肠系膜白斑菌生物合成氧化锌纳米颗粒的影响。右旋精抗细菌性皮肤感染

A. Aman
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引用次数: 1

摘要

目前的研究包括一种不同寻常的方法,利用伊拉克分离的益生菌肠系膜芽孢杆菌合成氧化锌纳米颗粒。dextranicum。采用x射线衍射(XRD)、原子力显微镜(AFM)、扫描电镜(SEM)、傅里叶变换红外光谱(FTIR)和能量色散x射线分析(EDX)对ZnO纳米颗粒进行了表征。结果表明,制备的ZnO纳米颗粒分散性好,稳定性好,呈球形,最大粒径在37 ~ 41 nm之间。本研究的目的是测定生物合成ZnO纳米颗粒对鲍曼不动杆菌、肺炎克雷伯菌、铜绿假单胞菌和金黄色葡萄球菌等细菌性皮肤感染的抗菌和抗毒因子性能。通过测定最小抑菌浓度(MIC)评价其抑菌活性,MIC范围在(25 ~ 50)mg/mL之间,并测定了对被试细菌溶血素、脲酶、花青苷产生和生物膜形成的抑毒因子。结果表明,生物合成氧化锌纳米粒子处理后,菌株产生溶血素、脲酶和花青苷的能力下降,72 h后形成生物膜的效果最好,对金黄色葡萄球菌(S9)的抑制率高达48.74%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Zinc Oxide Nanoparticles Biosynthesized by Leuconostoc Mesenteroides ssp. Dextranicum Against Bacterial Skin Infections
The current study included a unusual method for the biosynthesis of ZnO nanoparticles using Iraqi isolate a probiotic bacteria Leuconostoc mesenteroides ssp. dextranicum. The characterizations of ZnO nanoparticles were performed by Xray diffraction (XRD) Atomic Force Microscopy (AFM) technique, Scanning Electron Microscopic (SEM), Fourier Transform Infrared Spectroscopy (FTIR) and Energy-dispersive X-ray analysis (EDX) spectra. The results confirmed that the obtained ZnO nanoparticles are well dispersed, stable and spherical with maximum particles in size range within 37–41 nm in diameter. The aim of this study was to determine the antibacterial and antivirulence factors properties of biosynthesized ZnO nanoparticles against bacterial skin infections including Acinetobacter baumanii ,Klebsiella pneumonia, Pseudomonas aeruginosa and Staphylococcus aureus. The antibacterial activity was evaluated through the determination of the minimum inhibitory concentration (MIC), the results obtained suggested that the MIC ranged between (25 -50) mg/mL and the anti-virulence factors also determined against hemolysin, urease , pyocyanin production and biofilm formation of tested bacteria. Results showed that the ability of hemolysin, urease and pyocyanin production were decreased after treatment with biosynthesized ZnO nanoparticles, also the best effect has been shown in biofilm formation after 72 h for all isolates, with high inhibition 48.74% against Staphylococcus aureus (S9) .
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