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Signalling and Bioactive Metabolites from Streptomyces sp. RK44

Streptomyces remains one of the prolific sources of structural diversity, and a reservoir to mine for novel natural products. Continued screening for new Streptomyces strains in our laboratory led to the isolation of Streptomyces sp. RK44 from the underexplored areas of Kintampo waterfalls, Ghana, A...

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Autores principales: Fang, Qing, Maglangit, Fleurdeliz, Wu, Linrui, Ebel, Rainer, Kyeremeh, Kwaku, Andersen, Jeanette H., Annang, Frederick, Pérez-Moreno, Guiomar, Reyes, Fernando, Deng, Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037778/
https://www.ncbi.nlm.nih.gov/pubmed/31979050
http://dx.doi.org/10.3390/molecules25030460
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author Fang, Qing
Maglangit, Fleurdeliz
Wu, Linrui
Ebel, Rainer
Kyeremeh, Kwaku
Andersen, Jeanette H.
Annang, Frederick
Pérez-Moreno, Guiomar
Reyes, Fernando
Deng, Hai
author_facet Fang, Qing
Maglangit, Fleurdeliz
Wu, Linrui
Ebel, Rainer
Kyeremeh, Kwaku
Andersen, Jeanette H.
Annang, Frederick
Pérez-Moreno, Guiomar
Reyes, Fernando
Deng, Hai
author_sort Fang, Qing
collection PubMed
description Streptomyces remains one of the prolific sources of structural diversity, and a reservoir to mine for novel natural products. Continued screening for new Streptomyces strains in our laboratory led to the isolation of Streptomyces sp. RK44 from the underexplored areas of Kintampo waterfalls, Ghana, Africa. Preliminary screening of the metabolites from this strain resulted in the characterization of a new 2-alkyl-4-hydroxymethylfuran carboxamide (AHFA) 1 together with five known compounds, cyclo-(L-Pro-Gly) 2, cyclo-(L-Pro-L-Phe) 3, cyclo-(L-Pro-L-Val) 4, cyclo-(L-Leu-Hyp) 5, and deferoxamine E 6. AHFA 1, a methylenomycin (MMF) homolog, exhibited anti-proliferative activity (EC(50) = 89.6 µM) against melanoma A2058 cell lines. This activity, albeit weak is the first report amongst MMFs. Furthermore, the putative biosynthetic gene cluster (ahfa) was identified for the biosynthesis of AHFA 1. DFO-E 6 displayed potent anti-plasmodial activity (IC(50) = 1.08 µM) against P. falciparum 3D7. High-resolution electrospray ionization mass spectrometry (HR ESIMS) and molecular network assisted the targeted-isolation process, and tentatively identified six AHFA analogues, 7–12 and six siderophores 13–18.
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spelling pubmed-70377782020-03-10 Signalling and Bioactive Metabolites from Streptomyces sp. RK44 Fang, Qing Maglangit, Fleurdeliz Wu, Linrui Ebel, Rainer Kyeremeh, Kwaku Andersen, Jeanette H. Annang, Frederick Pérez-Moreno, Guiomar Reyes, Fernando Deng, Hai Molecules Article Streptomyces remains one of the prolific sources of structural diversity, and a reservoir to mine for novel natural products. Continued screening for new Streptomyces strains in our laboratory led to the isolation of Streptomyces sp. RK44 from the underexplored areas of Kintampo waterfalls, Ghana, Africa. Preliminary screening of the metabolites from this strain resulted in the characterization of a new 2-alkyl-4-hydroxymethylfuran carboxamide (AHFA) 1 together with five known compounds, cyclo-(L-Pro-Gly) 2, cyclo-(L-Pro-L-Phe) 3, cyclo-(L-Pro-L-Val) 4, cyclo-(L-Leu-Hyp) 5, and deferoxamine E 6. AHFA 1, a methylenomycin (MMF) homolog, exhibited anti-proliferative activity (EC(50) = 89.6 µM) against melanoma A2058 cell lines. This activity, albeit weak is the first report amongst MMFs. Furthermore, the putative biosynthetic gene cluster (ahfa) was identified for the biosynthesis of AHFA 1. DFO-E 6 displayed potent anti-plasmodial activity (IC(50) = 1.08 µM) against P. falciparum 3D7. High-resolution electrospray ionization mass spectrometry (HR ESIMS) and molecular network assisted the targeted-isolation process, and tentatively identified six AHFA analogues, 7–12 and six siderophores 13–18. MDPI 2020-01-22 /pmc/articles/PMC7037778/ /pubmed/31979050 http://dx.doi.org/10.3390/molecules25030460 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
Fang, Qing
Maglangit, Fleurdeliz
Wu, Linrui
Ebel, Rainer
Kyeremeh, Kwaku
Andersen, Jeanette H.
Annang, Frederick
Pérez-Moreno, Guiomar
Reyes, Fernando
Deng, Hai
Signalling and Bioactive Metabolites from Streptomyces sp. RK44
title Signalling and Bioactive Metabolites from Streptomyces sp. RK44
title_full Signalling and Bioactive Metabolites from Streptomyces sp. RK44
title_fullStr Signalling and Bioactive Metabolites from Streptomyces sp. RK44
title_full_unstemmed Signalling and Bioactive Metabolites from Streptomyces sp. RK44
title_short Signalling and Bioactive Metabolites from Streptomyces sp. RK44
title_sort signalling and bioactive metabolites from streptomyces sp. rk44
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037778/
https://www.ncbi.nlm.nih.gov/pubmed/31979050
http://dx.doi.org/10.3390/molecules25030460
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