Polyoxovanadate inhibition of: Escherichia coli growth shows a reverse correlation with Ca2+-ATPase inhibition
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Date
2019
Journal Title
Journal ISSN
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Publisher
Royal Society of Chemistry
Abstract
Recently, a global analysis of the structure-activity-relationship of a series of polyoxometalates (POMs) revealed that the most active POMs were ascribed to be polyoxovanadates (POVs), especially decavanadate (V<inf>10</inf>), which was very active against certain bacteria (Bijelic et al., Chem. Commun., 2018). The present study explores this observation and compares the effects of three POVs namely MnV<inf>11</inf>, MnV<inf>13</inf> and V<inf>10</inf> against Escherichia coli growth. It was observed that MnV<inf>11</inf> presents the lowest growth inhibition (GI<inf>50</inf>) value for Escherichia coli followed by the MnV<inf>13</inf> compound, being about 2 times lower than that of V<inf>10</inf>; respectively, the values obtained were 0.21, 0.27 and 0.58 mM. All three compounds were more effective than vanadate alone (GI<inf>50</inf> = 1.1 mM) and also than decaniobate, Nb<inf>10</inf> (GI<inf>50</inf> > 10 mM), an isostructural POM of V<inf>10</inf>. However, the POVs exhibiting the highest antibacterial activity (MnV<inf>11</inf>) were shown to have the lowest Ca2+-ATPase inhibitor capacity (IC<inf>50</inf> = 58 ?M) whereas decavanadate, which was also very active against this membranar ATPase (IC<inf>50</inf> = 15 ?M), was less active against bacterial growth, suggesting that POV inhibition of ion pumps might not be associated with the inhibition of Escherichia coli growth. This journal is © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
Description
Keywords
adenosine triphosphatase (calcium), ammonium vanadate, calcium ionophore, decavanadate, polyoxovanadate, sarcoplasmic reticulum calcium transporting adenosine triphosphatase, unclassified drug, vanadic acid, antibacterial activity, Article, calcium homeostasis, cell culture, controlled study, densitometry, depolymerization, drug decomposition, drug potency, drug solubility, enzyme activity, enzyme inhibition, Escherichia coli, GI50, Helicobacter pylori, IC50, nonhuman, optical density, polyacrylamide gel electrophoresis, protein synthesis inhibition, sarcoplasmic reticulum, solubilization, Streptococcus pneumoniae, structure activity relation, turbidity, ultraviolet visible spectroscopy
Citation
New Journal of Chemistry, 2019, 43, 45, pp. 17577-17587
