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胞外聚合物对蛋白核小球藻砷积累的影响。

Effect of extracellular polymeric substances on arsenic accumulation in Chlorella pyrenoidosa.

机构信息

College of Environmental and Resource Sciences, Zhejiang University, 866 Yuhangtang Road, Hangzhou, Zhejiang Province 310058, China; National Demonstration Center for Experimental Environment and Resources Education (Zhejiang University), Hangzhou 310058, China.

College of Environmental and Resource Sciences, Zhejiang University, 866 Yuhangtang Road, Hangzhou, Zhejiang Province 310058, China.

出版信息

Sci Total Environ. 2020 Feb 20;704:135368. doi: 10.1016/j.scitotenv.2019.135368. Epub 2019 Nov 23.

Abstract

Inorganic arsenic (iAs) in its dominant dissolved phase in the environment is known to pose major threats to ecological and human health. While the biological effects in many arsenic-bearing freshwaters have been extensively studied, the behavior and bioaccumulation of dissolved iAS in the presence of extracellular polymeric substances (EPS) still remains to be a critical knowledge gap. In this study, the uptakes and kinetic characteristics of iAs were studied using Chlorella pyrenoidosa (a typical freshwater green algae) by addressing the different effects of EPS on arsenite (As) and arsenate (As). The arsenic uptake capacity increased as the exposure concentration increased from 0 to 300 µmol L, and the uptake rate constants (K) in the Bio-dynamic model were greater for As than As (0.63-11.57 L g h vs. 0.44-5.43 L g h). The toxic effects as mitigated by EPS were observed through the morphological changes of algal cells by TEM and SEM. When compared with the EPS-free algal cells (EPS-F), EPS-covered cells (EPS-C) had a higher arsenic adsorption capacity through EPS-enhanced surface adsorption and reduced intracellular uptake. The overall decrease (35% and 23.3% for As and As, respectively) in the maximum uptake capacity in intact algae cells favors cell's tolerance to the toxic effects of iAs. These observed discrepancies between As and As and between EPS-C and EPS-F were further elucidated through morphological images (TEM and SEM) and molecular/atomic spectroscopic data that combine three-dimensional excitation-emission matrix fluorescence spectroscopy (3D-EEM), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Altogether, the spectroscopic evidence revealed the interactions of iAs with C-O-C, C-O-H and -NH functional groups in EPS' tyrosine- and tryptophan-like proteins as the binding sites. Overall, this study for the first time provides comprehensive evidence on the iAs-EPS interactions. Such insights will benefit our understanding of the biogeochemical processes of iAs and the strategic development of bioremediation techniques involving microalgae in the natural and engineered systems.

摘要

环境中以溶解态为主的无机砷 (iAs) 对生态和人类健康构成重大威胁。虽然含砷的淡水生物效应已得到广泛研究,但在细胞外聚合物 (EPS) 存在的情况下,溶解态 iAs 的行为和生物累积仍然是一个关键的知识空白。在这项研究中,通过研究 EPS 对亚砷酸盐 (As) 和砷酸盐 (As) 的不同影响,使用蛋白核小球藻 (一种典型的淡水绿藻) 研究了 iAs 的吸收和动力学特性。砷的吸收能力随着暴露浓度从 0 增加到 300 μmol/L 而增加,生物动力学模型中的吸收速率常数 (K) 对 As 的吸收大于对 As 的吸收 (0.63-11.57 L g h 对 0.44-5.43 L g h)。通过 TEM 和 SEM 观察到 EPS 对藻细胞形态的改变,减轻了砷的毒性效应。与无 EPS 的藻细胞 (EPS-F) 相比,EPS 覆盖的细胞 (EPS-C) 通过 EPS 增强的表面吸附和减少的细胞内摄取具有更高的砷吸附能力。完整藻类细胞中最大吸收能力的总体下降 (As 为 35%,As 为 23.3%) 有利于细胞对 iAs 毒性效应的耐受。通过三维激发-发射矩阵荧光光谱 (3D-EEM)、傅里叶变换红外光谱 (FTIR) 和 X 射线光电子能谱 (XPS) 相结合的形态图像 (TEM 和 SEM) 和分子/原子光谱数据,进一步阐明了 As 和 As 之间以及 EPS-C 和 EPS-F 之间的这些差异。总之,光谱证据表明 iAs 与 EPS 中天冬氨酸-和色氨酸样蛋白中的 C-O-C、C-O-H 和-NH 官能团相互作用作为结合位点。总的来说,这项研究首次提供了 iAs-EPS 相互作用的综合证据。这些见解将有助于我们理解 iAs 的生物地球化学过程,以及涉及自然和工程系统中微藻的生物修复技术的战略发展。

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