Stress response of Microcystis aeruginosa to chlorine during transportation: The significance of surface-adsorbed organic matter

Jing Qi, Yuancheng Jiang, Rong Ni,Xi Wang,Chengzhi Hu,Jiuhui Qu

WATER RESEARCH(2024)

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摘要
The desorption of surface -adsorbed organic matter (S-AOM) without damaging algal cells was reported to be the key to destabilizing Microcystis aeruginosa (M. aeruginosa) cells while avoiding intracellular organic matter (IOM) release in our previous study. However, a temporal effect was found from spontaneous and continuous damage to algal cells even after quenching. This study aims to demonstrate the mechanism of the temporal inactivation effect and the stress response exhibited by chlorine -oxidized algal cells, and finally guide the prechlorination process for algae -laden water at water sources. Chlorine was proved to cause oxidative stress to M. aeruginosa cells, and result in a rapid increase in intracellular reactive oxygen species (ROS) levels. S-AOM appeared to have a protective effect on algal cells against oxidative damage, as evidenced by the maintenance of algal cell integrity and activated antioxidant enzymes. In addition, the activity of Caspase 3, a key protease for the execution of programmed cell death (PCD), was significantly enhanced during prechlorination. Cellular chromatin condensation and DNA fragmentation occurred in the early stages of PCD in algal cells. Therefore, the pre-treatment of algae -laden water at water sources, even with low chlorine doses, can induce a risk of significant algal cell death during the water transfer process due to activation of the PCD process, resulting in a higher health risk for drinking water. These findings indicate that both the dosage of chlorine and the duration of the transportation process should be considered during the prechlorination of algae -laden water, which can provide an important basis for avoiding increasing the risk to drinking water safety.
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关键词
Surface -adsorbed organic matter,Microcystis aeruginosa,Prechlorination,Stress response,Programmed cell death
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