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用于研究大肠杆菌K-12中硝酸盐和亚硝酸盐响应性NarX-NarL和NarQ-NarP双组分调节系统的合成乳糖操纵子替代物。

Synthetic lac operator substitutions for studying the nitrate- and nitrite-responsive NarX-NarL and NarQ-NarP two-component regulatory systems of Escherichia coli K-12.

作者信息

Stewart Valley, Bledsoe Peggy J

机构信息

Section of Microbiology, University of California, Davis, California 95616-8665, USA.

出版信息

J Bacteriol. 2003 Apr;185(7):2104-11. doi: 10.1128/JB.185.7.2104-2111.2003.

Abstract

The NarX and NarQ sensor-histidine kinases control phosphorylation of the NarL and NarP response regulators in response to the respiratory oxidants nitrate and nitrite. Target operon transcription is activated by the Fnr protein in response to anaerobiosis, and it is further activated and/or repressed by the phospho-NarL and phospho-NarP proteins, which bind to heptamer DNA sequences. The location and arrangement of heptamers vary widely among different target operon control regions. We have constructed a series of monocopy lac operon control region constructs in which the primary operator O1-lac has been replaced by 7-2-7 heptamer pairs from the nrfA, nirB, napF, and fdnG operon control regions. These constructs provide tools for dissecting various aspects of ligand interactions with sensor-kinases, sensor interactions with response regulators, and phospho-response regulator interactions with DNA targets. Expression of the lacZ gene from these constructs was repressed to various degrees by nitrate and nitrite. In response to nitrate, the nrfA and nirB operon 7-2-7 heptamer pairs at operator O1 each mediated greater than 100-fold repression of lacZ gene expression, whereas the napF operon 7-2-7 heptamer pair mediated approximately tenfold repression. Introduction of narL, narP, narX, and narQ null alleles in various combinations allowed the in vivo interactions between different sensor-regulator pairs to be evaluated and compared.

摘要

NarX和NarQ传感组氨酸激酶可控制NarL和NarP反应调节因子的磷酸化,以响应呼吸性氧化剂硝酸盐和亚硝酸盐。靶操纵子转录由Fnr蛋白响应厌氧状态而激活,并且它会被与七聚体DNA序列结合的磷酸化NarL和磷酸化NarP蛋白进一步激活和/或抑制。七聚体的位置和排列在不同的靶操纵子控制区域之间差异很大。我们构建了一系列单拷贝lac操纵子控制区域构建体,其中主要操纵基因O1-lac已被来自nrfA、nirB、napF和fdnG操纵子控制区域的7-2-7七聚体对所取代。这些构建体为剖析配体与传感激酶的相互作用、传感蛋白与反应调节因子的相互作用以及磷酸化反应调节因子与DNA靶标的相互作用的各个方面提供了工具。这些构建体中lacZ基因的表达受到硝酸盐和亚硝酸盐不同程度的抑制。响应硝酸盐时,操纵基因O1处的nrfA和nirB操纵子7-2-7七聚体对各自介导lacZ基因表达超过100倍的抑制,而napF操纵子7-2-7七聚体对介导约10倍的抑制。以各种组合引入narL、narP、narX和narQ无效等位基因,可以评估和比较不同传感调节因子对之间的体内相互作用。

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