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Biologically active drimane derivatives isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis

Four previously undescribed drimane sesquiterpenoids were isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis along with two compounds that were previously reported as synthetic or biotransformation compounds but not as natural products. The constitution and re...

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Autores principales: Mitschke, Nico, Chemutai Sum, Winnie, Hassan, Khadija, Kirchenwitz, Marco, Schrey, Hedda, Gerhards, Luca, Kellner, Harald, Stradal, Theresia E. B., Matasyoh, Josphat C., Stadler, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468952/
https://www.ncbi.nlm.nih.gov/pubmed/37664205
http://dx.doi.org/10.1039/d3ra04204a
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author Mitschke, Nico
Chemutai Sum, Winnie
Hassan, Khadija
Kirchenwitz, Marco
Schrey, Hedda
Gerhards, Luca
Kellner, Harald
Stradal, Theresia E. B.
Matasyoh, Josphat C.
Stadler, Marc
author_facet Mitschke, Nico
Chemutai Sum, Winnie
Hassan, Khadija
Kirchenwitz, Marco
Schrey, Hedda
Gerhards, Luca
Kellner, Harald
Stradal, Theresia E. B.
Matasyoh, Josphat C.
Stadler, Marc
author_sort Mitschke, Nico
collection PubMed
description Four previously undescribed drimane sesquiterpenoids were isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis along with two compounds that were previously reported as synthetic or biotransformation compounds but not as natural products. The constitution and relative configuration of these compounds was determined based on high-resolution electrospray ionization mass spectrometry as well as by 1D and 2D nuclear magnetic resonance spectroscopy. The absolute configurations were established based on exemplary calculation of circular dichroism spectra and comparison with measured data as well as on biogenetic considerations. The biological activities of the isolated compounds were assessed in antimicrobial, cytotoxicity and neurotrophic assays. 10-Methoxycarbonyl-10-norisodrimenin (3) exhibited weak activity against the Gram-positive bacterium Staphylococcus aureus and the zygomycete Mucor hiemalis with minimal inhibitory concentrations of 66.7 μg mL(−1). In addition, compound 3 showed weak inhibition of the mammalian cell line KB3.1 (human endocervical adenocarcinoma) with a half maximal inhibitory concentration of 21.2 μM. The neurotrophic activities of 15-hydroxyisodrimenin (1) and 10-carboxy-10-norisodrimenin (5) were assed in neurite outgrowth and real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) assays. When supplemented with 5 ng mL(−1) nerve growth factor (NGF), the drimanes 1 and 5 induced neurite outgrowth in PC-12 (rat pheochromocytoma) cells compared to cells solely treated with NGF. As evaluated by RT-qPCR, compounds 1 and 5 also increased NGF and brain-derived neurotrophic factor expression levels in 1321N1 astrocytoma cells. Interestingly, the current study only represents the second report on neurotrophic activities of this widespread class of terpenoids. The only other available study deals with Cyathus africanus, another basidiomycete that can produce drimanes and cyathanes, but is only distantly related to Dentipellis and the Hericiaceae.
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spelling pubmed-104689522023-09-01 Biologically active drimane derivatives isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis Mitschke, Nico Chemutai Sum, Winnie Hassan, Khadija Kirchenwitz, Marco Schrey, Hedda Gerhards, Luca Kellner, Harald Stradal, Theresia E. B. Matasyoh, Josphat C. Stadler, Marc RSC Adv Chemistry Four previously undescribed drimane sesquiterpenoids were isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis along with two compounds that were previously reported as synthetic or biotransformation compounds but not as natural products. The constitution and relative configuration of these compounds was determined based on high-resolution electrospray ionization mass spectrometry as well as by 1D and 2D nuclear magnetic resonance spectroscopy. The absolute configurations were established based on exemplary calculation of circular dichroism spectra and comparison with measured data as well as on biogenetic considerations. The biological activities of the isolated compounds were assessed in antimicrobial, cytotoxicity and neurotrophic assays. 10-Methoxycarbonyl-10-norisodrimenin (3) exhibited weak activity against the Gram-positive bacterium Staphylococcus aureus and the zygomycete Mucor hiemalis with minimal inhibitory concentrations of 66.7 μg mL(−1). In addition, compound 3 showed weak inhibition of the mammalian cell line KB3.1 (human endocervical adenocarcinoma) with a half maximal inhibitory concentration of 21.2 μM. The neurotrophic activities of 15-hydroxyisodrimenin (1) and 10-carboxy-10-norisodrimenin (5) were assed in neurite outgrowth and real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) assays. When supplemented with 5 ng mL(−1) nerve growth factor (NGF), the drimanes 1 and 5 induced neurite outgrowth in PC-12 (rat pheochromocytoma) cells compared to cells solely treated with NGF. As evaluated by RT-qPCR, compounds 1 and 5 also increased NGF and brain-derived neurotrophic factor expression levels in 1321N1 astrocytoma cells. Interestingly, the current study only represents the second report on neurotrophic activities of this widespread class of terpenoids. The only other available study deals with Cyathus africanus, another basidiomycete that can produce drimanes and cyathanes, but is only distantly related to Dentipellis and the Hericiaceae. The Royal Society of Chemistry 2023-08-31 /pmc/articles/PMC10468952/ /pubmed/37664205 http://dx.doi.org/10.1039/d3ra04204a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Mitschke, Nico
Chemutai Sum, Winnie
Hassan, Khadija
Kirchenwitz, Marco
Schrey, Hedda
Gerhards, Luca
Kellner, Harald
Stradal, Theresia E. B.
Matasyoh, Josphat C.
Stadler, Marc
Biologically active drimane derivatives isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis
title Biologically active drimane derivatives isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis
title_full Biologically active drimane derivatives isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis
title_fullStr Biologically active drimane derivatives isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis
title_full_unstemmed Biologically active drimane derivatives isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis
title_short Biologically active drimane derivatives isolated from submerged cultures of the wood-inhabiting basidiomycete Dentipellis fragilis
title_sort biologically active drimane derivatives isolated from submerged cultures of the wood-inhabiting basidiomycete dentipellis fragilis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468952/
https://www.ncbi.nlm.nih.gov/pubmed/37664205
http://dx.doi.org/10.1039/d3ra04204a
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