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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...

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Autores principales: de Martino, M. Teresa, Tonin, Fabio, Bloemendal, Victor R. L. J., Hanefeld, Ulf, Rutjes, Floris P. J. T., van Hest, Jan C. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
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.
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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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