Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B

Autores
Celiz, Gustavo; Martearena, Maria Rita; Scaroni, Elsa Elda; Daz, Mirta Elizabeth
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Alkyl prunin esters are new compounds, which are soluble in lipophilic media. They possess antioxidant and antibacterial properties, so they may have useful applications. The current work studied the kinetic of prunin 6'. -O-laurate synthesis catalysed by Novozym 435 from vinyl laurate and prunin in acetone completely solubilised, forming colloids or scattered in solid state, according to its concentration in the reaction media.The kinetic study was determined at 50°C using initial concentrations between 20 and 220mM for prunin and between 20 and 4000mM (solvent free system) for vinyl laurate. When prunin completely solubilised or forming colloids was used, a model based on mechanism ordered Bi Bi without inhibition, neither by alcohol nor acyl group, which was the best fit in the initial rate data. The determined model was used to simulate initial reaction rate and these values were plotted against the experimental data. The model was consistent with the experimental data (slope 0.97±0.01, R2 0.993, n=72), even on solvent-free systems.
Fil: Celiz, Gustavo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina
Fil: Martearena, Maria Rita. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina
Fil: Scaroni, Elsa Elda. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina
Fil: Daz, Mirta Elizabeth. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina
Materia
Alkyl Prunin Ester
Kinetic Study
Lipase
Transesterification
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/59414
Acceder
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oai_identifier_str oai:ri.conicet.gov.ar:11336/59414
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase BCeliz, GustavoMartearena, Maria RitaScaroni, Elsa EldaDaz, Mirta ElizabethAlkyl Prunin EsterKinetic StudyLipaseTransesterificationhttps://purl.org/becyt/ford/2.9https://purl.org/becyt/ford/2Alkyl prunin esters are new compounds, which are soluble in lipophilic media. They possess antioxidant and antibacterial properties, so they may have useful applications. The current work studied the kinetic of prunin 6'. -O-laurate synthesis catalysed by Novozym 435 from vinyl laurate and prunin in acetone completely solubilised, forming colloids or scattered in solid state, according to its concentration in the reaction media.The kinetic study was determined at 50°C using initial concentrations between 20 and 220mM for prunin and between 20 and 4000mM (solvent free system) for vinyl laurate. When prunin completely solubilised or forming colloids was used, a model based on mechanism ordered Bi Bi without inhibition, neither by alcohol nor acyl group, which was the best fit in the initial rate data. The determined model was used to simulate initial reaction rate and these values were plotted against the experimental data. The model was consistent with the experimental data (slope 0.97±0.01, R2 0.993, n=72), even on solvent-free systems.Fil: Celiz, Gustavo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; ArgentinaFil: Martearena, Maria Rita. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; ArgentinaFil: Scaroni, Elsa Elda. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; ArgentinaFil: Daz, Mirta Elizabeth. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; ArgentinaElsevier Science Sa2012-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/59414Celiz, Gustavo; Martearena, Maria Rita; Scaroni, Elsa Elda; Daz, Mirta Elizabeth; Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B; Elsevier Science Sa; Biochemical Engineering Journal; 69; 12-2012; 69-741369-703XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.bej.2012.08.008info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S1369703X12002392info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:29:22Zoai:ri.conicet.gov.ar:11336/59414instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:29:22.972CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B
title Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B
spellingShingle Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B
Celiz, Gustavo
Alkyl Prunin Ester
Kinetic Study
Lipase
Transesterification
title_short Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B
title_full Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B
title_fullStr Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B
title_full_unstemmed Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B
title_sort Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B
dc.creator.none.fl_str_mv Celiz, Gustavo
Martearena, Maria Rita
Scaroni, Elsa Elda
Daz, Mirta Elizabeth
author Celiz, Gustavo
author_facet Celiz, Gustavo
Martearena, Maria Rita
Scaroni, Elsa Elda
Daz, Mirta Elizabeth
author_role author
author2 Martearena, Maria Rita
Scaroni, Elsa Elda
Daz, Mirta Elizabeth
author2_role author
author
author
dc.subject.none.fl_str_mv Alkyl Prunin Ester
Kinetic Study
Lipase
Transesterification
topic Alkyl Prunin Ester
Kinetic Study
Lipase
Transesterification
purl_subject.fl_str_mv https://purl.org/becyt/ford/2.9
https://purl.org/becyt/ford/2
dc.description.none.fl_txt_mv Alkyl prunin esters are new compounds, which are soluble in lipophilic media. They possess antioxidant and antibacterial properties, so they may have useful applications. The current work studied the kinetic of prunin 6'. -O-laurate synthesis catalysed by Novozym 435 from vinyl laurate and prunin in acetone completely solubilised, forming colloids or scattered in solid state, according to its concentration in the reaction media.The kinetic study was determined at 50°C using initial concentrations between 20 and 220mM for prunin and between 20 and 4000mM (solvent free system) for vinyl laurate. When prunin completely solubilised or forming colloids was used, a model based on mechanism ordered Bi Bi without inhibition, neither by alcohol nor acyl group, which was the best fit in the initial rate data. The determined model was used to simulate initial reaction rate and these values were plotted against the experimental data. The model was consistent with the experimental data (slope 0.97±0.01, R2 0.993, n=72), even on solvent-free systems.
Fil: Celiz, Gustavo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina
Fil: Martearena, Maria Rita. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina
Fil: Scaroni, Elsa Elda. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina
Fil: Daz, Mirta Elizabeth. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina
description Alkyl prunin esters are new compounds, which are soluble in lipophilic media. They possess antioxidant and antibacterial properties, so they may have useful applications. The current work studied the kinetic of prunin 6'. -O-laurate synthesis catalysed by Novozym 435 from vinyl laurate and prunin in acetone completely solubilised, forming colloids or scattered in solid state, according to its concentration in the reaction media.The kinetic study was determined at 50°C using initial concentrations between 20 and 220mM for prunin and between 20 and 4000mM (solvent free system) for vinyl laurate. When prunin completely solubilised or forming colloids was used, a model based on mechanism ordered Bi Bi without inhibition, neither by alcohol nor acyl group, which was the best fit in the initial rate data. The determined model was used to simulate initial reaction rate and these values were plotted against the experimental data. The model was consistent with the experimental data (slope 0.97±0.01, R2 0.993, n=72), even on solvent-free systems.
publishDate 2012
dc.date.none.fl_str_mv 2012-12
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/59414
Celiz, Gustavo; Martearena, Maria Rita; Scaroni, Elsa Elda; Daz, Mirta Elizabeth; Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B; Elsevier Science Sa; Biochemical Engineering Journal; 69; 12-2012; 69-74
1369-703X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/59414
identifier_str_mv Celiz, Gustavo; Martearena, Maria Rita; Scaroni, Elsa Elda; Daz, Mirta Elizabeth; Kinetic study of the alkyl flavonoid ester prunin 6'-O-laurate synthesis in acetone catalysed by immobilised Candida antarctica lipase B; Elsevier Science Sa; Biochemical Engineering Journal; 69; 12-2012; 69-74
1369-703X
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.bej.2012.08.008
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S1369703X12002392
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier Science Sa
publisher.none.fl_str_mv Elsevier Science Sa
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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score 13.070432

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