The combination of covalent and ionic exchange immobilizations enables the coimmobilization on vinyl sulfone activated supports and the reuse of the most stable immobilized enzyme

The coimmobilization of lipases from Rhizomucor miehei (RML) and Candida antarctica (CALB) has been intended using agarose beads activated with divinyl sulfone. CALB could be immobilized on this support, while RML was not. However, RML was ionically exchanged on this support blocked with ethylendiam...

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Published in:International Journal of Biological Macromolecules
Main Authors: Arana Peña, Sara, Carballares, Diego, Morellon Sterling, Roberto, Rocha Martin, Javier, Fernandez Lafuente, Roberto
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier 2021
Subjects:
Online Access:https://eprints.ucm.es/id/eprint/72694/
https://eprints.ucm.es/id/eprint/72694/1/Ara%C3%B1a-Pe%C3%B1a,%20Sara%20et%20al.%202021.%20The%20combination%20of%20covalent%20and%20ionic%20exchange%20immobilizations%20enables.pdf
https://doi.org/10.1016/j.ijbiomac.2021.12.148
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spelling ftunivcmadrid:oai:www.ucm.es:72694 2023-05-15T13:45:45+02:00 The combination of covalent and ionic exchange immobilizations enables the coimmobilization on vinyl sulfone activated supports and the reuse of the most stable immobilized enzyme Arana Peña, Sara Carballares, Diego Morellon Sterling, Roberto Rocha Martin, Javier Fernandez Lafuente, Roberto 2021-12-30 application/pdf https://eprints.ucm.es/id/eprint/72694/ https://eprints.ucm.es/id/eprint/72694/1/Ara%C3%B1a-Pe%C3%B1a,%20Sara%20et%20al.%202021.%20The%20combination%20of%20covalent%20and%20ionic%20exchange%20immobilizations%20enables.pdf https://doi.org/10.1016/j.ijbiomac.2021.12.148 en eng Elsevier https://eprints.ucm.es/id/eprint/72694/1/Ara%C3%B1a-Pe%C3%B1a,%20Sara%20et%20al.%202021.%20The%20combination%20of%20covalent%20and%20ionic%20exchange%20immobilizations%20enables.pdf cc_by_nc_nd info:eu-repo/semantics/openAccess CC-BY-NC-ND Biología molecular Bioquímica info:eu-repo/semantics/article PeerReviewed 2021 ftunivcmadrid https://doi.org/10.1016/j.ijbiomac.2021.12.148 2022-10-18T23:07:45Z The coimmobilization of lipases from Rhizomucor miehei (RML) and Candida antarctica (CALB) has been intended using agarose beads activated with divinyl sulfone. CALB could be immobilized on this support, while RML was not. However, RML was ionically exchanged on this support blocked with ethylendiamine. Therefore, both enzymes could be coimmobilized on the same particle, CALB covalently using the vinyl sulfone groups, and RML via anionic exchange on the aminated blocked support. However, immobilized RML was far less stable than immobilized CALB. To avoid the discarding of CALB (that maintained 90% of the initial activity after RML inactivation), a strategy was developed. Inactivated RML was desorbed from the support using ammonium sulfate and 1% Triton X-100 at pH 7.0. That way, 5 cycles of RML thermal inactivation, discharge of the inactivated enzyme and re-immobilization of a fresh sample of RML could be performed. In the last cycle, immobilized CALB activity was still over 90% of the initial one. Thus, the strategy permits that enzymes can be coimmobilized on vinyl sulfone supports even if one of them cannot be immobilized on it, and also permits the reuse of the most stable enzyme (if it is irreversibly attached to the support). Article in Journal/Newspaper Antarc* Antarctica Universidad Complutense de Madrid (UCM): E-Prints Complutense Triton ENVELOPE(-55.615,-55.615,49.517,49.517) International Journal of Biological Macromolecules 199 51 60
institution Open Polar
collection Universidad Complutense de Madrid (UCM): E-Prints Complutense
op_collection_id ftunivcmadrid
language English
topic Biología molecular
Bioquímica
spellingShingle Biología molecular
Bioquímica
Arana Peña, Sara
Carballares, Diego
Morellon Sterling, Roberto
Rocha Martin, Javier
Fernandez Lafuente, Roberto
The combination of covalent and ionic exchange immobilizations enables the coimmobilization on vinyl sulfone activated supports and the reuse of the most stable immobilized enzyme
topic_facet Biología molecular
Bioquímica
description The coimmobilization of lipases from Rhizomucor miehei (RML) and Candida antarctica (CALB) has been intended using agarose beads activated with divinyl sulfone. CALB could be immobilized on this support, while RML was not. However, RML was ionically exchanged on this support blocked with ethylendiamine. Therefore, both enzymes could be coimmobilized on the same particle, CALB covalently using the vinyl sulfone groups, and RML via anionic exchange on the aminated blocked support. However, immobilized RML was far less stable than immobilized CALB. To avoid the discarding of CALB (that maintained 90% of the initial activity after RML inactivation), a strategy was developed. Inactivated RML was desorbed from the support using ammonium sulfate and 1% Triton X-100 at pH 7.0. That way, 5 cycles of RML thermal inactivation, discharge of the inactivated enzyme and re-immobilization of a fresh sample of RML could be performed. In the last cycle, immobilized CALB activity was still over 90% of the initial one. Thus, the strategy permits that enzymes can be coimmobilized on vinyl sulfone supports even if one of them cannot be immobilized on it, and also permits the reuse of the most stable enzyme (if it is irreversibly attached to the support).
format Article in Journal/Newspaper
author Arana Peña, Sara
Carballares, Diego
Morellon Sterling, Roberto
Rocha Martin, Javier
Fernandez Lafuente, Roberto
author_facet Arana Peña, Sara
Carballares, Diego
Morellon Sterling, Roberto
Rocha Martin, Javier
Fernandez Lafuente, Roberto
author_sort Arana Peña, Sara
title The combination of covalent and ionic exchange immobilizations enables the coimmobilization on vinyl sulfone activated supports and the reuse of the most stable immobilized enzyme
title_short The combination of covalent and ionic exchange immobilizations enables the coimmobilization on vinyl sulfone activated supports and the reuse of the most stable immobilized enzyme
title_full The combination of covalent and ionic exchange immobilizations enables the coimmobilization on vinyl sulfone activated supports and the reuse of the most stable immobilized enzyme
title_fullStr The combination of covalent and ionic exchange immobilizations enables the coimmobilization on vinyl sulfone activated supports and the reuse of the most stable immobilized enzyme
title_full_unstemmed The combination of covalent and ionic exchange immobilizations enables the coimmobilization on vinyl sulfone activated supports and the reuse of the most stable immobilized enzyme
title_sort combination of covalent and ionic exchange immobilizations enables the coimmobilization on vinyl sulfone activated supports and the reuse of the most stable immobilized enzyme
publisher Elsevier
publishDate 2021
url https://eprints.ucm.es/id/eprint/72694/
https://eprints.ucm.es/id/eprint/72694/1/Ara%C3%B1a-Pe%C3%B1a,%20Sara%20et%20al.%202021.%20The%20combination%20of%20covalent%20and%20ionic%20exchange%20immobilizations%20enables.pdf
https://doi.org/10.1016/j.ijbiomac.2021.12.148
long_lat ENVELOPE(-55.615,-55.615,49.517,49.517)
geographic Triton
geographic_facet Triton
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
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op_rights cc_by_nc_nd
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