Solvent-Free Lipase-Catalyzed Synthesis of Technical-Grade Sugar Esters and Evaluation of Their Physicochemical and Bioactive Properties

Technical-grade oleic acid esters of sucrose and fructose were prepared using solvent-free biocatalysis at 65 °C, without any downstream purification applied, and their physicochemical and bioactivity-related properties were evaluated and compared to a commercially available sucrose laurate emulsifi...

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Published in:Catalysts
Main Authors: Ran Ye, Douglas G. Hayes, Rachel Burton, Anjun Liu, Federico M. Harte, Yuemeng Wang
Format: Article in Journal/Newspaper
Language:English
Published: MDPI AG 2016
Subjects:
Online Access:https://doi.org/10.3390/catal6060078
https://doaj.org/article/8d7be3537bcc4dc1ae9233a62f521848
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spelling ftdoajarticles:oai:doaj.org/article:8d7be3537bcc4dc1ae9233a62f521848 2023-05-15T13:58:55+02:00 Solvent-Free Lipase-Catalyzed Synthesis of Technical-Grade Sugar Esters and Evaluation of Their Physicochemical and Bioactive Properties Ran Ye Douglas G. Hayes Rachel Burton Anjun Liu Federico M. Harte Yuemeng Wang 2016-05-01T00:00:00Z https://doi.org/10.3390/catal6060078 https://doaj.org/article/8d7be3537bcc4dc1ae9233a62f521848 EN eng MDPI AG http://www.mdpi.com/2073-4344/6/6/78 https://doaj.org/toc/2073-4344 2073-4344 doi:10.3390/catal6060078 https://doaj.org/article/8d7be3537bcc4dc1ae9233a62f521848 Catalysts, Vol 6, Iss 6, p 78 (2016) antimicrobial activity antitumor activity emulsification high-pressure homogenation lipase sugar-fatty acid esters surfactants Chemical technology TP1-1185 Chemistry QD1-999 article 2016 ftdoajarticles https://doi.org/10.3390/catal6060078 2022-12-31T12:34:51Z Technical-grade oleic acid esters of sucrose and fructose were prepared using solvent-free biocatalysis at 65 °C, without any downstream purification applied, and their physicochemical and bioactivity-related properties were evaluated and compared to a commercially available sucrose laurate emulsifier. To increase the conversion of sucrose and fructose oleate, prepared previously using solvent-free lipase-catalyzed esterification catalyzed by Rhizomucor miehei lipase (81% and 83% ester, respectively), the enzymatic reaction conditions was continued using CaSO4 to control the reactor’s air headspace and a lipase (from Candida antarctica B) with a hydrophobic immobilization matrix to provide an ultralow water activity, and high-pressure homogenation, to form metastable suspensions of 2.0–3.3 micron sized saccharide particles in liquid-phase reaction media. These measures led to increased ester content of 89% and 96% for reactions involving sucrose and fructose, respectively. The monoester content among the esters decreased from 90% to <70% due to differences in regioselectivity between the lipases. The resultant technical-grade sucrose and fructose lowered the surface tension to <30 mN/m, and possessed excellent emulsification capability and stability over 36 h using hexadecane and dodecane as oils, comparable to that of sucrose laurate and Tween® 80). The technical-grade sugar esters, particularly fructose oleate, more effectively inhibited gram-positive foodborne pathogens (Lactobacillus plantarum, Pediococcus pentosaceus and Bacillus subtilis). Furthermore, all three sugar esters displayed antitumor activity, particularly the two sucrose esters. This study demonstrates the importance of controlling the biocatalysts’ water activity to achieve high conversion, the impact of a lipase’s regioselectivity in dictating product distribution, and the use of solvent-free biocatalysis to important biobased surfactants useful in foods, cosmetics, personal care products, and medicine. Article in Journal/Newspaper Antarc* Antarctica Directory of Open Access Journals: DOAJ Articles Catalysts 6 6 78
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic antimicrobial activity
antitumor activity
emulsification
high-pressure homogenation
lipase
sugar-fatty acid esters
surfactants
Chemical technology
TP1-1185
Chemistry
QD1-999
spellingShingle antimicrobial activity
antitumor activity
emulsification
high-pressure homogenation
lipase
sugar-fatty acid esters
surfactants
Chemical technology
TP1-1185
Chemistry
QD1-999
Ran Ye
Douglas G. Hayes
Rachel Burton
Anjun Liu
Federico M. Harte
Yuemeng Wang
Solvent-Free Lipase-Catalyzed Synthesis of Technical-Grade Sugar Esters and Evaluation of Their Physicochemical and Bioactive Properties
topic_facet antimicrobial activity
antitumor activity
emulsification
high-pressure homogenation
lipase
sugar-fatty acid esters
surfactants
Chemical technology
TP1-1185
Chemistry
QD1-999
description Technical-grade oleic acid esters of sucrose and fructose were prepared using solvent-free biocatalysis at 65 °C, without any downstream purification applied, and their physicochemical and bioactivity-related properties were evaluated and compared to a commercially available sucrose laurate emulsifier. To increase the conversion of sucrose and fructose oleate, prepared previously using solvent-free lipase-catalyzed esterification catalyzed by Rhizomucor miehei lipase (81% and 83% ester, respectively), the enzymatic reaction conditions was continued using CaSO4 to control the reactor’s air headspace and a lipase (from Candida antarctica B) with a hydrophobic immobilization matrix to provide an ultralow water activity, and high-pressure homogenation, to form metastable suspensions of 2.0–3.3 micron sized saccharide particles in liquid-phase reaction media. These measures led to increased ester content of 89% and 96% for reactions involving sucrose and fructose, respectively. The monoester content among the esters decreased from 90% to <70% due to differences in regioselectivity between the lipases. The resultant technical-grade sucrose and fructose lowered the surface tension to <30 mN/m, and possessed excellent emulsification capability and stability over 36 h using hexadecane and dodecane as oils, comparable to that of sucrose laurate and Tween® 80). The technical-grade sugar esters, particularly fructose oleate, more effectively inhibited gram-positive foodborne pathogens (Lactobacillus plantarum, Pediococcus pentosaceus and Bacillus subtilis). Furthermore, all three sugar esters displayed antitumor activity, particularly the two sucrose esters. This study demonstrates the importance of controlling the biocatalysts’ water activity to achieve high conversion, the impact of a lipase’s regioselectivity in dictating product distribution, and the use of solvent-free biocatalysis to important biobased surfactants useful in foods, cosmetics, personal care products, and medicine.
format Article in Journal/Newspaper
author Ran Ye
Douglas G. Hayes
Rachel Burton
Anjun Liu
Federico M. Harte
Yuemeng Wang
author_facet Ran Ye
Douglas G. Hayes
Rachel Burton
Anjun Liu
Federico M. Harte
Yuemeng Wang
author_sort Ran Ye
title Solvent-Free Lipase-Catalyzed Synthesis of Technical-Grade Sugar Esters and Evaluation of Their Physicochemical and Bioactive Properties
title_short Solvent-Free Lipase-Catalyzed Synthesis of Technical-Grade Sugar Esters and Evaluation of Their Physicochemical and Bioactive Properties
title_full Solvent-Free Lipase-Catalyzed Synthesis of Technical-Grade Sugar Esters and Evaluation of Their Physicochemical and Bioactive Properties
title_fullStr Solvent-Free Lipase-Catalyzed Synthesis of Technical-Grade Sugar Esters and Evaluation of Their Physicochemical and Bioactive Properties
title_full_unstemmed Solvent-Free Lipase-Catalyzed Synthesis of Technical-Grade Sugar Esters and Evaluation of Their Physicochemical and Bioactive Properties
title_sort solvent-free lipase-catalyzed synthesis of technical-grade sugar esters and evaluation of their physicochemical and bioactive properties
publisher MDPI AG
publishDate 2016
url https://doi.org/10.3390/catal6060078
https://doaj.org/article/8d7be3537bcc4dc1ae9233a62f521848
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source Catalysts, Vol 6, Iss 6, p 78 (2016)
op_relation http://www.mdpi.com/2073-4344/6/6/78
https://doaj.org/toc/2073-4344
2073-4344
doi:10.3390/catal6060078
https://doaj.org/article/8d7be3537bcc4dc1ae9233a62f521848
op_doi https://doi.org/10.3390/catal6060078
container_title Catalysts
container_volume 6
container_issue 6
container_start_page 78
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