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dc.contributor.author
Origone, Anabella Lucía

dc.contributor.author
Barberis, Sonia Esther

dc.contributor.author
Illanes, Andrés
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Guzmán, Fanny
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Camí, Gerardo Enrique

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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
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ASCLEPIAS CURASSAVICA L.
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ENZYMATIC SYNTHESIS OF PEPTIDES
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POROUS SILICA SUPPORTS
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PROTEASES IMMOBILIZATION
dc.subject.classification
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
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