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苜蓿根瘤菌nifA和fixK基因的氧调节体外转录

Oxygen-regulated in vitro transcription of Rhizobium meliloti nifA and fixK genes.

作者信息

Reyrat J M, David M, Blonski C, Boistard P, Batut J

机构信息

Laboratoire de Biologie Moléculaire des Relations Plantes-Microorganismes, CNRS-INRA, France.

出版信息

J Bacteriol. 1993 Nov;175(21):6867-72. doi: 10.1128/jb.175.21.6867-6872.1993.

Abstract

Oxygen concentration regulates the expression of nitrogen fixation genes in the symbiotic bacterium Rhizobium meliloti. We demonstrate that two proteins, FixL and FixJ, that belong to the two-component family of regulatory proteins are necessary and sufficient for oxygen-regulated in vitro transcription of the two key regulatory genes, nifA and fixK. We show directly that FixJ is a transcriptional activator, working in conjunction with the RNA polymerase sigma 70 holoenzyme. Addition of FixL122, a soluble form of the sensor FixL protein, to the transcription assay enhanced FixJ transcriptional activity in response to low oxygen concentration. This enhancement of FixJ activity was correlated with FixJ phosphorylation.

摘要

氧浓度调节共生细菌苜蓿根瘤菌中固氮基因的表达。我们证明,属于双组分调节蛋白家族的两种蛋白FixL和FixJ,对于两个关键调节基因nifA和fixK的氧调节体外转录是必需且充分的。我们直接表明,FixJ是一种转录激活因子,与RNA聚合酶σ70全酶协同作用。将传感器FixL蛋白的可溶形式FixL122添加到转录试验中,可增强FixJ在低氧浓度下的转录活性。FixJ活性的这种增强与FixJ磷酸化相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f06d/206811/90b673263de6/jbacter00063-0146-a.jpg

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