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Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum

The volatiles emitted by the ascomycetes Hypoxylon griseobrunneum and Hypoxylon macrocarpum (Hypoxylaceae, Xylariales) were collected by use of a closed-loop stripping apparatus (CLSA) and analysed by GC–MS. The main compound class of both species were polysubstituted benzene derivatives. Their stru...

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Autores principales: Rinkel, Jan, Babczyk, Alexander, Wang, Tao, Stadler, Marc, Dickschat, Jeroen S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296411/
https://www.ncbi.nlm.nih.gov/pubmed/30591821
http://dx.doi.org/10.3762/bjoc.14.277
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author Rinkel, Jan
Babczyk, Alexander
Wang, Tao
Stadler, Marc
Dickschat, Jeroen S
author_facet Rinkel, Jan
Babczyk, Alexander
Wang, Tao
Stadler, Marc
Dickschat, Jeroen S
author_sort Rinkel, Jan
collection PubMed
description The volatiles emitted by the ascomycetes Hypoxylon griseobrunneum and Hypoxylon macrocarpum (Hypoxylaceae, Xylariales) were collected by use of a closed-loop stripping apparatus (CLSA) and analysed by GC–MS. The main compound class of both species were polysubstituted benzene derivatives. Their structures could only be unambiguously determined by comparison to all isomers with different substitution patterns. The substitution pattern of the main compound from H. griseobrunneum, the new natural product 2,4,5-trimethylanisole, was explainable by a polyketide biosynthesis mechanism that was supported by a feeding experiment with (methyl-(2)H(3))methionine.
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spelling pubmed-62964112018-12-27 Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum Rinkel, Jan Babczyk, Alexander Wang, Tao Stadler, Marc Dickschat, Jeroen S Beilstein J Org Chem Full Research Paper The volatiles emitted by the ascomycetes Hypoxylon griseobrunneum and Hypoxylon macrocarpum (Hypoxylaceae, Xylariales) were collected by use of a closed-loop stripping apparatus (CLSA) and analysed by GC–MS. The main compound class of both species were polysubstituted benzene derivatives. Their structures could only be unambiguously determined by comparison to all isomers with different substitution patterns. The substitution pattern of the main compound from H. griseobrunneum, the new natural product 2,4,5-trimethylanisole, was explainable by a polyketide biosynthesis mechanism that was supported by a feeding experiment with (methyl-(2)H(3))methionine. Beilstein-Institut 2018-12-04 /pmc/articles/PMC6296411/ /pubmed/30591821 http://dx.doi.org/10.3762/bjoc.14.277 Text en Copyright © 2018, Rinkel et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Rinkel, Jan
Babczyk, Alexander
Wang, Tao
Stadler, Marc
Dickschat, Jeroen S
Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum
title Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum
title_full Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum
title_fullStr Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum
title_full_unstemmed Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum
title_short Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum
title_sort volatiles from the hypoxylaceous fungi hypoxylon griseobrunneum and hypoxylon macrocarpum
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296411/
https://www.ncbi.nlm.nih.gov/pubmed/30591821
http://dx.doi.org/10.3762/bjoc.14.277
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