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天蓝色链霉菌GlnR调控子:新GlnR靶标的鉴定及GlnR在放线菌氮代谢中核心作用的证据

The Streptomyces coelicolor GlnR regulon: identification of new GlnR targets and evidence for a central role of GlnR in nitrogen metabolism in actinomycetes.

作者信息

Tiffert Yvonne, Supra Petra, Wurm Reinhild, Wohlleben Wolfgang, Wagner Rolf, Reuther Jens

机构信息

Mikrobiologie/Biotechnologie, Institut für Mikrobiologie, Fakultät für Biologie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 28, D-72076 Tübingen, Germany.

出版信息

Mol Microbiol. 2008 Feb;67(4):861-80. doi: 10.1111/j.1365-2958.2007.06092.x. Epub 2008 Jan 7.

Abstract

Streptomyces coelicolor GlnR is a global regulator that controls genes involved in nitrogen metabolism. By genomic screening 10 new GlnR targets were identified, including enzymes for ammonium assimilation (glnII, gdhA), nitrite reduction (nirB), urea cleavage (ureA) and a number of biochemically uncharacterized proteins (SCO0255, SCO0888, SCO2195, SCO2400, SCO2404, SCO7155). For the GlnR regulon, a GlnR binding site which comprises the sequence gTnAc-n(6)-GaAAc-n(6)-GtnAC-n(6)-GAAAc-n(6) has been found. Reverse transcription analysis of S. coelicolor and the S. coelicolor glnR mutant revealed that GlnR activates or represses the expression of its target genes. Furthermore, glnR expression itself was shown to be nitrogen-dependent. Physiological studies of S. coelicolor and the S. coelicolor glnR mutant with ammonium and nitrate as the sole nitrogen source revealed that GlnR is not only involved in ammonium assimilation but also in ammonium supply. blast analysis demonstrated that GlnR-homologous proteins are present in different actinomycetes containing the glnA gene with the conserved GlnR binding site. By DNA binding studies, it was furthermore demonstrated that S. coelicolor GlnR is able to interact with these glnA upstream regions. We therefore suggest that GlnR-mediated regulation is not restricted to Streptomyces but constitutes a regulon conserved in many actinomycetes.

摘要

天蓝色链霉菌GlnR是一种全局调节因子,可控制参与氮代谢的基因。通过基因组筛选,鉴定出10个新的GlnR靶标,包括铵同化酶(glnII、gdhA)、亚硝酸盐还原酶(nirB)、尿素裂解酶(ureA)以及一些生化特性未明确的蛋白质(SCO0255、SCO0888、SCO2195、SCO2400、SCO2404、SCO7155)。对于GlnR调控子,已发现一个GlnR结合位点,其序列为gTnAc-n(6)-GaAAc-n(6)-GtnAC-n(6)-GAAAc-n(6)。对天蓝色链霉菌及其glnR突变体的逆转录分析表明,GlnR可激活或抑制其靶基因的表达。此外,glnR表达本身显示出氮依赖性。以铵和硝酸盐作为唯一氮源对天蓝色链霉菌及其glnR突变体进行的生理学研究表明,GlnR不仅参与铵同化,还参与铵供应。blast分析表明,在含有具有保守GlnR结合位点的glnA基因的不同放线菌中存在GlnR同源蛋白。通过DNA结合研究进一步证明,天蓝色链霉菌GlnR能够与这些glnA上游区域相互作用。因此,我们认为GlnR介导的调控不仅限于链霉菌,而是构成了许多放线菌中保守的调控子。

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