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A Mechanistic View of the Light-Induced Synthesis of Silver Nanoparticles Using Extracellular Polymeric Substances of Chlamydomonas reinhardtii
In the current study, extracellular polymeric substances (EPS) of Chlamydomonas reinhardtii and photon energy biosynthetically converted Ag(+) to silver nanoparticles (AgNPs). The reaction mechanism began with the non-photon-dependent adsorption of Ag(+) to EPS biomolecules. An electron from the EPS...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804166/ https://www.ncbi.nlm.nih.gov/pubmed/31569641 http://dx.doi.org/10.3390/molecules24193506 |
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author | Rahman, Ashiqur Kumar, Shishir Bafana, Adarsh Lin, Julia Dahoumane, Si Amar Jeffryes, Clayton |
author_facet | Rahman, Ashiqur Kumar, Shishir Bafana, Adarsh Lin, Julia Dahoumane, Si Amar Jeffryes, Clayton |
author_sort | Rahman, Ashiqur |
collection | PubMed |
description | In the current study, extracellular polymeric substances (EPS) of Chlamydomonas reinhardtii and photon energy biosynthetically converted Ag(+) to silver nanoparticles (AgNPs). The reaction mechanism began with the non-photon-dependent adsorption of Ag(+) to EPS biomolecules. An electron from the EPS biomolecules was then donated to reduce Ag(+) to Ag(0), while a simultaneous release of H(+) acidified the reaction mixture. The acidification of the media and production rate of AgNPs increased with increasing light intensity, indicating the light-dependent nature of the AgNP synthesis process. In addition, the extent of Ag(+) disappearance from the aqueous phase and the AgNP production rate were both dependent on the quantity of EPS in the reaction mixture, indicating Ag(+) adsorption to EPS as an important step in AgNP production. Following the reaction, stabilization of the NPs took place as a function of EPS concentration. The shifts in the intensities and positions of the functional groups, detected by Fourier-transform infrared spectroscopy (FTIR), indicated the potential functional groups in the EPS that reduced Ag(+), capped Ag(0), and produced stable AgNPs. Based on these findings, a hypothetic three-step, EPS-mediated biosynthesis mechanism, which includes a light-independent adsorption of Ag(+), a light-dependent reduction of Ag(+) to Ag(0), and an EPS concentration-dependent stabilization of Ag(0) to AgNPs, has been proposed. |
format | Online Article Text |
id | pubmed-6804166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68041662019-11-18 A Mechanistic View of the Light-Induced Synthesis of Silver Nanoparticles Using Extracellular Polymeric Substances of Chlamydomonas reinhardtii Rahman, Ashiqur Kumar, Shishir Bafana, Adarsh Lin, Julia Dahoumane, Si Amar Jeffryes, Clayton Molecules Article In the current study, extracellular polymeric substances (EPS) of Chlamydomonas reinhardtii and photon energy biosynthetically converted Ag(+) to silver nanoparticles (AgNPs). The reaction mechanism began with the non-photon-dependent adsorption of Ag(+) to EPS biomolecules. An electron from the EPS biomolecules was then donated to reduce Ag(+) to Ag(0), while a simultaneous release of H(+) acidified the reaction mixture. The acidification of the media and production rate of AgNPs increased with increasing light intensity, indicating the light-dependent nature of the AgNP synthesis process. In addition, the extent of Ag(+) disappearance from the aqueous phase and the AgNP production rate were both dependent on the quantity of EPS in the reaction mixture, indicating Ag(+) adsorption to EPS as an important step in AgNP production. Following the reaction, stabilization of the NPs took place as a function of EPS concentration. The shifts in the intensities and positions of the functional groups, detected by Fourier-transform infrared spectroscopy (FTIR), indicated the potential functional groups in the EPS that reduced Ag(+), capped Ag(0), and produced stable AgNPs. Based on these findings, a hypothetic three-step, EPS-mediated biosynthesis mechanism, which includes a light-independent adsorption of Ag(+), a light-dependent reduction of Ag(+) to Ag(0), and an EPS concentration-dependent stabilization of Ag(0) to AgNPs, has been proposed. MDPI 2019-09-27 /pmc/articles/PMC6804166/ /pubmed/31569641 http://dx.doi.org/10.3390/molecules24193506 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rahman, Ashiqur Kumar, Shishir Bafana, Adarsh Lin, Julia Dahoumane, Si Amar Jeffryes, Clayton A Mechanistic View of the Light-Induced Synthesis of Silver Nanoparticles Using Extracellular Polymeric Substances of Chlamydomonas reinhardtii |
title | A Mechanistic View of the Light-Induced Synthesis of Silver Nanoparticles Using Extracellular Polymeric Substances of Chlamydomonas reinhardtii |
title_full | A Mechanistic View of the Light-Induced Synthesis of Silver Nanoparticles Using Extracellular Polymeric Substances of Chlamydomonas reinhardtii |
title_fullStr | A Mechanistic View of the Light-Induced Synthesis of Silver Nanoparticles Using Extracellular Polymeric Substances of Chlamydomonas reinhardtii |
title_full_unstemmed | A Mechanistic View of the Light-Induced Synthesis of Silver Nanoparticles Using Extracellular Polymeric Substances of Chlamydomonas reinhardtii |
title_short | A Mechanistic View of the Light-Induced Synthesis of Silver Nanoparticles Using Extracellular Polymeric Substances of Chlamydomonas reinhardtii |
title_sort | mechanistic view of the light-induced synthesis of silver nanoparticles using extracellular polymeric substances of chlamydomonas reinhardtii |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804166/ https://www.ncbi.nlm.nih.gov/pubmed/31569641 http://dx.doi.org/10.3390/molecules24193506 |
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