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Biosynthetic Conversion of Ag+ to highly Stable Ag0 Nanoparticles by Wild Type and Cell Wall Deficient Strains of Chlamydomonas reinhardtii

机译:野生型和莱茵衣藻细胞壁缺陷菌株对Ag +到高度稳定的Ag0纳米颗粒的生物合成转化。

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摘要

In the current study, two different strains of the green, freshwater microalga Chlamydomonas reinhardtii bioreduced Ag+ to silver nanoparticles (AgNPs), which have applications in biosensors, biomaterials, and therapeutic and diagnostic tools. The bioreduction takes place in cell cultures of C. reinhardtii at ambient temperature and atmospheric pressure, thus eliminating the need for specialized equipment, harmful reducing agents or the generation of toxic byproducts. In addition to the visual changes in the cell culture, the production of AgNPs was confirmed by the characteristic surface plasmon resonance (SPR) band in the range of 415–425 nm using UV-Vis spectrophotometry and further evolution of the SPR peaks were studied by comparing the peak intensity at maximum absorbance over time. X-ray diffraction (XRD) determined that the NPs were Ag0. Micrographs from transmission electron microscopy (TEM) revealed that 97 ± 2% AgNPs were <10 nm in diameter. Ag+ to AgNP conversion was determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES). The AgNPs were stable over time in the cell culture media, acetone, NaCl and reagent alcohol solutions. This was verified by a negligible change in the features of the SPR band after t > 300 days of storage at 4 °C.
机译:在当前的研究中,两种不同的绿色淡水微藻莱茵衣藻生物还原了Ag + 到银纳米颗粒(AgNPs),它们在生物传感器,生物材料以及治疗和诊断工具中都有应用。生物还原在环境温度和大气压下在莱茵衣藻的细胞培养中进行,因此无需专用设备,有害还原剂或有毒副产物的产生。除了细胞培养中的视觉变化外,还通过紫外可见分光光度法在415-425 nm范围内的特征表面等离子体共振(SPR)谱带确认了AgNP的产生,并通过SPR峰的进一步演化进行了研究。比较随时间变化的最大吸收峰强度。 X射线衍射(XRD)分析表明NPs为Ag 0 。透射电子显微镜(TEM)的显微照片显示,97±2%AgNP的直径小于10 nm。通过电感耦合等离子体原子发射光谱法(ICP-AES)确定从Ag + 到AgNP的转化。 AgNP在细胞培养基,丙酮,NaCl和试剂酒精溶液中随时间稳定。在4°C下储存t> 300天后,SPR谱带的特征变化微不足道,从而证明了这一点。

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