Toxicity mechanisms and synergies of silver nanoparticles in 2,4-dichlorophenol degradation by Phanerochaete chrysosporium
[Display omitted] •Synergies of AgNPs at low doses (0–60μM) in 2,4-DCP biodegradation were observed.•Maximum degradation rates of 2,4-DCP were more than 94% at low-level AgNPs.•AgNPs-mediated toxicity to P. chrysosporium arised from the “Trojan-horse” effects.•2,4-DCP was completely degraded into CO...
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| Published in | Journal of hazardous materials Vol. 321; pp. 37 - 46 |
|---|---|
| Main Authors | , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Netherlands
Elsevier B.V
05.01.2017
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| Subjects | |
| Online Access | Get full text |
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| Abstract | [Display omitted]
•Synergies of AgNPs at low doses (0–60μM) in 2,4-DCP biodegradation were observed.•Maximum degradation rates of 2,4-DCP were more than 94% at low-level AgNPs.•AgNPs-mediated toxicity to P. chrysosporium arised from the “Trojan-horse” effects.•2,4-DCP was completely degraded into CO2 and H2O at optimum conditions.•Amino, carboxyl, carbonyl and sulfur-containing groups assist in Ag transportation.
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. |
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| AbstractList | 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
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 CO
and H
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
to Ag
. [Display omitted] •Synergies of AgNPs at low doses (0–60μM) in 2,4-DCP biodegradation were observed.•Maximum degradation rates of 2,4-DCP were more than 94% at low-level AgNPs.•AgNPs-mediated toxicity to P. chrysosporium arised from the “Trojan-horse” effects.•2,4-DCP was completely degraded into CO2 and H2O at optimum conditions.•Amino, carboxyl, carbonyl and sulfur-containing groups assist in Ag transportation. 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. 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 (0-60 mu M) 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. 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.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. 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. |
| Author | Wu, Jing Zhu, Yuan Zeng, Guangming Guo, Zhi He, Kai Chen, Guiqiu Zhang, Lihua Song, Zhongxian Hu, Liang Huang, Zhenzhen |
| Author_xml | – sequence: 1 givenname: Zhenzhen surname: Huang fullname: Huang, Zhenzhen organization: College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China – sequence: 2 givenname: Guiqiu surname: Chen fullname: Chen, Guiqiu email: gqchen@hnu.edu.cn organization: College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China – sequence: 3 givenname: Guangming surname: Zeng fullname: Zeng, Guangming email: zgming@hnu.edu.cn organization: College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China – sequence: 4 givenname: Zhi surname: Guo fullname: Guo, Zhi organization: College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China – sequence: 5 givenname: Kai surname: He fullname: He, Kai organization: College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China – sequence: 6 givenname: Liang surname: Hu fullname: Hu, Liang organization: College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China – sequence: 7 givenname: Jing surname: Wu fullname: Wu, Jing organization: College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China – sequence: 8 givenname: Lihua surname: Zhang fullname: Zhang, Lihua organization: College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China – sequence: 9 givenname: Yuan surname: Zhu fullname: Zhu, Yuan organization: College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China – sequence: 10 givenname: Zhongxian surname: Song fullname: Song, Zhongxian organization: Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming 650500, PR China |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27607931$$D View this record in MEDLINE/PubMed |
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| Keywords | Biodegradation 2,4-Dichlorophenol Phanerochaete chrysosporium Silver nanoparticles Synergies |
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•Synergies of AgNPs at low doses (0–60μM) in 2,4-DCP biodegradation were observed.•Maximum degradation rates of 2,4-DCP were more than 94% at... Mechanisms of silver nanoparticles-mediated toxicity to Phanerochaete chrysosporium and the influence of silver nanoparticles (AgNPs) on the biodegradation of... |
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| SubjectTerms | 2,4-Dichlorophenol Biodegradation Biodegradation, Environmental carbon dioxide Chlorophenols - metabolism cytotoxicity dechlorination Degradation Dose-Response Relationship, Drug Drug Synergism Exposure Fourier transform infrared spectroscopy hydroxyl radicals Metal Nanoparticles - toxicity moieties Nanoparticles nanosilver Nanostructure Oxidation-Reduction Phanerochaete - drug effects Phanerochaete - metabolism Phanerochaete chrysosporium Silver Silver - metabolism Silver - pharmacology Silver - toxicity Silver nanoparticles silver nitrate Synergies Toxicity |
| Title | Toxicity mechanisms and synergies of silver nanoparticles in 2,4-dichlorophenol degradation by Phanerochaete chrysosporium |
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