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

Motivated by recent studies that documented changes in fullerene toxicity after chemical transformation, C60 aggregates (nC60) were subject to UVC irradiation at monochromatic 254 nm and subsequently evaluated for antibacterial and bactericidal properties against Escherichia coli. The nC60 treated w...

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Published inEnvironmental science & technology Vol. 45; no. 22; pp. 9627 - 9633
Main Authors Cho, Min, Snow, Samuel D, Hughes, Joseph B, Kim, Jae-Hong
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 15.11.2011
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ISSN0013-936X
1520-5851
1520-5851
DOI10.1021/es202269r

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Abstract Motivated by recent studies that documented changes in fullerene toxicity after chemical transformation, C60 aggregates (nC60) were subject to UVC irradiation at monochromatic 254 nm and subsequently evaluated for antibacterial and bactericidal properties against Escherichia coli. The nC60 treated with UVC irradiation, referred to herein as UVC-irradiated C60, did not directly inhibit bacterial growth at concentrations up to 20 mg/L. In the presence of UVA and visible light, however, UVC-irradiated C60 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 C60 diffusing through E. coli cell membrane and producing hydroxyl radicals within the cell. Further study on water-soluble C60 derivatives and possible transformative processes is, therefore, recommended based on the environmental implications of results presented herein that nC60 exposed to UVC irradiation is more toxic than parent nC60.
AbstractList 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 C(60) 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).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 C(60) 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).
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 C(60) 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).
Motivated by recent studies that documented changes in fullerene toxicity after chemical transformation, C60 aggregates (nC60) were subject to UVC irradiation at monochromatic 254 nm and subsequently evaluated for antibacterial and bactericidal properties against Escherichia coli. The nC60 treated with UVC irradiation, referred to herein as UVC-irradiated C60, did not directly inhibit bacterial growth at concentrations up to 20 mg/L. In the presence of UVA and visible light, however, UVC-irradiated C60 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 C60 diffusing through E. coli cell membrane and producing hydroxyl radicals within the cell. Further study on water-soluble C60 derivatives and possible transformative processes is, therefore, recommended based on the environmental implications of results presented herein that nC60 exposed to UVC irradiation is more toxic than parent nC60.
Author Cho, Min
Hughes, Joseph B
Kim, Jae-Hong
Snow, Samuel D
AuthorAffiliation Chonbuk National University
Georgia Institute of Technology
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Issue 22
Keywords Microbiology
Toxicity
Escherichia coli
Atomic cluster
Disinfection
UVC radiation
Ultraviolet irradiation
Pathogenic
Metabolic inactivation
Fullerenes
Bacteria
Water pollution
Biological contamination
Nanostructured materials
Enterobacteriaceae
Gram negative bacteria
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Snippet Motivated by recent studies that documented changes in fullerene toxicity after chemical transformation, C60 aggregates (nC60) were subject to UVC irradiation...
Motivated by recent studies that documented changes in fullerene toxicity after chemical transformation, C(60) aggregates (nC(60)) were subject to UVC...
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SubjectTerms Anti-Bacterial Agents - chemistry
Anti-Bacterial Agents - pharmacology
Applied sciences
Biological and physicochemical phenomena
Environmental Processes
Escherichia coli - drug effects
Escherichia coli - growth & development
Escherichia coli Infections - drug therapy
Exact sciences and technology
Fullerenes - chemistry
Fullerenes - pharmacology
Humans
Kinetics
Natural water pollution
Photochemical Processes
Pollution
Ultraviolet Rays
Water treatment and pollution
Title Escherichia coli Inactivation by UVC-Irradiated C60: Kinetics and Mechanisms
URI http://dx.doi.org/10.1021/es202269r
https://www.ncbi.nlm.nih.gov/pubmed/21999435
https://www.proquest.com/docview/904008063
Volume 45
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