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Toxicity mechanisms and synergies of silver nanoparticles in 2,4-dichlorophenol degradation by Phanerochaete chrysosporium.

Identifieur interne : 000147 ( Main/Exploration ); précédent : 000146; suivant : 000148

Toxicity mechanisms and synergies of silver nanoparticles in 2,4-dichlorophenol degradation by Phanerochaete chrysosporium.

Auteurs : Zhenzhen Huang [République populaire de Chine] ; Guiqiu Chen [République populaire de Chine] ; Guangming Zeng [République populaire de Chine] ; Zhi Guo [République populaire de Chine] ; Kai He [République populaire de Chine] ; Liang Hu [République populaire de Chine] ; Jing Wu [République populaire de Chine] ; Lihua Zhang [République populaire de Chine] ; Yuan Zhu [République populaire de Chine] ; Zhongxian Song [République populaire de Chine]

Source :

RBID : pubmed:27607931

Descripteurs français

English descriptors

Abstract

Mechanisms of silver nanoparticles-mediated toxicity to Phanerochaete chrysosporium and the influence of silver nanoparticles (AgNPs) on the biodegradation of 2,4-dichlorophenol (2,4-DCP) have been systematically investigated. AgNPs at low doses (0-60μM) have greatly enhanced the degradation ability of P. chrysosporium to 2,4-DCP with the maximum degradation rates of more than 94%, exhibiting excellent synergies between AgNPs and P. chrysosporium in the degradation of 2,4-DCP. Meanwhile, removal of total Ag was also at high levels and highly pH dependent. However, significant inhibition was highlighted on 2,4-DCP biodegradation and Ag removal upon treatment with AgNPs at high doses and AgNO3 at low-level exposure. Results also suggested that AgNPs-induced cytotoxicity could arise from the "Trojan-horse" mechanism executing particle effects, ion effects, or both, ruling out extracellularly released Ag+. Moreover, under relatively low concentrations of AgNPs exposure, 2,4-DCP was broken into linear chain organics, and eventually turned into CO2 and H2O through reductive dechlorination and reaction with hydroxyl radicals. FTIR analysis showed that amino, carboxyl, carbonyl, and sulfur-containing functional groups played crucial roles in Ag transportation and the reduction of Ag+ to Ag0.

DOI: 10.1016/j.jhazmat.2016.08.075
PubMed: 27607931


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<term>Dose-Response Relationship, Drug (MeSH)</term>
<term>Drug Synergism (MeSH)</term>
<term>Metal Nanoparticles (toxicity)</term>
<term>Oxidation-Reduction (MeSH)</term>
<term>Phanerochaete (drug effects)</term>
<term>Phanerochaete (metabolism)</term>
<term>Silver (metabolism)</term>
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<term>Silver (toxicity)</term>
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<term>Argent (toxicité)</term>
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<term>Dépollution biologique de l'environnement (MeSH)</term>
<term>Nanoparticules métalliques (toxicité)</term>
<term>Oxydoréduction (MeSH)</term>
<term>Phanerochaete (effets des médicaments et des substances chimiques)</term>
<term>Phanerochaete (métabolisme)</term>
<term>Relation dose-effet des médicaments (MeSH)</term>
<term>Synergie des médicaments (MeSH)</term>
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<term>Silver</term>
</keywords>
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<term>Phanerochaete</term>
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<term>Silver</term>
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<term>Oxydoréduction</term>
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<div type="abstract" xml:lang="en">Mechanisms of silver nanoparticles-mediated toxicity to Phanerochaete chrysosporium and the influence of silver nanoparticles (AgNPs) on the biodegradation of 2,4-dichlorophenol (2,4-DCP) have been systematically investigated. AgNPs at low doses (0-60μM) have greatly enhanced the degradation ability of P. chrysosporium to 2,4-DCP with the maximum degradation rates of more than 94%, exhibiting excellent synergies between AgNPs and P. chrysosporium in the degradation of 2,4-DCP. Meanwhile, removal of total Ag was also at high levels and highly pH dependent. However, significant inhibition was highlighted on 2,4-DCP biodegradation and Ag removal upon treatment with AgNPs at high doses and AgNO
<sub>3</sub>
at low-level exposure. Results also suggested that AgNPs-induced cytotoxicity could arise from the "Trojan-horse" mechanism executing particle effects, ion effects, or both, ruling out extracellularly released Ag
<sup>+</sup>
. Moreover, under relatively low concentrations of AgNPs exposure, 2,4-DCP was broken into linear chain organics, and eventually turned into CO
<sub>2</sub>
and H
<sub>2</sub>
O through reductive dechlorination and reaction with hydroxyl radicals. FTIR analysis showed that amino, carboxyl, carbonyl, and sulfur-containing functional groups played crucial roles in Ag transportation and the reduction of Ag
<sup>+</sup>
to Ag
<sup>0</sup>
.</div>
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<Day>05</Day>
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<Title>Journal of hazardous materials</Title>
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<ArticleTitle>Toxicity mechanisms and synergies of silver nanoparticles in 2,4-dichlorophenol degradation by Phanerochaete chrysosporium.</ArticleTitle>
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<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.jhazmat.2016.08.075</ELocationID>
<Abstract>
<AbstractText>Mechanisms of silver nanoparticles-mediated toxicity to Phanerochaete chrysosporium and the influence of silver nanoparticles (AgNPs) on the biodegradation of 2,4-dichlorophenol (2,4-DCP) have been systematically investigated. AgNPs at low doses (0-60μM) have greatly enhanced the degradation ability of P. chrysosporium to 2,4-DCP with the maximum degradation rates of more than 94%, exhibiting excellent synergies between AgNPs and P. chrysosporium in the degradation of 2,4-DCP. Meanwhile, removal of total Ag was also at high levels and highly pH dependent. However, significant inhibition was highlighted on 2,4-DCP biodegradation and Ag removal upon treatment with AgNPs at high doses and AgNO
<sub>3</sub>
at low-level exposure. Results also suggested that AgNPs-induced cytotoxicity could arise from the "Trojan-horse" mechanism executing particle effects, ion effects, or both, ruling out extracellularly released Ag
<sup>+</sup>
. Moreover, under relatively low concentrations of AgNPs exposure, 2,4-DCP was broken into linear chain organics, and eventually turned into CO
<sub>2</sub>
and H
<sub>2</sub>
O through reductive dechlorination and reaction with hydroxyl radicals. FTIR analysis showed that amino, carboxyl, carbonyl, and sulfur-containing functional groups played crucial roles in Ag transportation and the reduction of Ag
<sup>+</sup>
to Ag
<sup>0</sup>
.</AbstractText>
<CopyrightInformation>Copyright © 2016 Elsevier B.V. All rights reserved.</CopyrightInformation>
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<Affiliation>College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China; Key Laboratory of Environmental Biology and Pollution Control (Hunan University), Ministry of Education, Changsha 410082, PR China.</Affiliation>
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<LastName>Chen</LastName>
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<Affiliation>College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China; Key Laboratory of Environmental Biology and Pollution Control (Hunan University), Ministry of Education, Changsha 410082, PR China. Electronic address: gqchen@hnu.edu.cn.</Affiliation>
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<DescriptorName UI="D020075" MajorTopicYN="N">Phanerochaete</DescriptorName>
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<QualifierName UI="Q000633" MajorTopicYN="Y">toxicity</QualifierName>
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<Keyword MajorTopicYN="N">2,4-Dichlorophenol</Keyword>
<Keyword MajorTopicYN="N">Biodegradation</Keyword>
<Keyword MajorTopicYN="N">Phanerochaete chrysosporium</Keyword>
<Keyword MajorTopicYN="N">Silver nanoparticles</Keyword>
<Keyword MajorTopicYN="N">Synergies</Keyword>
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<Day>01</Day>
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<Year>2016</Year>
<Month>08</Month>
<Day>29</Day>
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<Month>08</Month>
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<name sortKey="He, Kai" sort="He, Kai" uniqKey="He K" first="Kai" last="He">Kai He</name>
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<name sortKey="Zhu, Yuan" sort="Zhu, Yuan" uniqKey="Zhu Y" first="Yuan" last="Zhu">Yuan Zhu</name>
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