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在应对铁缺乏时,AraC样转录调节因子DhbR是布鲁氏菌2308中2,3 - 二羟基苯甲酸生物合成基因最大程度表达所必需的。

The AraC-like transcriptional regulator DhbR is required for maximum expression of the 2,3-dihydroxybenzoic acid biosynthesis genes in Brucella abortus 2308 in response to iron deprivation.

作者信息

Anderson Eric S, Paulley James T, Roop R Martin

机构信息

Department of Microbiology and Immunology, East Carolina University School of Medicine, 600 Moye Boulevard, Greenville, NC 27834, USA.

出版信息

J Bacteriol. 2008 Mar;190(5):1838-42. doi: 10.1128/JB.01551-07. Epub 2007 Dec 21.

DOI:10.1128/JB.01551-07
PMID:18156262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2258684/
Abstract

Phenotypic evaluation of isogenic mutants derived from Brucella abortus 2308 indicates that the AlcR homolog DhbR (2,3-dihydroxybenzoic acid [2,3-DHBA] biosynthesis regulator) modulates the expression of the genes involved in 2,3-DHBA production, employing 2,3-DHBA or brucebactin as a coinducer.

摘要

源自流产布鲁氏菌2308的同基因突变体的表型评估表明,AlcR同源物DhbR(2,3-二羟基苯甲酸[2,3-DHBA]生物合成调节因子)利用2,3-DHBA或brucebactin作为共诱导剂来调节参与2,3-DHBA产生的基因的表达。

相似文献

1
The AraC-like transcriptional regulator DhbR is required for maximum expression of the 2,3-dihydroxybenzoic acid biosynthesis genes in Brucella abortus 2308 in response to iron deprivation.在应对铁缺乏时,AraC样转录调节因子DhbR是布鲁氏菌2308中2,3 - 二羟基苯甲酸生物合成基因最大程度表达所必需的。
J Bacteriol. 2008 Mar;190(5):1838-42. doi: 10.1128/JB.01551-07. Epub 2007 Dec 21.
2
Genetic organization and iron-responsive regulation of the Brucella abortus 2,3-dihydroxybenzoic acid biosynthesis operon, a cluster of genes required for wild-type virulence in pregnant cattle.流产布鲁氏菌2,3-二羟基苯甲酸生物合成操纵子的遗传组织与铁响应调控,该操纵子是孕牛野生型毒力所需的一组基因。
Infect Immun. 2003 Apr;71(4):1794-803. doi: 10.1128/IAI.71.4.1794-1803.2003.
3
Irr regulates brucebactin and 2,3-dihydroxybenzoic acid biosynthesis, and is implicated in the oxidative stress resistance and intracellular survival of Brucella abortus.Irr调节brucebactin和2,3-二羟基苯甲酸的生物合成,并与牛布鲁氏菌的氧化应激抗性和细胞内存活有关。
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The siderophore 2,3-dihydroxybenzoic acid is not required for virulence of Brucella abortus in BALB/c mice.2,3-二羟基苯甲酸这种铁载体对于布鲁氏菌在BALB/c小鼠中的致病性并非必需。
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Production of the siderophore 2,3-dihydroxybenzoic acid is required for wild-type growth of Brucella abortus in the presence of erythritol under low-iron conditions in vitro.在体外低铁条件下,布鲁氏菌在赤藓糖醇存在时野生型生长需要产生铁载体2,3 - 二羟基苯甲酸。
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Brucella abortus strain 2308 produces brucebactin, a highly efficient catecholic siderophore.流产布鲁氏菌2308菌株产生brucebactin,一种高效的儿茶酚型铁载体。
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Identification of 2,3-dihydroxybenzoic acid as a Brucella abortus siderophore.鉴定2,3 - 二羟基苯甲酸为流产布鲁氏菌的铁载体。
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Effect of entF deletion on iron acquisition and erythritol metabolism by Brucella abortus 2308.entF 缺失对布鲁氏菌 2308 铁摄取和赤藓糖醇代谢的影响。
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Brucella abortus siderophore 2,3-dihydroxybenzoic acid (DHBA) facilitates intracellular survival of the bacteria.流产布鲁氏菌铁载体2,3-二羟基苯甲酸(DHBA)有助于该细菌在细胞内存活。
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The bhuQ gene encodes a heme oxygenase that contributes to the ability of Brucella abortus 2308 to use heme as an iron source and is regulated by Irr.bhuQ基因编码一种血红素加氧酶,该酶有助于布鲁氏菌2308利用血红素作为铁源,并受Irr调控。
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本文引用的文献

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Brucella abortus requires the heme transporter BhuA for maintenance of chronic infection in BALB/c mice.布鲁氏菌流产亚种在BALB/c小鼠中维持慢性感染需要血红素转运蛋白BhuA。
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PchR-box recognition by the AraC-type regulator PchR of Pseudomonas aeruginosa requires the siderophore pyochelin as an effector.铜绿假单胞菌的AraC型调节因子PchR对PchR-box的识别需要铁载体绿脓菌素作为效应物。
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Genetic organization and iron-responsive regulation of the Brucella abortus 2,3-dihydroxybenzoic acid biosynthesis operon, a cluster of genes required for wild-type virulence in pregnant cattle.流产布鲁氏菌2,3-二羟基苯甲酸生物合成操纵子的遗传组织与铁响应调控,该操纵子是孕牛野生型毒力所需的一组基因。
Infect Immun. 2003 Apr;71(4):1794-803. doi: 10.1128/IAI.71.4.1794-1803.2003.
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RirA, an iron-responsive regulator in the symbiotic bacterium Rhizobium leguminosarum.RirA,一种豆科根瘤菌共生细菌中的铁响应调节因子。
Microbiology (Reading). 2002 Dec;148(Pt 12):4059-4071. doi: 10.1099/00221287-148-12-4059.
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Brucella abortus siderophore 2,3-dihydroxybenzoic acid (DHBA) facilitates intracellular survival of the bacteria.流产布鲁氏菌铁载体2,3-二羟基苯甲酸(DHBA)有助于该细菌在细胞内存活。
Microb Pathog. 2002 May;32(5):239-48. doi: 10.1006/mpat.2002.0500.