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α-氨基膦酸酯的合成及分子对接研究作为潜在的多靶点抗菌药物。

Synthesis and molecular docking study of α-aminophosphonates as potential multi-targeting antibacterial agents.

机构信息

Beijing Key Laboratory of Ionic Liquids Clean Process, CAS Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academy of Sciences, 100190 Beijing, China; College of Chemical Engineering, University of Chinese Academy of Sciences, 19 A Yuquan Road, 100049 Beijing, China; School of Chemistry and Chemical Engineering, University of Chinese Academy of Sciences, 100049 Beijing, China.

College of Chemical Engineering, University of Chinese Academy of Sciences, 19 A Yuquan Road, 100049 Beijing, China; CAS Key Laboratory of Green Process and Engineering & State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China; Aquatic microbiology department, Faculty of Chemistry, University of Duisburg-Essen, 45141 Essen, Germany.

出版信息

J Hazard Mater. 2024 Mar 5;465:133203. doi: 10.1016/j.jhazmat.2023.133203. Epub 2023 Dec 12.

Abstract

Antibacterial compounds that reduce extracellular polymeric substances (EPS) are needed to avoid bacterial biofilms in water pipelines. Herein, green one-pot synthesis of α-aminophosphonates (α-Amp) [A-G] was achieved by using ionic liquid (IL) as a Lewis acid catalyst. The synthesized α-Amp analogues were tested against different bacteria such as Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa. The representative [B] analogue showed an efficient antibacterial effect with MIC values of 3.13 μg/mL for E. coli, P. aeruginosa, and 6.25 μg/mL for B. subtilis. Additionally, a strong ability to eliminate the mature bacterial biofilm, with super-MIC values of 12.5 μg/mL for E. coli, P. aeruginosa, and 25 μg/mL for B. subtilis. Moreover, bacterial cell disruption by ROS formation was also tested, and the compound [B] revealed the highest ROS level compared to other compounds and the control, and efficiently destroyed the extracellular polymeric substances (EPS). The docking study confirmed strong interactions between [B] analogue and protein structures with a binding affinity of -6.65 kCal/mol for the lyase protein of gram-positive bacteria and -6.46 kCal/mol for DNA gyrase of gram-negative bacteria. The results showed that α-Amp moiety is a promising candidate for developing novel antibacterial and anti-biofilm agents for clean water supply.

摘要

需要具有减少胞外聚合物 (EPS) 作用的抗菌化合物,以避免水管中的细菌生物膜。本文采用离子液体 (IL) 作为路易斯酸催化剂,实现了α-氨基膦酸酯 (α-Amp) [A-G] 的绿色一锅法合成。所合成的α-Amp 类似物针对枯草芽孢杆菌、大肠杆菌和铜绿假单胞菌等不同细菌进行了测试。代表性 [B] 类似物表现出有效的抗菌作用,对大肠杆菌、铜绿假单胞菌的 MIC 值分别为 3.13μg/mL 和 6.25μg/mL,对枯草芽孢杆菌的 MIC 值为 6.25μg/mL。此外,它还具有很强的消除成熟细菌生物膜的能力,对大肠杆菌、铜绿假单胞菌的超 MIC 值分别为 12.5μg/mL 和 25μg/mL,对枯草芽孢杆菌的超 MIC 值为 25μg/mL。此外,还测试了 ROS 形成引起的细菌细胞破坏,与其他化合物和对照相比,化合物 [B] 显示出最高的 ROS 水平,并有效地破坏了胞外聚合物物质 (EPS)。对接研究证实了 [B] 类似物与蛋白质结构之间的强相互作用,与革兰氏阳性菌的裂解酶蛋白的结合亲和力为-6.65 kCal/mol,与革兰氏阴性菌的 DNA 拓扑异构酶 II 的结合亲和力为-6.46 kCal/mol。结果表明,α-Amp 部分是开发新型抗菌和抗生物膜剂以提供清洁水供应的有前途的候选物。

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