Biotransformation of disperse dyes using nitroreductase immobilized on magnetic particles modified with tosyl group: Identification of products by LC-MS-MS and theoretical studies conducted with DNA

Detalhes bibliográficos
Autor(a) principal: Franco, Jefferson Honorio [UNESP]
Data de Publicação: 2018
Outros Autores: da Silva, Bianca F. [UNESP], de Castro, Alexandre A., Ramalho, Teodorico C., Pividori, María Isabel, Zanoni, Maria Valnice Boldrin [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.envpol.2018.07.054
http://hdl.handle.net/11449/180169
Resumo: The present work evaluates the action of nitroreductase enzyme immobilized on Tosylactivated magnetic particles (MP-Tosyl) on three disperse dyes which contain nitro and azo groups. The dyes included Disperse Red 73 (DR 73), Disperse Red 78 (DR 78), and Disperse Red 167 (DR 167). The use of a magnet enabled the rapid and easy removal of the immobilized enzyme after biotransformation; this facilitated the identification of the products generated using high-performance liquid chromatography with diode array detector (HPLC-DAD) and mass spectrometry (LC-MS/MS). The main products formed by the in vitro biotransformation were identified as the product of nitro group reduction to the correspondent amine groups, which were denoted as follows: 50% of 2-(2-(4-((2-cyanoethyl)(ethyl)amino)phenyl)hydrazinyl)-5-nitrobenzonitrile, 98% of 3-((4-((4-amino-2-chlorophenyl) diazenyl)phenyl) (ethyl)amino)propanenitrile and 99% of (3-acetamido-4 - ((4-amino-2-chlorophenyl) diazenyl) phenyl) azanediyl) bis (ethane-2,1-diyl) for DR 73, DR 78 and DR 167, respectively. Based on the docking studies, the dyes investigated were found to be biotransformed by nitroreductase enzyme due to their favorable interaction with the active site of the enzyme. Theoretical results show that DR73 dye exhibits a relatively lower rate of degradation; this is attributed to the cyanide substituent which affects the electron density of the azo group. The docking studies also indicate that all the dyes presented significant reactivity towards DNA. However, Disperse Red 73 was found to exhibit a substantially higher reactivity compared to the other dyes; this implies that the dye possesses a relatively higher mutagenic power. The docking results also show that DR 73, DR 78 and DR 167 may be harmful to both humans and the environment, since the mutagenicity of nitro compounds is associated with the products formed during the reduction of nitro groups. These products can interact with biomolecules, including DNA, causing toxic and mutagenic effects. To sum up, the results point out that both the original textile dyes and their degradation products may pose serious risks to human health and the environment at large.
id UNSP_1c3363bc2d65e8d545dcfb39cc36cc57
oai_identifier_str oai:repositorio.unesp.br:11449/180169
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Biotransformation of disperse dyes using nitroreductase immobilized on magnetic particles modified with tosyl group: Identification of products by LC-MS-MS and theoretical studies conducted with DNABiotransformationDisperse dyes degradationEnzyme immobilized onto magnetiteNitroreductaseThe present work evaluates the action of nitroreductase enzyme immobilized on Tosylactivated magnetic particles (MP-Tosyl) on three disperse dyes which contain nitro and azo groups. The dyes included Disperse Red 73 (DR 73), Disperse Red 78 (DR 78), and Disperse Red 167 (DR 167). The use of a magnet enabled the rapid and easy removal of the immobilized enzyme after biotransformation; this facilitated the identification of the products generated using high-performance liquid chromatography with diode array detector (HPLC-DAD) and mass spectrometry (LC-MS/MS). The main products formed by the in vitro biotransformation were identified as the product of nitro group reduction to the correspondent amine groups, which were denoted as follows: 50% of 2-(2-(4-((2-cyanoethyl)(ethyl)amino)phenyl)hydrazinyl)-5-nitrobenzonitrile, 98% of 3-((4-((4-amino-2-chlorophenyl) diazenyl)phenyl) (ethyl)amino)propanenitrile and 99% of (3-acetamido-4 - ((4-amino-2-chlorophenyl) diazenyl) phenyl) azanediyl) bis (ethane-2,1-diyl) for DR 73, DR 78 and DR 167, respectively. Based on the docking studies, the dyes investigated were found to be biotransformed by nitroreductase enzyme due to their favorable interaction with the active site of the enzyme. Theoretical results show that DR73 dye exhibits a relatively lower rate of degradation; this is attributed to the cyanide substituent which affects the electron density of the azo group. The docking studies also indicate that all the dyes presented significant reactivity towards DNA. However, Disperse Red 73 was found to exhibit a substantially higher reactivity compared to the other dyes; this implies that the dye possesses a relatively higher mutagenic power. The docking results also show that DR 73, DR 78 and DR 167 may be harmful to both humans and the environment, since the mutagenicity of nitro compounds is associated with the products formed during the reduction of nitro groups. These products can interact with biomolecules, including DNA, causing toxic and mutagenic effects. To sum up, the results point out that both the original textile dyes and their degradation products may pose serious risks to human health and the environment at large.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Institute of Chemistry - São Paulo State University “Julio de Mesquita Filho”-UNESP-Avenida Professor Francisco Degni, 55, QuitandinhaDepartment of Chemistry Federal University of LavrasGroup of Sensors and Biosensors Autonomous University of BarcelonaInstitute of Chemistry - São Paulo State University “Julio de Mesquita Filho”-UNESP-Avenida Professor Francisco Degni, 55, QuitandinhaCNPq: 200309/2015-3 400459/2012-4FAPESP: 2008/10449-7FAPESP: 2015/18109-4Universidade Estadual Paulista (Unesp)Federal University of LavrasAutonomous University of BarcelonaFranco, Jefferson Honorio [UNESP]da Silva, Bianca F. [UNESP]de Castro, Alexandre A.Ramalho, Teodorico C.Pividori, María IsabelZanoni, Maria Valnice Boldrin [UNESP]2018-12-11T17:38:27Z2018-12-11T17:38:27Z2018-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article863-871application/pdfhttp://dx.doi.org/10.1016/j.envpol.2018.07.054Environmental Pollution, v. 242, p. 863-871.1873-64240269-7491http://hdl.handle.net/11449/18016910.1016/j.envpol.2018.07.0542-s2.0-850530714892-s2.0-85053071489.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengEnvironmental Pollution1,6151,615info:eu-repo/semantics/openAccess2023-12-17T06:17:42Zoai:repositorio.unesp.br:11449/180169Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-17T06:17:42Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Biotransformation of disperse dyes using nitroreductase immobilized on magnetic particles modified with tosyl group: Identification of products by LC-MS-MS and theoretical studies conducted with DNA
title Biotransformation of disperse dyes using nitroreductase immobilized on magnetic particles modified with tosyl group: Identification of products by LC-MS-MS and theoretical studies conducted with DNA
spellingShingle Biotransformation of disperse dyes using nitroreductase immobilized on magnetic particles modified with tosyl group: Identification of products by LC-MS-MS and theoretical studies conducted with DNA
Franco, Jefferson Honorio [UNESP]
Biotransformation
Disperse dyes degradation
Enzyme immobilized onto magnetite
Nitroreductase
title_short Biotransformation of disperse dyes using nitroreductase immobilized on magnetic particles modified with tosyl group: Identification of products by LC-MS-MS and theoretical studies conducted with DNA
title_full Biotransformation of disperse dyes using nitroreductase immobilized on magnetic particles modified with tosyl group: Identification of products by LC-MS-MS and theoretical studies conducted with DNA
title_fullStr Biotransformation of disperse dyes using nitroreductase immobilized on magnetic particles modified with tosyl group: Identification of products by LC-MS-MS and theoretical studies conducted with DNA
title_full_unstemmed Biotransformation of disperse dyes using nitroreductase immobilized on magnetic particles modified with tosyl group: Identification of products by LC-MS-MS and theoretical studies conducted with DNA
title_sort Biotransformation of disperse dyes using nitroreductase immobilized on magnetic particles modified with tosyl group: Identification of products by LC-MS-MS and theoretical studies conducted with DNA
author Franco, Jefferson Honorio [UNESP]
author_facet Franco, Jefferson Honorio [UNESP]
da Silva, Bianca F. [UNESP]
de Castro, Alexandre A.
Ramalho, Teodorico C.
Pividori, María Isabel
Zanoni, Maria Valnice Boldrin [UNESP]
author_role author
author2 da Silva, Bianca F. [UNESP]
de Castro, Alexandre A.
Ramalho, Teodorico C.
Pividori, María Isabel
Zanoni, Maria Valnice Boldrin [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Federal University of Lavras
Autonomous University of Barcelona
dc.contributor.author.fl_str_mv Franco, Jefferson Honorio [UNESP]
da Silva, Bianca F. [UNESP]
de Castro, Alexandre A.
Ramalho, Teodorico C.
Pividori, María Isabel
Zanoni, Maria Valnice Boldrin [UNESP]
dc.subject.por.fl_str_mv Biotransformation
Disperse dyes degradation
Enzyme immobilized onto magnetite
Nitroreductase
topic Biotransformation
Disperse dyes degradation
Enzyme immobilized onto magnetite
Nitroreductase
description The present work evaluates the action of nitroreductase enzyme immobilized on Tosylactivated magnetic particles (MP-Tosyl) on three disperse dyes which contain nitro and azo groups. The dyes included Disperse Red 73 (DR 73), Disperse Red 78 (DR 78), and Disperse Red 167 (DR 167). The use of a magnet enabled the rapid and easy removal of the immobilized enzyme after biotransformation; this facilitated the identification of the products generated using high-performance liquid chromatography with diode array detector (HPLC-DAD) and mass spectrometry (LC-MS/MS). The main products formed by the in vitro biotransformation were identified as the product of nitro group reduction to the correspondent amine groups, which were denoted as follows: 50% of 2-(2-(4-((2-cyanoethyl)(ethyl)amino)phenyl)hydrazinyl)-5-nitrobenzonitrile, 98% of 3-((4-((4-amino-2-chlorophenyl) diazenyl)phenyl) (ethyl)amino)propanenitrile and 99% of (3-acetamido-4 - ((4-amino-2-chlorophenyl) diazenyl) phenyl) azanediyl) bis (ethane-2,1-diyl) for DR 73, DR 78 and DR 167, respectively. Based on the docking studies, the dyes investigated were found to be biotransformed by nitroreductase enzyme due to their favorable interaction with the active site of the enzyme. Theoretical results show that DR73 dye exhibits a relatively lower rate of degradation; this is attributed to the cyanide substituent which affects the electron density of the azo group. The docking studies also indicate that all the dyes presented significant reactivity towards DNA. However, Disperse Red 73 was found to exhibit a substantially higher reactivity compared to the other dyes; this implies that the dye possesses a relatively higher mutagenic power. The docking results also show that DR 73, DR 78 and DR 167 may be harmful to both humans and the environment, since the mutagenicity of nitro compounds is associated with the products formed during the reduction of nitro groups. These products can interact with biomolecules, including DNA, causing toxic and mutagenic effects. To sum up, the results point out that both the original textile dyes and their degradation products may pose serious risks to human health and the environment at large.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:38:27Z
2018-12-11T17:38:27Z
2018-11-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.envpol.2018.07.054
Environmental Pollution, v. 242, p. 863-871.
1873-6424
0269-7491
http://hdl.handle.net/11449/180169
10.1016/j.envpol.2018.07.054
2-s2.0-85053071489
2-s2.0-85053071489.pdf
url http://dx.doi.org/10.1016/j.envpol.2018.07.054
http://hdl.handle.net/11449/180169
identifier_str_mv Environmental Pollution, v. 242, p. 863-871.
1873-6424
0269-7491
10.1016/j.envpol.2018.07.054
2-s2.0-85053071489
2-s2.0-85053071489.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Environmental Pollution
1,615
1,615
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 863-871
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1803046986438410240