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Furanones and Anthranilic Acid Derivatives from the Endophytic Fungus Dendrothyrium variisporum
Extracts from an endophytic fungus isolated from the roots of the Algerian plant Globularia alypum showed prominent antimicrobial activity in a screening for novel antibiotics. The producer organism was identified as Dendrothyrium variisporum by means of morphological studies and molecular phylogene...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151570/ https://www.ncbi.nlm.nih.gov/pubmed/28991218 http://dx.doi.org/10.3390/molecules22101674 |
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author | Teponno, Rémy B. Noumeur, Sara R. Helaly, Soleiman E. Hüttel, Stephan Harzallah, Daoud Stadler, Marc |
author_facet | Teponno, Rémy B. Noumeur, Sara R. Helaly, Soleiman E. Hüttel, Stephan Harzallah, Daoud Stadler, Marc |
author_sort | Teponno, Rémy B. |
collection | PubMed |
description | Extracts from an endophytic fungus isolated from the roots of the Algerian plant Globularia alypum showed prominent antimicrobial activity in a screening for novel antibiotics. The producer organism was identified as Dendrothyrium variisporum by means of morphological studies and molecular phylogenetic methods. Studies on the secondary metabolite production of this strain in various culture media revealed that the major components from shake flasks were massarilactones D (1) and H (2) as well as two new furanone derivatives for which we propose the trivial names (5S)-cis-gregatin B (3) and graminin D (4). Scale-up of the fermentation in a 10 L bioreactor yielded massarilactone D and several further metabolites. Among those were three new anthranilic acid derivatives (5–7), two known anthranilic acid analogues (8 and 9) and three cyclopeptides (10–12). Their structures were elucidated on the basis of extensive spectroscopic analysis (1D- and 2D-NMR), high-resolution mass spectrometry (HRESIMS), and the application of the modified Mosher’s method. The isolated metabolites were tested for antimicrobial and cytotoxic activities against various bacteria, fungi, and two mammalian cell lines. The new Metabolite 5 and Compound 9 exhibited antimicrobial activity while Compound 9 showed cytotoxicity activity against KB3.1 cells. |
format | Online Article Text |
id | pubmed-6151570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61515702018-11-13 Furanones and Anthranilic Acid Derivatives from the Endophytic Fungus Dendrothyrium variisporum Teponno, Rémy B. Noumeur, Sara R. Helaly, Soleiman E. Hüttel, Stephan Harzallah, Daoud Stadler, Marc Molecules Article Extracts from an endophytic fungus isolated from the roots of the Algerian plant Globularia alypum showed prominent antimicrobial activity in a screening for novel antibiotics. The producer organism was identified as Dendrothyrium variisporum by means of morphological studies and molecular phylogenetic methods. Studies on the secondary metabolite production of this strain in various culture media revealed that the major components from shake flasks were massarilactones D (1) and H (2) as well as two new furanone derivatives for which we propose the trivial names (5S)-cis-gregatin B (3) and graminin D (4). Scale-up of the fermentation in a 10 L bioreactor yielded massarilactone D and several further metabolites. Among those were three new anthranilic acid derivatives (5–7), two known anthranilic acid analogues (8 and 9) and three cyclopeptides (10–12). Their structures were elucidated on the basis of extensive spectroscopic analysis (1D- and 2D-NMR), high-resolution mass spectrometry (HRESIMS), and the application of the modified Mosher’s method. The isolated metabolites were tested for antimicrobial and cytotoxic activities against various bacteria, fungi, and two mammalian cell lines. The new Metabolite 5 and Compound 9 exhibited antimicrobial activity while Compound 9 showed cytotoxicity activity against KB3.1 cells. MDPI 2017-10-09 /pmc/articles/PMC6151570/ /pubmed/28991218 http://dx.doi.org/10.3390/molecules22101674 Text en © 2017 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 Teponno, Rémy B. Noumeur, Sara R. Helaly, Soleiman E. Hüttel, Stephan Harzallah, Daoud Stadler, Marc Furanones and Anthranilic Acid Derivatives from the Endophytic Fungus Dendrothyrium variisporum |
title | Furanones and Anthranilic Acid Derivatives from the Endophytic Fungus Dendrothyrium variisporum |
title_full | Furanones and Anthranilic Acid Derivatives from the Endophytic Fungus Dendrothyrium variisporum |
title_fullStr | Furanones and Anthranilic Acid Derivatives from the Endophytic Fungus Dendrothyrium variisporum |
title_full_unstemmed | Furanones and Anthranilic Acid Derivatives from the Endophytic Fungus Dendrothyrium variisporum |
title_short | Furanones and Anthranilic Acid Derivatives from the Endophytic Fungus Dendrothyrium variisporum |
title_sort | furanones and anthranilic acid derivatives from the endophytic fungus dendrothyrium variisporum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151570/ https://www.ncbi.nlm.nih.gov/pubmed/28991218 http://dx.doi.org/10.3390/molecules22101674 |
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