Hossain Md Sabbir, Okino Tatsufumi
Graduate School of Environmental Science, Hokkaido University Sapporo 060-0810 Japan
Department of Environmental Science and Technology, Jashore University of Science and Technology Jashore-7408 Bangladesh.
RSC Adv. 2024 Apr 2;14(15):10452-10463. doi: 10.1039/d4ra00409d. eCollection 2024 Mar 26.
The cyanoremediation technique for heavy metal (HM) removal from wastewater using live cyanobacteria is promising to reduce the pollution risk both for the environment and human health. In this study, two widely recognized freshwater cyanobacteria, and sp., were used to explore their efficacy in HM (As(v), Cd(ii), Cr(vi), Pb(ii)) removal. The different optimum adsorption conditions were pH 8 and 7.5 for and sp., respectively, but the temperature (25 °C) and contact time (48 hours) were the same for both strains. Under these specified conditions, exhibited the capability to remove 25% of As(v), 78% of Cd(ii), 54% of Cr(vi), and 17% of Pb(ii), whereas sp. removed 77% of As(v), 57% of Cd(ii), 91% of Cr(vi), and 77% of Pb(ii) at different initial concentrations. Metal diversity interfered negatively with cyanobacterial growth, especially Cd(ii) and As(v), as measured by OD, dry biomass, chlorophyll a, and carotenoid production for both strains. Fourier transform infrared spectrum (FT-IR) analysis revealed the existence of diverse surface binding sites for HM adsorption, stemming from proteins and polysaccharides. Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray Spectroscopy (EDS) confirmed the presence of HMs on the surface of the cyanobacterial cells. Finally, the zeta potential results indicating alterations in the surface negative charges elucidated the adsorption mechanisms involved in the HM removal by both cyanobacteria. These results provided a comprehensive understanding of the HM adsorption mechanism by cyanobacteria, offering valuable theoretical insights that can be extrapolated to enhance our comprehension of the cyanoremediation mechanisms by various other cyanobacterial strains.
利用活的蓝藻从废水中去除重金属的蓝藻修复技术有望降低对环境和人类健康的污染风险。在本研究中,使用了两种广泛认可的淡水蓝藻,[具体名称1]和[具体名称2],来探索它们去除重金属(砷(Ⅴ)、镉(Ⅱ)、铬(Ⅵ)、铅(Ⅱ))的效果。[具体名称1]和[具体名称2]去除重金属的不同最佳吸附条件分别为pH 8和7.5,但两种菌株的温度(25℃)和接触时间(48小时)相同。在这些特定条件下,[具体名称1]能够去除25%的砷(Ⅴ)、78%的镉(Ⅱ)、54%的铬(Ⅵ)和17%的铅(Ⅱ),而[具体名称2]在不同初始浓度下分别去除了77%的砷(Ⅴ)、57%的镉(Ⅱ)、91%的铬(Ⅵ)和77%的铅(Ⅱ)。通过测量两种菌株的OD、干生物量、叶绿素a和类胡萝卜素产量发现,金属多样性对蓝藻生长有负面影响,尤其是镉(Ⅱ)和砷(Ⅴ)。傅里叶变换红外光谱(FT-IR)分析表明,蛋白质和多糖产生了多种用于重金属吸附的表面结合位点。扫描电子显微镜(SEM)和能量色散X射线光谱(EDS)证实了蓝藻细胞表面存在重金属。最后,ζ电位结果表明表面负电荷的变化阐明了两种蓝藻去除重金属所涉及的吸附机制。这些结果全面了解了蓝藻对重金属的吸附机制,提供了有价值的理论见解,可用于增进我们对其他各种蓝藻菌株蓝藻修复机制的理解。