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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7287710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT santinicolo streptavidinhostedorganocatalyticaldoladdition AT morrilllouisc streptavidinhostedorganocatalyticaldoladdition AT luklouisyp streptavidinhostedorganocatalyticaldoladdition |