CaLB Catalyzed Conversion of ε-Caprolactone in Aqueous Medium. Part 1: Immobilization of CaLB to Microgels

The enzymatic ring-opening polymerization of lactones is a method of increasing interest for the synthesis of biodegradable and biocompatible polymers. In the past it was shown that immobilization of Candida antarctica lipase B (CaLB) and the reaction medium play an important role in the polymerizat...

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Main Authors: Engel, Stefan, Höck, Heidi, Bocola, Marco, Keul, Helmut, Schwaneberg, Ulrich, Möller, Martin
Format: Article in Journal/Newspaper
Language:English
Published: Basel : MDPI 2016
Subjects:
Online Access:https://oa.tib.eu/renate/handle/123456789/8644
https://doi.org/10.34657/7682
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author Engel, Stefan
Höck, Heidi
Bocola, Marco
Keul, Helmut
Schwaneberg, Ulrich
Möller, Martin
author_facet Engel, Stefan
Höck, Heidi
Bocola, Marco
Keul, Helmut
Schwaneberg, Ulrich
Möller, Martin
author_sort Engel, Stefan
collection LeibnizOpen (The Leibniz Association)
description The enzymatic ring-opening polymerization of lactones is a method of increasing interest for the synthesis of biodegradable and biocompatible polymers. In the past it was shown that immobilization of Candida antarctica lipase B (CaLB) and the reaction medium play an important role in the polymerization ability especially of medium ring size lactones like ε-caprolactone (ε-CL). We investigated a route for the preparation of compartmentalized microgels based on poly(glycidol) in which CaLB was immobilized to increase its esterification ability. To find the ideal environment for CaLB, we investigated the acceptable water concentration and the accessibility for the monomer in model polymerizations in toluene and analyzed the obtained oligomers/polymers by NMR and SEC. We observed a sufficient accessibility for ε-CL to a toluene like hydrophobic phase imitating a hydrophobic microgel. Comparing free CaLB and Novozym® 435 we found that not the monomer concentration but rather the solubility of the enzyme, as well as the water concentration, strongly influences the equilibrium of esterification and hydrolysis. On the basis of these investigations, microgels of different polarity were prepared and successfully loaded with CaLB by physical entrapment. By comparison of immobilized and free CaLB, we demonstrated an effect of the hydrophobicity of the microenvironment of CaLB on its enzymatic activity. publishedVersion
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language English
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op_doi https://doi.org/10.34657/7682
op_rights CC BY 4.0 Unported
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op_source Polymers 8 (2016), Nr. 10
publishDate 2016
publisher Basel : MDPI
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spelling ftleibnizopen:oai:oai.leibnizopen.de:rTiJYIgBdbrxVwz6zmCQ 2025-01-16T19:07:54+00:00 CaLB Catalyzed Conversion of ε-Caprolactone in Aqueous Medium. Part 1: Immobilization of CaLB to Microgels Engel, Stefan Höck, Heidi Bocola, Marco Keul, Helmut Schwaneberg, Ulrich Möller, Martin 2016 application/pdf https://oa.tib.eu/renate/handle/123456789/8644 https://doi.org/10.34657/7682 eng eng Basel : MDPI CC BY 4.0 Unported https://creativecommons.org/licenses/by/4.0/ Polymers 8 (2016), Nr. 10 Candida antarctica lipase B enzyme immobilization Microgel Novozym® 435 Polyesterification ε-Caprolactone 540 article Text 2016 ftleibnizopen https://doi.org/10.34657/7682 2023-05-28T23:14:42Z The enzymatic ring-opening polymerization of lactones is a method of increasing interest for the synthesis of biodegradable and biocompatible polymers. In the past it was shown that immobilization of Candida antarctica lipase B (CaLB) and the reaction medium play an important role in the polymerization ability especially of medium ring size lactones like ε-caprolactone (ε-CL). We investigated a route for the preparation of compartmentalized microgels based on poly(glycidol) in which CaLB was immobilized to increase its esterification ability. To find the ideal environment for CaLB, we investigated the acceptable water concentration and the accessibility for the monomer in model polymerizations in toluene and analyzed the obtained oligomers/polymers by NMR and SEC. We observed a sufficient accessibility for ε-CL to a toluene like hydrophobic phase imitating a hydrophobic microgel. Comparing free CaLB and Novozym® 435 we found that not the monomer concentration but rather the solubility of the enzyme, as well as the water concentration, strongly influences the equilibrium of esterification and hydrolysis. On the basis of these investigations, microgels of different polarity were prepared and successfully loaded with CaLB by physical entrapment. By comparison of immobilized and free CaLB, we demonstrated an effect of the hydrophobicity of the microenvironment of CaLB on its enzymatic activity. publishedVersion Article in Journal/Newspaper Antarc* Antarctica LeibnizOpen (The Leibniz Association)
spellingShingle Candida antarctica lipase B
enzyme immobilization
Microgel
Novozym® 435
Polyesterification
ε-Caprolactone
540
Engel, Stefan
Höck, Heidi
Bocola, Marco
Keul, Helmut
Schwaneberg, Ulrich
Möller, Martin
CaLB Catalyzed Conversion of ε-Caprolactone in Aqueous Medium. Part 1: Immobilization of CaLB to Microgels
title CaLB Catalyzed Conversion of ε-Caprolactone in Aqueous Medium. Part 1: Immobilization of CaLB to Microgels
title_full CaLB Catalyzed Conversion of ε-Caprolactone in Aqueous Medium. Part 1: Immobilization of CaLB to Microgels
title_fullStr CaLB Catalyzed Conversion of ε-Caprolactone in Aqueous Medium. Part 1: Immobilization of CaLB to Microgels
title_full_unstemmed CaLB Catalyzed Conversion of ε-Caprolactone in Aqueous Medium. Part 1: Immobilization of CaLB to Microgels
title_short CaLB Catalyzed Conversion of ε-Caprolactone in Aqueous Medium. Part 1: Immobilization of CaLB to Microgels
title_sort calb catalyzed conversion of ε-caprolactone in aqueous medium. part 1: immobilization of calb to microgels
topic Candida antarctica lipase B
enzyme immobilization
Microgel
Novozym® 435
Polyesterification
ε-Caprolactone
540
topic_facet Candida antarctica lipase B
enzyme immobilization
Microgel
Novozym® 435
Polyesterification
ε-Caprolactone
540
url https://oa.tib.eu/renate/handle/123456789/8644
https://doi.org/10.34657/7682