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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...

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Autores principales: Kawana, Hideaki, Miwa, Toru, Honda, Yuki, Furuya, Toshiki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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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