Reversible Immobilization of Lipases on Heterofunctional Octyl-Amino Agarose Beads Prevents Enzyme Desorption
Two different heterofunctional octyl-amino supports have been prepared using ethylenediamine and hexylendiamine (OCEDA and OCHDA) and utilized to immobilize five lipases (lipases A (CALA) and B (CALB) from Candida antarctica, lipases from Thermomyces lanuginosus (TLL), from Rhizomucor miehei (RML) a...
Published in: | Molecules |
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Main Authors: | , , , , , , , , |
Format: | Text |
Language: | English |
Published: |
Multidisciplinary Digital Publishing Institute
2016
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Subjects: | |
Online Access: | https://doi.org/10.3390/molecules21050646 |
_version_ | 1821772657167695872 |
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author | Nazzoly Rueda Tiago Albuquerque Rocio Bartolome-Cabrero Laura Fernandez-Lopez Rodrigo Torres Claudia Ortiz Jose Dos Santos Oveimar Barbosa Roberto Fernandez-Lafuente |
author_facet | Nazzoly Rueda Tiago Albuquerque Rocio Bartolome-Cabrero Laura Fernandez-Lopez Rodrigo Torres Claudia Ortiz Jose Dos Santos Oveimar Barbosa Roberto Fernandez-Lafuente |
author_sort | Nazzoly Rueda |
collection | MDPI Open Access Publishing |
container_issue | 5 |
container_start_page | 646 |
container_title | Molecules |
container_volume | 21 |
description | Two different heterofunctional octyl-amino supports have been prepared using ethylenediamine and hexylendiamine (OCEDA and OCHDA) and utilized to immobilize five lipases (lipases A (CALA) and B (CALB) from Candida antarctica, lipases from Thermomyces lanuginosus (TLL), from Rhizomucor miehei (RML) and from Candida rugosa (CRL) and the phospholipase Lecitase Ultra (LU). Using pH 5 and 50 mM sodium acetate, the immobilizations proceeded via interfacial activation on the octyl layer, after some ionic bridges were established. These supports did not release enzyme when incubated at Triton X-100 concentrations that released all enzyme molecules from the octyl support. The octyl support produced significant enzyme hyperactivation, except for CALB. However, the activities of the immobilized enzymes were usually slightly higher using the new supports than the octyl ones. Thermal and solvent stabilities of LU and TLL were significantly improved compared to the OC counterparts, while in the other enzymes the stability decreased in most cases (depending on the pH value). As a general rule, OCEDA had lower negative effects on the stability of the immobilized enzymes than OCHDA and while in solvent inactivation the enzyme molecules remained attached to the support using the new supports and were released using monofunctional octyl supports, in thermal inactivations this only occurred in certain cases. |
format | Text |
genre | Antarc* Antarctica |
genre_facet | Antarc* Antarctica |
geographic | Rugosa Triton |
geographic_facet | Rugosa Triton |
id | ftmdpi:oai:mdpi.com:/1420-3049/21/5/646/ |
institution | Open Polar |
language | English |
long_lat | ENVELOPE(-61.250,-61.250,-62.633,-62.633) ENVELOPE(-55.615,-55.615,49.517,49.517) |
op_collection_id | ftmdpi |
op_coverage | agris |
op_doi | https://doi.org/10.3390/molecules21050646 |
op_relation | Molecular Diversity https://dx.doi.org/10.3390/molecules21050646 |
op_rights | https://creativecommons.org/licenses/by/4.0/ |
op_source | Molecules; Volume 21; Issue 5; Pages: 646 |
publishDate | 2016 |
publisher | Multidisciplinary Digital Publishing Institute |
record_format | openpolar |
spelling | ftmdpi:oai:mdpi.com:/1420-3049/21/5/646/ 2025-01-16T19:39:18+00:00 Reversible Immobilization of Lipases on Heterofunctional Octyl-Amino Agarose Beads Prevents Enzyme Desorption Nazzoly Rueda Tiago Albuquerque Rocio Bartolome-Cabrero Laura Fernandez-Lopez Rodrigo Torres Claudia Ortiz Jose Dos Santos Oveimar Barbosa Roberto Fernandez-Lafuente agris 2016-05-16 application/pdf https://doi.org/10.3390/molecules21050646 EN eng Multidisciplinary Digital Publishing Institute Molecular Diversity https://dx.doi.org/10.3390/molecules21050646 https://creativecommons.org/licenses/by/4.0/ Molecules; Volume 21; Issue 5; Pages: 646 heterofunctional supports octyl supports interfacial activation of lipases ion exchange enzyme hyperactivation reversible immobilization Text 2016 ftmdpi https://doi.org/10.3390/molecules21050646 2023-07-31T20:53:20Z Two different heterofunctional octyl-amino supports have been prepared using ethylenediamine and hexylendiamine (OCEDA and OCHDA) and utilized to immobilize five lipases (lipases A (CALA) and B (CALB) from Candida antarctica, lipases from Thermomyces lanuginosus (TLL), from Rhizomucor miehei (RML) and from Candida rugosa (CRL) and the phospholipase Lecitase Ultra (LU). Using pH 5 and 50 mM sodium acetate, the immobilizations proceeded via interfacial activation on the octyl layer, after some ionic bridges were established. These supports did not release enzyme when incubated at Triton X-100 concentrations that released all enzyme molecules from the octyl support. The octyl support produced significant enzyme hyperactivation, except for CALB. However, the activities of the immobilized enzymes were usually slightly higher using the new supports than the octyl ones. Thermal and solvent stabilities of LU and TLL were significantly improved compared to the OC counterparts, while in the other enzymes the stability decreased in most cases (depending on the pH value). As a general rule, OCEDA had lower negative effects on the stability of the immobilized enzymes than OCHDA and while in solvent inactivation the enzyme molecules remained attached to the support using the new supports and were released using monofunctional octyl supports, in thermal inactivations this only occurred in certain cases. Text Antarc* Antarctica MDPI Open Access Publishing Rugosa ENVELOPE(-61.250,-61.250,-62.633,-62.633) Triton ENVELOPE(-55.615,-55.615,49.517,49.517) Molecules 21 5 646 |
spellingShingle | heterofunctional supports octyl supports interfacial activation of lipases ion exchange enzyme hyperactivation reversible immobilization Nazzoly Rueda Tiago Albuquerque Rocio Bartolome-Cabrero Laura Fernandez-Lopez Rodrigo Torres Claudia Ortiz Jose Dos Santos Oveimar Barbosa Roberto Fernandez-Lafuente Reversible Immobilization of Lipases on Heterofunctional Octyl-Amino Agarose Beads Prevents Enzyme Desorption |
title | Reversible Immobilization of Lipases on Heterofunctional Octyl-Amino Agarose Beads Prevents Enzyme Desorption |
title_full | Reversible Immobilization of Lipases on Heterofunctional Octyl-Amino Agarose Beads Prevents Enzyme Desorption |
title_fullStr | Reversible Immobilization of Lipases on Heterofunctional Octyl-Amino Agarose Beads Prevents Enzyme Desorption |
title_full_unstemmed | Reversible Immobilization of Lipases on Heterofunctional Octyl-Amino Agarose Beads Prevents Enzyme Desorption |
title_short | Reversible Immobilization of Lipases on Heterofunctional Octyl-Amino Agarose Beads Prevents Enzyme Desorption |
title_sort | reversible immobilization of lipases on heterofunctional octyl-amino agarose beads prevents enzyme desorption |
topic | heterofunctional supports octyl supports interfacial activation of lipases ion exchange enzyme hyperactivation reversible immobilization |
topic_facet | heterofunctional supports octyl supports interfacial activation of lipases ion exchange enzyme hyperactivation reversible immobilization |
url | https://doi.org/10.3390/molecules21050646 |