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One‐step selective affinity purification and immobilization of His‐tagged enzyme by recyclable magnetic nanoparticles
The NiFe(2)O(4) magnetic nanoparticles (NF‐MNPs) were prepared for one‐step selective affinity purification and immobilization of His‐tagged recombinant glucose dehydrogenase (GluDH). The prepared nanoparticles were characterized by a Fourier‐transform infrared spectrophotometer and microscopy. The...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8182278/ https://www.ncbi.nlm.nih.gov/pubmed/34140847 http://dx.doi.org/10.1002/elsc.202000093 |
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author | Zhou, Li‐Jian Li, Rui‐Fang Li, Xue‐Yong Zhang, Ye‐Wang |
author_facet | Zhou, Li‐Jian Li, Rui‐Fang Li, Xue‐Yong Zhang, Ye‐Wang |
author_sort | Zhou, Li‐Jian |
collection | PubMed |
description | The NiFe(2)O(4) magnetic nanoparticles (NF‐MNPs) were prepared for one‐step selective affinity purification and immobilization of His‐tagged recombinant glucose dehydrogenase (GluDH). The prepared nanoparticles were characterized by a Fourier‐transform infrared spectrophotometer and microscopy. The immobilization and purification of His‐tagged GluDH on NF‐MNPs were investigated. The optimal immobilization conditions were obtained that mixed cell lysis and carriers in a ratio of 0.13 in pH 8.0 Tris‐HCl buffer at 30℃ and incubated for 2 h. The highest activity recovery and protein bindings were 71.39% and 38.50 μg mg(–1) support, respectively. The immobilized GluDH exhibited high thermostability, pH‐stability and it can retain more than 65% of the initial enzyme after 10 cycles for the conversion of glucose to gluconolactone. Comparing with a commercial Ni‐NTA resin, the NF‐MNPs displayed a higher specific affinity with His‐tagged recombinant GluDH. |
format | Online Article Text |
id | pubmed-8182278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81822782021-06-16 One‐step selective affinity purification and immobilization of His‐tagged enzyme by recyclable magnetic nanoparticles Zhou, Li‐Jian Li, Rui‐Fang Li, Xue‐Yong Zhang, Ye‐Wang Eng Life Sci Research Articles The NiFe(2)O(4) magnetic nanoparticles (NF‐MNPs) were prepared for one‐step selective affinity purification and immobilization of His‐tagged recombinant glucose dehydrogenase (GluDH). The prepared nanoparticles were characterized by a Fourier‐transform infrared spectrophotometer and microscopy. The immobilization and purification of His‐tagged GluDH on NF‐MNPs were investigated. The optimal immobilization conditions were obtained that mixed cell lysis and carriers in a ratio of 0.13 in pH 8.0 Tris‐HCl buffer at 30℃ and incubated for 2 h. The highest activity recovery and protein bindings were 71.39% and 38.50 μg mg(–1) support, respectively. The immobilized GluDH exhibited high thermostability, pH‐stability and it can retain more than 65% of the initial enzyme after 10 cycles for the conversion of glucose to gluconolactone. Comparing with a commercial Ni‐NTA resin, the NF‐MNPs displayed a higher specific affinity with His‐tagged recombinant GluDH. John Wiley and Sons Inc. 2021-05-04 /pmc/articles/PMC8182278/ /pubmed/34140847 http://dx.doi.org/10.1002/elsc.202000093 Text en © 2021 The Authors. Engineering in Life Sciences published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Zhou, Li‐Jian Li, Rui‐Fang Li, Xue‐Yong Zhang, Ye‐Wang One‐step selective affinity purification and immobilization of His‐tagged enzyme by recyclable magnetic nanoparticles |
title | One‐step selective affinity purification and immobilization of His‐tagged enzyme by recyclable magnetic nanoparticles |
title_full | One‐step selective affinity purification and immobilization of His‐tagged enzyme by recyclable magnetic nanoparticles |
title_fullStr | One‐step selective affinity purification and immobilization of His‐tagged enzyme by recyclable magnetic nanoparticles |
title_full_unstemmed | One‐step selective affinity purification and immobilization of His‐tagged enzyme by recyclable magnetic nanoparticles |
title_short | One‐step selective affinity purification and immobilization of His‐tagged enzyme by recyclable magnetic nanoparticles |
title_sort | one‐step selective affinity purification and immobilization of his‐tagged enzyme by recyclable magnetic nanoparticles |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8182278/ https://www.ncbi.nlm.nih.gov/pubmed/34140847 http://dx.doi.org/10.1002/elsc.202000093 |
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