大肠杆菌d8纳米银的细胞外生物合成、优化、表征和抗菌潜力

M. M. N. El-Dein, Z. Baka, M. Abou-Dobara, A. El‐Sayed, M. El-Zahed
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引用次数: 14

摘要

本研究重点利用大肠杆菌D8 (MF06257)粗代谢物优化银纳米颗粒(AgNPs)的胞外生物合成和抗菌效率。该菌株是从埃及达米埃塔市的一条污水流中分离出来的。制备AgNPs的最佳条件为温度35℃,pH 7,硝酸银1.5mM。在室温(25±2℃)和光照条件下,培养滤液在1-2分钟内检测AgNPs的生物合成。采用紫外可见光谱(最大吸光度为429 nm)、x射线衍射(XRD)图(晶体平面为110、111、200、211、220和311)、透射电子显微镜(TEM) (AgNPs为6 ~ 17 nm的球形)、傅里叶变换红外(FTIR)光谱(对称胺和不对称胺的波段分别为3421.1和2962.13 cm-1,芳族和脂肪族(C-N)的伸缩振动带分别存在于1392.35和1122.37 cm-1波段),Zeta电位分析仪(AgNPs具有负电荷值;-33.6 mV)和体积大小分布(封盖剂包裹AgNPs的存在,平均尺寸为136.0-294.3 nm)。硝酸还原酶(NR)作为优化生产的重要伙伴(NR的产率达到2.18 U/ml)。研究表明,AgNPs是金黄色葡萄球菌、大肠杆菌、铜绿假单胞菌、交替孢霉、尖孢镰刀菌和黄曲霉的有效抑制剂。用透射电镜研究了AgNPs的抑菌活性。TEM显微图显示对金黄色葡萄球菌细胞增殖有抑制作用。在尖孢霉的情况下,检测到处理后的细胞大小减小,形成粘液基质将菌丝细胞连接在一起,出现大液泡,脂滴和细胞质内容物严重泄漏。AgNPs对金黄色葡萄球菌和白色念珠菌的MIC值分别为6.25μg/ml和50 μg/ml。此外,AgNPs与氟康唑联用具有协同效应,对黑曲霉、黄曲霉和尖孢镰刀菌的杀伤面积明显增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EXTRACELLULAR BIOSYNTHESIS, OPTIMIZATION, CHARACTERIZATION AND ANTIMICROBIAL POTENTIAL OF ESCHERICHIA COLI D8 SILVER NANOPARTICLES
This study highlights the optimization of extracellular biosynthesis and antimicrobial efficiency of silver nanoparticles (AgNPs) using the crude metabolite of Escherichia coli D8 (MF06257) strain. The bacterial strain had been isolated from a sewage water stream located in Damietta City, Egypt. The optimum conditions for AgNPs production were at temperature 35°C, pH 7 and 1.5mM silver nitrate. The AgNPs biosynthesis was detected in culture filtrate within 1-2 minutes at room temperature (25±2°C) and sunlight. The characterization of AgNPs was studied by UV-Vis spectroscopy (maximum absorbance at 429 nm), X-ray diffraction (XRD) pattern (crystal planes were 110, 111, 200, 211, 220, and 311), transmission electron microscopy (TEM) (AgNPs were spherical in shape ranging from 6 to 17 nm), Fourier transform-infrared (FTIR) spectroscopy (the bands of symmetric and asymmetric amines were assigned at 3421.1 and 2962.13 cm-1, the stretching vibration band of aromatic and aliphatic (C-N) exist at 1392.35 and 1122.37 cm-1 bands), Zeta potential analyser (AgNPs had a negative charge value; -33.6 mV) and size distribution by volume (the presence of capping agent enveloping the AgNPs with a mean size of 136.0-294.3 nm). Nitrate reductase (NR) was assayed as an important partner in the optimized production (the rate of NR reached to 2.18 U/ml). The study demonstrated that AgNPs are potent inhibitors of Staphylococcus aureus, E. coli, Pseudomonas aeruginosa, Alternaria alternata, Fusarium oxysporum and Aspergillus flavus. The antimicrobial activity of AgNPs was studied by TEM. TEM micrographs showed an inhibition of S. aureus cell multiplication. In case of F. oxysporum, a reduction in the size of treated cells, formation of a mucilage matrix connecting the hyphal cells together, the appearance of a big vacuole, lipid droplets an a severe leakage of cytoplasmic contents were detected. AgNPs exhibited MIC values of 6.25μg/ml and 50 μg/ml against S. aureus and Candida albicans, respectively. In addition, AgNPs showed synergy effects by their combination with fluconazole that increased fold areas especially against A. niger, A. flavus and F. oxysporum.
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