Successive cycles of utilization of novozym 435 in three different reaction systems
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , , , |
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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Brazilian Journal of Chemical Engineering |
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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 |
_version_ |
1754213173438709760 |