Physicochemical stability of antilisterial proteins from P. polymyxa Kp10 as potential food biopreservative

Listeria monocytogenes has continuously become a significant threat to consumers worldwide. The use of chemical-derived preservatives that are commonly associated with safety and nutritional issues has prompted the use of natural-based preservatives as a better alternative. Many bacterial strains including Paenibacillus polymyxa Kp10 have been reported to produce various antimicrobial proteins and compounds that are considered more natural. However, their stability in various physicochemical conditions should be examined before being applied in various types of food. In this study, the stability of four previously identified antilisterial proteins in P. polymyxa Kp10 upon exposure to several physicochemical conditions was examined. More than 80% residual antilisterial activity is conserved upon heat and proteinase K treatment. But, sensitivity to 24 h trypsin digestion has been observed. P1 and P2 proteins (histone-like DNA binding proteins HU) were sensitive to alkaline pH (pH 10-12) as compared with other proteins. More than 70% and 97% residual antilisterial activity were recovered after incubation in raw beef homogenates and simulated meat gravy model, respectively. However, the antilisterial activity of most proteins was highly compromised in chicken and salmon meat homogenates, and UHT cow milk. Inoculation of these proteins into Listeria-contaminated simulated meat gravy showed that all proteins exerted a bactericidal action against L. monocytogenes. P1 and P2 shared almost similar antilisterial activity rates, while P4 was the most potent antilisterial protein. The findings in this study could provide important preliminary data for future applications of these proteins as preservative in food products especially beef-based meat products.     

On the absence of global solutions for quantum versions of Schrödinger equations and systems

We, first, consider the quantum version of the nonlinear Schrödinger equation

$i^q{D}_{q|t}u(t,x)+\Delta u(qt,x)=\lambda |u(qt,x){|}^p,t>0,x\in {\mathbb{R}}^N,$

where $0<q<1$, $i^q$ is the principal value of $i^q$, $D_{q|t}$ is the $q$-derivative with respect to $t$, $\Delta$ is the Laplacian operator in ${\mathbb{R}}^N$, $\lambda \in ??\left\{0\right\}$, $p>1$, and $u(t,x)$ is a complex-valued function. Sufficient conditions for the nonexistence of global weak solution to the considered equation are obtained under suitable initial data. Next, we study the system of nonlinear coupled equations

$i^q{D}_{q|t}u(t,x)+\Delta u(qt,x)=\lambda |v(qt,x){|}^p,t>0,x\in {\mathbb{R}}^N,$

$i^q{D}_{q|t}v(t,x)+\Delta v(qt,x)=\lambda |u(qt,x){|}^m,t>0,x\in {\mathbb{R}}^N,$     

Chemometric Characterization of Eight Monovarietal Algerian Virgin Olive Oils

Differences in triacylglycerol, fatty acid, squalene, and tocopherol compositions were demonstrated between 8 varieties of virgin olive oils (Aberkane, Aguenaou, Aharoun, Aimel, Bouchouk Guergour, Bouichret, Chemlal, and Sigoise) from Petite Kabylie area, north eastern Algeria. Fatty acid and triacylglycerol morphotypes characterized each variety. A principal component analysis, based on triacylglycerol, fatty acid, and squalene compositions, differentiates between varieties. Minor fatty acids and squalene, usually not taken into account individually in authentication studies, are strongly involved in this differentiation, whereas the discriminant power of tocopherols is weak. Soft Independent Modeling of Class Analogy classification using chemical compositions as variables showed a high potential to authenticate the varietal origin of Algerian virgin olive oils.     

Iron oxide supported sulfated TiO2 nanotube catalysts for NO reduction with propane

Sulfated TiO₂ nanotubes and a series of iron oxide loaded sulfated TiO₂ nanotubes catalysts with different iron oxide loadings (1 wt%, 3 wt%, 5 wt% and 7 wt%) were prepared and calcined at 400 °C. The physico-chemical properties of the catalysts were studied by using XRD, N₂-physisorption, Raman spectroscopy, SEM-EDX, TEM, XPS, and pyridine adsorption using FTIR and H₂-TPR techniques. It was observed that iron oxide was highly dispersed on the sulfated TiO₂ nanotube support due to its strong interaction. The activity of these catalysts in the catalytic removal of NO with propane was also studied in the temperature range of 300–500 °C. Highest activity (90% NO conversion) was observed with 5 wt% iron oxide supported on sulfated TiO₂ catalyst at 450 °C. Selective catalytic reduction of NO activity of the catalysts was correlated with iron oxide loading, reducibility, and the Brönsted and Lewis acid sites of the catalysts. The catalyst also showed good stability under studied reaction conditions that no deactivation was observed during the 50 h of reaction.     

Radiation-induced Grafting of Acrylic Acid and Vinyl Acetate Monomers onto Heavy-duty Poly(ethylene–vinyl acetate) Films

The preparation of graft films was carried out by direct radiation-induced graft polymerization of acrylic acid and vinyl acetate comonomer onto heavy-duty poly(ethylene–vinyl acetate) films. The effect of various comonomer compositions on the degree of grafting was investigated. The characterization and some selected properties of the graft copolymers prepared were studied. Thermal stability, mechanical and electrical properties of the films showed great promise for some practical applications. © of SCI.     

Synthesis of Novel Tetra(µ3-Methoxo) Bridged with [Cu(II)-O-Cd(II)] Double-Open-Cubane Cluster: XRD/HSA-Interactions,Spectral and Oxidizing Properties

A new double-open-cubane core Cd(II)-O-Cu(II) bimetallic ligand mixed cluster of type [Cl₂Cu₄Cd₂(NNO)₆(NN)₂(NO₃)₂].CH₃CN was made available in EtOH/CH₃CN solution. The 1-hydroxymethyl-3,5-dimethylpyrazole (NNOH) and 3,5-dimethylpyrazole (NNH) act as N,O-polydentate anion ligands in coordinating the Cu(II) and Cd(II) centers. The structure of the cluster in the solid state was proved by XRD study and confirmed in the liquid state by UV-vis analysis. The XRD result supported the construction of two octahedral and one square pyramid geometries types around the four Cu(II) centers and only octahedral geometry around Cd(II) two centers. Interestingly, NNOH ligand acts as a tetra-µ³-oxo and tri-µ²-oxo ligand; meanwhile, the N-N in NNH acts as classical bidentate anion/neutral ligands. The interactions in the lattice were detected experimentally by the XRD-packing result and computed via Hirschfeld surface analysis (HSA). The UV-vis., FT-IR and Energy Dispersive X-ray (EDX), supported the desired double-open cubane cluster composition. The oxidation potential of the desired cluster was evaluated using a 3,5-DTB-catechol 3,5-DTB-quinone as a catecholase model reaction.     

CuII Pyrazolyl-Benzimidazole Dinuclear Complexes with Remarkable Antioxidant Activity

Three dinuclear coordination complexes generated from 1-n-butyl-2-((5-methyl-1H-pyrazole-3-yl)methyl)-1H-benzimidazole ( L ), have been synthesized and characterized spectroscopically and structurally by single crystal X-ray diffraction analysis. Reaction with iron(II) chloride and then copper(II) nitrate led to a co-crystal containing 78 % of [Cu(NO₃)(μ-Cl)( L’ )]₂ ( C₁ ) and 22 % of [Cu(NO₃)(μ-NO₃)( L’ )]₂ ( C₂ ), where L was oxidized to a new ligand L^’ . A mechanism is provided. Reaction with copper chloride led to the dinuclear complex [Cu(Cl)(μ-Cl)( L) ]₂ ( C₃ ). The presence of N−H⋅⋅⋅O and C−H⋅⋅⋅O intermolecular interactions in the crystal structure of C₁ and C₂ , and C−H⋅⋅⋅N and C−H⋅⋅⋅Cl hydrogen bonding in the crystal structure of C₃ led to supramolecular structures that were confirmed by Hirshfeld surface analysis. The ligands and their complexes were tested for free radical scavenging activity and ferric reducing antioxidant power. The complex C₁ / C₂ shows remarkable antioxidant activities as compared to the ligand L and reference compounds.