Coimmobilization of different lipases: Simple layer by layer enzyme spatial ordering
This paper shows the step by step coimmobilization of up to five different enzymes following two different orders in the coimmobilization to alter the effect of substrate diffusion limitations. The enzymes were the lipases A and B from Candida antarctica, the lipases from Rhizomocur miehei and, Them...
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ftunifrgnorteir:oai:https://repositorio.ufrn.br:123456789/45068 2024-02-11T09:57:27+01:00 Coimmobilization of different lipases: Simple layer by layer enzyme spatial ordering Peña, Sara Arana Rios, Nathalia Saraiva Sanchez, Carmen Mendez Lokha, Yuliya Carballares, Diego Gonçalves, Luciana Rocha Barros Lafuente, Roberto Fernandez 2021-11-29T21:16:03Z https://repositorio.ufrn.br/handle/123456789/45068 https://doi.org/10.1016/j.ijbiomac.2019.10.087 en eng Elsevier ARANA-PEÑA, Sara; RIOS, Nathalia S.; MENDEZ-SANCHEZ, Carmen; LOKHA, Yuliya; CARBALLARES, Diego; GONÇALVES, Luciana R.B.; FERNANDEZ-LAFUENTE, Roberto. Coimmobilization of different lipases: simple layer by layer enzyme spatial ordering. International Journal Of Biological Macromolecules, [S.L.], v. 145, p. 856-864, fev. 2020. Disponível em: https://www.sciencedirect.com/science/article/abs/pii/S0141813019371466?via%3Dihub#!. Acesso em: 29 nov. 2021. https://doi.org/10.1016/j.ijbiomac.2019.10.087. 0141-8130 https://repositorio.ufrn.br/handle/123456789/45068 doi:10.1016/j.ijbiomac.2019.10.087 Enzyme coimmobilization Enzyme ordering Combilipases article 2021 ftunifrgnorteir https://doi.org/10.1016/j.ijbiomac.2019.10.087 2024-01-21T00:37:58Z This paper shows the step by step coimmobilization of up to five different enzymes following two different orders in the coimmobilization to alter the effect of substrate diffusion limitations. The enzymes were the lipases A and B from Candida antarctica, the lipases from Rhizomocur miehei and, Themomyces lanuginosus and the phospholipase Lecitase Ultra. The utilized strategy was a layer by layer immobilization, coating the immobilized enzymes with polyethylenimine followed by the crosslinking of the enzyme and PEI with glutaraldehyde to prevent enzyme release, and them adding a new lipase layer. The use of previously inactivated biocatalysts (using diethyl p-nitrophenylphosphate) permitted to visualize the immobilization of each enzyme layer, which was later confirmed by SDS-PAGE. This also confirmed the successful and complete covalent crosslinking of the glutaraldehyde treated enzyme layers. Activity of the combibiocatalysts was followed using diverse substrates. The protocol was successful and permitted to immobilize in an ordered way the 5 different enzymes in a down-up distribution 2030-12 Article in Journal/Newspaper Antarc* Antarctica Universidade Federal do Rio Grande do Norte: Repositório Institucional (RI UFRN) International Journal of Biological Macromolecules 145 856 864 |
institution |
Open Polar |
collection |
Universidade Federal do Rio Grande do Norte: Repositório Institucional (RI UFRN) |
op_collection_id |
ftunifrgnorteir |
language |
English |
topic |
Enzyme coimmobilization Enzyme ordering Combilipases |
spellingShingle |
Enzyme coimmobilization Enzyme ordering Combilipases Peña, Sara Arana Rios, Nathalia Saraiva Sanchez, Carmen Mendez Lokha, Yuliya Carballares, Diego Gonçalves, Luciana Rocha Barros Lafuente, Roberto Fernandez Coimmobilization of different lipases: Simple layer by layer enzyme spatial ordering |
topic_facet |
Enzyme coimmobilization Enzyme ordering Combilipases |
description |
This paper shows the step by step coimmobilization of up to five different enzymes following two different orders in the coimmobilization to alter the effect of substrate diffusion limitations. The enzymes were the lipases A and B from Candida antarctica, the lipases from Rhizomocur miehei and, Themomyces lanuginosus and the phospholipase Lecitase Ultra. The utilized strategy was a layer by layer immobilization, coating the immobilized enzymes with polyethylenimine followed by the crosslinking of the enzyme and PEI with glutaraldehyde to prevent enzyme release, and them adding a new lipase layer. The use of previously inactivated biocatalysts (using diethyl p-nitrophenylphosphate) permitted to visualize the immobilization of each enzyme layer, which was later confirmed by SDS-PAGE. This also confirmed the successful and complete covalent crosslinking of the glutaraldehyde treated enzyme layers. Activity of the combibiocatalysts was followed using diverse substrates. The protocol was successful and permitted to immobilize in an ordered way the 5 different enzymes in a down-up distribution 2030-12 |
format |
Article in Journal/Newspaper |
author |
Peña, Sara Arana Rios, Nathalia Saraiva Sanchez, Carmen Mendez Lokha, Yuliya Carballares, Diego Gonçalves, Luciana Rocha Barros Lafuente, Roberto Fernandez |
author_facet |
Peña, Sara Arana Rios, Nathalia Saraiva Sanchez, Carmen Mendez Lokha, Yuliya Carballares, Diego Gonçalves, Luciana Rocha Barros Lafuente, Roberto Fernandez |
author_sort |
Peña, Sara Arana |
title |
Coimmobilization of different lipases: Simple layer by layer enzyme spatial ordering |
title_short |
Coimmobilization of different lipases: Simple layer by layer enzyme spatial ordering |
title_full |
Coimmobilization of different lipases: Simple layer by layer enzyme spatial ordering |
title_fullStr |
Coimmobilization of different lipases: Simple layer by layer enzyme spatial ordering |
title_full_unstemmed |
Coimmobilization of different lipases: Simple layer by layer enzyme spatial ordering |
title_sort |
coimmobilization of different lipases: simple layer by layer enzyme spatial ordering |
publisher |
Elsevier |
publishDate |
2021 |
url |
https://repositorio.ufrn.br/handle/123456789/45068 https://doi.org/10.1016/j.ijbiomac.2019.10.087 |
genre |
Antarc* Antarctica |
genre_facet |
Antarc* Antarctica |
op_relation |
ARANA-PEÑA, Sara; RIOS, Nathalia S.; MENDEZ-SANCHEZ, Carmen; LOKHA, Yuliya; CARBALLARES, Diego; GONÇALVES, Luciana R.B.; FERNANDEZ-LAFUENTE, Roberto. Coimmobilization of different lipases: simple layer by layer enzyme spatial ordering. International Journal Of Biological Macromolecules, [S.L.], v. 145, p. 856-864, fev. 2020. Disponível em: https://www.sciencedirect.com/science/article/abs/pii/S0141813019371466?via%3Dihub#!. Acesso em: 29 nov. 2021. https://doi.org/10.1016/j.ijbiomac.2019.10.087. 0141-8130 https://repositorio.ufrn.br/handle/123456789/45068 doi:10.1016/j.ijbiomac.2019.10.087 |
op_doi |
https://doi.org/10.1016/j.ijbiomac.2019.10.087 |
container_title |
International Journal of Biological Macromolecules |
container_volume |
145 |
container_start_page |
856 |
op_container_end_page |
864 |
_version_ |
1790609746875645952 |