Actinobacterial Research Laboratory, Department of Microbiology, Periyar University, Periyar Palkalai Nagar, Salem 636 011, Tamil Nadu, India.
Department of Bacteriology, National Institute for Research in Tuberculosis, Chennai, 600 031, Tamil Nadu, India.
Colloids Surf B Biointerfaces. 2013 Nov 1;111:680-7. doi: 10.1016/j.colsurfb.2013.06.045. Epub 2013 Jul 5.
Actinobacteria- mediated synthesis of silver nanoparticles (AgNPs) is a reliable, eco-friendly and important aspect of nanobiotechnology. In this study, aqueous silver ions, which were exposed to an actinobacterial biomass of Streptomyces naganishii (MA7), were reduced to form stable AgNPs under optimised conditions. The microbially synthesised AgNPs were characterised by UV-Vis spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), selected area electron diffraction (SAED), energy dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), atomic force microscopy (AFM) and high- resolution transmission electron microscopy (HR-TEM). The size (5-50 nm) and shape (spherical) of the AgNPs were determined. The biosynthesised AgNPs exhibited good bactericidal, anti-biofouling, antioxidant and cytotoxic effects with regards to the HeLa cell line. A single protein band with a molecular weight of 44 kDa was obtained after partial purification of the culture filtrate via polyacrylamide gel electrophoresis. The potent actinobacterial strain was identified by its molecular (16s rRNA sequencing), phenotypic and cultural characteristics. The current study demonstrated the potential use of the extremophilic actinobacterial strain of S. naganishii (MA7) as a novel source for AgNPs synthesis with improved biomedical applications.
放线菌介导的银纳米粒子(AgNPs)合成是纳米生物技术的一个可靠、环保和重要方面。在这项研究中,将处于优化条件下的水合银离子暴露于链霉菌(Streptomyces naganishii)(MA7)的放线菌生物质中,银离子被还原形成稳定的 AgNPs。通过紫外可见分光光度法、傅里叶变换红外(FT-IR)光谱、X 射线衍射(XRD)、选区电子衍射(SAED)、能量色散 X 射线能谱(EDX)、扫描电子显微镜(SEM)、原子力显微镜(AFM)和高分辨率透射电子显微镜(HR-TEM)对微生物合成的 AgNPs 进行了表征。AgNPs 的尺寸(5-50nm)和形状(球形)。生物合成的 AgNPs 对 HeLa 细胞系表现出良好的杀菌、抗生物污损、抗氧化和细胞毒性作用。通过聚丙烯酰胺凝胶电泳对培养滤液进行部分纯化后,得到一条分子量为 44kDa 的单一蛋白带。通过分子(16s rRNA 测序)、表型和培养特征对具有潜在能力的放线菌进行了鉴定。本研究表明,极端嗜热放线菌 S. naganishii(MA7)菌株具有作为新型 AgNPs 合成来源的潜力,具有改善的生物医学应用。