Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubes
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1038/s41598-021-00841-2 http://hdl.handle.net/11449/222793 |
Resumo: | l-asparaginase (ASNase, EC 3.5.1.1) is an enzyme that catalyzes the l-asparagine hydrolysis into l-aspartic acid and ammonia, being mainly applied in pharmaceutical and food industries. However, some disadvantages are associated with its free form, such as the ASNase short half-life, which may be overcome by enzyme immobilization. In this work, the immobilization of ASNase by adsorption over pristine and modified multi-walled carbon nanotubes (MWCNTs) was investigated, the latter corresponding to functionalized MWCNTs through a hydrothermal oxidation treatment. Different operating conditions, including pH, contact time and ASNase/MWCNT mass ratio, as well as the operational stability of the immobilized ASNase, were evaluated. For comparison purposes, data regarding the ASNase immobilization with pristine MWCNT was detailed. The characterization of the ASNase-MWCNT bioconjugate was addressed using different techniques, namely Transmission Electron Microscopy (TEM), Thermogravimetric Analysis (TGA) and Raman spectroscopy. Functionalized MWCNTs showed promising results, with an immobilization yield and a relative recovered activity of commercial ASNase above 95% under the optimized adsorption conditions (pH 8, 60 min of contact and 1.5 × 10–3 g mL−1 of ASNase). The ASNase-MWCNT bioconjugate also showed improved enzyme operational stability (6 consecutive reaction cycles without activity loss), paving the way for its use in industrial processes. |
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Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubesl-asparaginase (ASNase, EC 3.5.1.1) is an enzyme that catalyzes the l-asparagine hydrolysis into l-aspartic acid and ammonia, being mainly applied in pharmaceutical and food industries. However, some disadvantages are associated with its free form, such as the ASNase short half-life, which may be overcome by enzyme immobilization. In this work, the immobilization of ASNase by adsorption over pristine and modified multi-walled carbon nanotubes (MWCNTs) was investigated, the latter corresponding to functionalized MWCNTs through a hydrothermal oxidation treatment. Different operating conditions, including pH, contact time and ASNase/MWCNT mass ratio, as well as the operational stability of the immobilized ASNase, were evaluated. For comparison purposes, data regarding the ASNase immobilization with pristine MWCNT was detailed. The characterization of the ASNase-MWCNT bioconjugate was addressed using different techniques, namely Transmission Electron Microscopy (TEM), Thermogravimetric Analysis (TGA) and Raman spectroscopy. Functionalized MWCNTs showed promising results, with an immobilization yield and a relative recovered activity of commercial ASNase above 95% under the optimized adsorption conditions (pH 8, 60 min of contact and 1.5 × 10–3 g mL−1 of ASNase). The ASNase-MWCNT bioconjugate also showed improved enzyme operational stability (6 consecutive reaction cycles without activity loss), paving the way for its use in industrial processes.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Fundação para a Ciência e a TecnologiaCICECO-Aveiro Institute of Materials Department of Chemistry University of AveiroLaboratory of Separation and Reaction Engineering - Laboratory of Catalysis and Materials (LSRE-LCM) Department of Chemical Engineering Faculty of Engineering University of Porto, Rua do Dr. Roberto FriasDepartment of Engineering Bioprocess and Biotechnology School of Pharmaceutical Sciences São Paulo State University (Unesp)Department of Engineering Bioprocess and Biotechnology School of Pharmaceutical Sciences São Paulo State University (Unesp)FAPESP: 2018/06908-8Fundação para a Ciência e a Tecnologia: POCI-01-0145-FEDER-031268Fundação para a Ciência e a Tecnologia: UIDB/50011/2020University of AveiroUniversity of PortoUniversidade Estadual Paulista (UNESP)Almeida, Mafalda R.Cristóvão, Raquel O.Barros, Maria A.Nunes, João C. F.Boaventura, Rui A. R.Loureiro, José M.Faria, Joaquim L.Neves, Márcia C.Freire, Mara G.Santos-Ebinuma, Valéria C. [UNESP]Tavares, Ana P. M.Silva, Cláudia G.2022-04-28T19:46:42Z2022-04-28T19:46:42Z2021-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1038/s41598-021-00841-2Scientific Reports, v. 11, n. 1, 2021.2045-2322http://hdl.handle.net/11449/22279310.1038/s41598-021-00841-22-s2.0-85118451348Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengScientific Reportsinfo:eu-repo/semantics/openAccess2022-04-28T19:46:42Zoai:repositorio.unesp.br:11449/222793Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:03:16.042070Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubes |
title |
Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubes |
spellingShingle |
Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubes Almeida, Mafalda R. |
title_short |
Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubes |
title_full |
Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubes |
title_fullStr |
Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubes |
title_full_unstemmed |
Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubes |
title_sort |
Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubes |
author |
Almeida, Mafalda R. |
author_facet |
Almeida, Mafalda R. Cristóvão, Raquel O. Barros, Maria A. Nunes, João C. F. Boaventura, Rui A. R. Loureiro, José M. Faria, Joaquim L. Neves, Márcia C. Freire, Mara G. Santos-Ebinuma, Valéria C. [UNESP] Tavares, Ana P. M. Silva, Cláudia G. |
author_role |
author |
author2 |
Cristóvão, Raquel O. Barros, Maria A. Nunes, João C. F. Boaventura, Rui A. R. Loureiro, José M. Faria, Joaquim L. Neves, Márcia C. Freire, Mara G. Santos-Ebinuma, Valéria C. [UNESP] Tavares, Ana P. M. Silva, Cláudia G. |
author2_role |
author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
University of Aveiro University of Porto Universidade Estadual Paulista (UNESP) |
dc.contributor.author.fl_str_mv |
Almeida, Mafalda R. Cristóvão, Raquel O. Barros, Maria A. Nunes, João C. F. Boaventura, Rui A. R. Loureiro, José M. Faria, Joaquim L. Neves, Márcia C. Freire, Mara G. Santos-Ebinuma, Valéria C. [UNESP] Tavares, Ana P. M. Silva, Cláudia G. |
description |
l-asparaginase (ASNase, EC 3.5.1.1) is an enzyme that catalyzes the l-asparagine hydrolysis into l-aspartic acid and ammonia, being mainly applied in pharmaceutical and food industries. However, some disadvantages are associated with its free form, such as the ASNase short half-life, which may be overcome by enzyme immobilization. In this work, the immobilization of ASNase by adsorption over pristine and modified multi-walled carbon nanotubes (MWCNTs) was investigated, the latter corresponding to functionalized MWCNTs through a hydrothermal oxidation treatment. Different operating conditions, including pH, contact time and ASNase/MWCNT mass ratio, as well as the operational stability of the immobilized ASNase, were evaluated. For comparison purposes, data regarding the ASNase immobilization with pristine MWCNT was detailed. The characterization of the ASNase-MWCNT bioconjugate was addressed using different techniques, namely Transmission Electron Microscopy (TEM), Thermogravimetric Analysis (TGA) and Raman spectroscopy. Functionalized MWCNTs showed promising results, with an immobilization yield and a relative recovered activity of commercial ASNase above 95% under the optimized adsorption conditions (pH 8, 60 min of contact and 1.5 × 10–3 g mL−1 of ASNase). The ASNase-MWCNT bioconjugate also showed improved enzyme operational stability (6 consecutive reaction cycles without activity loss), paving the way for its use in industrial processes. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-12-01 2022-04-28T19:46:42Z 2022-04-28T19:46:42Z |
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/10.1038/s41598-021-00841-2 Scientific Reports, v. 11, n. 1, 2021. 2045-2322 http://hdl.handle.net/11449/222793 10.1038/s41598-021-00841-2 2-s2.0-85118451348 |
url |
http://dx.doi.org/10.1038/s41598-021-00841-2 http://hdl.handle.net/11449/222793 |
identifier_str_mv |
Scientific Reports, v. 11, n. 1, 2021. 2045-2322 10.1038/s41598-021-00841-2 2-s2.0-85118451348 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Scientific Reports |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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 |
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1808129387839619072 |