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Sustainable Approach for Peroxygenase-Catalyzed Oxidation Reactions Using Hydrogen Peroxide Generated from Spent Coffee Grounds and Tea Leaf Residues
[Image: see text] Peroxygenases are promising catalysts for use in the oxidation of chemicals as they catalyze the direct oxidation of a variety of compounds under ambient conditions using hydrogen peroxide (H(2)O(2)) as an oxidant. Although the use of peroxygenases provides a simple method for oxid...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201881/ https://www.ncbi.nlm.nih.gov/pubmed/35721909 http://dx.doi.org/10.1021/acsomega.2c02186 |
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author | Kawana, Hideaki Miwa, Toru Honda, Yuki Furuya, Toshiki |
author_facet | Kawana, Hideaki Miwa, Toru Honda, Yuki Furuya, Toshiki |
author_sort | Kawana, Hideaki |
collection | PubMed |
description | [Image: see text] Peroxygenases are promising catalysts for use in the oxidation of chemicals as they catalyze the direct oxidation of a variety of compounds under ambient conditions using hydrogen peroxide (H(2)O(2)) as an oxidant. Although the use of peroxygenases provides a simple method for oxidation of chemicals, the anthraquinone process currently used to produce H(2)O(2) requires significant energy input and generates considerable waste, which negatively affects process sustainability and production costs. Thus, generating H(2)O(2) for peroxygenases on site using an environmentally benign method would be advantageous. Here, we utilized spent coffee grounds (SCGs) and tea leaf residues (TLRs) for the production of H(2)O(2). These waste biomass products reacted with molecular oxygen and effectively generated H(2)O(2) in sodium phosphate buffer. The resulting H(2)O(2) was utilized by the bacterial P450 peroxygenase, CYP152A1. Both SCG-derived and TLR-derived H(2)O(2) promoted the CYP152A1-catalyzed oxidation of 4-methoxy-1-naphthol to Russig’s blue as a model reaction. In addition, when CYP152A1 was incubated with styrene, the SCG and TLR solutions enabled the synthesis of styrene oxide and phenylacetaldehyde. This new approach using waste biomass provides a simple, cost-effective, and sustainable oxidation method that should be readily applicable to other peroxygenases for the synthesis of a variety of valuable chemicals. |
format | Online Article Text |
id | pubmed-9201881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92018812022-06-17 Sustainable Approach for Peroxygenase-Catalyzed Oxidation Reactions Using Hydrogen Peroxide Generated from Spent Coffee Grounds and Tea Leaf Residues Kawana, Hideaki Miwa, Toru Honda, Yuki Furuya, Toshiki ACS Omega [Image: see text] Peroxygenases are promising catalysts for use in the oxidation of chemicals as they catalyze the direct oxidation of a variety of compounds under ambient conditions using hydrogen peroxide (H(2)O(2)) as an oxidant. Although the use of peroxygenases provides a simple method for oxidation of chemicals, the anthraquinone process currently used to produce H(2)O(2) requires significant energy input and generates considerable waste, which negatively affects process sustainability and production costs. Thus, generating H(2)O(2) for peroxygenases on site using an environmentally benign method would be advantageous. Here, we utilized spent coffee grounds (SCGs) and tea leaf residues (TLRs) for the production of H(2)O(2). These waste biomass products reacted with molecular oxygen and effectively generated H(2)O(2) in sodium phosphate buffer. The resulting H(2)O(2) was utilized by the bacterial P450 peroxygenase, CYP152A1. Both SCG-derived and TLR-derived H(2)O(2) promoted the CYP152A1-catalyzed oxidation of 4-methoxy-1-naphthol to Russig’s blue as a model reaction. In addition, when CYP152A1 was incubated with styrene, the SCG and TLR solutions enabled the synthesis of styrene oxide and phenylacetaldehyde. This new approach using waste biomass provides a simple, cost-effective, and sustainable oxidation method that should be readily applicable to other peroxygenases for the synthesis of a variety of valuable chemicals. American Chemical Society 2022-06-01 /pmc/articles/PMC9201881/ /pubmed/35721909 http://dx.doi.org/10.1021/acsomega.2c02186 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Kawana, Hideaki Miwa, Toru Honda, Yuki Furuya, Toshiki Sustainable Approach for Peroxygenase-Catalyzed Oxidation Reactions Using Hydrogen Peroxide Generated from Spent Coffee Grounds and Tea Leaf Residues |
title | Sustainable Approach for Peroxygenase-Catalyzed Oxidation
Reactions Using Hydrogen Peroxide Generated from Spent Coffee Grounds
and Tea Leaf Residues |
title_full | Sustainable Approach for Peroxygenase-Catalyzed Oxidation
Reactions Using Hydrogen Peroxide Generated from Spent Coffee Grounds
and Tea Leaf Residues |
title_fullStr | Sustainable Approach for Peroxygenase-Catalyzed Oxidation
Reactions Using Hydrogen Peroxide Generated from Spent Coffee Grounds
and Tea Leaf Residues |
title_full_unstemmed | Sustainable Approach for Peroxygenase-Catalyzed Oxidation
Reactions Using Hydrogen Peroxide Generated from Spent Coffee Grounds
and Tea Leaf Residues |
title_short | Sustainable Approach for Peroxygenase-Catalyzed Oxidation
Reactions Using Hydrogen Peroxide Generated from Spent Coffee Grounds
and Tea Leaf Residues |
title_sort | sustainable approach for peroxygenase-catalyzed oxidation
reactions using hydrogen peroxide generated from spent coffee grounds
and tea leaf residues |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201881/ https://www.ncbi.nlm.nih.gov/pubmed/35721909 http://dx.doi.org/10.1021/acsomega.2c02186 |
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