Estudo da influência do solvente, carboidrato e ácido graxo na síntese enzimática de ésteres de açúcares

Detalhes bibliográficos
Autor(a) principal: Paula,Ariela V. de
Data de Publicação: 2005
Outros Autores: Barboza,Jayne C. de Souza, Castro,Heizir F. de
Tipo de documento: Artigo
Idioma: por
Título da fonte: Química Nova (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422005000500011
Resumo: The aim of this work was to gain knowledge of enzymatic processes for the synthesis fatty acid esters of sugar, with the objective to develop an enzymatic process for the preparation of non-toxic biodegradable surface-active agents derived entirely from renewable resources. A wide range of data were collected for reaction conditions involving different sugars (glucose, fructose and sucrose), fatty acids (oleic, palmitic, lauric), solvents (hexane, heptane and t-butanol) and different sources of lipases in both free and immobilized forms. As a solvent t-butanol provided the best conditions to create a catalytic liquid phase in which the reaction occurs. Sugars were preferentially esterified in the following order: fructose > glucose > sucrose, depending on the enzyme preparation. For fructose no influence was found concerning de acyl donor and similar rates were achieved for all tested fatty acids. Ester synthesis was maximized for substrates containing fructose, lauric or oleic acids, t-butanol and lipase from porcine pancreas immobilized on polysiloxane-polyvinyl alcohol particles. Under such conditions molar conversions were higher than 50%.
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spelling Estudo da influência do solvente, carboidrato e ácido graxo na síntese enzimática de ésteres de açúcareslipasecarbohydrateestersThe aim of this work was to gain knowledge of enzymatic processes for the synthesis fatty acid esters of sugar, with the objective to develop an enzymatic process for the preparation of non-toxic biodegradable surface-active agents derived entirely from renewable resources. A wide range of data were collected for reaction conditions involving different sugars (glucose, fructose and sucrose), fatty acids (oleic, palmitic, lauric), solvents (hexane, heptane and t-butanol) and different sources of lipases in both free and immobilized forms. As a solvent t-butanol provided the best conditions to create a catalytic liquid phase in which the reaction occurs. Sugars were preferentially esterified in the following order: fructose > glucose > sucrose, depending on the enzyme preparation. For fructose no influence was found concerning de acyl donor and similar rates were achieved for all tested fatty acids. Ester synthesis was maximized for substrates containing fructose, lauric or oleic acids, t-butanol and lipase from porcine pancreas immobilized on polysiloxane-polyvinyl alcohol particles. Under such conditions molar conversions were higher than 50%.Sociedade Brasileira de Química2005-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422005000500011Química Nova v.28 n.5 2005reponame:Química Nova (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0100-40422005000500011info:eu-repo/semantics/openAccessPaula,Ariela V. deBarboza,Jayne C. de SouzaCastro,Heizir F. depor2005-09-23T00:00:00Zoai:scielo:S0100-40422005000500011Revistahttps://www.scielo.br/j/qn/ONGhttps://old.scielo.br/oai/scielo-oai.phpquimicanova@sbq.org.br1678-70640100-4042opendoar:2005-09-23T00:00Química Nova (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Estudo da influência do solvente, carboidrato e ácido graxo na síntese enzimática de ésteres de açúcares
title Estudo da influência do solvente, carboidrato e ácido graxo na síntese enzimática de ésteres de açúcares
spellingShingle Estudo da influência do solvente, carboidrato e ácido graxo na síntese enzimática de ésteres de açúcares
Paula,Ariela V. de
lipase
carbohydrate
esters
title_short Estudo da influência do solvente, carboidrato e ácido graxo na síntese enzimática de ésteres de açúcares
title_full Estudo da influência do solvente, carboidrato e ácido graxo na síntese enzimática de ésteres de açúcares
title_fullStr Estudo da influência do solvente, carboidrato e ácido graxo na síntese enzimática de ésteres de açúcares
title_full_unstemmed Estudo da influência do solvente, carboidrato e ácido graxo na síntese enzimática de ésteres de açúcares
title_sort Estudo da influência do solvente, carboidrato e ácido graxo na síntese enzimática de ésteres de açúcares
author Paula,Ariela V. de
author_facet Paula,Ariela V. de
Barboza,Jayne C. de Souza
Castro,Heizir F. de
author_role author
author2 Barboza,Jayne C. de Souza
Castro,Heizir F. de
author2_role author
author
dc.contributor.author.fl_str_mv Paula,Ariela V. de
Barboza,Jayne C. de Souza
Castro,Heizir F. de
dc.subject.por.fl_str_mv lipase
carbohydrate
esters
topic lipase
carbohydrate
esters
description The aim of this work was to gain knowledge of enzymatic processes for the synthesis fatty acid esters of sugar, with the objective to develop an enzymatic process for the preparation of non-toxic biodegradable surface-active agents derived entirely from renewable resources. A wide range of data were collected for reaction conditions involving different sugars (glucose, fructose and sucrose), fatty acids (oleic, palmitic, lauric), solvents (hexane, heptane and t-butanol) and different sources of lipases in both free and immobilized forms. As a solvent t-butanol provided the best conditions to create a catalytic liquid phase in which the reaction occurs. Sugars were preferentially esterified in the following order: fructose > glucose > sucrose, depending on the enzyme preparation. For fructose no influence was found concerning de acyl donor and similar rates were achieved for all tested fatty acids. Ester synthesis was maximized for substrates containing fructose, lauric or oleic acids, t-butanol and lipase from porcine pancreas immobilized on polysiloxane-polyvinyl alcohol particles. Under such conditions molar conversions were higher than 50%.
publishDate 2005
dc.date.none.fl_str_mv 2005-10-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422005000500011
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422005000500011
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv 10.1590/S0100-40422005000500011
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Química Nova v.28 n.5 2005
reponame:Química Nova (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Química Nova (Online)
collection Química Nova (Online)
repository.name.fl_str_mv Química Nova (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv quimicanova@sbq.org.br
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