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Polymer-Coated Mesoporous Carbon as Enzyme Platform for Oxidation of Bisphenol A in Organic Solvents
[Image: see text] Bisphenol A (BPA) is not only a widely used chemical but also a toxic pollutant, and its biodegradation in an aqueous environment is hard due to its near insolubility in water. While the enzyme tyrosinase can oxidize BPA in organic solvents, it does so only very slowly. In the pres...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787886/ https://www.ncbi.nlm.nih.gov/pubmed/31616819 http://dx.doi.org/10.1021/acsomega.9b01945 |
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author | Wu, Lidong Ji, Xiang Kong, Jing |
author_facet | Wu, Lidong Ji, Xiang Kong, Jing |
author_sort | Wu, Lidong |
collection | PubMed |
description | [Image: see text] Bisphenol A (BPA) is not only a widely used chemical but also a toxic pollutant, and its biodegradation in an aqueous environment is hard due to its near insolubility in water. While the enzyme tyrosinase can oxidize BPA in organic solvents, it does so only very slowly. In the present study, we have found that in toluene the catalytic activity of tyrosinase deposited onto coated mesoporous carbon is significantly enhanced when the support is precoated with polyethylenimine. The resultant enzymatically formed o-quinone is both easily recoverable and potentially useful monomer. As a particular example, the o-quinone readily reacts with diamine in toluene to form poly(amino-quinone) polymers, which are suitable for anticorrosion, energy storage, or biosensor applications. |
format | Online Article Text |
id | pubmed-6787886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-67878862019-10-15 Polymer-Coated Mesoporous Carbon as Enzyme Platform for Oxidation of Bisphenol A in Organic Solvents Wu, Lidong Ji, Xiang Kong, Jing ACS Omega [Image: see text] Bisphenol A (BPA) is not only a widely used chemical but also a toxic pollutant, and its biodegradation in an aqueous environment is hard due to its near insolubility in water. While the enzyme tyrosinase can oxidize BPA in organic solvents, it does so only very slowly. In the present study, we have found that in toluene the catalytic activity of tyrosinase deposited onto coated mesoporous carbon is significantly enhanced when the support is precoated with polyethylenimine. The resultant enzymatically formed o-quinone is both easily recoverable and potentially useful monomer. As a particular example, the o-quinone readily reacts with diamine in toluene to form poly(amino-quinone) polymers, which are suitable for anticorrosion, energy storage, or biosensor applications. American Chemical Society 2019-09-27 /pmc/articles/PMC6787886/ /pubmed/31616819 http://dx.doi.org/10.1021/acsomega.9b01945 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Wu, Lidong Ji, Xiang Kong, Jing Polymer-Coated Mesoporous Carbon as Enzyme Platform for Oxidation of Bisphenol A in Organic Solvents |
title | Polymer-Coated Mesoporous Carbon as Enzyme Platform
for Oxidation of Bisphenol A in Organic Solvents |
title_full | Polymer-Coated Mesoporous Carbon as Enzyme Platform
for Oxidation of Bisphenol A in Organic Solvents |
title_fullStr | Polymer-Coated Mesoporous Carbon as Enzyme Platform
for Oxidation of Bisphenol A in Organic Solvents |
title_full_unstemmed | Polymer-Coated Mesoporous Carbon as Enzyme Platform
for Oxidation of Bisphenol A in Organic Solvents |
title_short | Polymer-Coated Mesoporous Carbon as Enzyme Platform
for Oxidation of Bisphenol A in Organic Solvents |
title_sort | polymer-coated mesoporous carbon as enzyme platform
for oxidation of bisphenol a in organic solvents |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787886/ https://www.ncbi.nlm.nih.gov/pubmed/31616819 http://dx.doi.org/10.1021/acsomega.9b01945 |
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