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Biosynthetic Pathways of Ergot Alkaloids
Ergot alkaloids are nitrogen-containing natural products belonging to indole alkaloids. The best known producers are fungi of the phylum Ascomycota, e.g., Claviceps, Epichloë, Penicillium and Aspergillus species. According to their structures, ergot alkaloids can be divided into three groups: clavin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280535/ https://www.ncbi.nlm.nih.gov/pubmed/25513893 http://dx.doi.org/10.3390/toxins6123281 |
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author | Gerhards, Nina Neubauer, Lisa Tudzynski, Paul Li, Shu-Ming |
author_facet | Gerhards, Nina Neubauer, Lisa Tudzynski, Paul Li, Shu-Ming |
author_sort | Gerhards, Nina |
collection | PubMed |
description | Ergot alkaloids are nitrogen-containing natural products belonging to indole alkaloids. The best known producers are fungi of the phylum Ascomycota, e.g., Claviceps, Epichloë, Penicillium and Aspergillus species. According to their structures, ergot alkaloids can be divided into three groups: clavines, lysergic acid amides and peptides (ergopeptines). All of them share the first biosynthetic steps, which lead to the formation of the tetracyclic ergoline ring system (except the simplest, tricyclic compound: chanoclavine). Different modifications on the ergoline ring by specific enzymes result in an abundance of bioactive natural products, which are used as pharmaceutical drugs or precursors thereof. From the 1950s through to recent years, most of the biosynthetic pathways have been elucidated. Gene clusters from several ergot alkaloid producers have been identified by genome mining and the functions of many of those genes have been demonstrated by knock-out experiments or biochemical investigations of the overproduced enzymes. |
format | Online Article Text |
id | pubmed-4280535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-42805352015-01-21 Biosynthetic Pathways of Ergot Alkaloids Gerhards, Nina Neubauer, Lisa Tudzynski, Paul Li, Shu-Ming Toxins (Basel) Review Ergot alkaloids are nitrogen-containing natural products belonging to indole alkaloids. The best known producers are fungi of the phylum Ascomycota, e.g., Claviceps, Epichloë, Penicillium and Aspergillus species. According to their structures, ergot alkaloids can be divided into three groups: clavines, lysergic acid amides and peptides (ergopeptines). All of them share the first biosynthetic steps, which lead to the formation of the tetracyclic ergoline ring system (except the simplest, tricyclic compound: chanoclavine). Different modifications on the ergoline ring by specific enzymes result in an abundance of bioactive natural products, which are used as pharmaceutical drugs or precursors thereof. From the 1950s through to recent years, most of the biosynthetic pathways have been elucidated. Gene clusters from several ergot alkaloid producers have been identified by genome mining and the functions of many of those genes have been demonstrated by knock-out experiments or biochemical investigations of the overproduced enzymes. MDPI 2014-12-10 /pmc/articles/PMC4280535/ /pubmed/25513893 http://dx.doi.org/10.3390/toxins6123281 Text en © 2014 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 license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Gerhards, Nina Neubauer, Lisa Tudzynski, Paul Li, Shu-Ming Biosynthetic Pathways of Ergot Alkaloids |
title | Biosynthetic Pathways of Ergot Alkaloids |
title_full | Biosynthetic Pathways of Ergot Alkaloids |
title_fullStr | Biosynthetic Pathways of Ergot Alkaloids |
title_full_unstemmed | Biosynthetic Pathways of Ergot Alkaloids |
title_short | Biosynthetic Pathways of Ergot Alkaloids |
title_sort | biosynthetic pathways of ergot alkaloids |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280535/ https://www.ncbi.nlm.nih.gov/pubmed/25513893 http://dx.doi.org/10.3390/toxins6123281 |
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