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2-Hydroxysorangiadenosine: Structure and Biosynthesis of a Myxobacterial Sesquiterpene–Nucleoside

Myxobacteria represent an under-investigated source for biologically active natural products featuring intriguing structural moieties with potential applications, e.g., in the pharmaceutical industry. Sorangiadenosine and the here-discovered 2-hydroxysorangiadenosine are myxobacterial sesquiterpene–...

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Autores principales: Okoth, Dorothy A., Hug, Joachim J., Garcia, Ronald, Spröer, Cathrin, Overmann, Jörg, Müller, Rolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321100/
https://www.ncbi.nlm.nih.gov/pubmed/32527018
http://dx.doi.org/10.3390/molecules25112676
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author Okoth, Dorothy A.
Hug, Joachim J.
Garcia, Ronald
Spröer, Cathrin
Overmann, Jörg
Müller, Rolf
author_facet Okoth, Dorothy A.
Hug, Joachim J.
Garcia, Ronald
Spröer, Cathrin
Overmann, Jörg
Müller, Rolf
author_sort Okoth, Dorothy A.
collection PubMed
description Myxobacteria represent an under-investigated source for biologically active natural products featuring intriguing structural moieties with potential applications, e.g., in the pharmaceutical industry. Sorangiadenosine and the here-discovered 2-hydroxysorangiadenosine are myxobacterial sesquiterpene–nucleosides with an unusual structural moiety, a bicyclic eudesmane-type sesquiterpene. As the biosynthesis of these rare terpene–nucleoside hybrid natural products remains elusive, we investigated secondary metabolomes and genomes of several 2-hydroxysorangiadenosine-producing myxobacteria. We report the isolation and full structure elucidation of 2-hydroxysorangiadenosine and its cytotoxic and antibiotic activities and propose a biosynthetic pathway in the myxobacterium Vitiosangium cumulatum MCy10943(T).
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spelling pubmed-73211002020-07-06 2-Hydroxysorangiadenosine: Structure and Biosynthesis of a Myxobacterial Sesquiterpene–Nucleoside Okoth, Dorothy A. Hug, Joachim J. Garcia, Ronald Spröer, Cathrin Overmann, Jörg Müller, Rolf Molecules Article Myxobacteria represent an under-investigated source for biologically active natural products featuring intriguing structural moieties with potential applications, e.g., in the pharmaceutical industry. Sorangiadenosine and the here-discovered 2-hydroxysorangiadenosine are myxobacterial sesquiterpene–nucleosides with an unusual structural moiety, a bicyclic eudesmane-type sesquiterpene. As the biosynthesis of these rare terpene–nucleoside hybrid natural products remains elusive, we investigated secondary metabolomes and genomes of several 2-hydroxysorangiadenosine-producing myxobacteria. We report the isolation and full structure elucidation of 2-hydroxysorangiadenosine and its cytotoxic and antibiotic activities and propose a biosynthetic pathway in the myxobacterium Vitiosangium cumulatum MCy10943(T). MDPI 2020-06-09 /pmc/articles/PMC7321100/ /pubmed/32527018 http://dx.doi.org/10.3390/molecules25112676 Text en © 2020 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
Okoth, Dorothy A.
Hug, Joachim J.
Garcia, Ronald
Spröer, Cathrin
Overmann, Jörg
Müller, Rolf
2-Hydroxysorangiadenosine: Structure and Biosynthesis of a Myxobacterial Sesquiterpene–Nucleoside
title 2-Hydroxysorangiadenosine: Structure and Biosynthesis of a Myxobacterial Sesquiterpene–Nucleoside
title_full 2-Hydroxysorangiadenosine: Structure and Biosynthesis of a Myxobacterial Sesquiterpene–Nucleoside
title_fullStr 2-Hydroxysorangiadenosine: Structure and Biosynthesis of a Myxobacterial Sesquiterpene–Nucleoside
title_full_unstemmed 2-Hydroxysorangiadenosine: Structure and Biosynthesis of a Myxobacterial Sesquiterpene–Nucleoside
title_short 2-Hydroxysorangiadenosine: Structure and Biosynthesis of a Myxobacterial Sesquiterpene–Nucleoside
title_sort 2-hydroxysorangiadenosine: structure and biosynthesis of a myxobacterial sesquiterpene–nucleoside
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321100/
https://www.ncbi.nlm.nih.gov/pubmed/32527018
http://dx.doi.org/10.3390/molecules25112676
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