Studies on DNA fragmentation and cell integrity of rapidly hydroxyl radical inactivated Microcystis aeruginosa

铜绿微囊藻 细胞内 化学 DNA断裂 羟基自由基 DNA损伤 碎片(计算) DNA 细胞外 彗星试验 微生物学 分子生物学 生物化学 细胞凋亡 程序性细胞死亡 激进的 生物 细菌 蓝藻 遗传学 生态学
作者
Qilin Zheng,Changqing Tian,Yubo Zhang,Mindong Bai,Pengyu Liang,Yongning Bian
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:454: 140414-140414 被引量:18
标识
DOI:10.1016/j.cej.2022.140414
摘要

• Cells of rapidly •OH-inactivated M. aeruginosa maintained their integrity. • The surge in intracellular •OH was a crucial factor for rapid •OH-inactivation. • •OH-inactivation was mainly caused by DNA fragmentation. • Direct action of •OH on the DNA was verified by the increase of marker 8-OHdG to 1.4 times. Microcystis aeruginosa ( M. aeruginosa ) blooms occur frequently in freshwater lakes and reservoirs, posing a great threaten to drinking water safety. When using conventional oxidants remedy toxic algae, there is an unavoidable shortage leading to cell rupture and release of intracellular organic matter (IOM), thus causing more serious hazard to water safety. In this study, with the synergistic effect of strong ionisation discharge and hydrodynamic cavitation, hydroxyl radical (•OH) were generated and injected into cells to inactivate M. aeruginosa within 3 s. •OH-inactivated M. aeruginosa was intact without rupture and exhibited a 39% increase in DOC due to the degradation of the components of the cell wall and extracellular matrix. For comparison, ClO 2 inactivated M. aeruginosa after 10 min of exposure, which induced cell rupture and a 113% increase in DOC due to the release of IOM. Meanwhile, in •OH-inactivated M. aeruginosa , intracellular •OH was increased to 2 times according to the detection by fluorescence probe and the DNA oxidative damage biomarker 8-hydroxy-2’-deoxyguanosine increased to 1.4 times according to the enzyme-linked immunosorbent assay, confirming the direct action of •OH on the DNA. And •OH induced DNA fragmentation in cells of M. aeruginosa was identified by comet assay and TUNEL assay, finding a 464% increase in the DNA tail length, and 96.71% of the cells showed DNA phosphatediester bond cleavage. In summary, the main reason for the rapid •OH-inactivation of M. aeruginosa is DNA fragmentation, which may represent a new method for the safely and efficient control of harmful algal blooms.
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