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Título

Signalling and bioactive metabolites from Streptomyces sp. RK44

AutorFang, Q.; Maglangit, F.; Wu, L.; Ebel, R.; Kyeremeh, K.; Andersen, J.H.; Annang, F.; Pérez-Moreno, Guiomar; Reyes, F.; Deng, H.
Palabras claveAHFA
methylenomycin
MMFs
signalling molecules
Streptomyces sp. RK44
Anticancer
Antimalaria
Fecha de publicación2020
EditorMolecular Diversity Preservation International
CitaciónMolecules 25 (2020)
ResumenStreptomyces 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-LeuHyp) 5, and deferoxamine E 6. AHFA 1, a methylenomycin (MMF) homolog, exhibited antiproliferative activity (EC50 = 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 (IC50 = 1.08µM) 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.
Versión del editorhttp://dx.doi.org/10.3390/molecules25030460
URIhttp://hdl.handle.net/10261/216684
DOI10.3390/molecules25030460
Identificadoresdoi: 10.3390/molecules25030460
issn: 1420-3049
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