Successive cycles of utilization of novozym 435 in three different reaction systems

Detalhes bibliográficos
Autor(a) principal: Lerin,L.
Data de Publicação: 2011
Outros Autores: Ceni,G., Richett,A., Kubiak,G., Oliveira,J. Vladimir, Toniazzo,G., Treichel,H., Oestreicher,E. G., Oliveira,D.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Chemical Engineering
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322011000200002
Resumo: The main focus of this work was to investigate the residual esterification activity and the product conversion after 10 successive cycles of utilization of a commercial lipase in three systems: esterification of 2-ethyl hexanol and palmitic acid in a solvent-free system; esterification of ascorbic acid and palmitic acid in tert-butanol; and transesterification of glycerol and methyl benzoate in 2-propanol. These systems were chosen based on previous results by our research group in terms of product conversion. Before scale-up, there is a need for evaluating several cycles of utilization of the biocatalyst. The esterification of 2-ethyl hexanol showed that after 10 cycles the enzyme retained 90% of its activity. The system consisting of ascorbic acid, palmitic acid, Novozym 435 and tert-butanol showed that a reduction in enzyme activity was accompanied by a reduction in reaction conversion; the same behavior was not observed for the third system.
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spelling Successive cycles of utilization of novozym 435 in three different reaction systemsLipaseTransesterificationReuseThe main focus of this work was to investigate the residual esterification activity and the product conversion after 10 successive cycles of utilization of a commercial lipase in three systems: esterification of 2-ethyl hexanol and palmitic acid in a solvent-free system; esterification of ascorbic acid and palmitic acid in tert-butanol; and transesterification of glycerol and methyl benzoate in 2-propanol. These systems were chosen based on previous results by our research group in terms of product conversion. Before scale-up, there is a need for evaluating several cycles of utilization of the biocatalyst. The esterification of 2-ethyl hexanol showed that after 10 cycles the enzyme retained 90% of its activity. The system consisting of ascorbic acid, palmitic acid, Novozym 435 and tert-butanol showed that a reduction in enzyme activity was accompanied by a reduction in reaction conversion; the same behavior was not observed for the third system.Brazilian Society of Chemical Engineering2011-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322011000200002Brazilian Journal of Chemical Engineering v.28 n.2 2011reponame:Brazilian Journal of Chemical Engineeringinstname:Associação Brasileira de Engenharia Química (ABEQ)instacron:ABEQ10.1590/S0104-66322011000200002info:eu-repo/semantics/openAccessLerin,L.Ceni,G.Richett,A.Kubiak,G.Oliveira,J. VladimirToniazzo,G.Treichel,H.Oestreicher,E. G.Oliveira,D.eng2011-07-04T00:00:00Zoai:scielo:S0104-66322011000200002Revistahttps://www.scielo.br/j/bjce/https://old.scielo.br/oai/scielo-oai.phprgiudici@usp.br||rgiudici@usp.br1678-43830104-6632opendoar:2011-07-04T00:00Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)false
dc.title.none.fl_str_mv Successive cycles of utilization of novozym 435 in three different reaction systems
title Successive cycles of utilization of novozym 435 in three different reaction systems
spellingShingle Successive cycles of utilization of novozym 435 in three different reaction systems
Lerin,L.
Lipase
Transesterification
Reuse
title_short Successive cycles of utilization of novozym 435 in three different reaction systems
title_full Successive cycles of utilization of novozym 435 in three different reaction systems
title_fullStr Successive cycles of utilization of novozym 435 in three different reaction systems
title_full_unstemmed Successive cycles of utilization of novozym 435 in three different reaction systems
title_sort Successive cycles of utilization of novozym 435 in three different reaction systems
author Lerin,L.
author_facet Lerin,L.
Ceni,G.
Richett,A.
Kubiak,G.
Oliveira,J. Vladimir
Toniazzo,G.
Treichel,H.
Oestreicher,E. G.
Oliveira,D.
author_role author
author2 Ceni,G.
Richett,A.
Kubiak,G.
Oliveira,J. Vladimir
Toniazzo,G.
Treichel,H.
Oestreicher,E. G.
Oliveira,D.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Lerin,L.
Ceni,G.
Richett,A.
Kubiak,G.
Oliveira,J. Vladimir
Toniazzo,G.
Treichel,H.
Oestreicher,E. G.
Oliveira,D.
dc.subject.por.fl_str_mv Lipase
Transesterification
Reuse
topic Lipase
Transesterification
Reuse
description The main focus of this work was to investigate the residual esterification activity and the product conversion after 10 successive cycles of utilization of a commercial lipase in three systems: esterification of 2-ethyl hexanol and palmitic acid in a solvent-free system; esterification of ascorbic acid and palmitic acid in tert-butanol; and transesterification of glycerol and methyl benzoate in 2-propanol. These systems were chosen based on previous results by our research group in terms of product conversion. Before scale-up, there is a need for evaluating several cycles of utilization of the biocatalyst. The esterification of 2-ethyl hexanol showed that after 10 cycles the enzyme retained 90% of its activity. The system consisting of ascorbic acid, palmitic acid, Novozym 435 and tert-butanol showed that a reduction in enzyme activity was accompanied by a reduction in reaction conversion; the same behavior was not observed for the third system.
publishDate 2011
dc.date.none.fl_str_mv 2011-06-01
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=S0104-66322011000200002
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322011000200002
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0104-66322011000200002
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 Brazilian Society of Chemical Engineering
publisher.none.fl_str_mv Brazilian Society of Chemical Engineering
dc.source.none.fl_str_mv Brazilian Journal of Chemical Engineering v.28 n.2 2011
reponame:Brazilian Journal of Chemical Engineering
instname:Associação Brasileira de Engenharia Química (ABEQ)
instacron:ABEQ
instname_str Associação Brasileira de Engenharia Química (ABEQ)
instacron_str ABEQ
institution ABEQ
reponame_str Brazilian Journal of Chemical Engineering
collection Brazilian Journal of Chemical Engineering
repository.name.fl_str_mv Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)
repository.mail.fl_str_mv rgiudici@usp.br||rgiudici@usp.br
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