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Calligonum comosum and Fusarium sp. extracts as bio-mediator in silver nanoparticles formation: characterization antioxidant and antibacterial capability

机译:Calligonum comosum and Fusarium sp。提取物作为银纳米颗粒形成过程中的生物介质:表征抗氧化剂和抗菌能力

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摘要

In the current study, extracellular biosynthesis of silver nanoparticles (AgNPs) was carried out using aqueous extracts of green Calligonum comosum stem, besides Fusarium sp. Synthesized AgNPs were characterized using ultraviolet (UV)–Vis spectrophotometer, transmission electron microscopy (TEM) and zeta potential. Moreover, biosynthesized AgNPs were estimated for the scavenging ability on DPPH radical as well as tested for their antibacterial activity using well diffusion method against Gram-positive bacteria Staphylococcus aureus. On the other hand, DNA content from untreated and AgNPs treated bacterial cells was evaluated by (UV)–Vis spectrophotometer and agarose gel electrophoresis. Results revealed the formation of AgNPs, which was first detected by color change of the reaction mixture. The characteristic surface plasmon resonance absorption was detected at 450 and 410 nm for the plant and myco-synthesized AgNPs. Furthermore, TEM micrograph and zeta sizer showed formation of spherical particles with an average size of about 105.8 and 228.4 nm for plant and myco-synthesized AgNPs, respectively. Plant-synthesized AgNPs exhibited higher scavenging of DPPH radicals than that of the myco-synthesized one. For bactericidal action, plant-synthesized AgNPs showed higher inhibition zone compared with myco-synthesized one, which was negatively correlated with the nanoparticle size. Furthermore, low DNA concentration was detected for AgNPs treated bacteria, which might be a consequence of inactivation for DNA replication. Further experimental work is required to find out if there is any correlation between nanoparticles size and efficacy against bacteria.
机译:在当前的研究中,除镰孢属(Fusarium sp。)外,还使用绿色的Calligonum comosum茎的水提物进行银纳米颗粒(AgNPs)的细胞外生物合成。合成的AgNPs使用紫外(UV)-可见分光光度计,透射电子显微镜(TEM)和ζ电位进行表征。此外,估计生物合成的AgNPs对DPPH自由基的清除能力,并使用针对革兰氏阳性细菌金黄色葡萄球菌的良好扩散方法测试其抗菌活性。另一方面,通过(UV)-Vis分光光度计和琼脂糖凝胶电泳评估了未经处理和经AgNPs处理的细菌细胞的DNA含量。结果揭示了AgNP的形成,其首先通过反应混合物的颜色变化来检测。在植物和霉菌合成的AgNPs的450和410nm处检测到了特征性的表面等离子体共振吸收。此外,TEM显微照片和zeta粒度仪显示出球形颗粒的形成,分别用于植物和霉菌合成的AgNPs的平均大小分别约为105.8和228.4 nm。与真菌合成的植物相比,植物合成的AgNPs清除DPPH自由基的能力更高。对于杀菌作用,与真菌合成的植物相比,植物合成的AgNPs表现出更高的抑制区,而抑制区与纳米颗粒大小负相关。此外,检测到用AgNPs处理的细菌的DNA浓度低,这可能是DNA复制失活的结果。需要进一步的实验工作,以发现纳米粒子的大小与抗细菌功效之间是否存在任何关联。

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