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1
Heat shock-dependent transcriptional activation of the metA gene of Escherichia coli.大肠杆菌metA基因的热休克依赖性转录激活。
J Bacteriol. 1995 Mar;177(5):1374-9. doi: 10.1128/jb.177.5.1374-1379.1995.
2
Adaptation of Escherichia coli to elevated temperatures: the metA gene product is a heat shock protein.大肠杆菌对高温的适应性:metA基因产物是一种热休克蛋白。
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3
[Genetic regulation of the heat-shock response in Escherichia coli].[大肠杆菌热休克反应的遗传调控]
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4
Stress-induced expression of the Escherichia coli phage shock protein operon is dependent on sigma 54 and modulated by positive and negative feedback mechanisms.应激诱导的大肠杆菌噬菌体休克蛋白操纵子的表达依赖于σ54,并受正反馈和负反馈机制调节。
Genes Dev. 1991 Oct;5(10):1912-23. doi: 10.1101/gad.5.10.1912.
5
A distinct segment of the sigma 32 polypeptide is involved in DnaK-mediated negative control of the heat shock response in Escherichia coli.西格玛32多肽的一个独特片段参与了大肠杆菌中DnaK介导的热休克反应的负调控。
Proc Natl Acad Sci U S A. 1994 Oct 25;91(22):10280-4. doi: 10.1073/pnas.91.22.10280.
6
Methionine biosynthesis in Agrobacterium tumefaciens: study of the first enzyme.根瘤农杆菌蛋氨酸生物合成途径:第一酶的研究。
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7
Heat shock regulatory gene rpoH mRNA level increases after heat shock in Escherichia coli.热休克调节基因rpoH的mRNA水平在大肠杆菌热休克后升高。
J Bacteriol. 1986 Dec;168(3):1155-8. doi: 10.1128/jb.168.3.1155-1158.1986.
8
Transcription of the ibpB heat-shock gene is under control of sigma(32)- and sigma(54)-promoters, a third regulon of heat-shock response.ibpB热休克基因的转录受σ(32)和σ(54)启动子的控制,这是热休克反应的第三个调控子。
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Enzyme-catalyzed acylation of homoserine: mechanistic characterization of the Escherichia coli metA-encoded homoserine transsuccinylase.酶催化的高丝氨酸酰化作用:大肠杆菌metA编码的高丝氨酸转琥珀酰酶的机制表征
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Transcriptional regulation of stress-inducible genes in procaryotes.原核生物中应激诱导基因的转录调控
EXS. 1996;77:165-81. doi: 10.1007/978-3-0348-9088-5_11.

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MetA is a "thermal fuse" that inhibits growth and protects Escherichia coli at elevated temperatures.MetA 是一种“热熔断物”,可在高温下抑制大肠杆菌的生长并对其提供保护。
Cell Rep. 2022 Aug 30;40(9):111290. doi: 10.1016/j.celrep.2022.111290.
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Heat-responsive and time-resolved transcriptome and metabolome analyses of Escherichia coli uncover thermo-tolerant mechanisms.热响应和时分辨转录组和代谢组分析揭示了大肠杆菌的耐热机制。
Sci Rep. 2020 Oct 19;10(1):17715. doi: 10.1038/s41598-020-74606-8.
3
Heat shock and prolonged heat stress attenuate neurotoxin and sporulation gene expression in group I Clostridium botulinum strain ATCC 3502.热休克和长时间热应激会减弱I型肉毒梭菌ATCC 3502菌株中神经毒素和芽孢形成基因的表达。
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Stabilization of homoserine-O-succinyltransferase (MetA) decreases the frequency of persisters in Escherichia coli under stressful conditions.高丝氨酸-O-琥珀酰基转移酶(MetA)的稳定化降低了应激条件下大肠杆菌中持留菌的频率。
PLoS One. 2014 Oct 17;9(10):e110504. doi: 10.1371/journal.pone.0110504. eCollection 2014.
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Potential for development of an Escherichia coli-based biosensor for assessing bioavailable methionine: a review.基于大肠杆菌的生物传感器评估生物可利用蛋氨酸的发展潜力:综述。
Sensors (Basel). 2010;10(4):3562-84. doi: 10.3390/s100403562. Epub 2010 Apr 8.
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Regulated proteolysis in Gram-negative bacteria--how and when?革兰氏阴性细菌中的调控蛋白水解——如何及何时发生?
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7
Analysis of protein expression profiles of Halobacillus dabanensis D-8T under optimal and high salinity conditions.达坂盐芽孢杆菌D-8T在最适盐度和高盐度条件下的蛋白质表达谱分析
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8
Regulon and promoter analysis of the E. coli heat-shock factor, sigma32, reveals a multifaceted cellular response to heat stress.大肠杆菌热休克因子sigma32的调控子和启动子分析揭示了细胞对热应激的多方面反应。
Genes Dev. 2006 Jul 1;20(13):1776-89. doi: 10.1101/gad.1428206.
9
The Escherichia coli proteome: past, present, and future prospects.大肠杆菌蛋白质组:过去、现在及未来展望
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10
DegS is necessary for virulence and is among extraintestinal Escherichia coli genes induced in murine peritonitis.DegS对于毒力是必需的,并且属于在小鼠腹膜炎中诱导表达的肠外大肠杆菌基因。
Infect Immun. 2003 Jun;71(6):3088-96. doi: 10.1128/IAI.71.6.3088-3096.2003.

本文引用的文献

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Mutants of Escherichia coli requiring methionine or vitamin B12.需要甲硫氨酸或维生素B12的大肠杆菌突变体。
J Bacteriol. 1950 Jul;60(1):17-28. doi: 10.1128/jb.60.1.17-28.1950.
2
Transcription of the Escherichia coli rrnB P1 promoter by the heat shock RNA polymerase (E sigma 32) in vitro.体外热休克RNA聚合酶(E sigma 32)对大肠杆菌rrnB P1启动子的转录。
J Bacteriol. 1993 Feb;175(3):661-8. doi: 10.1128/jb.175.3.661-668.1993.
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Regulation of the Escherichia coli heat-shock response.大肠杆菌热休克反应的调控
Mol Microbiol. 1993 Aug;9(4):671-80. doi: 10.1111/j.1365-2958.1993.tb01727.x.
4
Heat shock regulatory gene htpR influences rates of protein degradation and expression of the lon gene in Escherichia coli.热休克调节基因htpR影响大肠杆菌中蛋白质降解速率和lon基因的表达。
Proc Natl Acad Sci U S A. 1984 Nov;81(21):6647-51. doi: 10.1073/pnas.81.21.6647.
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The htpR gene product of E. coli is a sigma factor for heat-shock promoters.大肠杆菌的htpR基因产物是热休克启动子的一种σ因子。
Cell. 1984 Sep;38(2):383-90. doi: 10.1016/0092-8674(84)90493-8.
6
Transcription from a heat-inducible promoter causes heat shock regulation of the sigma subunit of E. coli RNA polymerase.来自热诱导启动子的转录导致大肠杆菌RNA聚合酶σ亚基的热休克调节。
Cell. 1984 Sep;38(2):371-81. doi: 10.1016/0092-8674(84)90492-6.
7
Overlapping promoters transcribed by bacillus subtilis sigma 55 and sigma 37 RNA polymerase holoenzymes during growth and stationary phases.枯草芽孢杆菌σ55和σ37 RNA聚合酶全酶在生长和稳定期转录的重叠启动子。
J Biol Chem. 1984 Jul 10;259(13):8619-25.
8
Structure and autoregulation of the metJ regulatory gene in Escherichia coli.大肠杆菌中metJ调控基因的结构与自动调节
J Biol Chem. 1984 Nov 25;259(22):14282-5.
9
Regulatory region of the metA gene of Escherichia coli K-12.大肠杆菌K-12 metA基因的调控区域。
J Bacteriol. 1984 Dec;160(3):1158-62. doi: 10.1128/jb.160.3.1158-1162.1984.
10
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.

大肠杆菌metA基因的热休克依赖性转录激活。

Heat shock-dependent transcriptional activation of the metA gene of Escherichia coli.

作者信息

Biran D, Brot N, Weissbach H, Ron E Z

机构信息

Department of Molecular Microbiology and Biotechnology, Tel-Aviv University, Israel.

出版信息

J Bacteriol. 1995 Mar;177(5):1374-9. doi: 10.1128/jb.177.5.1374-1379.1995.

DOI:10.1128/jb.177.5.1374-1379.1995
PMID:7868613
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC176745/
Abstract

In Escherichia coli, the growth rate at elevated temperatures is controlled by the availability of endogenous methionine, which is limited because of the temperature sensitivity of the metA gene product, homoserine transsuccinylase (HTS). In order to determine the relationship between this control mechanism and the heat shock response, we estimated the cellular levels of HTS during heat shock by Western (immunoblot) analysis and found an increase following induction by temperature shift and by addition of ethanol or cadmium ions. The elevated level of HTS was a result of transcriptional activation of the metA gene. This activation was heat shock dependent, as it did not take place in rpoH mutants, and probably specific to the metA gene, as another gene of the methionine regulon (metE) was not activated. These results suggest a metabolic link between the two systems that control the response of E. coli to elevated temperatures: the metA gene, which codes for the enzyme responsible for regulating cell growth as a function of temperature elevation (HTS), is transcriptionally activated by the heat shock response.

摘要

在大肠杆菌中,高温下的生长速率受内源性甲硫氨酸可用性的控制,由于metA基因产物高丝氨酸转琥珀酰酶(HTS)对温度敏感,内源性甲硫氨酸的量有限。为了确定这种控制机制与热休克反应之间的关系,我们通过蛋白质免疫印迹分析估计了热休克期间HTS的细胞水平,发现温度变化、添加乙醇或镉离子诱导后其水平升高。HTS水平的升高是metA基因转录激活的结果。这种激活依赖于热休克,因为它在rpoH突变体中不发生,并且可能是metA基因特有的,因为甲硫氨酸调节子的另一个基因(metE)未被激活。这些结果表明,控制大肠杆菌对高温反应的两个系统之间存在代谢联系:编码负责根据温度升高调节细胞生长的酶(HTS)的metA基因,被热休克反应转录激活。