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Hauptverfasser: Maglangit, Fleurdeliz, Fang, Qing, Tabudravu, Jioji N, Kyeremeh, Kwaku, Jaspars, Marcel, Deng, Hai
Format: Artículo científico
Sprache:en
Veröffentlicht: Molecules (Basel, Switzerland) 2025
Schlagworte:
Online-Zugang:https://pubmed.ncbi.nlm.nih.gov/39860176/
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author Maglangit, Fleurdeliz
Fang, Qing
Tabudravu, Jioji N
Kyeremeh, Kwaku
Jaspars, Marcel
Deng, Hai
author_facet Maglangit, Fleurdeliz
Fang, Qing
Tabudravu, Jioji N
Kyeremeh, Kwaku
Jaspars, Marcel
Deng, Hai
Maglangit, Fleurdeliz
Fang, Qing
Tabudravu, Jioji N
Kyeremeh, Kwaku
Jaspars, Marcel
Deng, Hai
collection PubMed - marine biology
contents Isolation and Bioactivity of Natural Products from sp. MA37. Maglangit, Fleurdeliz Fang, Qing Tabudravu, Jioji N Kyeremeh, Kwaku Jaspars, Marcel Deng, Hai Streptomyces Biological Products Humans Siderophores Antineoplastic Agents MCF-7 Cells Cell Line, Tumor Molecular Structure Deferoxamine The isolation and characterization of bioactive metabolites from species continue to represent a vital area of research, given their potential in natural product drug discovery. In this study, we characterize a new siderophore called legonoxamine I, together with a known compound, streptimidone, from the talented soil bacterium sp. MA37, using chromatographic techniques and spectroscopic analysis. Legonoxamine I is a new holo-siderophore, which is likely to be a derailed product from the biosynthetic pathway of legonoxamine A. We also demonstrate that legonoxamine A possesses potent anticancer activity (IC = 2.2 µM), exhibiting a remarkable ~30-fold increase in potency against MCF-7 ATCC HTB-22 breast cancer cells compared to desferrioxamine B, a structural analogue of legonoxamine A (IC = 61.1 µM). Comparing the structural difference between legonoxamine A and desferrioxamine B, it is deduced that the phenylacetyl moiety in legonoxamine A may have contributed significantly to its enhanced potency. Our findings contribute to the growing library of -derived metabolites and underscore the genus' potential as a promising source of lead compounds.
format Artículo científico
id pubmed_39860176
institution PubMed
language en
publishDate 2025
publisher Molecules (Basel, Switzerland)
record_format pubmed
spellingShingle Isolation and Bioactivity of Natural Products from sp. MA37.
Maglangit, Fleurdeliz
Fang, Qing
Tabudravu, Jioji N
Kyeremeh, Kwaku
Jaspars, Marcel
Deng, Hai
Streptomyces
Biological Products
Humans
Siderophores
Antineoplastic Agents
MCF-7 Cells
Cell Line, Tumor
Molecular Structure
Deferoxamine
Isolation and Bioactivity of Natural Products from sp. MA37. Maglangit, Fleurdeliz Fang, Qing Tabudravu, Jioji N Kyeremeh, Kwaku Jaspars, Marcel Deng, Hai Streptomyces Biological Products Humans Siderophores Antineoplastic Agents MCF-7 Cells Cell Line, Tumor Molecular Structure Deferoxamine The isolation and characterization of bioactive metabolites from species continue to represent a vital area of research, given their potential in natural product drug discovery. In this study, we characterize a new siderophore called legonoxamine I, together with a known compound, streptimidone, from the talented soil bacterium sp. MA37, using chromatographic techniques and spectroscopic analysis. Legonoxamine I is a new holo-siderophore, which is likely to be a derailed product from the biosynthetic pathway of legonoxamine A. We also demonstrate that legonoxamine A possesses potent anticancer activity (IC = 2.2 µM), exhibiting a remarkable ~30-fold increase in potency against MCF-7 ATCC HTB-22 breast cancer cells compared to desferrioxamine B, a structural analogue of legonoxamine A (IC = 61.1 µM). Comparing the structural difference between legonoxamine A and desferrioxamine B, it is deduced that the phenylacetyl moiety in legonoxamine A may have contributed significantly to its enhanced potency. Our findings contribute to the growing library of -derived metabolites and underscore the genus' potential as a promising source of lead compounds.
title Isolation and Bioactivity of Natural Products from sp. MA37.
topic Streptomyces
Biological Products
Humans
Siderophores
Antineoplastic Agents
MCF-7 Cells
Cell Line, Tumor
Molecular Structure
Deferoxamine
url https://pubmed.ncbi.nlm.nih.gov/39860176/