Department of Chemical and Biochemical Engineering, College of Chemistry and Chemical Engineering, and The Key Laboratory for Synthetic Biotechnology of Xiamen City, Xiamen University , Xiamen, P. R. China.
Environ Sci Technol. 2014 Jul 1;48(13):7469-76. doi: 10.1021/es4055077. Epub 2014 Jun 13.
Microcosm experiments were conducted to investigate the mechanism of microbial-mediated As mobilization from high arsenic tailing sediments amended with nanoparticles (NPs). The addition of SiO2 NPs could substantially stimulate arsenic mobilization in the sodium acetate amendment sediments. However, the addition of Fe2O3 and Fe3O4 NPs restrained arsenic release because these NPs resulted in Fe-As coprecipiate. Moreover, NP additions in sediments amended with sodium acetate as the electron donor clearly promoted microbial dissimilatory iron reduction. Nearly 4 times the Fe(II) (11.67-12.87 mg·L(-1)) from sediments amended with NPs and sodium acetate was released compared to sediments amended with only sodium acetate (3.49 mg·L(-1)). Based on molecular fingerprinting and sequencing analyses, the NP additions could potentially change the sediment bacterial community composition and increase the abundance of Fe(III) and As(V) reduction bacteria. Several potential NP-stimulated bacteria were related to Geobacter, Anaeromyxobacter, Clostridium, and Alicyclobacillus. The findings offer a relatively comprehensive assessment of NP (e.g., Fe2O3, Fe3O4, and SiO2) effects on sediment bacterial communities and As mobilization.
开展微宇宙实验以研究纳米颗粒(NPs)添加条件下从高砷尾矿沉积物中微生物介导的砷迁移机制。SiO2 NPs 的添加可显著刺激乙酸钠添加沉积物中的砷迁移。然而,Fe2O3 和 Fe3O4 NPs 的添加抑制了砷的释放,因为这些 NPs 导致了 Fe-As 共沉淀。此外,在以乙酸钠作为电子供体的沉积物中添加 NPs 明显促进了微生物异化铁还原。与仅添加乙酸钠的沉积物相比(3.49 mg·L(-1)),添加 NPs 和乙酸钠的沉积物中释放出的 Fe(II)(11.67-12.87 mg·L(-1))增加了近 4 倍。基于分子指纹图谱和测序分析,NP 的添加可能会改变沉积物细菌群落组成,并增加 Fe(III) 和 As(V)还原细菌的丰度。一些潜在的受 NP 刺激的细菌与 Geobacter、Anaeromyxobacter、Clostridium 和 Alicyclobacillus 有关。这些发现为 NPs(例如 Fe2O3、Fe3O4 和 SiO2)对沉积物细菌群落和砷迁移的影响提供了相对全面的评估。