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Boron NMR as a Method to Screen Natural Product Libraries for B-Containing Compounds
[Image: see text] Natural products are biologically relevant metabolites exploited for biomedicine and biotechnology. The frequent reisolation of known natural products questions whether existing discovery models are still capable of identifying novel compounds. As innovative NMR-based screening tec...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088847/ https://www.ncbi.nlm.nih.gov/pubmed/35472262 http://dx.doi.org/10.1021/acs.orglett.2c00885 |
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author | Macho, Jocelyn M. Blue, Riley M. Lee, Hsiau-Wei MacMillan, John B. |
author_facet | Macho, Jocelyn M. Blue, Riley M. Lee, Hsiau-Wei MacMillan, John B. |
author_sort | Macho, Jocelyn M. |
collection | PubMed |
description | [Image: see text] Natural products are biologically relevant metabolites exploited for biomedicine and biotechnology. The frequent reisolation of known natural products questions whether existing discovery models are still capable of identifying novel compounds. As innovative NMR-based screening techniques can help overcome these challenges, we applied a phase cycling composite pulse sequence to (11)B NMR experiments to enhance their sensitivity to screen libraries for novel boron-containing molecules. Aplasmomycin and autoinducer-2 were detected in crude and enhanced microbial fractions, via their boron signals, as proof of concept. Subsequently, a screen of 21 crude plant and 50 crude marine microbial extracts were chosen at random and analyzed with the optimized (11)B experiment for feasibility as a high throughput discovery method. Eight of the plant samples and 13 of the microbial samples were identified as boron-containing, suggesting that there is a higher presence of boron metabolites available from natural sources than previously known due to a lack of appropriate discovery methods. As a result, we believe that this optimized (11)B NMR experiment can serve as a robust method for quick and facile discovery of novel boron-containing metabolites from a variety of natural sources. |
format | Online Article Text |
id | pubmed-9088847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90888472023-04-26 Boron NMR as a Method to Screen Natural Product Libraries for B-Containing Compounds Macho, Jocelyn M. Blue, Riley M. Lee, Hsiau-Wei MacMillan, John B. Org Lett [Image: see text] Natural products are biologically relevant metabolites exploited for biomedicine and biotechnology. The frequent reisolation of known natural products questions whether existing discovery models are still capable of identifying novel compounds. As innovative NMR-based screening techniques can help overcome these challenges, we applied a phase cycling composite pulse sequence to (11)B NMR experiments to enhance their sensitivity to screen libraries for novel boron-containing molecules. Aplasmomycin and autoinducer-2 were detected in crude and enhanced microbial fractions, via their boron signals, as proof of concept. Subsequently, a screen of 21 crude plant and 50 crude marine microbial extracts were chosen at random and analyzed with the optimized (11)B experiment for feasibility as a high throughput discovery method. Eight of the plant samples and 13 of the microbial samples were identified as boron-containing, suggesting that there is a higher presence of boron metabolites available from natural sources than previously known due to a lack of appropriate discovery methods. As a result, we believe that this optimized (11)B NMR experiment can serve as a robust method for quick and facile discovery of novel boron-containing metabolites from a variety of natural sources. American Chemical Society 2022-04-26 2022-05-06 /pmc/articles/PMC9088847/ /pubmed/35472262 http://dx.doi.org/10.1021/acs.orglett.2c00885 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Macho, Jocelyn M. Blue, Riley M. Lee, Hsiau-Wei MacMillan, John B. Boron NMR as a Method to Screen Natural Product Libraries for B-Containing Compounds |
title | Boron NMR as a Method to Screen Natural Product Libraries
for B-Containing Compounds |
title_full | Boron NMR as a Method to Screen Natural Product Libraries
for B-Containing Compounds |
title_fullStr | Boron NMR as a Method to Screen Natural Product Libraries
for B-Containing Compounds |
title_full_unstemmed | Boron NMR as a Method to Screen Natural Product Libraries
for B-Containing Compounds |
title_short | Boron NMR as a Method to Screen Natural Product Libraries
for B-Containing Compounds |
title_sort | boron nmr as a method to screen natural product libraries
for b-containing compounds |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088847/ https://www.ncbi.nlm.nih.gov/pubmed/35472262 http://dx.doi.org/10.1021/acs.orglett.2c00885 |
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