DES-Based Biocatalysis as a Green Alternative for the l-menthyl Ester Production Based on l-menthol Acylation

The deep eutectic solvent (DES)-based biocatalysis of l-menthol acylation was designed for the production of fatty acid l-menthyl ester (FME) using fatty acid methyl ester (FAME). The biocatalytic reaction was assisted by a lipase enzyme in the DES reaction medium. ւՒ-menthol and fatty acids (e.g.,...

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Published in:Molecules
Main Authors: Sabina Ion, Florentina Olănescu, Florina Teodorescu, Robert Tincu, Daniela Gheorghe, Vasile I. Pârvulescu, Mădălina Tudorache
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2022
Subjects:
DES
Online Access:https://doi.org/10.3390/molecules27165273
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spelling ftmdpi:oai:mdpi.com:/1420-3049/27/16/5273/ 2023-08-20T04:01:36+02:00 DES-Based Biocatalysis as a Green Alternative for the l-menthyl Ester Production Based on l-menthol Acylation Sabina Ion Florentina Olănescu Florina Teodorescu Robert Tincu Daniela Gheorghe Vasile I. Pârvulescu Mădălina Tudorache agris 2022-08-18 application/pdf https://doi.org/10.3390/molecules27165273 EN eng Multidisciplinary Digital Publishing Institute Organic Chemistry https://dx.doi.org/10.3390/molecules27165273 https://creativecommons.org/licenses/by/4.0/ Molecules; Volume 27; Issue 16; Pages: 5273 biocatalysis DES l -menthol fatty acid l -menthyl ester (FME) immobilized lipase Text 2022 ftmdpi https://doi.org/10.3390/molecules27165273 2023-08-01T06:07:29Z The deep eutectic solvent (DES)-based biocatalysis of l-menthol acylation was designed for the production of fatty acid l-menthyl ester (FME) using fatty acid methyl ester (FAME). The biocatalytic reaction was assisted by a lipase enzyme in the DES reaction medium. ւՒ-menthol and fatty acids (e.g., CA—caprylic acid; OA—oleic acid; LiA—linoleic acid; and LnA—linolenic acid) were combined in the binary mixture of DES. In this way, the DES provided a nonpolar environment for requested homogeneity of a biocatalytic system with reduced impact on the environment. The screening of lipase enzyme demonstrated better performance of immobilized lipase compared with powdered lipase. The performance of the biocatalytic system was evaluated for different DES compositions (type and concentration of the acid component). l-menthol:CA = 73:27 molar ratio allowed it to reach a maximum conversion of 95% methyl lauric ester (MLE) using a NV (Candida antarctica lipase B immobilized on acrylic resin) lipase biocatalyst. The recyclability of biocatalysts under optimum conditions of the system was also evaluated (more than 80% recovered biocatalytic activity was achieved for the tested biocatalysts after five reaction cycles). DES mixtures were characterized based on differential scanning calorimetry (DSC) and refractive index analysis. Text Antarc* Antarctica MDPI Open Access Publishing Molecules 27 16 5273
institution Open Polar
collection MDPI Open Access Publishing
op_collection_id ftmdpi
language English
topic biocatalysis
DES
l -menthol
fatty acid
l -menthyl ester (FME)
immobilized lipase
spellingShingle biocatalysis
DES
l -menthol
fatty acid
l -menthyl ester (FME)
immobilized lipase
Sabina Ion
Florentina Olănescu
Florina Teodorescu
Robert Tincu
Daniela Gheorghe
Vasile I. Pârvulescu
Mădălina Tudorache
DES-Based Biocatalysis as a Green Alternative for the l-menthyl Ester Production Based on l-menthol Acylation
topic_facet biocatalysis
DES
l -menthol
fatty acid
l -menthyl ester (FME)
immobilized lipase
description The deep eutectic solvent (DES)-based biocatalysis of l-menthol acylation was designed for the production of fatty acid l-menthyl ester (FME) using fatty acid methyl ester (FAME). The biocatalytic reaction was assisted by a lipase enzyme in the DES reaction medium. ւՒ-menthol and fatty acids (e.g., CA—caprylic acid; OA—oleic acid; LiA—linoleic acid; and LnA—linolenic acid) were combined in the binary mixture of DES. In this way, the DES provided a nonpolar environment for requested homogeneity of a biocatalytic system with reduced impact on the environment. The screening of lipase enzyme demonstrated better performance of immobilized lipase compared with powdered lipase. The performance of the biocatalytic system was evaluated for different DES compositions (type and concentration of the acid component). l-menthol:CA = 73:27 molar ratio allowed it to reach a maximum conversion of 95% methyl lauric ester (MLE) using a NV (Candida antarctica lipase B immobilized on acrylic resin) lipase biocatalyst. The recyclability of biocatalysts under optimum conditions of the system was also evaluated (more than 80% recovered biocatalytic activity was achieved for the tested biocatalysts after five reaction cycles). DES mixtures were characterized based on differential scanning calorimetry (DSC) and refractive index analysis.
format Text
author Sabina Ion
Florentina Olănescu
Florina Teodorescu
Robert Tincu
Daniela Gheorghe
Vasile I. Pârvulescu
Mădălina Tudorache
author_facet Sabina Ion
Florentina Olănescu
Florina Teodorescu
Robert Tincu
Daniela Gheorghe
Vasile I. Pârvulescu
Mădălina Tudorache
author_sort Sabina Ion
title DES-Based Biocatalysis as a Green Alternative for the l-menthyl Ester Production Based on l-menthol Acylation
title_short DES-Based Biocatalysis as a Green Alternative for the l-menthyl Ester Production Based on l-menthol Acylation
title_full DES-Based Biocatalysis as a Green Alternative for the l-menthyl Ester Production Based on l-menthol Acylation
title_fullStr DES-Based Biocatalysis as a Green Alternative for the l-menthyl Ester Production Based on l-menthol Acylation
title_full_unstemmed DES-Based Biocatalysis as a Green Alternative for the l-menthyl Ester Production Based on l-menthol Acylation
title_sort des-based biocatalysis as a green alternative for the l-menthyl ester production based on l-menthol acylation
publisher Multidisciplinary Digital Publishing Institute
publishDate 2022
url https://doi.org/10.3390/molecules27165273
op_coverage agris
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source Molecules; Volume 27; Issue 16; Pages: 5273
op_relation Organic Chemistry
https://dx.doi.org/10.3390/molecules27165273
op_rights https://creativecommons.org/licenses/by/4.0/
op_doi https://doi.org/10.3390/molecules27165273
container_title Molecules
container_volume 27
container_issue 16
container_start_page 5273
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