4.7 Article

Oxidative stress in the cyanobacterium Microcystis aeruginosa PCC 7813: Comparison of different analytical cell stress detection assays

Journal

CHEMOSPHERE
Volume 269, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2020.128766

Keywords

Cyanobacteria; Fluorescence; Microcystin; Water treatment; Hydrogen peroxide

Funding

  1. Engineering and Physical Sciences Research Council (EPSRC) [EP/P029280/1]
  2. Coordination for the Improvement of Higher Education Personnel - CAPES [PROEX 20/2016, PrInt 88887.311806/2018-00]
  3. Brazilian National Research Council-e CNPq [403116/2016-3, 304164/2017-8]
  4. Ceara Research Support Foundation - FUNCAP [PNE-0112-00042.01.00/16]
  5. EPSRC [EP/P029280/1] Funding Source: UKRI

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Cyanobacterial blooms pose a danger to human and animal health due to cyanotoxins, and traditional water treatment methods struggle to remove cyanobacterial cells efficiently. Hydrogen peroxide has been shown to suppress cyanobacterial growth effectively, with photosynthetic activity proving to be the most suitable method for rapid oxidative cell stress detection in cyanobacteria. Combined methods are recommended for efficient water treatment management.
Cyanobacterial blooms are observed when high cell densities occur and are often dangerous to human and animal health due to the presence of cyanotoxins. Conventional drinking water treatment technology struggles to efficiently remove cyanobacterial cells and their metabolites during blooms, increasing costs and decreasing water quality. Although field applications of hydrogen peroxide have been shown to successfully suppress cyanobacterial growth, a rapid and accurate measure of the effect of oxidative stress on cyanobacterial cells is required. In the current study, H2O2 (5 and 20 mg L-1) was used to induce oxidative stress in Microcystis aeruginosa PCC 7813. Cell density, quantumyield of photosystem II, minimal fluorescence and microcystin (MC-LR, -LY, -LW, -LF) concentrations were compared when evaluating M. aeruginosa cellular stress. Chlorophyll content (determined by minimal fluorescence) decreased by 10% after 48 h while cell density was reduced by 97% after 24 h in samples treated with 20 mg L-1 H2O2. Photosystem II quantum yield (photosynthetic activity) indicated cyanobacteria cell stress within 6 h, which was considerably faster than the other methods. Intracellular microcystins (MC-LR, -LY, -LW and -LF) were reduced by at least 96% after 24 h of H2O2 treatment. No increase in extracellular microcystin concentration was detected, which suggests that the intracellular microcystins released into the surrounding water were completely removed by the hydrogen peroxide. Thus, photosynthetic activity was deemed the most suitable and rapid method for oxidative cell stress detection in cyanobacteria, however, an approach using combined methods is recomended for efficient water treatment management. Crown Copyright (C) 2020 Published by Elsevier Ltd. All rights reserved.

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