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本文引用的文献

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Escherichia coli physiology in Luria-Bertani broth.大肠杆菌在吕氏肉汤中的生理学特性。
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2
The intracellular concentration of acetyl phosphate in Escherichia coli is sufficient for direct phosphorylation of two-component response regulators.大肠杆菌中乙酰磷酸的细胞内浓度足以使双组分响应调节因子直接磷酸化。
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Novel gene members in the Pho regulon of Escherichia coli.大肠杆菌Pho调节子中的新基因成员。
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Mechanism of activation for transcription factor PhoB suggested by different modes of dimerization in the inactive and active states.转录因子PhoB在非活性状态和活性状态下通过不同二聚化模式实现激活的机制。
Structure. 2005 Sep;13(9):1353-63. doi: 10.1016/j.str.2005.06.006.
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Role of the 'cre/blr-tag' DNA sequence in regulation of gene expression by the Aeromonas hydrophila beta-lactamase regulator, BlrA.
J Antimicrob Chemother. 2004 Feb;53(2):197-202. doi: 10.1093/jac/dkh077. Epub 2004 Jan 16.
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Genetic linkage of the penicillinase gene, amp, and blrAB, encoding the regulator of beta-lactamase expression in Aeromonas spp.青霉素酶基因(amp)与blrAB的遗传连锁,blrAB编码气单胞菌属中β-内酰胺酶表达的调节因子。
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Transcriptome analysis of all two-component regulatory system mutants of Escherichia coli K-12.大肠杆菌K-12所有双组分调节系统突变体的转录组分析
Mol Microbiol. 2002 Oct;46(1):281-91. doi: 10.1046/j.1365-2958.2002.03170.x.
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Tandem DNA recognition by PhoB, a two-component signal transduction transcriptional activator.PhoB对串联DNA的识别,一种双组分信号转导转录激活因子。
Structure. 2002 May;10(5):701-13. doi: 10.1016/s0969-2126(02)00761-x.
9
Escherichia coli CreBC is a global regulator of gene expression that responds to growth in minimal media.大肠杆菌CreBC是一种基因表达的全局调节因子,可响应在基本培养基中的生长。
J Biol Chem. 2001 Jul 20;276(29):26955-61. doi: 10.1074/jbc.M011186200. Epub 2001 May 11.
10
The unphosphorylated receiver domain of PhoB silences the activity of its output domain.PhoB的未磷酸化受体结构域会使其输出结构域的活性沉默。
J Bacteriol. 2000 Dec;182(23):6592-7. doi: 10.1128/JB.182.23.6592-6597.2000.

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。

Defining the growth conditions and promoter-proximal DNA sequences required for activation of gene expression by CreBC in Escherichia coli.

作者信息

Cariss S James L, Tayler Amy E, Avison Matthew B

机构信息

Department of Cellular & Molecular Medicine, University of Bristol, School of Medical Sciences, University Walk, Bristol BS8 1TD, United Kingdom.

出版信息

J Bacteriol. 2008 Jun;190(11):3930-9. doi: 10.1128/JB.00108-08. Epub 2008 Mar 28.

DOI:10.1128/JB.00108-08
PMID:18375564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2395042/
Abstract

CreBC is a two-component system that controls the expression of a number of genes in Escherichia coli (called the cre regulon) that encode diverse functions, including intermediary metabolic enzymes. Using a reporter construct, we have shown that cre regulon gene expression is activated during growth in minimal media when glycolytic carbon sources are being fermented. It also is activated during aerobic growth when fermentation products are being used as carbon sources. CreB and CreC are essential for the activation of cre regulon gene expression, but CreA and CreD, encoded as part of the creABCD gene cluster, are not. CreB binds to a TTCACnnnnnnTTCAC direct repeat (the cre tag) in vitro, and this sequence, which is associated with cre regulon gene promoters, is required for the control of gene expression in vivo. These observations support the hypothesis that CreBC is a functional two-component system involved in the metabolic control of transcription in E. coli and confirm that CreB is a DNA binding transcriptional regulator.

摘要

CreBC是一种双组分系统,可控制大肠杆菌中许多基因(称为cre调节子)的表达,这些基因编码多种功能,包括中间代谢酶。使用报告构建体,我们已经表明,当糖酵解碳源被发酵时,cre调节子基因表达在基本培养基中生长期间被激活。当发酵产物被用作碳源时,它在有氧生长期间也被激活。CreB和CreC对于cre调节子基因表达的激活至关重要,但作为creABCD基因簇一部分编码的CreA和CreD则不然。CreB在体外与TTCACnnnnnnTTCAC直接重复序列(cre标签)结合,并且该序列与cre调节子基因启动子相关,是体内基因表达控制所必需的。这些观察结果支持以下假设:CreBC是一种参与大肠杆菌转录代谢控制的功能性双组分系统,并证实CreB是一种DNA结合转录调节因子。