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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Cloning, overexpression, purification of bacteriocin enterocin-B and structural analysis, interaction determination of enterocin-A, B against pathogenic bacteria and human cancer cells
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Cloning, overexpression, purification of bacteriocin enterocin-B and structural analysis, interaction determination of enterocin-A, B against pathogenic bacteria and human cancer cells

机译:克隆,过度表达,纯化的菌肠肠蛋白-B和结构分析,肠素-A,B对致病菌和人癌细胞的相互作用测定

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In this present study, a gene (ent-B) encoding the bacteriocin enterocin-B was cloned, overexpressed and purified from Enterococcus faecium port. The molecular weight of the bacteriocin enterocin-B was observed around 7.2 kDa and exhibited antimicrobial activity against several human pathogenic bacteria. The antimicrobial activity of cloned enterocin-B was increased effectively by combining with another bacteriocin enterocin-A from the same microorganism. Protein-protein docking and molecular dynamics simulation studies revealed that the bacteriocin enterocin-B is interacting with enterocin-A and formation of a heterodimer (enterocin A + B). The heterodimer of bacteriocin enterocin-A + B exhibited potential anti-bacterial, anti-biofilm activity against Staphylococcus aureus, Acinetobacter baumannii, Listeria monocytogenes and Escherichia coli. The bacteriocin enterocin-B, A and heterodimer of bacteriocin enterocin A + B showed no haemolysis on human RBC cells. This is the first report that the cell growth inhibitory activity of the bacteriocin enterocin B against HeLa, HT-29 and AGS human cancer cells and this cell growth inhibitory activity was significantly increased when cancer cells treated with the heterodimer of bacteriocins enterocin-A + B. The cell growth inhibitory activity of the bacteriocin enterocin-B and the heterodimer of bacteriocin enterocin-A + B were not observed in non-cancerous INT-407 cells (intestinal epithelial cells). (C) 2018 Published by Elsevier B.V.
机译:在此研究中,将编码细菌肠道菌素-B的基因(ENT-B)克隆,过表达,并且从屎肠球菌端口纯化。细菌素肠道菌素-B的分子量为7.2左右kDa的观察,显示出抗微生物活性的几种人病原性细菌。克隆肠道菌素B的抗菌活性是通过用另一种细菌素肠道菌素-A从相同的微生物组合有效地增加。蛋白质 - 蛋白质对接和分子动力学模拟的研究显示,细菌肠道菌素-B与肠道菌素-A和形成异二聚体(肠道菌素A + B)进行交互。细菌肠道菌素-A + B的异源二聚体表现出潜在的抗细菌,抗生物膜活性的对金黄色葡萄球菌,鲍曼不动杆菌,李斯特菌和大肠杆菌。细菌素肠道菌素-B,A和细菌肠道菌素A + B的异源二聚体显示出对人RBC细胞没有溶血。这是第一份报告,对海拉细菌素肠道菌素B,HT-29和的细胞生长抑制活性AGS人癌细胞和该细胞的生长抑制活性显著增加当与细菌素的异源二聚体处理过的癌细胞肠道菌素-A + B 。在非癌INT-407细胞(肠上皮细胞)中没有观察到细菌素肠道菌素-B的细胞生长抑制活性和细菌肠道菌素-A + B的异源二聚体。 (c)2018由elestvier b.v出版。

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