Department of Biotechnology, Noida Institute of Engineering and Technology, Greater Noida, India.
Department of Microbiology, Swami Shraddhanand College, University of Delhi, Delhi, India.
Water Environ Res. 2021 Nov;93(11):2727-2739. doi: 10.1002/wer.1629. Epub 2021 Sep 15.
The present study utilized Aspergillus spp. for the synthesis of silver nanoparticles (AgNPs); the developed AgNPs were categorized using analytical techniques, that is, ultraviolet-visible (UV-vis) spectrophotometer, Zeta-potential, dynamic light scattering (DLS), and transmission electron microscopy (TEM). A sharp peak of 463 nm highlighted the synthesis of AgNPs; further Zeta-potential of -16 mV indicates stability of synthesized AgNPs. The TEM micrograph showed spherical and hexagonal shapes of synthesized AgNPs of 6-25 nm. The photocatalytic activity of fungal-mediated AgNPs was evaluated for degradation of reactive yellow dye in the concentration range of 20-100 mg L . The results showed efficient degradation of dye using AgNPs in short span of time. For antibacterial activity, synthesized AgNPs, antibiotic, and AgNPs + antibiotic were tested. As per results, the zone of inhibition (ZOI) of AgNPs showed the values of 13 and 10 mm for Escherichia coli and Staphylococcus aureus, respectively. Further, the ZOI of penicillin highlighted the values of 18 and 17 mm for E. coli and S. aureus, respectively. When AgNPs and penicillin were used in combination, a clear synergistic effect was observed; the ZOI showed 0.49- and 0.36-fold increase in area against E. coli and S. aureus, respectively, in comparison with penicillin or AgNPs alone. Further, the leftover biomass (retentate biomass) was used to decolorize the reactive yellow dye at different initial concentration ranging from 20 to 100 mg L . It was observed that 1 g L retentate biomass (B ) can effectively remove 82%-100% dye at 20 and 100 mg L initial dye concentration. Results also indicated that with increase in initial reactive dye concentration from 20 to 100 mg L , the decolorization capacity of retentate biomass (B ) (at 0.2 g L ) decreased from 79.2% to 32.3%. However, the use of AgNPs synthesized leftover fungal biomass can be a good option for up taking the additional dyes/contaminants, and also as leftover biomass can be utilized effectively, it can prove to be an excellent approach for environment safety. As the literature studies did not mentioned the further use of retentate biomass, the present study provides an excellent approach for further research on this aspect. PRACTITIONER POINTS: Synthesis of AgNPs from Aspergillus spp. and characterized with the help of a U.V-vis spectrophotometer, a zeta potential, DLS and TEM. The developed AgNPs were used for antibacterial and dye degradation activity. The left over (retentate) fungal biomass was used further for additional dye degradation activity.
本研究利用曲霉属(Aspergillus spp.)合成了银纳米粒子(AgNPs);通过分析技术,即紫外-可见分光光度计、Zeta 电位、动态光散射(DLS)和透射电子显微镜(TEM)对所制备的 AgNPs 进行分类。463nm 处的尖锐峰值表明 AgNPs 的合成;进一步的 Zeta 电位为-16mV 表明合成的 AgNPs 的稳定性。TEM 显微照片显示合成的 AgNPs 呈球形和六方形状,粒径为 6-25nm。研究评估了真菌介导的 AgNPs 的光催化活性,用于在 20-100mg/L 浓度范围内降解活性黄染料。结果表明,AgNPs 在短时间内有效地降解了染料。对于抗菌活性,测试了合成的 AgNPs、抗生素和 AgNPs+抗生素。结果表明,AgNPs 对大肠杆菌和金黄色葡萄球菌的抑菌圈(ZOI)分别为 13 和 10mm。此外,青霉素的抑菌圈(ZOI)分别为大肠杆菌和金黄色葡萄球菌的 18 和 17mm。当 AgNPs 和青霉素联合使用时,观察到明显的协同作用;与单独使用青霉素或 AgNPs 相比,ZOI 对大肠杆菌和金黄色葡萄球菌的面积分别增加了 0.49 倍和 0.36 倍。此外,剩余的生物质(保留物生物质)用于在不同的初始浓度(20-100mg/L)下对活性黄染料进行脱色。结果表明,1g/L 的保留物生物质(B)可以在 20 和 100mg/L 的初始染料浓度下有效去除 82%-100%的染料。结果还表明,随着初始反应性染料浓度从 20mg/L 增加到 100mg/L,保留物生物质(B)(在 0.2g/L)的脱色能力从 79.2%降低到 32.3%。然而,使用合成的曲霉属 leftover 生物质的 AgNPs 可以是吸收额外染料/污染物的好选择,而且由于可以有效地利用 leftover 生物质,因此它可以成为环境安全的绝佳方法。由于文献研究没有提到进一步使用保留物生物质,本研究为这方面的进一步研究提供了一个极好的方法。从业者要点:从曲霉属(Aspergillus spp.)合成 AgNPs 并借助 U.V-vis 分光光度计、Zeta 电位、DLS 和 TEM 进行表征。所开发的 AgNPs 用于抗菌和染料降解活性。剩余的(保留物)真菌生物质进一步用于额外的染料降解活性。