Enzymatic synthesis optimization of isoamyl butyrate from fusel oil
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , |
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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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 |
_version_ |
1799317397911371776 |