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Antimicrobial Mechanism and Identification of the Proteins Mediated by Extracts from Asphaltum punjabianum and Myrtus communis

机译:沥青旁遮普菌和Myrtus Communis提取物介导的抗菌机制及鉴定蛋白质

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Myrtus communis (“myrtle”) and Asphaltum punjabianum (“shilajeet”) are a medicinal plant and a long-term-humified dead plant material, respectively. We studied their antibacterial and anticandidal activities against Pseudomonas aeruginosa , Escherichia coli , Staphylococcus aureus , and Candida albicans . The activities of the aqueous extracts of the studied materials were measured using agar-well diffusion methods. Furthermore, proteomic analysis of treated microbial cells was conducted to identify affected proteins. The results showed both antibacterial and anticandidal activities for the myrtle extract (ME), while the shilajeet extract (SE) showed antibacterial activity only. The highest antimicrobial activity was observed against E. coli among the microbes tested; therefore, it was taken as the model for the proteomic analysis to identify the antimicrobial mechanism of ME and SE using two-dimensional electrophoresis. Upregulation of expression of 42 proteins and downregulation of expression of 6 proteins were observed in E. coli treated with ME, whereas 12 upregulated and 104 downregulated proteins were detected in E. coli treated with SE, in comparison with the control. About 85% of identified expressed proteins were from the cytoplasm and 15% from microbial cell walls, indicating the penetration of extracts inside cells. A higher percentage of expressed proteins was recorded for enzymatic activity. Our findings suggest that the major targets of the antibacterial action were proteins involved in the outer membrane, oxidative stress, and metabolism. Our data might reveal new targets for antimicrobial agents.
机译:Myrtus Communis(“Myrtle”)和沥青旁遮普(“Shilajeet”)分别是一种药用植物和长期令人满意的死亡植物材料。我们研究了对抗菌和预油段的抗菌和反混活动,对抗铜绿假单胞菌,大肠杆菌,金黄色葡萄球菌和念珠菌念珠菌。使用琼脂 - 孔扩散方法测量研究的含水提取物的活性。此外,进行了处理的微生物细胞的蛋白质组学分析以鉴定受影响的蛋白质。结果表明,Myrtle提取物(ME)的抗菌和反线性活性,而Shilajeet提取物仅显示抗菌活性。观察到最高抗微生物活性对抗e。在测试的微生物中的Coli;因此,作为蛋白质组学分析的模型,以鉴定ME和SE的抗微生物机制使用二维电泳。在 e中观察到42个蛋白表达和6例蛋白表达下调的表达的上调。用我处理的大肠杆菌,而在 e中检测到12个上调和104个下调蛋白质。与对照相比,用SE治疗的大肠杆菌。大约85%的已鉴定的表达蛋白质来自细胞质和15%来自微生物细胞壁,表明提取物内部的渗透。记录更高百分比的表达蛋白质以进行酶活性。我们的研究结果表明,抗菌作用的主要目标是参与外膜,氧化应激和代谢的蛋白质。我们的数据可能会揭示抗微生物剂的新目标。

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