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Compartmentalized cross-linked enzyme nano aggregates (c-CLEnAs) toward pharmaceutical transformations
A new immobilization strategy using compartmentalized nanoreactors is herein reported for two biocatalytic processes: (1) N-acetylneuraminate lyase (NAL) is internalized in NAL-c-CLEnAs and used in a continuous flow aldol condensation of N-acetyl-d-mannosamine with sodium pyruvate to N-acetylneurami...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034143/ https://www.ncbi.nlm.nih.gov/pubmed/35478789 http://dx.doi.org/10.1039/d1ra04332c |
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author | de Martino, M. Teresa Tonin, Fabio Bloemendal, Victor R. L. J. Hanefeld, Ulf Rutjes, Floris P. J. T. van Hest, Jan C. M. |
author_facet | de Martino, M. Teresa Tonin, Fabio Bloemendal, Victor R. L. J. Hanefeld, Ulf Rutjes, Floris P. J. T. van Hest, Jan C. M. |
author_sort | de Martino, M. Teresa |
collection | PubMed |
description | A new immobilization strategy using compartmentalized nanoreactors is herein reported for two biocatalytic processes: (1) N-acetylneuraminate lyase (NAL) is internalized in NAL-c-CLEnAs and used in a continuous flow aldol condensation of N-acetyl-d-mannosamine with sodium pyruvate to N-acetylneuraminic acid; (2) two hydroxysteroid dehydrogenases (HSDH) 7α- and 7β-HSDH are incorporated in c-CLEnAs and used in a two-step cascade batch synthesis of ursodeoxycholic acid (UDCA). The versatile use of c-CLEnA demonstrates that this immobilization methodology is a valuable addition to the toolbox of synthetic chemists. |
format | Online Article Text |
id | pubmed-9034143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90341432022-04-26 Compartmentalized cross-linked enzyme nano aggregates (c-CLEnAs) toward pharmaceutical transformations de Martino, M. Teresa Tonin, Fabio Bloemendal, Victor R. L. J. Hanefeld, Ulf Rutjes, Floris P. J. T. van Hest, Jan C. M. RSC Adv Chemistry A new immobilization strategy using compartmentalized nanoreactors is herein reported for two biocatalytic processes: (1) N-acetylneuraminate lyase (NAL) is internalized in NAL-c-CLEnAs and used in a continuous flow aldol condensation of N-acetyl-d-mannosamine with sodium pyruvate to N-acetylneuraminic acid; (2) two hydroxysteroid dehydrogenases (HSDH) 7α- and 7β-HSDH are incorporated in c-CLEnAs and used in a two-step cascade batch synthesis of ursodeoxycholic acid (UDCA). The versatile use of c-CLEnA demonstrates that this immobilization methodology is a valuable addition to the toolbox of synthetic chemists. The Royal Society of Chemistry 2021-06-21 /pmc/articles/PMC9034143/ /pubmed/35478789 http://dx.doi.org/10.1039/d1ra04332c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry de Martino, M. Teresa Tonin, Fabio Bloemendal, Victor R. L. J. Hanefeld, Ulf Rutjes, Floris P. J. T. van Hest, Jan C. M. Compartmentalized cross-linked enzyme nano aggregates (c-CLEnAs) toward pharmaceutical transformations |
title | Compartmentalized cross-linked enzyme nano aggregates (c-CLEnAs) toward pharmaceutical transformations |
title_full | Compartmentalized cross-linked enzyme nano aggregates (c-CLEnAs) toward pharmaceutical transformations |
title_fullStr | Compartmentalized cross-linked enzyme nano aggregates (c-CLEnAs) toward pharmaceutical transformations |
title_full_unstemmed | Compartmentalized cross-linked enzyme nano aggregates (c-CLEnAs) toward pharmaceutical transformations |
title_short | Compartmentalized cross-linked enzyme nano aggregates (c-CLEnAs) toward pharmaceutical transformations |
title_sort | compartmentalized cross-linked enzyme nano aggregates (c-clenas) toward pharmaceutical transformations |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034143/ https://www.ncbi.nlm.nih.gov/pubmed/35478789 http://dx.doi.org/10.1039/d1ra04332c |
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