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蛋白质包覆银纳米颗粒的仿生合成与表征

Biomimetic synthesis and characterisation of protein capped silver nanoparticles.

作者信息

Sanghi Rashmi, Verma Preeti

机构信息

Facility for Ecological and Analytical Testing, Indian Institute of Technology Kanpur, Kanpur, India.

出版信息

Bioresour Technol. 2009 Jan;100(1):501-4. doi: 10.1016/j.biortech.2008.05.048. Epub 2008 Jul 14.

Abstract

A controlled and up-scalable route for the biosynthesis of silver nanopartilces (NPs) mediated by fungal proteins of Coriolus versicolor has been undertaken for the first time. The fungus when challenged with silver nitrate solution accumulated silver NPs on its surface in 72h which could be reduced to 1h by tailoring the reaction conditions. Under alkaline conditions, the reaction was much faster and could easily proceed at room temperature even without stirring. The resulting Ag NPs displayed controllable structural and optical properties depending on the experimental parameters such as pH and reaction temperatures. The average size, morphology, and structure of particles were determined by AFM, TEM, XRD and UV/Visible absorption spectrophotometry. Fourier transform infrared study disclosed that the amino groups were bound to the particles, which was accountable for the stability of NPs. It further confirmed the presence of protein as the stabilizing and capping agent surrounding the silver NPs. Experiments were conducted both with, media in which fungus was initially harvested and that of pristine fungal mycelium alone. Under normal conditions, in the case of media extracellular synthesis took place whereby other than the fungal proteins, glucose was also responsible for the reduction. In the case of fungal mycelium, the intracellular formation of Ag NPs, could be tailored to give both intracellular and extracellular Ag NPs under alkaline conditions whereby the surface S-H groups of the fungus played a major role.

摘要

首次采用了一种可控且可扩大规模的途径,用于由云芝真菌蛋白介导的银纳米颗粒(NPs)的生物合成。当用硝酸银溶液挑战该真菌时,其在72小时内在其表面积累了银纳米颗粒,通过调整反应条件可将时间缩短至1小时。在碱性条件下,反应速度更快,即使不搅拌也能在室温下轻松进行。所得的银纳米颗粒根据诸如pH值和反应温度等实验参数显示出可控的结构和光学性质。通过原子力显微镜(AFM)、透射电子显微镜(TEM)、X射线衍射(XRD)和紫外/可见吸收分光光度法确定了颗粒的平均尺寸、形态和结构。傅里叶变换红外研究表明,氨基与颗粒结合,这是纳米颗粒稳定性的原因。它进一步证实了蛋白质作为围绕银纳米颗粒的稳定和封端剂的存在。实验分别使用最初收获真菌的培养基和仅使用原始真菌菌丝体的培养基进行。在正常条件下,在培养基的情况下发生细胞外合成,除了真菌蛋白外,葡萄糖也负责还原。在真菌菌丝体的情况下,银纳米颗粒的细胞内形成可以在碱性条件下进行调整,以产生细胞内和细胞外的银纳米颗粒,其中真菌的表面S-H基团起主要作用。

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