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Individual and Combined Effects of Extracellular Polymeric Substances and Whole Cell Components of Chlamydomonas reinhardtii on Silver Nanoparticle Synthesis and Stability

机译:莱茵衣藻胞外聚合物和全细胞组分对银纳米颗粒合成和稳定性的个体和联合作用

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摘要

The fresh water microalga Chlamydomonas reinhardtii bioreduced Ag+ to silver nanoparticles (AgNPs) via three biosynthetic routes in a process that could be a more sustainable alternative to conventionally produced AgNPs. The AgNPs were synthesized in either the presence of whole cell cultures, an exopolysaccharide (EPS)-containing cell culture supernatant, or living cells that had been separated from the EPS-containing supernatant and then washed before being suspended again in fresh media. While AgNPs were produced by all three methods, the washed cultures had no supernatant-derived EPS and produced only unstable AgNPs, thus the supernatant-EPS was shown to be necessary to cap and stabilize the biogenic AgNPs. TEM images showed stable AgNPs were mostly spherical and showed a bimodal size distribution about the size ranges of 3.0 ± 1.3 nm and 19.2 ± 5.0 nm for whole cultures and 3.5 ± 0.6 nm and 17.4 ± 2.6 nm for EPS only. Moreover, selected area electron diffraction pattern of these AgNPs confirmed their polycrystalline nature. FTIR of the as-produced AgNPs identified polysaccharides, polyphenols and proteins were responsible for the observed differences in the AgNP stability, size and shape. Additionally, Raman spectroscopy indicated carboxylate and amine groups were bound to the AgNP surface.
机译:淡水藻类莱茵衣藻通过三种生物合成途径将Ag + 生物还原为银纳米颗粒(AgNPs),该过程可能是常规生产的AgNPs的更可持续的替代方法。在全细胞培养物,含胞外多糖(EPS)的细胞培养上清液或已经从含EPS的上清液中分离出来的活细胞存在下进行合成,然后洗涤,然后再次悬浮于新鲜培养基中,即可合成AgNP。尽管通过所有三种方法均可生产AgNP,但洗涤后的培养物却没有上清液衍生的EPS,而仅产生不稳定的AgNPs,因此,上清液EPS被证明是封闭和稳定生物AgNP所必需的。 TEM图像显示稳定的AgNPs大多为球形,整个培养物的双峰尺寸分布在3.0±1.3 nm和19.2±5.0 nm范围内,而EPS则只有3.5±0.6 nm和17.4±2.6 nm。而且,这些AgNP的选定区域电子衍射图证实了它们的多晶性质。所产生的AgNP的FTIR鉴定为多糖,多酚和蛋白质是造成观察到的AgNP稳定性,大小和形状差异的原因。另外,拉曼光谱表明羧酸根和胺基与AgNP表面结合。

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