首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Interplay between CedA, rpoB and double stranded DNA: A step towards understanding CedA mediated cell division in E. coli
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Interplay between CedA, rpoB and double stranded DNA: A step towards understanding CedA mediated cell division in E. coli

机译:CEDA,RPOB和双链DNA之间的相互作用:迈为在大肠杆菌中了解CEDA介导细胞分裂的步骤

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Cell division is compromised in DnaAcos mutant E. coli cells due to chromosome over-replication. In these cells, CedA acts as a regulatory protein and initiates cell division by a hitherto unknown mechanism. CedA, a double stranded DNA binding protein, interacts with various subunits of RNA polymerase complex,. including rpoB. To reveal how this concert between CedA, rpoB and DNA brings about cell division in E. coli, we performed biophysical and in silico analysis and obtained mechanistic insights. Interaction between CedA and rpoB was shown by circular dichroism spectrometry and in silico docking experiments. Further, CedA and rpoB were allowed to interact individually to a selected DNA and their binding was monitored by fluorescence spectroscopy. The binding constants of these interactions as determined by BioLayer Interferometry clearly show that rpoB binds to DNA with higher affinity (K-D2 = 1.0E-12 M) as compared to CedA (K-D2=9.58E-09M). These findings were supported by docking analysis where 12 intermolecular H-bonds were formed in rpoB-DNA complex as compared to 4 in CedA-DNA complex. Based on our data we propose that in E. coli cells chromosome over-replication signals CedA to recruit rpoB to specific DNA site(s), which initiates transcription of cell division regulatory elements. (C) 2017 Elsevier B.V. All rights reserved.
机译:由于染色体过度复制,细胞分裂在DNAAcos突变体大肠杆菌中受到损害。在这些细胞中,CEDA充当调节蛋白,并通过迄今未知的机制引发细胞分裂。 CEDA,双链DNA结合蛋白,与RNA聚合酶复合物的各种亚基相互作用。包括RPOB。为了揭示CEDA,RPOB和DNA之间的这种音乐会如何在大肠杆菌中引入细胞分裂,我们进行了生物物理和硅分析并获得了机械洞察力。 CEDA和RPOB之间的相互作用由圆形二分频谱光谱和硅基粘接实验显示。此外,使CEDA和RPOB被单独与所选DNA相互作用,并通过荧光光谱监测它们的结合。由Biolayer干涉测定法测定的这些相互作用的结合常数清楚地表明,与CEDA(K-D2 = 9.58E-09M)相比,RPOB与具有较高亲和力(K-D2 = <0E-12M)的DNA结合。通过对接分析支持这些发现,其中在RPOB-DNA复合物中形成12个分子间H键,与CEDA-DNA复合物相比。基于我们的数据,我们提出在大肠杆菌细胞染色体上过度复制信号CEDA募集RPOB至特异性DNA位点,其引发细胞分裂调节元件的转录。 (c)2017年Elsevier B.V.保留所有权利。

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