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Physical and genetic structure of the glpD-malT interval of the Escherichia coli K-12 chromosome. Identification of two new structural genes of the glp-regulon.

作者信息

Schweizer H, Sweet G, Larson T J

出版信息

Mol Gen Genet. 1986 Mar;202(3):488-92. doi: 10.1007/BF00333282.

DOI:10.1007/BF00333282
PMID:3012272
Abstract

A transducing lambda phage carrying glpD''lacZ, glpR, and malT was isolated from a strain harboring a glpD''lacZ fusion. Comparison of restriction endonuclease cleavage patterns of DNA isolated from this phage with that of the previously cloned malT region (Raibaud and Schwartz 1980) facilitated the construction of recombinant plasmids carrying different portions of the glpD-malT region. Results of minicell analysis and complementation studies showed that this region of the chromosome encodes at least five polypeptides. These included the previously identified glpD, glpR, and malT gene products. In addition, two new structural genes of the glp regulon (glpE and glpG) located between the glpD and glpR genes were identified. Hybrid plasmids carrying glpD''lacZ and glpR''lacZ fusions were constructed. Restriction endonuclease cleavage analysis of these two plasmids demonstrated that glpD and glpR are divergently transcribed.

摘要

相似文献

1
Physical and genetic structure of the glpD-malT interval of the Escherichia coli K-12 chromosome. Identification of two new structural genes of the glp-regulon.
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2
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5
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6
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J Bacteriol. 2001 Oct;183(19):5675-83. doi: 10.1128/JB.183.19.5675-5683.2001.
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本文引用的文献

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Identification of the glpT-encoded sn-glycerol-3-phosphate permease of Escherichia coli, an oligomeric integral membrane protein.大肠杆菌中由glpT编码的sn-甘油-3-磷酸通透酶的鉴定,一种寡聚整合膜蛋白。
J Bacteriol. 1982 Dec;152(3):1008-21. doi: 10.1128/jb.152.3.1008-1021.1982.
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Linkage map of Escherichia coli K-12, edition 7.大肠杆菌K-12连锁图谱,第7版。
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Lambda placMu: a transposable derivative of bacteriophage lambda for creating lacZ protein fusions in a single step.
远距离作用对大肠杆菌K-12编码sn-甘油3-磷酸脱氢酶的glpD基因转录的负调控
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Repressor for the sn-glycerol 3-phosphate regulon of Escherichia coli K-12: primary structure and identification of the DNA-binding domain.大肠杆菌K-12的sn-甘油-3-磷酸调节子的阻遏物:一级结构及DNA结合结构域的鉴定
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Regulation of glycerol metabolism in Pseudomonas aeruginosa: characterization of the glpR repressor gene.铜绿假单胞菌中甘油代谢的调控:glpR阻遏基因的特性分析
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Functions of the gene products of Escherichia coli.大肠杆菌基因产物的功能。
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Structures of the promoter and operator of the glpD gene encoding aerobic sn-glycerol-3-phosphate dehydrogenase of Escherichia coli K-12.大肠杆菌K-12中编码好氧甘油-3-磷酸脱氢酶的glpD基因启动子和操纵子的结构
J Bacteriol. 1988 Sep;170(9):4209-15. doi: 10.1128/jb.170.9.4209-4215.1988.
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Cloning and characterization of the aerobic sn-glycerol-3-phosphate dehydrogenase structural gene glpD of Escherichia coli K-12.大肠杆菌K-12需氧型sn-甘油-3-磷酸脱氢酶结构基因glpD的克隆与特性分析
J Bacteriol. 1987 Feb;169(2):507-13. doi: 10.1128/jb.169.2.507-513.1987.
9
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J Bacteriol. 1990 Jan;172(1):179-84. doi: 10.1128/jb.172.1.179-184.1990.
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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.
λplacMu:一种噬菌体λ的可转座衍生物,用于一步构建lacZ蛋白融合体。
J Bacteriol. 1984 Jun;158(3):1084-93. doi: 10.1128/jb.158.3.1084-1093.1984.
4
Mapping of two ugp genes coding for the pho regulon-dependent sn-glycerol-3-phosphate transport system of Escherichia coli.编码大肠杆菌磷酸调节子依赖性sn-甘油-3-磷酸转运系统的两个ugp基因的定位
J Bacteriol. 1982 Jun;150(3):1164-71. doi: 10.1128/jb.150.3.1164-1171.1982.
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Construction and characterization of new cloning vehicles. VI. Plasmid pBR329, a new derivative of pBR328 lacking the 482-base-pair inverted duplication.新型克隆载体的构建与特性分析。VI. 质粒pBR329,pBR328的一种新衍生物,缺失482个碱基对的反向重复序列。
Gene. 1982 Jan;17(1):79-89. doi: 10.1016/0378-1119(82)90103-2.
6
Restriction map of the Escherichia coli malA region and identification of the malT product.大肠杆菌malA区域的限制酶切图谱及malT产物的鉴定
J Bacteriol. 1980 Aug;143(2):761-71. doi: 10.1128/jb.143.2.761-771.1980.
7
Cloning of the ugp region containing the structural genes for the pho regulon-dependent sn-glycerol-3-phosphate transport system of Escherichia coli.大肠杆菌中受pho调节子依赖的sn-甘油-3-磷酸转运系统结构基因所在的ugp区域的克隆。
Mol Gen Genet. 1983;192(1-2):177-86. doi: 10.1007/BF00327664.
8
In vitro gene fusions that join an enzymatically active beta-galactosidase segment to amino-terminal fragments of exogenous proteins: Escherichia coli plasmid vectors for the detection and cloning of translational initiation signals.将具有酶活性的β-半乳糖苷酶片段与外源蛋白质的氨基末端片段连接的体外基因融合:用于检测和克隆翻译起始信号的大肠杆菌质粒载体。
J Bacteriol. 1980 Aug;143(2):971-80. doi: 10.1128/jb.143.2.971-980.1980.
9
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.
10
Location of the maltose A and B loci on the genetic map of Escherichia coli.麦芽糖A和B基因座在大肠杆菌遗传图谱上的位置。
J Bacteriol. 1966 Oct;92(4):1083-9. doi: 10.1128/jb.92.4.1083-1089.1966.