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1
Control of bacterial alkaline phosphatase synthesis and variation in an Escherichia coli K-12 phoR mutant by adenyl cyclase, the cyclic AMP receptor protein, and the phoM operon.通过腺苷酸环化酶、环磷酸腺苷受体蛋白和phoM操纵子对大肠杆菌K-12 phoR突变体中细菌碱性磷酸酶合成及变异的控制
J Bacteriol. 1988 Mar;170(3):1092-102. doi: 10.1128/jb.170.3.1092-1102.1988.
2
Molecular cloning of the wild-type phoM operon in Escherichia coli K-12.大肠杆菌K-12中野生型phoM操纵子的分子克隆
J Bacteriol. 1988 Jan;170(1):279-88. doi: 10.1128/jb.170.1.279-288.1988.
3
Cloning and characterization of the alkaline phosphatase positive regulatory gene (phoM) of Escherichia coli.大肠杆菌碱性磷酸酶正调控基因(phoM)的克隆与特性分析
Mol Gen Genet. 1984;195(3):381-90. doi: 10.1007/BF00341438.
4
Control of phoR-dependent bacterial alkaline phosphatase clonal variation by the phoM region.phoM区域对phoR依赖性细菌碱性磷酸酶克隆变异的控制
J Bacteriol. 1987 Feb;169(2):900-3. doi: 10.1128/jb.169.2.900-903.1987.
5
Cloning of phoM, a gene involved in regulation of the synthesis of phosphate limitation inducible proteins in Escherichia coli K12.大肠杆菌K12中参与磷酸盐限制诱导蛋白合成调控的phoM基因的克隆。
Mol Gen Genet. 1984;195(1-2):190-4. doi: 10.1007/BF00332745.
6
Overlapping and separate controls on the phosphate regulon in Escherichia coli K12.大肠杆菌K12中磷酸调节子的重叠和独立调控
J Mol Biol. 1983 May 25;166(3):283-308. doi: 10.1016/s0022-2836(83)80086-2.
7
Mutants affected in alkaline phosphatase, expression: evidence for multiple positive regulators of the phosphate regulon in Escherichia coli.碱性磷酸酶表达受影响的突变体:大肠杆菌中磷酸调节子多个正调控因子的证据
Genetics. 1980 Oct;96(2):353-66. doi: 10.1093/genetics/96.2.353.
8
Bacterial alkaline phosphatase clonal variation in some Escherichia coli K-12 phoR mutant strains.一些大肠杆菌K-12 phoR突变菌株中细菌碱性磷酸酶的克隆变异。
J Bacteriol. 1986 Dec;168(3):1366-71. doi: 10.1128/jb.168.3.1366-1371.1986.
9
Negative regulation of adenylate cyclase gene (cya) expression by cyclic AMP-cyclic AMP receptor protein in Escherichia coli: studies with cya-lac protein and operon fusion plasmids.环腺苷酸-环腺苷酸受体蛋白对大肠杆菌中腺苷酸环化酶基因(cya)表达的负调控:利用cya-lac蛋白和操纵子融合质粒的研究
J Bacteriol. 1985 Nov;164(2):872-7. doi: 10.1128/jb.164.2.872-877.1985.
10
[Effect of mutation in phoB and phoM genes for the positive control of alkaline phosphatase biosynthesis on Escherichia coli envelope proteins].[phoB和phoM基因中的突变对碱性磷酸酶生物合成的正向调控作用对大肠杆菌包膜蛋白的影响]
Mol Biol (Mosk). 1986 Sep-Oct;20(5):1290-8.

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Effective Small Molecule Antibacterials from a Novel Anti-Protein Secretion Screen.通过新型抗蛋白质分泌筛选获得的有效小分子抗菌剂。
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Metabolic Regulation of a Bacterial Cell System with Emphasis on Escherichia coli Metabolism.细菌细胞系统的代谢调控,重点是大肠杆菌的代谢
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Proc Natl Acad Sci U S A. 2013 Oct 8;110(41):16592-7. doi: 10.1073/pnas.1315320110. Epub 2013 Sep 23.
6
Metabolic regulation of Escherichia coli and its phoB and phoR genes knockout mutants under phosphate and nitrogen limitations as well as at acidic condition.在磷和氮限制以及酸性条件下,对大肠杆菌及其 phoB 和 phoR 基因敲除突变体的代谢调控。
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7
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Mol Microbiol. 2008 Oct;70(2):494-506. doi: 10.1111/j.1365-2958.2008.06426.x. Epub 2008 Aug 29.
8
Defining the growth conditions and promoter-proximal DNA sequences required for activation of gene expression by CreBC in Escherichia coli.确定大肠杆菌中CreBC激活基因表达所需的生长条件和启动子近端DNA序列。
J Bacteriol. 2008 Jun;190(11):3930-9. doi: 10.1128/JB.00108-08. Epub 2008 Mar 28.
9
Inactivation of the pst system reduces the virulence of an avian pathogenic Escherichia coli O78 strain.pst系统的失活降低了禽致病性大肠杆菌O78菌株的毒力。
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10
Identification of a regulated alkaline phosphatase, a cell surface-associated lipoprotein, in Mycobacterium smegmatis.耻垢分枝杆菌中一种受调控的碱性磷酸酶(一种细胞表面相关脂蛋白)的鉴定。
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本文引用的文献

1
Mutants affected in alkaline phosphatase, expression: evidence for multiple positive regulators of the phosphate regulon in Escherichia coli.碱性磷酸酶表达受影响的突变体:大肠杆菌中磷酸调节子多个正调控因子的证据
Genetics. 1980 Oct;96(2):353-66. doi: 10.1093/genetics/96.2.353.
2
Phosphate-controlled gene expression in Escherichia coli K12 using Mudl-directed lacZ fusions.利用Mudl定向的lacZ融合技术研究大肠杆菌K12中磷酸盐控制的基因表达。
J Mol Biol. 1982 Jul 5;158(3):347-63. doi: 10.1016/0022-2836(82)90202-9.
3
Cyclic AMP receptor protein: role in transcription activation.环磷酸腺苷受体蛋白:在转录激活中的作用。
Science. 1984 May 25;224(4651):831-8. doi: 10.1126/science.6372090.
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Conditionally transposition-defective derivative of Mu d1(Amp Lac).Mu d1(Amp Lac)的条件性转座缺陷衍生物
J Bacteriol. 1984 Jul;159(1):130-7. doi: 10.1128/jb.159.1.130-137.1984.
5
Cloning and insertional inactivation of the dye (sfrA) gene, mutation of which affects sex factor F expression and dye sensitivity of Escherichia coli K-12.染料(sfrA)基因的克隆与插入失活,该基因的突变会影响性因子F的表达及大肠杆菌K-12对染料的敏感性。
J Bacteriol. 1983 Jun;154(3):1309-14. doi: 10.1128/jb.154.3.1309-1314.1983.
6
Determining the phoM map location in Escherichia coli K-12 by using a nearby transposon Tn10 insertion.通过利用附近的转座子Tn10插入来确定大肠杆菌K-12中phoM的图谱位置。
J Bacteriol. 1982 Apr;150(1):429-32. doi: 10.1128/jb.150.1.429-432.1982.
7
Use of bacteriophage transposon Mu d1 to determine the orientation for three proC-linked phosphate-starvation-inducible (psi) genes in Escherichia coli K-12.利用噬菌体转座子Mu d1确定大肠杆菌K-12中三个与proC相连的磷酸盐饥饿诱导(psi)基因的方向。
J Bacteriol. 1981 Apr;146(1):93-101. doi: 10.1128/jb.146.1.93-101.1981.
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Phase variation: evolution of a controlling element.相变:一种控制元件的进化
Science. 1980 Sep 19;209(4463):1370-4. doi: 10.1126/science.6251543.
9
General method, using Mu-Mud1 dilysogens, to determine the direction of transcription of and generate deletions in the glnA region of Escherichia coli.使用Mu-Mud1双溶原菌确定大肠杆菌谷氨酰胺合成酶基因(glnA)区域转录方向并产生缺失的通用方法。
J Bacteriol. 1981 Apr;146(1):260-8. doi: 10.1128/jb.146.1.260-268.1981.
10
Genetic characterization of mutations which affect catabolite-sensitive operons in Escherichia coli, including deletions of the gene for adenyl cyclase.影响大肠杆菌中分解代谢物敏感操纵子的突变的遗传特征分析,包括腺苷酸环化酶基因的缺失。
J Bacteriol. 1973 Nov;116(2):582-7. doi: 10.1128/jb.116.2.582-587.1973.

通过腺苷酸环化酶、环磷酸腺苷受体蛋白和phoM操纵子对大肠杆菌K-12 phoR突变体中细菌碱性磷酸酶合成及变异的控制

Control of bacterial alkaline phosphatase synthesis and variation in an Escherichia coli K-12 phoR mutant by adenyl cyclase, the cyclic AMP receptor protein, and the phoM operon.

作者信息

Wanner B L, Wilmes M R, Young D C

机构信息

Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907.

出版信息

J Bacteriol. 1988 Mar;170(3):1092-102. doi: 10.1128/jb.170.3.1092-1102.1988.

DOI:10.1128/jb.170.3.1092-1102.1988
PMID:3277944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC210878/
Abstract

Mutant phoR cells show a clonal variation phenotype with respect to bacterial alkaline phosphatase (BAP) synthesis. BAP clonal variation is characterized by an alternation between a Bap+ and Bap- phenotype. The switching is regulated by the phoM operon and the presence of glucose; the pho-510 mutant form of the phoM operon abolishes both BAP clonal variation and the effect of glucose (B.L. Wanner, J. Bacteriol. 169:900-903, 1987). In this paper we show that a mutation of the adenyl cyclase (cya) and the cyclic AMP receptor protein (crp) gene also abolish BAP clonal variation; either simultaneously reduces the amount of BAP made in phoR mutants. Also, the pho-510 mutation is epistatic; it increases BAP synthesis in delta cya phoR and delta crp phoR mutants. These data are consistent with the wild-type phoM operon having a negative, as well as a positive, regulatory role in gene expression. Furthermore, the data suggest that adenyl cyclase and Crp indirectly regulate BAP synthesis in a phoR mutant via an interaction with the phoM operon or its gene products. However, phoM operon expression was unaffected when tested with phoM operon lacZ transcriptional fusions. In addition, the switching Bap phenotype was not associated with an alternation in phoM operon expression.

摘要

突变型phoR细胞在细菌碱性磷酸酶(BAP)合成方面表现出克隆变异表型。BAP克隆变异的特征是Bap+和Bap-表型之间的交替。这种转换受phoM操纵子和葡萄糖的存在调控;phoM操纵子的pho - 510突变形式消除了BAP克隆变异和葡萄糖的影响(B.L. 万纳,《细菌学杂志》169:900 - 903,1987)。在本文中,我们表明腺苷酸环化酶(cya)和环腺苷酸受体蛋白(crp)基因的突变也消除了BAP克隆变异;二者同时降低了phoR突变体中BAP的合成量。此外,pho - 510突变是上位性的;它增加了δcya phoR和δcrp phoR突变体中BAP的合成。这些数据与野生型phoM操纵子在基因表达中具有负调控以及正调控作用一致。此外,数据表明腺苷酸环化酶和Crp通过与phoM操纵子或其基因产物的相互作用间接调节phoR突变体中BAP的合成。然而,用phoM操纵子lacZ转录融合体检测时,phoM操纵子的表达未受影响。此外,Bap表型的转换与phoM操纵子表达的交替无关。