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Streptavidin-Hosted Organocatalytic Aldol Addition

In this report, the streptavidin-biotin technology was applied to enable organocatalytic aldol addition. By attaching pyrrolidine to the valeric motif of biotin and introducing it to streptavidin (Sav), a protein-based organocatalytic system was created, and the aldol addition of acetone with p-nitr...

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Detalles Bibliográficos
Autores principales: Santi, Nicolò, Morrill, Louis C., Luk, Louis Y. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287710/
https://www.ncbi.nlm.nih.gov/pubmed/32466220
http://dx.doi.org/10.3390/molecules25102457
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author Santi, Nicolò
Morrill, Louis C.
Luk, Louis Y. P.
author_facet Santi, Nicolò
Morrill, Louis C.
Luk, Louis Y. P.
author_sort Santi, Nicolò
collection PubMed
description In this report, the streptavidin-biotin technology was applied to enable organocatalytic aldol addition. By attaching pyrrolidine to the valeric motif of biotin and introducing it to streptavidin (Sav), a protein-based organocatalytic system was created, and the aldol addition of acetone with p-nitrobenzaldehyde was tested. The conversion of substrate to product can be as high as 93%. Although the observed enantioselectivity was only moderate (33:67 er), further protein engineering efforts can be included to improve the selectivity. These results have proven the concept that Sav can be used to host stereoselective aldol addition.
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spelling pubmed-72877102020-06-15 Streptavidin-Hosted Organocatalytic Aldol Addition Santi, Nicolò Morrill, Louis C. Luk, Louis Y. P. Molecules Article In this report, the streptavidin-biotin technology was applied to enable organocatalytic aldol addition. By attaching pyrrolidine to the valeric motif of biotin and introducing it to streptavidin (Sav), a protein-based organocatalytic system was created, and the aldol addition of acetone with p-nitrobenzaldehyde was tested. The conversion of substrate to product can be as high as 93%. Although the observed enantioselectivity was only moderate (33:67 er), further protein engineering efforts can be included to improve the selectivity. These results have proven the concept that Sav can be used to host stereoselective aldol addition. MDPI 2020-05-25 /pmc/articles/PMC7287710/ /pubmed/32466220 http://dx.doi.org/10.3390/molecules25102457 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Santi, Nicolò
Morrill, Louis C.
Luk, Louis Y. P.
Streptavidin-Hosted Organocatalytic Aldol Addition
title Streptavidin-Hosted Organocatalytic Aldol Addition
title_full Streptavidin-Hosted Organocatalytic Aldol Addition
title_fullStr Streptavidin-Hosted Organocatalytic Aldol Addition
title_full_unstemmed Streptavidin-Hosted Organocatalytic Aldol Addition
title_short Streptavidin-Hosted Organocatalytic Aldol Addition
title_sort streptavidin-hosted organocatalytic aldol addition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287710/
https://www.ncbi.nlm.nih.gov/pubmed/32466220
http://dx.doi.org/10.3390/molecules25102457
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