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Bioconjugation of enzyme with silica microparticles: a promising platform for α-amylase partitioning
Here, we report the implementation of α-amylase conjugated silica microparticles for improvement of α-amylase partitioning in a PEG–organic salt-based aqueous two phase system. A direct reduction method was employed for the synthesis of silica microparticles with simultaneous introduction of α-amyla...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064637/ https://www.ncbi.nlm.nih.gov/pubmed/35515231 http://dx.doi.org/10.1039/c9ra02342a |
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author | Karimi, Maryam Abdolrahimi, Shiva Pazuki, Gholamreza |
author_facet | Karimi, Maryam Abdolrahimi, Shiva Pazuki, Gholamreza |
author_sort | Karimi, Maryam |
collection | PubMed |
description | Here, we report the implementation of α-amylase conjugated silica microparticles for improvement of α-amylase partitioning in a PEG–organic salt-based aqueous two phase system. A direct reduction method was employed for the synthesis of silica microparticles with simultaneous introduction of α-amylase. In this context, we synthesized three different silica α-amylase conjugated microparticles with variation of tetraethyl orthosilicate concentration, and thus the effect of final particle size and enzyme loading on partitioning was also studied. The partition coefficient ratio of α-amylase to Si:α-amylase of 2.186 : 21.701 validated an almost tenfold increase in separation. The microscopic structure of the system was thoroughly investigated in order to understand the extraction mechanism and any possible denaturation. Improved partition coefficients can be interpreted by the formation of α-amylase–silica–PEG carriers. Furthermore, circular dichroism (CD) spectra validated partial unfolding of the enzyme. |
format | Online Article Text |
id | pubmed-9064637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90646372022-05-04 Bioconjugation of enzyme with silica microparticles: a promising platform for α-amylase partitioning Karimi, Maryam Abdolrahimi, Shiva Pazuki, Gholamreza RSC Adv Chemistry Here, we report the implementation of α-amylase conjugated silica microparticles for improvement of α-amylase partitioning in a PEG–organic salt-based aqueous two phase system. A direct reduction method was employed for the synthesis of silica microparticles with simultaneous introduction of α-amylase. In this context, we synthesized three different silica α-amylase conjugated microparticles with variation of tetraethyl orthosilicate concentration, and thus the effect of final particle size and enzyme loading on partitioning was also studied. The partition coefficient ratio of α-amylase to Si:α-amylase of 2.186 : 21.701 validated an almost tenfold increase in separation. The microscopic structure of the system was thoroughly investigated in order to understand the extraction mechanism and any possible denaturation. Improved partition coefficients can be interpreted by the formation of α-amylase–silica–PEG carriers. Furthermore, circular dichroism (CD) spectra validated partial unfolding of the enzyme. The Royal Society of Chemistry 2019-06-10 /pmc/articles/PMC9064637/ /pubmed/35515231 http://dx.doi.org/10.1039/c9ra02342a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Karimi, Maryam Abdolrahimi, Shiva Pazuki, Gholamreza Bioconjugation of enzyme with silica microparticles: a promising platform for α-amylase partitioning |
title | Bioconjugation of enzyme with silica microparticles: a promising platform for α-amylase partitioning |
title_full | Bioconjugation of enzyme with silica microparticles: a promising platform for α-amylase partitioning |
title_fullStr | Bioconjugation of enzyme with silica microparticles: a promising platform for α-amylase partitioning |
title_full_unstemmed | Bioconjugation of enzyme with silica microparticles: a promising platform for α-amylase partitioning |
title_short | Bioconjugation of enzyme with silica microparticles: a promising platform for α-amylase partitioning |
title_sort | bioconjugation of enzyme with silica microparticles: a promising platform for α-amylase partitioning |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064637/ https://www.ncbi.nlm.nih.gov/pubmed/35515231 http://dx.doi.org/10.1039/c9ra02342a |
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