4.7 Article

Photocatalytic inactivation and destruction of harmful microalgae Karenia mikimotoi under visible-light irradiation: Insights into physiological response and toxicity assessment

期刊

ENVIRONMENTAL RESEARCH
卷 198, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.envres.2021.111295

关键词

Photocatalysis; Karenia mikimotoi; Marine microalgae; Physiological response; Inactivation mechanism

资金

  1. Science and Technology Program of Guangzhou, China [202002030177]
  2. Guangdong Basic and Applied Basic Research Foundation for Distinguished Young Scholars [2021B1515020063]
  3. National Natural Science Foundation of China [21607028, U1901210, 41606175]
  4. National Key Research and Development Program of China [2019YFC1804501]
  5. Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01Z032]

向作者/读者索取更多资源

This study attempted visible-light-driven photocatalytic inactivation of Karenia mikimotoi using g-C3N4/TiO2 immobilized films as a model photocatalyst for the first time, achieving a high inactivation efficiency of 64% within 60 minutes. The study also confirmed the excellent photo-stability and recyclability of the immobilized photocatalyst films. Moreover, the mechanisms study revealed the specific cell rupture process of the inactivated algal cells, as well as the physiological responses and detoxification mechanisms involved.
Harmful algal blooms (HABs) caused by Karenia mikimotoi have frequently happened in coastal waters worldwide, causing serious damages to marine ecosystems and economic losses. Photocatalysis has potential to in-situ inhibit algal growth using sustainable sunlight. However, the inactivation and detoxification mechanisms of microalgae in marine environment have not been systematically investigated. In this work, for the first time, visible-light-driven photocatalytic inactivation of K. mikimotoi was attempted using g-C3N4/TiO2 immobilized films as a model photocatalyst. The inactivation efficiency could reach 64% within 60 min, evaluated by realtime in vivo chlorophyll-a fluorometric method. The immobilized photocatalyst films also exhibited excellent photo-stability and recyclability. Mechanisms study indicated photo-generated h+ and 1O2 were the dominant reactive species. Algal cell rupture process was monitored by fluorescent microscope combined with SEM observation, which confirmed the damage of cell membrane followed by the leakage of the intracellular components including the entire cell nucleus. The physiological responses regarding up-regulation of antioxidant enzyme activity (i.e. CAT and SOD), intracellular ROSs level and lipid peroxidation were all observed. Moreover, the intracellular release profile and acute toxicity assessment indicated the toxic K. mikimotoi was successfully detoxified, and the released organic matter had no cytotoxicity. This work not only provides a potential new strategy for in-situ treatment of K. mikimotoi using sunlight at sea environments, but also creates avenue for understanding the inactivation and destruction mechanisms of marine microalgae treated by photocatalysis and the toxicity impacts on the marine environments.

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