银纳米颗粒对革兰氏阳性和革兰氏阴性临床分离株的基因毒性研究

Lakshmipathy Muthukrishnan, Anima Nanda
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引用次数: 12

摘要

近年来,随着绿色化学原理在合成方案中的应用,纳米银在生物医学和临床领域受到越来越多的关注。此外,随着各种微生物对抗生素耐药性的发生率增加,还需要一种有效的遏制战略,以防止它们在环境中逃逸。所谓的长生不老药(药物)证明了它的无能,一种有效的纳米生物技术方法已经冒险进入对抗这些病原体的领域。目的研究土壤细菌芽孢杆菌合成的生物纳米银对病原菌基因组DNA的毒性作用。方法利用细胞外细菌滤液合成纳米银。利用紫外-可见分光光度计、x射线衍射仪(XRD)、场发射扫描电镜(FESEM)和能量色散光谱(EDX)对SNPs进行了表征。采用Kirby Bauer盘片扩散法对病原菌的snp进行抑菌研究。用琼脂糖凝胶电泳法研究了snp对病原菌基因组DNA的毒性作用。结果证实了snp对基因组DNA的时间依赖性毒性作用。结论该snp对临床分离株具有潜在的抗菌活性。DNA片段被SNPs以剪切的形式观察到,这可能是由于与活性氧(ROS)的亲和力和复杂的形成趋势,这些活性氧(ROS)以磷酸盐的形式存在于核酸上,导致片段化。这种对从临床分离物中分离出的DNA的操作方法可能对基因改变的生物体具有守夜作用。
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Geno-toxic study of silver bio-nanoparticles toward Gram-positive and Gram-negative clinical isolates

Background

In recent years, with the implication of green chemistry principles in the synthesis protocol, nano silver is gaining much attention in biomedical and clinical field. Alongside, with the increased incidence of antibiotic(s) resistance among various microorganisms, there is also a need for an effective containment strategy to prevent their escape in the environment. The so called elixir (drug) proving its inability, an effective nano-biotechnological approach has ventured in to combat such pathogens.

Objective

To study the toxic effect of silver bio-nanoparticles synthesized using a soil bacterium, Bacillus sp. on genomic DNA isolated from pathogenic bacteria.

Methods

In this study, silver bio-nanoparticles (SNPs) were synthesized using extracellular bacterial filtrate. Characterization of SNPs was done using UV–vis spectrophotometer, X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and energy dispersive spectroscopy (EDX). Antibacterial study of SNPs toward the pathogenic bacteria was studied by Kirby Bauer's Disc diffusion method. The toxic effect of SNPs on the genomic DNA isolated from the pathogenic microorganisms was investigated by agarose gel electrophoresis.

Results

The time dependent toxic effect of SNPs on genomic DNA has been validated.

Conclusion

The SNPs exhibit potential antibacterial activity toward clinical isolates tested. DNA fragmentation by SNPs was observed in the form of shear may be due to the affinity and complex forming tendency with Reactive Oxygen Species (ROS) present as phosphates on nucleic acid resulting in fragmentation. This modus operandi toward DNA isolated from the clinical isolates might have a vigil over genetically altered organisms.

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