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首页> 外文期刊>International Journal of Nanomedicine >Extracellular biosynthesis of silver nanoparticles using the cell-free filtrate of nematophagous fungus Duddingtonia flagrans
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Extracellular biosynthesis of silver nanoparticles using the cell-free filtrate of nematophagous fungus Duddingtonia flagrans

机译:线虫真菌无鞭毛鞭毛鞭毛的无细胞滤液合成银纳米颗粒的细胞外生物

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摘要

The biosynthesis of metallic nanoparticles (NPs) using biological systems such as fungi has evolved to become an important area of nanobiotechnology. Herein, we report for the first time the extracellular synthesis of highly stable silver NPs (AgNPs) using the nematophagous fungus Duddingtonia flagrans (AC001). The fungal cell-free filtrate was analyzed by the Bradford method and 3,5-dinitrosalicylic acid assay and used to synthesize the AgNPs in the presence of a 1 mM AgNO3 solution. They have been characterized by UV–Vis spectroscopy, X-ray diffraction, transmission electron microscopy, dynamic light scattering, Zeta potential measurements, Fourier-transform infrared, and Raman spectroscopes. UV–Vis spectroscopy confirmed bioreduction, while X-ray diffractometry established the crystalline nature of the AgNPs. Dynamic light scattering and transmission electron microscopy images showed approximately 11, 38 nm monodisperse and quasispherical AgNPs. Zeta potential analysis was able to show a considerable stability of AgNPs. The N–H stretches in Fourier-transform infrared spectroscopy indicate the presence of protein molecules. The Raman bands suggest that chitinase was involved in the growth and stabilization of AgNPs, through the coating of the particles. Our results show that the NPs we synthesized have good stability, high yield, and monodispersion.
机译:利用诸如真菌的生物系统对金属纳米颗粒(NPs)进行生物合成已经发展成为纳米生物技术的重要领域。在本文中,我们首次报道了使用线虫真菌达丁顿鞭毛(AC001)的高度稳定的银NP(AgNP)的细胞外合成。用Bradford方法和3,5-二硝基水杨酸分析法分析无真菌的滤液,并在1 mM AgNO 3 溶液存在下用于合成AgNP。它们的特征在于紫外可见光谱,X射线衍射,透射电子显微镜,动态光散射,Zeta电位测量,傅立叶变换红外光谱和拉曼光谱仪。紫外可见光谱证实了生物还原作用,而X射线衍射确定了AgNPs的晶体性质。动态光散射和透射电子显微镜图像显示约11、38 nm单分散和准球形AgNP。 Zeta电位分析能够显示相当大的AgNP稳定性。傅立叶变换红外光谱中的N–H伸展表明存在蛋白质分子。拉曼谱带表明几丁质酶通过颗粒的涂层参与了AgNPs的生长和稳定。我们的结果表明,我们合成的NP具有良好的稳定性,高收率和单分散性。

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