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...
Published in: | International Journal of Biological Macromolecules |
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Language: | English |
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Elsevier
2021
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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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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 |
op_relation |
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 |
op_rights |
cc_by_nc_nd info:eu-repo/semantics/openAccess |
op_rightsnorm |
CC-BY-NC-ND |
op_doi |
https://doi.org/10.1016/j.ijbiomac.2021.12.148 |
container_title |
International Journal of Biological Macromolecules |
container_volume |
199 |
container_start_page |
51 |
op_container_end_page |
60 |
_version_ |
1766230535203454976 |