Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents - Datafile.xlsx ...

These are the research data and calculations supplemented to the paper: Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents. Mannosylerythritol lipids (MELs) are a promising group of biosurfactants due to their high fermentation yield, self- assembly and biologic...

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Main Authors: Cassimon, Jonas, Kovacs, Attila, Neyts, Erik C., Cornet, Iris, Billen, Pieter
Format: Dataset
Language:unknown
Published: figshare 2023
Subjects:
Online Access:https://dx.doi.org/10.6084/m9.figshare.24745593.v1
https://figshare.com/articles/dataset/Deacetylation_of_Mannosylerythritol_Lipids_in_Hydrophobic_Natural_Deep_Eutectic_Solvents_-_Datafile_xlsx/24745593/1
id ftdatacite:10.6084/m9.figshare.24745593.v1
record_format openpolar
spelling ftdatacite:10.6084/m9.figshare.24745593.v1 2024-01-28T09:59:59+01:00 Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents - Datafile.xlsx ... Cassimon, Jonas Kovacs, Attila Neyts, Erik C. Cornet, Iris Billen, Pieter 2023 https://dx.doi.org/10.6084/m9.figshare.24745593.v1 https://figshare.com/articles/dataset/Deacetylation_of_Mannosylerythritol_Lipids_in_Hydrophobic_Natural_Deep_Eutectic_Solvents_-_Datafile_xlsx/24745593/1 unknown figshare https://dx.doi.org/10.6084/m9.figshare.24745593 https://dx.doi.org/10.1002/ejoc.202300934 Creative Commons Attribution 4.0 International https://creativecommons.org/licenses/by/4.0/legalcode cc-by-4.0 Enzymes Organic green chemistry Natural products and bioactive compounds Biocatalysis and enzyme technology Industrial microbiology incl. biofeedstocks Dataset dataset 2023 ftdatacite https://doi.org/10.6084/m9.figshare.24745593.v110.6084/m9.figshare.2474559310.1002/ejoc.202300934 2024-01-04T22:49:58Z These are the research data and calculations supplemented to the paper: Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents. Mannosylerythritol lipids (MELs) are a promising group of biosurfactants due to their high fermentation yield, self- assembly and biological activity. During fermentation by Pseudozyma aphidis, a mixture of MELs with different levels of acylation is formed, of which the fully deacetylated form is the most valuable. In order to reduce the environmental impact of deacetylation, an enzymatic process using natural deep eutectic solvents (NADES) has been developed. We tested the deacetylation of a purified MELs mixture with immobilized Candida antarctica lipase B enzyme and 2-ethylhexanol as co-substrate in 140 h reactions with different NADES. We identified hydrophobic NADES systems with similar yields and kinetics as in pure 2-ethylhexanol solvent. Our results indicate that deacetylation of MELs mixtures in NADES as a solvent is possible with yields ... Dataset Antarc* Antarctica DataCite Metadata Store (German National Library of Science and Technology)
institution Open Polar
collection DataCite Metadata Store (German National Library of Science and Technology)
op_collection_id ftdatacite
language unknown
topic Enzymes
Organic green chemistry
Natural products and bioactive compounds
Biocatalysis and enzyme technology
Industrial microbiology incl. biofeedstocks
spellingShingle Enzymes
Organic green chemistry
Natural products and bioactive compounds
Biocatalysis and enzyme technology
Industrial microbiology incl. biofeedstocks
Cassimon, Jonas
Kovacs, Attila
Neyts, Erik C.
Cornet, Iris
Billen, Pieter
Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents - Datafile.xlsx ...
topic_facet Enzymes
Organic green chemistry
Natural products and bioactive compounds
Biocatalysis and enzyme technology
Industrial microbiology incl. biofeedstocks
description These are the research data and calculations supplemented to the paper: Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents. Mannosylerythritol lipids (MELs) are a promising group of biosurfactants due to their high fermentation yield, self- assembly and biological activity. During fermentation by Pseudozyma aphidis, a mixture of MELs with different levels of acylation is formed, of which the fully deacetylated form is the most valuable. In order to reduce the environmental impact of deacetylation, an enzymatic process using natural deep eutectic solvents (NADES) has been developed. We tested the deacetylation of a purified MELs mixture with immobilized Candida antarctica lipase B enzyme and 2-ethylhexanol as co-substrate in 140 h reactions with different NADES. We identified hydrophobic NADES systems with similar yields and kinetics as in pure 2-ethylhexanol solvent. Our results indicate that deacetylation of MELs mixtures in NADES as a solvent is possible with yields ...
format Dataset
author Cassimon, Jonas
Kovacs, Attila
Neyts, Erik C.
Cornet, Iris
Billen, Pieter
author_facet Cassimon, Jonas
Kovacs, Attila
Neyts, Erik C.
Cornet, Iris
Billen, Pieter
author_sort Cassimon, Jonas
title Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents - Datafile.xlsx ...
title_short Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents - Datafile.xlsx ...
title_full Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents - Datafile.xlsx ...
title_fullStr Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents - Datafile.xlsx ...
title_full_unstemmed Deacetylation of Mannosylerythritol Lipids in Hydrophobic Natural Deep Eutectic Solvents - Datafile.xlsx ...
title_sort deacetylation of mannosylerythritol lipids in hydrophobic natural deep eutectic solvents - datafile.xlsx ...
publisher figshare
publishDate 2023
url https://dx.doi.org/10.6084/m9.figshare.24745593.v1
https://figshare.com/articles/dataset/Deacetylation_of_Mannosylerythritol_Lipids_in_Hydrophobic_Natural_Deep_Eutectic_Solvents_-_Datafile_xlsx/24745593/1
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_relation https://dx.doi.org/10.6084/m9.figshare.24745593
https://dx.doi.org/10.1002/ejoc.202300934
op_rights Creative Commons Attribution 4.0 International
https://creativecommons.org/licenses/by/4.0/legalcode
cc-by-4.0
op_doi https://doi.org/10.6084/m9.figshare.24745593.v110.6084/m9.figshare.2474559310.1002/ejoc.202300934
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