Escherichia coli Inactivation by UVC-Irradiated C60: Kinetics and Mechanisms

被引:21
作者
Cho, Min [1 ,2 ]
Snow, Samuel D. [1 ]
Hughes, Joseph B. [1 ]
Kim, Jae-Hong [1 ]
机构
[1] Georgia Inst Technol, Sch Civil & Environm Engn, Atlanta, GA 30332 USA
[2] Chonbuk Natl Univ, Div Biotechnol, Adv Inst Environm & Biosci, Coll Environm & Bioresource Sci, Iksan 570752, Jeonbuk, South Korea
基金
美国国家科学基金会; 新加坡国家研究基金会;
关键词
TITANIUM-DIOXIDE; AQUEOUS-PHASE; FULLERENE DERIVATIVES; BACTERICIDAL ACTIVITY; PROTEIN OXIDATION; WATER SUSPENSION; CLUSTERS; TIO2; PHOTOCHEMISTRY; TRANSFORMATION;
D O I
10.1021/es202269r
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Motivated by recent studies that documented changes in fullerene toxicity after chemical transformation, C-60 aggregates (nC(60)) were subject to UVC irradiation at monochromatic 254 nm and subsequently evaluated for antibacterial and bactericidal properties against Escherichia coli. The nC(60) treated with UVC irradiation, referred to herein as UVC-irradiated C-60, did not directly inhibit bacterial growth at concentrations up to 20 mg/L. In the presence of UVA and visible light, however, UVC-irradiated C-60 rapidly inactivated E. coli, suggesting that photochemical production of reactive oxygen species (ROS) was involved. The use of ROS scavengers and probes determined that hydroxyl radicals were the primary ROS responsible for the E. coli inactivation. Results from protein release, lipid peroxidation, cell permeability, and intracellular enzyme assays suggest that the inactivation mechanism involves UVC-irradiated diffusing through E. coli cell membrane and producing hydroxyl radicals within the cell. Further study on water-soluble C-60 derivatives and possible transformative processes is, therefore, recommended based on the environmental implications of results presented herein that nC(60) exposed to UVC irradiation is more toxic than parent nC(60).
引用
收藏
页码:9627 / 9633
页数:7
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