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dc.contributor.author
Origone, Anabella Lucía  
dc.contributor.author
Barberis, Sonia Esther  
dc.contributor.author
Illanes, Andrés  
dc.contributor.author
Guzmán, Fanny  
dc.contributor.author
Camí, Gerardo Enrique  
dc.contributor.author
Liggieri, Constanza Silvina  
dc.contributor.author
Martínez, Ronny  
dc.contributor.author
Bernal, Cintia Claudia  
dc.date.available
2020-10-28T13:50:10Z  
dc.date.issued
2020-08  
dc.identifier.citation
Origone, Anabella Lucía; Barberis, Sonia Esther; Illanes, Andrés; Guzmán, Fanny; Camí, Gerardo Enrique; et al.; Improvement of enzymatic performance of Asclepias curassavica L. proteases by immobilization: Application to the synthesis of an antihypertensive peptide; Elsevier; Process Biochemistry; 95; 8-2020; 36-46  
dc.identifier.issn
1359-5113  
dc.identifier.uri
http://hdl.handle.net/11336/117038  
dc.description.abstract
The aim of this work was to study different immobilization strategies on silica supports in order to obtain robust biocatalysts from latex proteases of Asclepias curassavica L., a South American native plant. Immobilized enzyme performance was evaluated under harsh reaction conditions such as the synthesis of the antihypertensive peptide N-α-CBZ-Val-Gly-OH. Proteases from A. curassavica, named asclepain, were immobilized (0.51–5.56 mg of protein/ g of support) in non-functionalized silica (S), in glyoxyl-silica (GS) and in octyl-glyoxyl-silica (OGS), by adsorption, and multi-point covalent attachment on mono and hetero-functional supports, respectively, under previously determined optimal immobilization conditions. Immobilization yields were expressed as activity yield (Ya) and protein yield (Yp). Asclepain-OGS showed the highest Ya (178 ± 1.62 %) meaning an expressed activity 1.8 times higher than the offered activity, while Yp was 75 ± 0.4 %. Ya for asclepain-S and -GS were 64 ± 1.45 % and 16 ± 0.37 %, respectively. Best results were attributed to the ability of OGS support to guide the enzyme before covalent attachment, increasing its reactivity. Asclepain-OGS led to product yield of 95.5 ± 0.14 %, five times higher than soluble asclepain in the synthesis of N-α-CBZ-Val-Gly-OH, after 3 h in 30 % methanol in 0.1 M Tris-HCl buffer pH 8.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
ANTIHYPERTENSIVE PEPTIDE  
dc.subject
ASCLEPIAS CURASSAVICA L.  
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ENZYMATIC SYNTHESIS OF PEPTIDES  
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POROUS SILICA SUPPORTS  
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PROTEASES IMMOBILIZATION  
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Bioprocesamiento Tecnológico, Biocatálisis, Fermentación  
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Biotecnología Industrial  
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INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Improvement of enzymatic performance of Asclepias curassavica L. proteases by immobilization: Application to the synthesis of an antihypertensive peptide  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2020-07-22T15:40:40Z  
dc.journal.volume
95  
dc.journal.pagination
36-46  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Origone, Anabella Lucía. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Física Aplicada "Dr. Jorge Andrés Zgrablich". Universidad Nacional de San Luis. Facultad de Ciencias Físico Matemáticas y Naturales. Instituto de Física Aplicada "Dr. Jorge Andrés Zgrablich"; Argentina. Universidad de La Serena; Chile. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Departamento de Farmacia. Laboratorio de Bromatología; Argentina  
dc.description.fil
Fil: Barberis, Sonia Esther. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Física Aplicada "Dr. Jorge Andrés Zgrablich". Universidad Nacional de San Luis. Facultad de Ciencias Físico Matemáticas y Naturales. Instituto de Física Aplicada "Dr. Jorge Andrés Zgrablich"; Argentina. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Departamento de Farmacia. Laboratorio de Bromatología; Argentina  
dc.description.fil
Fil: Illanes, Andrés. Pontificia Universidad Católica de Valparaíso. Escuela de Ingeniería Bioquímica; Chile  
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Fil: Guzmán, Fanny. Pontificia Universidad Católica de Valparaíso; Chile  
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Fil: Camí, Gerardo Enrique. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina  
dc.description.fil
Fil: Liggieri, Constanza Silvina. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Departamento de Ciencias Biológicas. Laboratorio de Investigación de Proteínas Vegetales; Argentina. Universidad Maimónides. Centro de Estudios Biomédicos, Básicos, Aplicados y Desarrollo. Departamento de Ciencias Biológicas y Biomédicas; Argentina  
dc.description.fil
Fil: Martínez, Ronny. Universidad de La Serena; Chile  
dc.description.fil
Fil: Bernal, Cintia Claudia. Universidad de La Serena; Chile  
dc.journal.title
Process Biochemistry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S1359511320302294  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.procbio.2020.05.013