Murugesan Vignesh, Palanivel Pargovan, Ramesh Gokul, Ganesh Dwarakesh, Michael Helan Soundra Rani, Bandhumy Lingam Shivakumar, Sivaraman Rathish Kumar
Department of Biotechnology, Sri Ramakrishna College of Arts & Science, Coimbatore, Tamil Nadu, India.
Department of Biotechnology, Manonmaniam Sundaranar University, Tirunelveli, India.
Front Pharmacol. 2025 Mar 12;16:1555542. doi: 10.3389/fphar.2025.1555542. eCollection 2025.
Multidrug-resistant bacterial pathogen has emerged as a significant global health challenge, underscoring the urgent need to identify and develop alternative therapeutic agents including plant natural products. In this study, the extract from plant extract was analyzed for antibacterial properties against and component composition.
The plant extract was obtained from leaves of and its antibacterial activity against was determined in Kirby-Bauer disc diffusion assay. In this assay, the activity of the extract was tested at two different concentrations of 50 and 100 μg/mL. The minimum inhibitory concentration (MIC) of the extract against was used with its MIC values against Vero cells to determine the selectivity index. GC-MS determined the phytochemical composition of the plant extract. The property of different extract components to bind the target receptor Penicillin Binding Protein 2a (7KIS) was assessed studies including docking and molecular dynamics (MD) analyses. In these analyses, the stability and interaction dynamics of the Penicillin Binding Protein 2a (7KIS) protein complexed with selected extract components.
The plant extracts had antibacterial activity against , with inhibition zones measuring 13 mm and 19 mm for 50 and 100 μg/mL concentrations, respectively. The MIC of the plant extract was determined to be 20 μg/mL, while its selectivity index was 4.54, indicating its antibiotic potential. One extract component, 2, 4-di-tert-butylphenol compound holds a binding affinity of -6.2 kcal/mol in molecular docking studies. MD simulations revealed stable binding interactions between the 7KIS protein and the tested ligands, characterized by reduced atomic fluctuations and energetically favorable binding profiles.
This study showed that extract has a robust antibacterial potential against . Furthermore, GC-MS profiling molecular docking, and dynamic simulation data showed that such antibacterial potential might be attributed to its one component, 2, 4-di-tert-butylphenol. Further, and studies are needed to show the applicability of bioactive compounds from in combating resistant bacterial pathogens.
多重耐药性细菌病原体已成为一项重大的全球卫生挑战,凸显了识别和开发包括植物天然产物在内的替代治疗剂的迫切需求。在本研究中,对一种植物提取物进行了分析,以检测其对[具体细菌名称未给出]的抗菌特性及成分组成。
该植物提取物取自[植物名称未给出]的叶子,并通过Kirby-Bauer纸片扩散法测定其对[具体细菌名称未给出]的抗菌活性。在该试验中,提取物在50和100μg/mL两种不同浓度下进行活性测试。提取物对[具体细菌名称未给出]的最低抑菌浓度(MIC)及其对Vero细胞的MIC值用于确定选择性指数。气相色谱-质谱联用(GC-MS)测定了植物提取物的植物化学成分。通过包括对接和分子动力学(MD)分析在内的[具体研究方法未详细说明]研究,评估了不同提取物成分与靶标受体青霉素结合蛋白2a(7KIS)结合的特性。在这些分析中,研究了青霉素结合蛋白2a(7KIS)与选定提取物成分复合后的稳定性和相互作用动力学。
该植物提取物对[具体细菌名称未给出]具有抗菌活性,50和100μg/mL浓度下的抑菌圈分别为13mm和19mm。植物提取物的MIC测定为20μg/mL,其选择性指数为4.54,表明其具有抗生素潜力。在分子对接研究中,一种提取物成分2,4-二叔丁基苯酚化合物的结合亲和力为-6.2 kcal/mol。分子动力学模拟揭示了7KIS蛋白与测试配体之间稳定的结合相互作用,其特征为原子波动减少且结合图谱在能量上有利。
本研究表明[植物名称未给出]提取物对[具体细菌名称未给出]具有强大的抗菌潜力。此外,GC-MS分析、分子对接和动态模拟数据表明,这种抗菌潜力可能归因于其一种成分2,4-二叔丁基苯酚。此外,还需要进一步的[具体研究未详细说明]研究来证明[植物名称未给出]中的生物活性化合物在对抗耐药细菌病原体方面的适用性。