Enzymatic synthesis optimization of isoamyl butyrate from fusel oil

Detalhes bibliográficos
Autor(a) principal: Anschau, Andréia
Data de Publicação: 2021
Outros Autores: Huerta, Katira da Mota, Rêgo , Tatiane Vieira, Oliveira , Janaina Mardioni Gonçalves de, Borba, Carina Molins, Kalil, Susana Juliano, Burkert, Carlos André Veiga, Burkert, Janaína Fernandes de Medeiros
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Acta Scientiarum Biological Sciences
Texto Completo: http://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/54966
Resumo: Many food, cosmetic and pharmaceutical industries have increased their interest in short-chain esters due to their flavor properties. From the industrial standpoint, enzyme reactions are the most economical strategy to reach green products with neither toxicity nor damage to human health. Isoamyl butyrate (pear flavor) was synthesized by isoamyl alcohol (a byproduct of alcohol production) and butyric acid with the use of the immobilized lipase Lipozyme TL IM and hexane as solvents. Reaction variables (temperature, butyric acid concentration, isoamyl alcohol:butyric acid molar ratio and enzyme concentration) were investigated in ester conversion (%), concentration (mol L-1) and productivity (mmol ester g-1 mixture . h), by applying a sequential strategy of the Fractional Factorial Design (FFD) and the Central Composite Rotatable Design (CCRD). High isoamyl butyrate conversion of 95.8% was achieved at 24 hours. At 3 hours, the highest isoamyl butyrate concentration (1.64 mol L-1) and productivity (0.19 mmol ester g-1 mixture . h) were obtained under different reaction conditions. Due to high specificity and selectivity of lipases, process parameters of this study and their interaction with the Lipozyme TL IM are fundamental to understand and optimize the system so as to achieve maximum yield to scale up. Results show that fusel oil may be recycled by the green chemistry process proposed by this study.
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spelling Enzymatic synthesis optimization of isoamyl butyrate from fusel oilaroma ester; esterification; immobilized lipase; organic mediaMany food, cosmetic and pharmaceutical industries have increased their interest in short-chain esters due to their flavor properties. From the industrial standpoint, enzyme reactions are the most economical strategy to reach green products with neither toxicity nor damage to human health. Isoamyl butyrate (pear flavor) was synthesized by isoamyl alcohol (a byproduct of alcohol production) and butyric acid with the use of the immobilized lipase Lipozyme TL IM and hexane as solvents. Reaction variables (temperature, butyric acid concentration, isoamyl alcohol:butyric acid molar ratio and enzyme concentration) were investigated in ester conversion (%), concentration (mol L-1) and productivity (mmol ester g-1 mixture . h), by applying a sequential strategy of the Fractional Factorial Design (FFD) and the Central Composite Rotatable Design (CCRD). High isoamyl butyrate conversion of 95.8% was achieved at 24 hours. At 3 hours, the highest isoamyl butyrate concentration (1.64 mol L-1) and productivity (0.19 mmol ester g-1 mixture . h) were obtained under different reaction conditions. Due to high specificity and selectivity of lipases, process parameters of this study and their interaction with the Lipozyme TL IM are fundamental to understand and optimize the system so as to achieve maximum yield to scale up. Results show that fusel oil may be recycled by the green chemistry process proposed by this study.Universidade Estadual De Maringá2021-04-20info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/5496610.4025/actascibiolsci.v43i1.54966Acta Scientiarum. Biological Sciences; Vol 43 (2021): Publicação contínua; e54966Acta Scientiarum. Biological Sciences; v. 43 (2021): Publicação contínua; e549661807-863X1679-9283reponame:Acta Scientiarum Biological Sciencesinstname:Universidade Estadual de Maringá (UEM)instacron:UEMenghttp://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/54966/751375151977Copyright (c) 2021 Acta Scientiarum. Biological Scienceshttp://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessAnschau, AndréiaHuerta, Katira da Mota Rêgo , Tatiane Vieira Oliveira , Janaina Mardioni Gonçalves deBorba, Carina MolinsKalil, Susana Juliano Burkert, Carlos André Veiga Burkert, Janaína Fernandes de Medeiros 2022-02-17T21:58:49Zoai:periodicos.uem.br/ojs:article/54966Revistahttp://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSciPUBhttp://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/oai||actabiol@uem.br1807-863X1679-9283opendoar:2022-02-17T21:58:49Acta Scientiarum Biological Sciences - Universidade Estadual de Maringá (UEM)false
dc.title.none.fl_str_mv Enzymatic synthesis optimization of isoamyl butyrate from fusel oil
title Enzymatic synthesis optimization of isoamyl butyrate from fusel oil
spellingShingle Enzymatic synthesis optimization of isoamyl butyrate from fusel oil
Anschau, Andréia
aroma ester; esterification; immobilized lipase; organic media
title_short Enzymatic synthesis optimization of isoamyl butyrate from fusel oil
title_full Enzymatic synthesis optimization of isoamyl butyrate from fusel oil
title_fullStr Enzymatic synthesis optimization of isoamyl butyrate from fusel oil
title_full_unstemmed Enzymatic synthesis optimization of isoamyl butyrate from fusel oil
title_sort Enzymatic synthesis optimization of isoamyl butyrate from fusel oil
author Anschau, Andréia
author_facet Anschau, Andréia
Huerta, Katira da Mota
Rêgo , Tatiane Vieira
Oliveira , Janaina Mardioni Gonçalves de
Borba, Carina Molins
Kalil, Susana Juliano
Burkert, Carlos André Veiga
Burkert, Janaína Fernandes de Medeiros
author_role author
author2 Huerta, Katira da Mota
Rêgo , Tatiane Vieira
Oliveira , Janaina Mardioni Gonçalves de
Borba, Carina Molins
Kalil, Susana Juliano
Burkert, Carlos André Veiga
Burkert, Janaína Fernandes de Medeiros
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Anschau, Andréia
Huerta, Katira da Mota
Rêgo , Tatiane Vieira
Oliveira , Janaina Mardioni Gonçalves de
Borba, Carina Molins
Kalil, Susana Juliano
Burkert, Carlos André Veiga
Burkert, Janaína Fernandes de Medeiros
dc.subject.por.fl_str_mv aroma ester; esterification; immobilized lipase; organic media
topic aroma ester; esterification; immobilized lipase; organic media
description Many food, cosmetic and pharmaceutical industries have increased their interest in short-chain esters due to their flavor properties. From the industrial standpoint, enzyme reactions are the most economical strategy to reach green products with neither toxicity nor damage to human health. Isoamyl butyrate (pear flavor) was synthesized by isoamyl alcohol (a byproduct of alcohol production) and butyric acid with the use of the immobilized lipase Lipozyme TL IM and hexane as solvents. Reaction variables (temperature, butyric acid concentration, isoamyl alcohol:butyric acid molar ratio and enzyme concentration) were investigated in ester conversion (%), concentration (mol L-1) and productivity (mmol ester g-1 mixture . h), by applying a sequential strategy of the Fractional Factorial Design (FFD) and the Central Composite Rotatable Design (CCRD). High isoamyl butyrate conversion of 95.8% was achieved at 24 hours. At 3 hours, the highest isoamyl butyrate concentration (1.64 mol L-1) and productivity (0.19 mmol ester g-1 mixture . h) were obtained under different reaction conditions. Due to high specificity and selectivity of lipases, process parameters of this study and their interaction with the Lipozyme TL IM are fundamental to understand and optimize the system so as to achieve maximum yield to scale up. Results show that fusel oil may be recycled by the green chemistry process proposed by this study.
publishDate 2021
dc.date.none.fl_str_mv 2021-04-20
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/54966
10.4025/actascibiolsci.v43i1.54966
url http://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/54966
identifier_str_mv 10.4025/actascibiolsci.v43i1.54966
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/54966/751375151977
dc.rights.driver.fl_str_mv Copyright (c) 2021 Acta Scientiarum. Biological Sciences
http://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2021 Acta Scientiarum. Biological Sciences
http://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Estadual De Maringá
publisher.none.fl_str_mv Universidade Estadual De Maringá
dc.source.none.fl_str_mv Acta Scientiarum. Biological Sciences; Vol 43 (2021): Publicação contínua; e54966
Acta Scientiarum. Biological Sciences; v. 43 (2021): Publicação contínua; e54966
1807-863X
1679-9283
reponame:Acta Scientiarum Biological Sciences
instname:Universidade Estadual de Maringá (UEM)
instacron:UEM
instname_str Universidade Estadual de Maringá (UEM)
instacron_str UEM
institution UEM
reponame_str Acta Scientiarum Biological Sciences
collection Acta Scientiarum Biological Sciences
repository.name.fl_str_mv Acta Scientiarum Biological Sciences - Universidade Estadual de Maringá (UEM)
repository.mail.fl_str_mv ||actabiol@uem.br
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