Ayed S. Al-Shihri

Di- and Tri-valent Metal Ions Interactions with Four Biodegradable Hydroxamate and Cataecholate Siderophores: New Insights into Their Complexation Equilibria

The interaction of a number of divalent and trivalent metal ions [iron(III), chromium(III) copper(II), cobalt(II) and nickel(II)] with four isolated and purified microbial catecholate and hydroxamate siderophores was studied using the pH-potentiometric technique to investigate the complexation behavior of these systems as these systems could mimic many biological interactions of the siderophore chelating agent. The protonation constants of these new siderophore analogues as well their binary complex species stability constants were determined using the Hyperquad 2008 estimation model program. From the determined stability constants of the metal complex species, the concentration distribution of the various metal ion complex species involving isolated siderophore analogues in solutions was estimated using the HySS 2009 modeling program. The complex species distribution diagrams were plotted and discussed. Additionally, the Gibbs energies and the molecular structures of the formed complex species were evaluated and predicted using Gaussian 09 software for molecular modeling and density functional theory calculations.

Microbial production of four biodegradable siderophores under submerged fermentation

Four siderophore analogues were isolated and purified from Escherichia coli, Bacillus spp. ST13, and Streptomyces pilosus microorganisms under some specific submerged fermentation conditions. In order to evaluate the highest production of this siderophore analogues through the growth, a rapid spectrophotometric screening semi-quantitative method was used, in which interestingly the analogues were isolated in its own form not its iron chelate. After chromatographic separation, the chemical structures of the isolated and purified siderophores were illustrated using detailed spectroscopic techniques. The biodegradation studies were done on that four novel isolated and purified siderophores following OECD protocols. In addition, the bioactivities of these siderophores and their iron complexes were examined and evaluated.

Spherical NiO Nanoparticles (SNPs): Synthesis, Characterization, and Optical Properties

Spherical NiO nanoparticles have been synthesized by a simple and modified solvothermal method using NiCl2·6H2O and urea. After the precursor was calcined in the air, NiO could be obtained. Structural, optical, and morphological characterizations were done by x-ray powder diffraction, ultraviolet–visible (UV–vis) spectroscopy, and scanning electron microscopy. Fourier-transform infrared (FTIR) studies show a broad absorption around 422–425 cm−1 corresponding to a surface-active mode, indicating the nanocrystalline nature of the oxide. The values of some important physical parameters of material are determined, such as refractive index (n), dielectric constant (ϵ), ratio of molar volume (Vm) and molar refraction (Rm), and metallization criterion (M(n)).

Biodegradable siderophores: survey on their production, chelating and complexing properties

Abstract The academic and industrial research on the interactions of complexing agents with the environment has received more attention for more than half a century ago and has always been concerned with the applications of chelating agents in the environment. In contrast, in recent years, an increasing scholarly interest has been demonstrated in the chemical and biological degradation of chelating agents. This is reflected by the increasing number of chelating agents-related publications between 1950 and middle of 2016. Consequently, the discovery of new green biodegradable chelating agents is of great importance and has an impact in the non-biodegradable chelating agent’s replacement with their green chemistry analogs. To acquire iron, many bacteria growing aerobically, including marine species, produce siderophores, which are low-molecular-weight compounds produced to facilitate acquisition of iron. To date and to the best of our knowledge, this is a concise and complete review article of the current and previous relevant studies conducted in the field of production, purification of siderophore compounds and their metal complexes, and their roles in biology and medicine.

Bioactivities of Novel Metal Complexes Involving B Vitamins and Glycine

Abstract In this work twelve novel mixed ligand complexes were synthesized. The complexes were formed between a metal ion (Cu(II), Cd(II), Mn(II), Fe(III), Ni(II), Pb(II)) and vitamins (B 3 and B 9) as primary ligands, and glycine as secondary ligand. Melting points, conductivities, and magnetic susceptibilities of the synthesized complexes were determined and the complexes were subjected to elemental analyses. The presence of coordination water molecules in the complex was also supported by TG/DTG thermal analysis. Full elucidation of the molecular structures for the synthesized mixed ligand complexes were confirmed using detailed spectroscopic IR, 1H-, 13C-NMR, and XRD techniques. In addition, cytotoxic and antioxidant activities of the twelve synthesized solid complexes were tested to evaluate their bioactivities.

Platinum and vanadate Bioactive Complexes of Glycoside Naringin and Phenolates

Abstract Platinum(II) and vanadium(V) solid binary and ternary complexes involving naringin, a flavanone glycoside in found in grapefruit, and some phenolic acids were synthesized and fully characterized using detailed structural and spectroscopic analysis techniques such as IR, NMR, and SEM techniques. The magnetic susceptibility results as well line drawings of the platinum and vanadium complexes showed four-coordinate square-planar and remarkable low-spin diamagnetic species; which is in agreement with the structures proposed. The cytotoxic activities of the binary and ternary vanadium and platinum metal complexes of phenolic acids and naringin were tested and evaluated against HepG2 (human hepatocellular carcinoma), MCF-7 (human breast adenocarcinoma), and HCT116 (human colorectal carcinoma) tumor cell lines. Also, their antioxidant activities were examined by free radical scavenging assay. The relationship between the chemical structure of the synthesized complexes and their biological influence was studied and evaluated.

Inner-sphere oxidation of 2-aminomethylpyridinecobalt(II) complex by N-bromosuccinimide

The kinetics of the oxidation of the 2-aminomethylpyridineCoII complex by N-bromosuccinimide (NBS), have been studied in aqueous solutions under various conditions, and obey the following rate law:Rate = [NBS][Co(L)(H2O)2]2+[k2+k3/[H+]]An inner-sphere mechanism is proposed for the oxidation pathway for both protonated and deprotonated complex species, with the formation of an intermediate, which is slowly converted into the final oxidation products. The reaction rate is increased by increasing the pH, T, [complex], and decreased by increasing ionic strength over the range studied.