Shreaz, S. and Shiekh, R. A. and Raja, V. and Wani, W. A. and Behbehani, J. M. (2016) Impaired ergosterol biosynthesis mediated fungicidal activity of Co(II) complex with ligand derived from cinnamaldehyde. Chemico-Biological Interactions, 247 . pp. 64-74. ISSN 0009-2797
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Abstract
In this study, we have used aldehyde function of cinnamaldehyde to synthesize N, N′-Bis (cinnamaldehyde) ethylenediimine [C20H20N2] and Co(II) complex of the type [Co(C40H40N4)Cl2]. The structures of the synthesized compounds were determined on the basis of physiochemical analysis and spectroscopic data (1H NMR, FTIR, UV-visible and mass spectra) along with molar conductivity measurements. Anticandidal activity of cinnamaldehyde its ligand [L] and Co(II) complex was investigated by determining MIC80, time-kill kinetics, disc diffusion assay and ergosterol extraction and estimation assay. Ligand [L] and Co(II) complex are found to be 4.55 and 21.0 folds more efficient than cinnamaldehyde in a liquid medium. MIC80 of Co(II) complex correlated well with ergosterol inhibition suggesting ergosterol biosynthesis to be the primary site of action. In comparison to fluconazole, the test compounds showed limited toxicity against H9c2 rat cardiac myoblasts. In confocal microscopy propidium iodide (PI) penetrates the yeast cells when treated with MIC of metal complex, indicating a disruption of cell membrane that results in imbibition of dye. TEM analysis of metal complex treated cells exhibited notable alterations or damage to the cell membrane and the cell wall. The structural disorganization within the cell cytoplasm was noted. It was concluded that fungicidal activity of Co(II) complex originated from loss of membrane integrity and a decrease in ergosterol content is only one consequence of this.
Item Type: | Article |
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Uncontrolled Keywords: | cinnamaldehyde, copper complex, ergosterol, fluconazole, Schiff base, acrolein, cinnamaldehyde, cobalt, ergosterol, fungicide, ligand, animal cell, Article, Candida, conductance, confocal laser microscopy, confocal microscopy, controlled study, disk diffusion, drug structure, fungal strain, fungicidal activity, fungus growth, growth inhibition, infrared spectroscopy, ligand binding, lipogenesis, lipophilicity, mass spectrometry, nonhuman, physical chemistry, proton nuclear magnetic resonance, rat, transmission electron microscopy, analogs and derivatives, animal, biosynthesis, cell line, chemistry, electrospray mass spectrometry, infrared spectrophotometry, Acrolein, Animals, Cell Line, Cobalt, Ergosterol, Fungicides, Industrial, Ligands, Microscopy, Electron, Transmission, Proton Magnetic Resonance Spectroscopy, Rats, Spectrometry, Mass, Electrospray Ionization, Spectrophotometry, Infrared |
Subjects: | T Technology > TP Chemical technology |
Divisions: | Chemical Engineering |
ID Code: | 73732 |
Deposited By: | Haliza Zainal |
Deposited On: | 18 Nov 2017 03:26 |
Last Modified: | 18 Nov 2017 03:26 |
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