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从地衣芽孢杆菌中分离得到的一种新型化合物的抗菌活性及其在鱼类细菌性疾病治疗中的应用:一种基于计算机的方法。

Antibacterial activity of a novel compound isolated from Bacillus licheniformis for treating bacterial infections in fishes: An in-silico approach.

机构信息

Center for Nanobiotechnology, Vellore Institute of Technology (VIT), Vellore, 632014, Tamil Nadu, India.

Bioinformatics Programming Laboratory, Department of Biotechnology, School of Biosciences and Technology, Vellore Institute of Technology (VIT), Vellore, 632014, India.

出版信息

Mol Cell Biochem. 2023 Dec;478(12):2609-2620. doi: 10.1007/s11010-023-04687-2. Epub 2023 Mar 9.

Abstract

Aeromonas hydrophila is a fish pathogen which is widely associated with diseases related to freshwater fishes. Vibrio parahemolyticus is a major globally emerging marine pathogen. Seven novel compounds were extracted from the ethyl acetate extract of Bacillus licheniformis, a novel marine bacterium isolated from marine actinomycetes. The compounds were identified using Gas Chromatography-Mass Spectroscopy (GC-MS). Only one bioactive compound having potent antibacterial activity was virtually screened to understand its drug-like property according to Lipinski's rule. The core proteins, 3L6E and 3RYL from the pathogens, A. hydrophila and V. parahemolyticus were targeted for drug discovery. In the present in-silico approach, Phenol,2,4-Bis(1,1-Dimethylethyl) a potent bioactive compound present in Bacillus licheniformis was used to prevent the infection due to the two pathogens. Further, using this bioactive compound, molecular docking was done to block their specific target proteins. This bioactive compound satisfied all the five rules of Lipinski. Molecular docking result revealed the best binding efficacy of Phenol,2,4-Bis(1,1-Dimethylethyl) against 3L6E and 3RYL with - 4.24 kcal/mol and - 4.82 kcal/mol, respectively. Molecular dynamics (MD) simulations were also executed to determine the binding modes as well as the stability of the protein-ligand docking complexes in the dynamic structure. The in vitro toxicity analysis of this potent bioactive compound against Artemia salina was carried out, revealing the non-toxic nature of B. licheniformis ethyl acetate extract. Thus, the bioactive compound of B. licheniformis was found to be a potent antibacterial agent against A. hydrophila and V. parahemolyticus.

摘要

气单胞菌是一种广泛与淡水鱼类疾病相关的鱼类病原体。副溶血性弧菌是一种主要的全球新兴海洋病原体。从海洋放线菌中分离到的新型海洋细菌地衣芽孢杆菌中提取了 7 种新型化合物。这些化合物通过气相色谱-质谱联用(GC-MS)进行鉴定。根据 Lipinski 规则,仅虚拟筛选出一种具有强大抗菌活性的生物活性化合物来了解其类药性。从病原体气单胞菌和副溶血性弧菌中,针对核心蛋白 3L6E 和 3RYL 进行药物发现。在目前的计算方法中,使用地衣芽孢杆菌中存在的一种有效的生物活性化合物对苯二酚,2,4-双(1,1-二甲基乙基)来预防两种病原体引起的感染。此外,使用这种生物活性化合物进行分子对接以阻止它们的特定靶蛋白。这种生物活性化合物符合 Lipinski 的所有 5 条规则。分子对接结果显示,对苯二酚,2,4-双(1,1-二甲基乙基)对 3L6E 和 3RYL 的最佳结合效果分别为-4.24 kcal/mol 和-4.82 kcal/mol。还进行了分子动力学(MD)模拟,以确定蛋白质-配体对接复合物在动态结构中的结合模式和稳定性。对这种有效的生物活性化合物对卤虫的体外毒性分析表明,地衣芽孢杆菌乙酸乙酯提取物没有毒性。因此,地衣芽孢杆菌的生物活性化合物被发现是一种有效的抗气单胞菌和副溶血性弧菌的抗菌剂。

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