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Impact of reactive oxygen species on cell activity and structural integrity of Gram-positive and Gram-negative bacteria in electrochemical disinfection system

化学 Zeta电位 肽聚糖 金黄色葡萄球菌 乳酸脱氢酶 细菌 大肠杆菌 微生物学 电化学 细菌细胞结构 细胞壁 羟基自由基 核化学 生物化学 生物 纳米技术 电极 材料科学 纳米颗粒 抗氧化剂 物理化学 基因 遗传学
作者
Junke Zhang,Peidong Su,Huihuang Chen,Meng Qiao,Bo Yang,Xu Zhao
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:451: 138879-138879 被引量:73
标识
DOI:10.1016/j.cej.2022.138879
摘要

High efficiency, eco-friendly, and without disinfection byproducts rendered the hydroxyl radical-dominated electrochemical process a promising disinfection technology. Inconsistent disinfection performances have been reported for Gram-positive (G+) and Gram-negative (G−) bacteria in *OH-dominated disinfection system. To thoroughly present and elucidate the different responses of G+ and G−, Fe-Co/CA cathode and Ru-Ir/Ti anode was fabricated. Under 22.73 mA/cm2, E. coli were completely inactivated within 45 min, while there were about 2 logs of S. aureus were inactivated. Moreover, the sublethal injury of E. coli outperformed that of S. aureus as well. However, when E. coli and S. aureus coexisted, the disinfection efficiencies were inhibited for both E. coli and S. aureus. The subcellular damage of E. coli and S. aureus were different as well. With the reaction, cell surface hydrophobicity for both E. coli and S. aureus increased. However, E. coli obtained increased negative zeta potential after treatment, which promoted the development of electrochemical disinfection, while S. aureus obtained decreased negative zeta potential which resulted in significant agglomeration. The determination of malondialdehyde (MDA), phosphate concentration, and the leakage of Lactate dehydrogenase (LDH), as well as the degradation of protein, TOC, and nucleic acid, and SEM observation, illustrated the cell well and cell outer membrane were the first barrier to OH-dominated disinfection. The thick and rigid cell wall and the stable structure of peptidoglycan (PGN) in S. aureus cells contributed to the high resistance of S. aureus.
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