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Soybean peroxidase-mediated degradation of an azo dye– a detailed mechanistic study

BACKGROUND: Peroxidases are emerging as an important class of enzymes that can be used for the efficient degradation of organic pollutants. However, detailed studies identifying the various intermediates produced and the mechanisms involved in the enzyme-mediated pollutant degradation are not widely...

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Autores principales: Ali, Liaquat, Algaithi, Rowdha, Habib, Hosam M, Souka, Usama, Rauf, Muhammad A, Ashraf, S Salman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028748/
https://www.ncbi.nlm.nih.gov/pubmed/24308857
http://dx.doi.org/10.1186/1471-2091-14-35
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author Ali, Liaquat
Algaithi, Rowdha
Habib, Hosam M
Souka, Usama
Rauf, Muhammad A
Ashraf, S Salman
author_facet Ali, Liaquat
Algaithi, Rowdha
Habib, Hosam M
Souka, Usama
Rauf, Muhammad A
Ashraf, S Salman
author_sort Ali, Liaquat
collection PubMed
description BACKGROUND: Peroxidases are emerging as an important class of enzymes that can be used for the efficient degradation of organic pollutants. However, detailed studies identifying the various intermediates produced and the mechanisms involved in the enzyme-mediated pollutant degradation are not widely published. RESULTS: In the present study, the enzymatic degradation of an azo dye (Crystal Ponceau 6R, CP6R) was studied using commercially available soybean peroxidase (SBP) enzyme. Several operational parameters affecting the enzymatic degradation of dye were evaluated and optimized, such as initial dye concentration, H(2)O(2) dosage, mediator amount and pH of the solution. Under optimized conditions, 40 ppm dye solution could be completely degraded in under one minute by SBP in the presence of H(2)O(2) and a redox mediator. Dye degradation was also confirmed using HPLC and TOC analyses, which showed that most of the dye was being mineralized to CO(2) in the process. CONCLUSIONS: Detailed analysis of metabolites, based on LC/MS results, showed that the enzyme-based degradation of the CP6R dye proceeded in two different reaction pathways- via symmetric azo bond cleavage as well as asymmetric azo bond breakage in the dye molecule. In addition, various critical transformative and oxidative steps such as deamination, desulfonation, keto-oxidation are explained on an electronic level. Furthermore, LC/MS/MS analyses confirmed that the end products in both pathways were small chain aliphatic carboxylic acids.
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spelling pubmed-40287482014-06-04 Soybean peroxidase-mediated degradation of an azo dye– a detailed mechanistic study Ali, Liaquat Algaithi, Rowdha Habib, Hosam M Souka, Usama Rauf, Muhammad A Ashraf, S Salman BMC Biochem Research Article BACKGROUND: Peroxidases are emerging as an important class of enzymes that can be used for the efficient degradation of organic pollutants. However, detailed studies identifying the various intermediates produced and the mechanisms involved in the enzyme-mediated pollutant degradation are not widely published. RESULTS: In the present study, the enzymatic degradation of an azo dye (Crystal Ponceau 6R, CP6R) was studied using commercially available soybean peroxidase (SBP) enzyme. Several operational parameters affecting the enzymatic degradation of dye were evaluated and optimized, such as initial dye concentration, H(2)O(2) dosage, mediator amount and pH of the solution. Under optimized conditions, 40 ppm dye solution could be completely degraded in under one minute by SBP in the presence of H(2)O(2) and a redox mediator. Dye degradation was also confirmed using HPLC and TOC analyses, which showed that most of the dye was being mineralized to CO(2) in the process. CONCLUSIONS: Detailed analysis of metabolites, based on LC/MS results, showed that the enzyme-based degradation of the CP6R dye proceeded in two different reaction pathways- via symmetric azo bond cleavage as well as asymmetric azo bond breakage in the dye molecule. In addition, various critical transformative and oxidative steps such as deamination, desulfonation, keto-oxidation are explained on an electronic level. Furthermore, LC/MS/MS analyses confirmed that the end products in both pathways were small chain aliphatic carboxylic acids. BioMed Central 2013-12-05 /pmc/articles/PMC4028748/ /pubmed/24308857 http://dx.doi.org/10.1186/1471-2091-14-35 Text en Copyright © 2013 Ali et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ali, Liaquat
Algaithi, Rowdha
Habib, Hosam M
Souka, Usama
Rauf, Muhammad A
Ashraf, S Salman
Soybean peroxidase-mediated degradation of an azo dye– a detailed mechanistic study
title Soybean peroxidase-mediated degradation of an azo dye– a detailed mechanistic study
title_full Soybean peroxidase-mediated degradation of an azo dye– a detailed mechanistic study
title_fullStr Soybean peroxidase-mediated degradation of an azo dye– a detailed mechanistic study
title_full_unstemmed Soybean peroxidase-mediated degradation of an azo dye– a detailed mechanistic study
title_short Soybean peroxidase-mediated degradation of an azo dye– a detailed mechanistic study
title_sort soybean peroxidase-mediated degradation of an azo dye– a detailed mechanistic study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028748/
https://www.ncbi.nlm.nih.gov/pubmed/24308857
http://dx.doi.org/10.1186/1471-2091-14-35
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