A. 1980 Dec;77(12):7372-6. doi: 10.1073/pnas.77.12.7372.
7
Escherichia coli K-12 F-prime factors, old and new.大肠杆菌K-12 F-prime因子,新旧情况
Bacteriol Rev. 1972 Dec;36(4):587-607. doi: 10.1128/br.36.4.587-607.1972.
8
Regulation of nitrogen fixation in Klebsiella pneumoniae: evidence for a role of glutamine synthetase as a regulator of nitrogenase synthesis.肺炎克雷伯菌中固氮作用的调控:谷氨酰胺合成酶作为固氮酶合成调节剂作用的证据。
J Bacteriol. 1974 Nov;120(2):815-21. doi: 10.1128/jb.120.2.815-821.1974.
9
Glutamine synthetase and the regulation of histidase formation in Klebsiella aerogenes.产气克雷伯菌中的谷氨酰胺合成酶与组氨酸酶形成的调控
J Biol Chem. 1973 Jun 25;248(12):4334-44.
10
Biochemical construction and selection of hybrid plasmids containing specific segments of the Escherichia coli genome.含有大肠杆菌基因组特定片段的杂交质粒的生化构建与筛选
Proc Natl Acad Sci U S A. 1975 Nov;72(11):4361-5. doi: 10.1073/pnas.72.11.4361.

大肠杆菌的复杂谷氨酰胺合成酶基因-谷氨酰胺基因-谷氨酰胺调节基因操纵子

Complex glnA-glnL-glnG operon of Escherichia coli.

作者信息

Pahel G, Rothstein D M, Magasanik B

出版信息

J Bacteriol. 1982 Apr;150(1):202-13. doi: 10.1128/jb.150.1.202-213.1982.

DOI:10.1128/jb.150.1.202-213.1982
PMID:6120929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC220100/
Abstract

The glnG gene product is both a positive regulator and a negative regulator of the expression of glnA, the structural gene for glutamine synthetase, as well as a positive regulator of the expression of a number of genes whose products are involved in the uptake and degradation of nitrogen-containing compounds. The regulation of beta-galactosidase in various strains containing a Mu d1 (lac bla) insertion within glnG leads to the following conclusions regarding the expression of this gene: (i) like the synthesis of glutamine synthetase, the synthesis of the glnG product is regulated in response to the nitrogen source; (ii) high-level expression of glnG under nitrogen-limiting growth conditions depends on transcription initiated at the glnA promoter; and (iii) there is a second, glnA-distal promoter for glnG, whose activity is negatively controlled by the glnG product. Thus, the glnG product regulates the synthesis of the glnG product at two distinct promoters (positively and negatively at the glnA promoter and negatively at the glnA-distal promoter). In addition, a high level of glnG product, corresponding to the level produced by initiation of transcription at the glnA promoter under nitrogen-limiting conditions, is necessary for activation of histidase synthesis. The lower level of glnG product originating from transcription initiated at the glnA-distal promoter is not sufficient to activate histidase synthesis, but is sufficient to activate fully and to repress glnA expression.

摘要

谷氨酰胺合成酶结构基因glnA的表达,其谷氨酰胺合成酶的产物既是正调控因子又是负调控因子,同时也是许多基因表达的正调控因子,这些基因的产物参与含氮化合物的摄取和降解。在含有glnG内Mu d1(lac bla)插入片段的各种菌株中对β-半乳糖苷酶的调控,得出了关于该基因表达的以下结论:(i)与谷氨酰胺合成酶的合成一样,glnG产物的合成受氮源调控;(ii)在氮限制生长条件下,glnG的高水平表达取决于从glnA启动子起始的转录;(iii)存在第二个位于glnA远端的glnG启动子,其活性受glnG产物的负调控。因此,glnG产物在两个不同的启动子处调控glnG产物的合成(在glnA启动子处正调控和负调控,在glnA远端启动子处负调控)。此外,高水平的glnG产物,对应于在氮限制条件下从glnA启动子起始转录所产生的水平,是激活组氨酸酶合成所必需的。源自glnA远端启动子起始转录的较低水平的glnG产物不足以激活组氨酸酶合成,但足以完全激活并抑制glnA表达。