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Effect of extracellular polymeric substances on arsenic accumulation Chlorella pyrenoidosa

机译:细胞外聚合物对砷积累小球藻的影响

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摘要

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~Ⅲ) and arsenate (As~Ⅴ). The arsenic uptake capacity increased as the exposure concentration increased from 0 to 300 nmol L~(-1) and the uptake rate constants (K_u) in the Bio-dynamic model were greater for As~Ⅴ than As~Ⅲ (0.63-11.57 L g~(-1) h-~(-1) vs. 0.44-5.43 L g~(-1) h~(-1)). 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~Ⅲ and As~Ⅴ, 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~Ⅲ and As~Ⅴ 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_2 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.
机译:众所周知,环境中处于溶解状态的无机砷(iAs)对生态和人类健康构成重大威胁。尽管已经对许多含砷淡水的生物学效应进行了广泛研究,但是在存在细胞外聚合物(EPS)的情况下溶解的iAS的行为和生物蓄积仍然是关键的知识缺口。本研究利用小球藻小球藻(一种典型的淡水绿藻)研究了iAs的吸收和动力学特性,探讨了EPS对亚砷酸盐(As〜Ⅲ)和砷酸盐(As〜Ⅴ)的不同影响。砷的吸收能力随着暴露浓度从0增加到300 nmol L〜(-1)而增加,并且在生物动力学模型中As〜Ⅴ的吸收速率常数(K_u)大于As〜Ⅲ(0.63-11.57 L g〜(-1)h ~~(-1)与0.44-5.43 L g〜(-1)h〜(-1))。通过TEM和SEM观察藻类细胞的形态变化,观察到EPS减轻的毒性作用。与不含EPS的藻类细胞(EPS-F)相比,EPS覆盖的细胞(EPS-C)通过EPS增强的表面吸附具有更高的砷吸附能力,并减少了细胞内摄取。完整藻类细胞最大吸收能力的总体下降(分别为As〜Ⅲ和As〜Ⅴ的35%和23.3%)有利于细胞对iAs毒性作用的耐受性。通过形态图像(TEM和SEM)以及结合三维激发-发射矩阵荧光光谱(3D)的分子/原子光谱数据进一步阐明了这些观测到的As〜Ⅲ和As〜Ⅴ之间以及EPS-C和EPS-F之间的差异。 -EEM),傅里叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)。总的来说,光谱学证据表明,iA与EPS酪氨酸和色氨酸样蛋白中的C-O-C,C-O-H和-NH_2官能团相互作用。总体而言,这项研究首次为iAs-EPS相互作用提供了全面的证据。这些见解将有助于我们了解iAs的生物地球化学过程,以及在自然和工程系统中涉及微藻的生物修复技术的战略发展。

著录项

  • 来源
    《The Science of the Total Environment》 |2020年第20期|135368.1-135368.13|共13页
  • 作者单位

    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;

    Department of Environmental Science University of Houston-Clear Lake Houston TX 77058 United States;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Green algae; Arsenite; Arsenate; Bioremediation; Kinetic characteristics;

    机译:绿藻;亚砷酸盐砷酸盐生物修复;动力学特性;

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