Continuous Flow Glycolipid Synthesis Using a Packed Bed Reactor

Glycolipids are a class of biodegradable biosurfactants that are non-toxic and based on renewables, making them a sustainable alternative to petrochemical surfactants. Enzymatic synthesis allows a tailor-made production of these versatile compounds using sugar and fatty acid building blocks with rat...

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Published in:Catalysts
Main Authors: Rebecca Hollenbach, Delphine Muller, André Delavault, Christoph Syldatk
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2022
Subjects:
Online Access:https://doi.org/10.3390/catal12050551
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spelling ftmdpi:oai:mdpi.com:/2073-4344/12/5/551/ 2023-08-20T04:01:50+02:00 Continuous Flow Glycolipid Synthesis Using a Packed Bed Reactor Rebecca Hollenbach Delphine Muller André Delavault Christoph Syldatk 2022-05-18 application/pdf https://doi.org/10.3390/catal12050551 EN eng Multidisciplinary Digital Publishing Institute Biocatalysis https://dx.doi.org/10.3390/catal12050551 https://creativecommons.org/licenses/by/4.0/ Catalysts; Volume 12; Issue 5; Pages: 551 continuous flow heterogenous biocatalysis packed bed reactor glycolipid biphasic system Candida antarctica Lipase B Text 2022 ftmdpi https://doi.org/10.3390/catal12050551 2023-08-01T05:05:02Z Glycolipids are a class of biodegradable biosurfactants that are non-toxic and based on renewables, making them a sustainable alternative to petrochemical surfactants. Enzymatic synthesis allows a tailor-made production of these versatile compounds using sugar and fatty acid building blocks with rationalized structures for targeted applications. Therefore, glycolipids can be comprehensively designed to outcompete conventional surfactants regarding their physicochemical properties. However, enzymatic glycolipid processes are struggling with both sugars and fatty acid solubilities in reaction media. Thus, continuous flow processes represent a powerful tool in designing efficient syntheses of sugar esters. In this study, a continuous enzymatic glycolipid production catalyzed by Novozyme 435® is presented as an unprecedented concept. A biphasic aqueous–organic system was investigated, allowing for the simultaneous solubilization of sugars and fatty acids. Owing to phase separation, the remaining non-acylated glucose was easily separated from the product stream and was refed to the reactor forming a closed-loop system. Productivity in the continuous process was higher compared to a batch one, with space–time yields of up to 1228 ± 65 µmol/L/h. A temperature of 70 °C resulted in the highest glucose-6-O-decanoate concentration in the Packed Bed Reactor (PBR). Consequently, the design of a continuous biocatalytic production is a step towards a more competitive glycolipid synthesis in the aim for industrialization. Text Antarc* Antarctica MDPI Open Access Publishing Catalysts 12 5 551
institution Open Polar
collection MDPI Open Access Publishing
op_collection_id ftmdpi
language English
topic continuous flow
heterogenous biocatalysis
packed bed reactor
glycolipid
biphasic system
Candida antarctica Lipase B
spellingShingle continuous flow
heterogenous biocatalysis
packed bed reactor
glycolipid
biphasic system
Candida antarctica Lipase B
Rebecca Hollenbach
Delphine Muller
André Delavault
Christoph Syldatk
Continuous Flow Glycolipid Synthesis Using a Packed Bed Reactor
topic_facet continuous flow
heterogenous biocatalysis
packed bed reactor
glycolipid
biphasic system
Candida antarctica Lipase B
description Glycolipids are a class of biodegradable biosurfactants that are non-toxic and based on renewables, making them a sustainable alternative to petrochemical surfactants. Enzymatic synthesis allows a tailor-made production of these versatile compounds using sugar and fatty acid building blocks with rationalized structures for targeted applications. Therefore, glycolipids can be comprehensively designed to outcompete conventional surfactants regarding their physicochemical properties. However, enzymatic glycolipid processes are struggling with both sugars and fatty acid solubilities in reaction media. Thus, continuous flow processes represent a powerful tool in designing efficient syntheses of sugar esters. In this study, a continuous enzymatic glycolipid production catalyzed by Novozyme 435® is presented as an unprecedented concept. A biphasic aqueous–organic system was investigated, allowing for the simultaneous solubilization of sugars and fatty acids. Owing to phase separation, the remaining non-acylated glucose was easily separated from the product stream and was refed to the reactor forming a closed-loop system. Productivity in the continuous process was higher compared to a batch one, with space–time yields of up to 1228 ± 65 µmol/L/h. A temperature of 70 °C resulted in the highest glucose-6-O-decanoate concentration in the Packed Bed Reactor (PBR). Consequently, the design of a continuous biocatalytic production is a step towards a more competitive glycolipid synthesis in the aim for industrialization.
format Text
author Rebecca Hollenbach
Delphine Muller
André Delavault
Christoph Syldatk
author_facet Rebecca Hollenbach
Delphine Muller
André Delavault
Christoph Syldatk
author_sort Rebecca Hollenbach
title Continuous Flow Glycolipid Synthesis Using a Packed Bed Reactor
title_short Continuous Flow Glycolipid Synthesis Using a Packed Bed Reactor
title_full Continuous Flow Glycolipid Synthesis Using a Packed Bed Reactor
title_fullStr Continuous Flow Glycolipid Synthesis Using a Packed Bed Reactor
title_full_unstemmed Continuous Flow Glycolipid Synthesis Using a Packed Bed Reactor
title_sort continuous flow glycolipid synthesis using a packed bed reactor
publisher Multidisciplinary Digital Publishing Institute
publishDate 2022
url https://doi.org/10.3390/catal12050551
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source Catalysts; Volume 12; Issue 5; Pages: 551
op_relation Biocatalysis
https://dx.doi.org/10.3390/catal12050551
op_rights https://creativecommons.org/licenses/by/4.0/
op_doi https://doi.org/10.3390/catal12050551
container_title Catalysts
container_volume 12
container_issue 5
container_start_page 551
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