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Self-Assembled Regenerated Silk Fibroin Microsphere-Embedded Fe(3)O(4) Magnetic Nanoparticles for Immobilization of Zymolyase
[Image: see text] Cytoplasm of Saccharomyces cerevisiae yeast cells contains a significant amount of desired intracellular products for both industrial utility and academic research. To recover intracellular compounds, it is necessary to break the yeast cells with high efficiency, which, under certa...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921612/ https://www.ncbi.nlm.nih.gov/pubmed/31867558 http://dx.doi.org/10.1021/acsomega.9b03491 |
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author | Xiao, Menglin Lv, Shanshan |
author_facet | Xiao, Menglin Lv, Shanshan |
author_sort | Xiao, Menglin |
collection | PubMed |
description | [Image: see text] Cytoplasm of Saccharomyces cerevisiae yeast cells contains a significant amount of desired intracellular products for both industrial utility and academic research. To recover intracellular compounds, it is necessary to break the yeast cells with high efficiency, which, under certain circumstances, requires the use of the lytic enzyme zymolyase to completely digest the cell walls. A promising strategy for zymolyase immobilization on silk fibroin (SF) was developed. SF/Fe(3)O(4) magnetic microspheres (MMs) were constructed by solvent (ethanol)-induced self-assembly of SF surrounding Fe(3)O(4) magnetic nanoparticles (MNs), which were synthesized by a coprecipitation method. Zymolyase was covalently bonded on the surface of the SF/Fe(3)O(4) MMs by a photochemical cross-linking method to produce robust biocatalysts of zymolyase/SF/Fe(3)O(4). The chemical, magnetic, and morphological properties of the MM supports and the immobilized zymolyase were investigated. Enzymolysis results demonstrated that the immobilized zymolyase showed good activity and stability for digesting yeast cell walls, and the biocatalyst can be readily recycled through convenient magnetic separation for reuse. At the optimum pH = 7.5, the immobilized zymolyase maintained 84% of the activity of the free zymolyase and retained 41% of its initial activity after four times of reuse. At unfavorable acidic pH = 4, the immobilized zymolyase retained 81% of its initial activity, while the free zymolyase showed no significant activity. Consequently, the SF/Fe(3)O(4) MMs exhibit superior performance in terms of immobilizing enzymes, which have a good prospect in the biological application. |
format | Online Article Text |
id | pubmed-6921612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-69216122019-12-20 Self-Assembled Regenerated Silk Fibroin Microsphere-Embedded Fe(3)O(4) Magnetic Nanoparticles for Immobilization of Zymolyase Xiao, Menglin Lv, Shanshan ACS Omega [Image: see text] Cytoplasm of Saccharomyces cerevisiae yeast cells contains a significant amount of desired intracellular products for both industrial utility and academic research. To recover intracellular compounds, it is necessary to break the yeast cells with high efficiency, which, under certain circumstances, requires the use of the lytic enzyme zymolyase to completely digest the cell walls. A promising strategy for zymolyase immobilization on silk fibroin (SF) was developed. SF/Fe(3)O(4) magnetic microspheres (MMs) were constructed by solvent (ethanol)-induced self-assembly of SF surrounding Fe(3)O(4) magnetic nanoparticles (MNs), which were synthesized by a coprecipitation method. Zymolyase was covalently bonded on the surface of the SF/Fe(3)O(4) MMs by a photochemical cross-linking method to produce robust biocatalysts of zymolyase/SF/Fe(3)O(4). The chemical, magnetic, and morphological properties of the MM supports and the immobilized zymolyase were investigated. Enzymolysis results demonstrated that the immobilized zymolyase showed good activity and stability for digesting yeast cell walls, and the biocatalyst can be readily recycled through convenient magnetic separation for reuse. At the optimum pH = 7.5, the immobilized zymolyase maintained 84% of the activity of the free zymolyase and retained 41% of its initial activity after four times of reuse. At unfavorable acidic pH = 4, the immobilized zymolyase retained 81% of its initial activity, while the free zymolyase showed no significant activity. Consequently, the SF/Fe(3)O(4) MMs exhibit superior performance in terms of immobilizing enzymes, which have a good prospect in the biological application. American Chemical Society 2019-12-05 /pmc/articles/PMC6921612/ /pubmed/31867558 http://dx.doi.org/10.1021/acsomega.9b03491 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Xiao, Menglin Lv, Shanshan Self-Assembled Regenerated Silk Fibroin Microsphere-Embedded Fe(3)O(4) Magnetic Nanoparticles for Immobilization of Zymolyase |
title | Self-Assembled
Regenerated Silk Fibroin Microsphere-Embedded
Fe(3)O(4) Magnetic Nanoparticles for Immobilization of Zymolyase |
title_full | Self-Assembled
Regenerated Silk Fibroin Microsphere-Embedded
Fe(3)O(4) Magnetic Nanoparticles for Immobilization of Zymolyase |
title_fullStr | Self-Assembled
Regenerated Silk Fibroin Microsphere-Embedded
Fe(3)O(4) Magnetic Nanoparticles for Immobilization of Zymolyase |
title_full_unstemmed | Self-Assembled
Regenerated Silk Fibroin Microsphere-Embedded
Fe(3)O(4) Magnetic Nanoparticles for Immobilization of Zymolyase |
title_short | Self-Assembled
Regenerated Silk Fibroin Microsphere-Embedded
Fe(3)O(4) Magnetic Nanoparticles for Immobilization of Zymolyase |
title_sort | self-assembled
regenerated silk fibroin microsphere-embedded
fe(3)o(4) magnetic nanoparticles for immobilization of zymolyase |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921612/ https://www.ncbi.nlm.nih.gov/pubmed/31867558 http://dx.doi.org/10.1021/acsomega.9b03491 |
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