Superior operational stability of immobilized l-asparaginase over surface-modified carbon nanotubes

Detalhes bibliográficos
Autor(a) principal: Almeida, Mafalda R.
Data de Publicação: 2021
Outros Autores: 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.
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.
id UNSP_91dd2334b00cd8e1f6d4bdad2cac55c4
oai_identifier_str oai:repositorio.unesp.br:11449/222793
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling 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:29462022-04-28T19:46:42Repositório 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
_version_ 1797790193993908224