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大肠杆菌谷氨酸依赖性耐酸基因gadA和gadBC在hns rpoS突变体中的转录表达

Transcriptional expression of Escherichia coli glutamate-dependent acid resistance genes gadA and gadBC in an hns rpoS mutant.

作者信息

Waterman Scott R, Small P L C

机构信息

Division of Human Immunology, Hanson Institute, Institute of Medical and Veterinary Science, Adelaide, South Australia, 5000, Australia.

出版信息

J Bacteriol. 2003 Aug;185(15):4644-7. doi: 10.1128/JB.185.15.4644-4647.2003.

DOI:10.1128/JB.185.15.4644-4647.2003
PMID:12867478
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC165754/
Abstract

Resistance to being killed by acidic environments with pH values lower than 3 is an important feature of both pathogenic and nonpathogenic Escherichia coli. The most potent E. coli acid resistance system utilizes two isoforms of glutamate decarboxylase encoded by gadA and gadB and a putative glutamate:gamma-aminobutyric acid antiporter encoded by gadC. The gad system is controlled by two repressors (H-NS and CRP), one activator (GadX), one repressor-activator (GadW), and two sigma factors (sigma(S) and sigma(70)). In contrast to results of previous reports, we demonstrate that gad transcription can be detected in an hns rpoS mutant strain of E. coli K-12, indicating that gad promoters can be initiated by sigma(70) in the absence of H-NS.

摘要

对pH值低于3的酸性环境具有抗性是致病性和非致病性大肠杆菌的一个重要特征。最有效的大肠杆菌酸抗性系统利用由gadA和gadB编码的两种谷氨酸脱羧酶同工型,以及由gadC编码的一种假定的谷氨酸:γ-氨基丁酸反向转运体。gad系统由两个阻遏物(H-NS和CRP)、一个激活剂(GadX)、一个阻遏物-激活剂(GadW)和两个σ因子(σ(S)和σ(70))控制。与之前报道的结果相反,我们证明在大肠杆菌K-12的hns rpoS突变株中可以检测到gad转录,这表明在没有H-NS的情况下,gad启动子可以由σ(70)启动。

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本文引用的文献

1
Collaborative regulation of Escherichia coli glutamate-dependent acid resistance by two AraC-like regulators, GadX and GadW (YhiW).两种AraC样调节因子GadX和GadW(YhiW)对大肠杆菌谷氨酸依赖性酸抗性的协同调节
J Bacteriol. 2002 Dec;184(24):7001-12. doi: 10.1128/JB.184.24.7001-7012.2002.
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Gene expression profiling of the pH response in Escherichia coli.大肠杆菌中pH响应的基因表达谱分析。
J Bacteriol. 2002 Dec;184(23):6551-8. doi: 10.1128/JB.184.23.6551-6558.2002.
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Functional characterization and regulation of gadX, a gene encoding an AraC/XylS-like transcriptional activator of the Escherichia coli glutamic acid decarboxylase system.gadX基因的功能表征与调控,该基因编码大肠杆菌谷氨酸脱羧酶系统的一种AraC/XylS样转录激活因子。
J Bacteriol. 2002 May;184(10):2603-13. doi: 10.1128/JB.184.10.2603-2613.2002.
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An activator of glutamate decarboxylase genes regulates the expression of enteropathogenic Escherichia coli virulence genes through control of the plasmid-encoded regulator, Per.谷氨酸脱羧酶基因激活剂通过控制质粒编码的调节因子Per来调节肠致病性大肠杆菌毒力基因的表达。
Mol Microbiol. 2001 Sep;41(5):1133-50. doi: 10.1046/j.1365-2958.2001.02570.x.
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Large-scale monitoring of pleiotropic regulation of gene expression by the prokaryotic nucleoid-associated protein, H-NS.对原核生物类核相关蛋白H-NS对基因表达的多效性调控进行大规模监测。
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6
Escherichia coli acid resistance: cAMP receptor protein and a 20 bp cis-acting sequence control pH and stationary phase expression of the gadA and gadBC glutamate decarboxylase genes.大肠杆菌的酸抗性:环腺苷酸受体蛋白和一个20碱基对的顺式作用序列控制gadA和gadBC谷氨酸脱羧酶基因在pH值和稳定期的表达。
Microbiology (Reading). 2001 Mar;147(Pt 3):709-715. doi: 10.1099/00221287-147-3-709.
7
The response to stationary-phase stress conditions in Escherichia coli: role and regulation of the glutamic acid decarboxylase system.大肠杆菌中对稳定期应激条件的应答:谷氨酸脱羧酶系统的作用与调控
Mol Microbiol. 1999 Jun;32(6):1198-211. doi: 10.1046/j.1365-2958.1999.01430.x.
8
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J Bacteriol. 1999 Jun;181(11):3525-35. doi: 10.1128/JB.181.11.3525-3535.1999.
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Mol Gen Genet. 1997 Oct;256(4):333-47. doi: 10.1007/s004380050577.