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首页> 外文期刊>Drug Design, Development and Therapy >Antibacterial of Dibenzo- p -Dioxi-2,8-Dicarboxylic Acid Against Pathogenic Oral Bacteria E. faecalis ATCC 29212 Peptide Pheromones: Quorum Sensing of in vitro and in silico Study
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Antibacterial of Dibenzo- p -Dioxi-2,8-Dicarboxylic Acid Against Pathogenic Oral Bacteria E. faecalis ATCC 29212 Peptide Pheromones: Quorum Sensing of in vitro and in silico Study

机译:抗菌性抗菌性抗菌性口腔细菌抗菌性抗菌剂E. FAECALIS ATCC 29212肽信息素:体外和硅研究的批量传感

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Background: Recently, it has emerged from the international scientific literature that quorum sensing (QS) is a promising way for the effective treatment of diseases caused by pathogenic bacteria. One of the crucial proteins in the QS system of Gram-positive bacteria is the pheromone. Some research has reported secondary metabolites from natural products capable of attenuating bacteria through the interruption of the quorum sensing system. One of the Indonesian herbal plants containing bioactive compounds is Sarang Semut ( Myrmecodia pendans ). A phenolic compound, dibenzo- p -dioxin-2,8-dicarboxylic acid, has been isolated from this plant which had antibacterial activity against Enterococcus faecalis . However, the molecular mechanism of it has not been known. Aim: The study in question aimed to predict the molecular action of the compound M. pendans against some proteins that act as a signal in the mediated QS of Gram-positive bacteria, called pheromones, including PrgQ, PrgX, PrgZ, and CcfA. Materials and Methods: The methods used in this in silico study were ligand-protein docking and virtual screening that were performed by some software and programs. The compound 1 and some positive controls act as ligand were subject binding to PrgQ, PrgX, PrgZ, and CcfA as proteins target, the ligands were free for blind docking. A framework was presented potency of phenolic compounds to inhibit the protein’s target from its affinity binding scores. Results: It was found thatcompound 1 was potential to inhibit all of the tested protein and gave the highest binding affinity to PrgX (? 9.2 kcal.mol? 1; the site at Phe59B, Phe59B, Asn63A, and Asn63B residue) and PrgZ (? 7.4 kcal.mol? 1; the site at Leu4B, Thr65A, Thr82A. Gln81A, and Val5B residue). Conclusion: It is proposed that compound 1 has a good activity to inhibit E. faecalis through its peptide pheromones in the QS system.
机译:背景:最近,它从国际科学文献中出现了法定感测(QS)是有效治疗致病菌引起的疾病的有希望的方式。 QS系统的QS阳性细菌系统中的一个关键蛋白是信息素。一些研究报告了通过仲裁传感系统的中断能够减弱细菌的天然产物中的次生代谢物。含有生物活性化合物的印度尼西亚草药植物之一是Sarang Sevut(Myrmecodia pendans)。酚类化合物二苯并苯-p-diOxin-2,8-二羧酸已从该植物中分离出对肠球菌粪便的抗菌活性。然而,它的分子机制尚不清楚。目的:有问题的研究旨在预测化合物M.Pendans对某些蛋白质的分子作用,该蛋白质在革兰氏阳性细菌的介导的QS中,称为信息素,包括PRGQ,PRGX,PRGZ和CCFA。材料和方法:其中在硅研究中使用的方法是由某些软件和程序执行的配体 - 蛋白对接和虚拟筛选。化合物1和一些阳性对照作为配体作为配体与PRGQ,PRGX,PRGZ和CCFA作为蛋白质靶标进行结合,使配体免于盲目对接。呈酚类化合物的效力呈效力,以抑制蛋白质的靶标的亲和力结合分数。结果:发现Compound 1是抑制所有测试蛋白的潜力,并给予PrGX的最高结合亲和力(α9.2kcal.molα1; PHE59B,PHE59B,ASN63A和ASN63B残留物的位点(? 7.4 kcal.mol?1; Leu4b,thr65a,thr82a的网站。gln81a和val5b残留物)。结论:提出了化合物1通过QS系统中的肽信息素抑制E.粪便的良好活性。

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