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Enhancement of Microbial Synthesis of GoldNanoparticles by Gamma Radiation

机译:γ辐射增强金纳米颗粒的微生物合成

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Aim: An eco-friendly protocol for the synthesis of gold nanoparticles (GNPs) using submerged liquid fermentation of fungus Pleurotus ostreatus was established.Methodology: Treatment of tetrachloro-auric acid (HAuCl4) solution with the free cell filtrate (FCF) of the fungus led to the reduction of the HAuCl4 ions and the formation of stable GNPs. These nanoparticles were characterized ?by ?Surface ?Plasmon ?Resonance ?(SPR) ?band ?at ?wavelength? 550 nm ?for ?GNPs. The components of the media needed for the fungal growth were optimized using factorial design.Results: The maximum SPR in UV-Vis spectra was recorded using a medium containing in (%); glucose (1), yeast (0.5), malt extract (0.5) and KNO_(3) (0.2) and incubation period 8 days, the temperature and pH were kept at 30°C and 6, respectively. The particles were characterized by UV/Vis spectroscopy, Transmission electron microscope (TEM), Dynamic light scattering (DLS), Fourier Transform and Infrared Spectroscopy (FT-IR). Exposure of fungal strain or FCF after mixing with Au+ to Gamma radiation showed 36% increase in the SPR band intensity of the synthesized GNPs compared to un-irradiated strain and FCF irradiated before mixing with Au+. The synthesized GNPs exhibited antimicrobial activity against both Gram negative and Gram positive bacteria, measured by well diffusion assay. Moreover, it also showed good anticancer activity against human Breast carcinoma (T47D) cells, Prostate carcinoma (PC3) cells and hepatocellular (HEPG2) cells using Trypan blue exclusion and Sulfo-Rhodamine B assay.Conclusion: The combined effect of both ?-radiation and proteins offers a highly efficient and inexpensive method for the synthesis of gold nanoparticles utilizing an edible mushroom, P. ostreatus for the bio- reduction of HAuCl_(4).
机译:目的:建立一种利用平菇平菇深层液体发酵法合成金纳米颗粒(GNPs)的环保方案。方法:用真菌的游离细胞滤液(FCF)处理四氯金酸(HAuCl4)溶液。导致HAuCl4离子的还原并形成稳定的GNP。这些纳米粒子的特征是“表面”,“等离子体”,“共振”(SPR),“波长”,“波长”。 550 nm-用于?GNP。结果:使用含(%)的培养基记录了UV-Vis光谱中的最大SPR,从而优化了真菌生长所需的培养基成分。葡萄糖(1),酵母(0.5),麦芽提取物(0.5)和KNO_(3)(0.2)以及潜伏期8天,温度和pH分别保持在30°C和6。通过UV / Vis光谱,透射电子显微镜(TEM),动态光散射(DLS),傅立叶变换和红外光谱(FT-IR)表征颗粒。与未经辐照的菌株和与Au +混合前辐照的FCF相比,与Au +混合后的真菌菌株或FCF暴露于Gamma辐射表明合成GNP的SPR带强度增加了36%。通过孔扩散测定法测量,合成的GNP对革兰氏阴性和革兰氏阳性细菌均显示出抗菌活性。此外,通过台盼蓝排除法和磺胺若丹明B检验,它对人乳腺癌(T47D)细胞,前列腺癌(PC3)细胞和肝细胞(HEPG2)细胞也显示出良好的抗癌活性。蛋白质和蛋白质为利用食用菌P. ostreatus进行HAuCl_(4)的生物还原提供了一种高效,廉价的金纳米颗粒合成方法。

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