Interrogating the Tailoring Steps of Pactamycin Biosynthesis and Accessing New Pactamycin Analogues

Pactamycin is a bacteria‐derived aminocyclitol antibiotic with a wide‐range of biological activity. Its chemical structure and potent biological activities have made it an interesting lead compound for drug discovery and development. Despite its unusual chemical structure, many aspects of its formation in nature remain elusive. Using a combination of genetic inactivation and metabolic analysis, we investigated the tailoring processes of pactamycin biosynthesis in Streptomyces pactum. The results provide insights into the sequence of events during the tailoring steps of pactamycin biosynthesis and explain the unusual production of various pactamycin analogues by S. pactum mutants. We also identified two new pactamycin analogues that have better selectivity indexes than pactamycin against malarial parasites.     

Synthesis,characterization and antimicrobial activity of colloidal copper nanoparticles stabilized by cationic thiol polyurethane surfactants

Metal nanoparticles have attracted considerable interest particularly because of the size dependence of physical and chemical properties and its enormous technological potential. Among different metal nanoparticles, copper nanoparticles have attracted great attention because copper is one of the most key metals in new technology. Chemical methods are used to synthesize copper nanoparticles. Chemical reduction is the most frequently applied method for the preparation of stable, colloidal dispersions in organic solvents. In this paper, the new cationic thiol polyurethane surfactants with different alkyl chain length were synthesized (PQ10, PQ14 and PQ18). The chemical structure of the synthesized surfactants was confirmed using infra-red spectroscopy (IR) and proton nuclear magnetic resonance spectroscopy (¹HNMR). Copper nanoparticles colloidal solution of 40–80 nm diameters was prepared using sodium borohydride in aqueous solution at room temperature as reducing agent. The synthesized surfactants decrease the aggreegation of copper nanoparticles. The nanostructure of the synthesized surfactant with copper nanoparticles with diameters ranging from 31.5 to 10.3 nm was prepared and characterized using ultra violet spectrophotometer (UV), infra-red spectroscopy (IR) and transmission electron microscope (TEM). The results declare formation and stabilization of copper nanoparticle using synthesized cationic surfactants. Antimicrobial activity of the synthesized cationic surfactants and their nanostructure with copper nanoparticles were evaluated against pathogenic bacteria and fungi.     

Blast furnace slags as functional fillers on rheological,thermal, and mechanical behavior of thermoplastics

Blast furnace slags (BFS) is a secondary byproduct of iron industry, which has a combination of acidic and basic oxides and show a complex, multiphase structure. If appropriately tailored, BFS could be an effective functional filler, improving the property profile of thermoplastics such as polypropylene (PP) and polystyrene (PS). As a raw material, the proposed filler may introduce both economic and ecological advantages, as it is considered an inexpensive secondary product rather than a natural resource. The current study aims at investigating the effect of incorporating BFS as a micro‐sized filler on the rheological, thermal, and mechanical behavior of PP and PS. BFS types in this study are air‐cooled, crystalline, and amorphous, grounded types. Both types are ground into 71, 40, and 20 μm batches and introduced in 10, 20, and 30 weight fractions via melt kneading. Mixtures are then formed into 4‐mm and 2‐mm thick plates via compression molding. Slight increase in rheological factors is observed with increasing filler loading. BFS hinders the crystallization of PP, resulting in slight increase of crystallization temperatures (T_c) and lowering of crystallization enthalpy (ΔH_c). No significant effect of filler on transition temperatures (T_g) is reported. Mechanically, BFS increases the tensile modulus of PP, but decreases its strength. For PS formulations, a modest toughening effect is observed by slag filler. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43021.     

Structural,magnetic, and optical properties of nano-sized Ni0.85Se

Nanocrystalline Ni_0.85Se was synthesized by a hydrothermal method. X-ray diffraction analysis by Rietveld method indicated that Ni_0.85Se has a NiAs-type hexagonal structure. Narrow crystallite size distribution with an average area-weighted size of 〈ɛ_F〉 = 8.5 nm is obtained by Warren-Averbach method. Structural analysis revealed deformed Se atoms octahedron with the shortest distance between Se atoms in adjacent planes 〈Se–Se〉_adj smaller than between nearest neighbors in layer plane 〈Se–Se〉_nea, and a rather short interatomic distance between the transition metal atoms 〈Ni–Ni〉. The optical property of Ni_0.85Se was studied by UV-spectroscopy. Magnetic measurement shows a ferromagnetic phase transition for Ni_0.85Se below 14 K.     

Crystallization behavior of iron- and boron-containing nepheline (Na2O·Al2O3·2SiO2) based model high-level nuclear waste glasses

This study focuses on understanding the relationship between iron redox, composition, and heat-treatment atmosphere in nepheline-based model high-level nuclear waste glasses. Glasses in the Na₂O–Al₂O₃–B₂O₃–Fe₂O₃–SiO₂ system with varying Al₂O₃/Fe₂O₃ and Na₂O/Fe₂O₃ ratios have been synthesized by melt-quench technique and studied for their crystallization behavior in different heating atmospheres—air, inert (N₂), and reducing (96%N₂–4%H₂). The compositional dependence of iron redox chemistry in glasses and the impact of heating environment and crystallization on iron coordination in glass-ceramics have been investigated by Mössbauer spectroscopy and vibrating sample magnetometry. While iron coordination in glasses and glass-ceramics changed as a function of glass chemistry, the heating atmosphere during crystallization exhibited minimal effect on iron redox. The change in heating atmosphere did not affect the phase assemblage but did affect the microstructural evolution. While glass-ceramics produced as a result of heat treatment in air and N₂ atmospheres developed a golden/brown colored iron-rich layer on their surface, those produced in a reducing atmosphere did not exhibit any such phenomenon. Furthermore, while this iron-rich layer was observed in glass-ceramics with varying Al₂O₃/Fe₂O₃ ratio, it was absent from glass-ceramics with varying Na₂O/Fe₂O₃ ratio. An explanation of these results has been provided on the basis of kinetics of diffusion of oxygen and network modifiers in the glasses under different thermodynamic conditions. The plausible implications of the formation of iron-rich layer on the surface of glass-ceramics on the chemical durability of high-level nuclear waste glasses have been discussed.     

Predicting trends in structural and physical properties of a model polymer with embedded natural fibers: Viability of molecular dynamics studies for a bottom up design

The effects of relatively high- and low-shear processing on the macroscopic and microscopic porosities of a standard packaging polymer—linear low density polyethylene (LLDPE) and its composites with pine flour are studied. The macroscopic porosities, represented by deviations of observed density from the theoretical density, primarily drive the trends in mechanical and solvent uptake properties. The microscopic porosities of the system, however, are independent of the processing method and pine flour concentration. Furthermore, by using molecular dynamics (MD), molecules of LLDPE and pine flour were constructed. The material properties of the molecules, specifically microporosity and elastic moduli, were compared to experiment. A semiempirical modeling approach was used to fit the simulated data to the experimental composite moduli. The model of Halpin and Tsai was found to be the most efficacious for this system, and the benefits of the combined MD-semiempirical modeling for bottom up design are discussed. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48189.     

Characterization and Beneficiation of Gold Mining By-products as Source of High-Quality Silica for High Technical Applications; Response Surface Studies and Optimization

Silicon - This paper aims to evaluate and upgrade the quality of quartz mining by-products through acid leaching process. The quartz samples were collected as gold mine by-products from El Sid-...     

Graft Copolymerization of Styrene‐Maleic Anhydride Onto Poly(Vinyl Chloride) and Its Cross‐linking by Toluene Diisocyanate: Characterization,Thermal, and Mechanical Properties

In this work, styrene‐maleic anhydride (St‐MA) copolymer was successfully grafted onto poly(vinyl chloride) (PVC) by means of chemical method in cyclohexanone medium. In this manner, the effects of various parameters such as total monomer content, monomers ratio, and initiator concentration on the grafting percentage (GP) and acid value (AV) were examined. The graft copolymers were characterized by Fourier‐transform infrared and nuclear magnetic resonance spectroscopy methods. Afterward, the cross‐linking reaction was carried out through MA hydrolysis and condensation reaction between maleic acid and produced diamines, by toluene diisocyanate (TDI) at the presence of hot water. The results showed that the GP and AV of PVC‐g‐(St‐MA) copolymers were considerably higher than those of PVC‐g‐MA and PVC‐g‐St with significant molecular weight. A gel content of 56% was attained with 1 phr TDI in PVC‐g‐(St‐MA) copolymer. The glass transition temperatures and mechanical properties of PVC‐g‐(St‐MA) samples were increased compared to pure PVC. Cross‐linked PVC‐g‐(St‐MA) showed improved mechanical properties than other samples, but the glass transition temperature of PVC backbone in this cross‐linked copolymer was disappeared due to its heavily dense structure. J. VINYL ADDIT. TECHNOL., 25:377–384, 2019. © 2019 Society of Plastics Engineers     

Synthesis of a novel inorganic cation exchanger based on molybdate: Applications for removal of Pb2+, Fe3+ and Mn2+ ions from polluted water

A novel manganese phosphomolybdate exchanger was synthesized, dried at different temperatures, and evaluated for the elimination of lead, iron, and manganese ions from aqueous solutions. The chemical structure of the cation exchanger was established using Fourier-transform infrared, scanning electron microscopy, Thermo gravimetric analysis/ Differential thermal analysis, and X-ray diffraction. The adsorption performance of the heavy metals Pb²⁺, Fe³⁺, and Mn²⁺ toward the synthesized material has been studied. The obtained outcomes show that the selectivity of the cationic exchanger was descending in this order, Pb²⁺ > Fe³⁺ > Mn²⁺. The highest adsorption capacity was shown to be decreased as drying temperature of the exchanger increases from 50°C to 800°C.     

Adsorptive Removal of Manganese Ions from Polluted Aqueous Media by Glauconite Clay-Functionalized Chitosan Nanocomposites

The presence of Mn(II) in water exceeding the permitted concentration limits declared by the World Health Organization (WHO) influences individuals, animals, and the ecosystem negatively. Therefore, there is a necessity for an efficient material to eliminate this potentially toxic element from wastewater. We herein focused on the adsorptive removal of Mn(II) ions from polluted aqueous media using natural Egyptian glauconite clay (G) and its nanocomposites with modified chitosan (CS). We applied modified chitosan with glutaraldehyde (GL), ethylenediaminetetraacetic acid (EDTA), sodium dodecyl sulfate (SDS), and cetyltrimethyl ammonium bromide (CTAB). The utilized nanocomposites were referred to as GL-CS/G, EDTA-GL-CS/G, SDS-CS/G, and CTAB-CS/G, respectively. The point of zero charge values of the materials were estimated. The adsorption properties of the G clay and its nanocomposites toward the removal of Mn(II) ions from polluted aqueous media as well as the adsorption mechanism were explored using a batch technique. The glauconite (G) and its nanocomposites: GL-CS/G, CTAB-CS/G, EDTA-GL-CS/G, and SDS-CS/G, exhibited maximum adsorption capacity values of 3.60, 24.0, 26.0, 27.0, and 27.9 mg g^?1, respectively. The adsorption results fitted well the Langmuir isotherm and pseudo-second-order kinetic models. The estimated thermodynamic parameters: ΔH° (from 1.03 to 5.55 kJ/mol) and ΔG° (from ? 14.5 to ? 18.8 kJ/mol), indicated that Mn(II) ion adsorption process was endothermic, spontaneous, and physisorption controlled. Furthermore, the obtained adsorption results are encouraging and revealing a great potentiality for using the modified adsorbents as accessible adsorbents for Mn(II) ion removal from polluted aqueous solutions, depending on their reusability, high stability, and good adsorption capacities.

Graphic Abstract