Strong Bragg gratings photoinduced by 633-nm illumination in evaporated As2Se3 thin films

Bragg gratings are used in several photonic devices to reflect, and thus to isolate, specific wavelengths of light. Gratings can be photoinduced in chalcogenide glasses by illumination of bandgap light in an interference pattern. We used holographic interferometry to create Bragg gratings in amorphous As2Se3 thin films with a period of 0.56 microm by illumination with 633-nm light. The quality of the gratings was tested in real time, and refractive-index modulations as high as 0.037 were measured. These gratings were found to be stable over a period of several months if they were kept in the dark.     

Ribozymomimetic Chemical Synthesis of Peptide Bond Using Phosphorous Acid/Oxirane Mediators

Abstract

A model system is created that mimics natural ribosome as well as the way of ribozyme action. It uses oxirane analogue as condensation reagent and H₃PO₃ as activator for the carboxyl group and as protecting reagent for the NH₂ function. In order to demonstrate the ability of the H₃PO₃/oxirane system to mimic natural peptide bond synthesis on the ribosome as well as to mimic the ribozyme synthesis and hydrolysis of an inter biomonomeric bond, four model compounds containing an amide bond were synthesized using phosphorous acid/oxirane mediators.

GRAPHICAL ABSTRACT     

Direct access to new β-d-galactofuranoconjugates: application to the synthesis of galactofuranosyl-l-cysteine and l-serine

Galactofuranose post-translational modifications, although quite rare, were detected in some biomolecules produced by parasites. While hexopyranosides were already linked to various peptides and proteins, few hexofuranosides have been artificially conjugated to amino acids. We thus report herein a robust glycosylation methodology to obtain S-alkyl, O-serine and S-cysteine-β-d-galactofuranosides starting from readily available galactofuranose donors. O-Acetyl, thioimidoyl and acetimidoyl donors were compared in terms of yields and selectivity when reacted with mercaptans, l-cysteine and l-serine. Acetimidates turned out to be the best notably for amino acids glycosylation.     

Synthesis,Antitumor and Antibacterial Studies of New Shortened Analogues of (KLAKLAK)2-NH2 and Their Conjugates Containing Unnatural Amino Acids

(1) Background: (KLAKLAK)₂ is a representative of the antimicrobial peptide group which also shows good anticancer properties. (2) Methods: Herein, we report synthesis using SPPS and characterization by HPLC/MS of a series of shortened analogues of (KLAKLAK)₂. They contain single sequence KLAKLAK as C-terminal amides. In addition, substitution of some natural amino acids with unnatural β-Ala and nor-Leu is realized. In addition, these structures are conjugated with second pharmacophore with well proven anticancer properties 1,8-naphthalimide or caffeic acid. Cytotoxicity, antiproliferative effect and antimicrobial activity of newly synthesized structures were studied. (3) Results: The obtained experimental results reveal significant selective index for substances with common chemical structure KLβAKLβAK-NH₂. The antibacterial properties of newly synthesized analogues at two different concentrations 10 μM and 20 μM, were tested against Gram-negative microorganisms Escherichia coli K12 407. Only two of the studied compounds KLAKLAK-NH₂ and the one conjugated with second pharmacophore 1,8-naphthalimide and unnatural amino acid nor-Leu showed moderate activity against tested strains at concentration of 20 μM. (4) Conclusions: The obtained results reveal that the introducing of 1,8-naphthalimideGly- and Caf- increase the cytotoxicity and antiproliferative activity of the peptides but not their selectivity. Only two compounds KLAKLAK-NH₂ and 1,8-naphthalimideGKnLAKnLAK-NH₂ show moderate activity against Escherichia coli K12 at low concentration of 20 μM.     

Synthesis and Biological Studies on (KLAKLAK)2-NH2 Analog Containing Unnatural Amino Acid β-Ala and Conjugates with Second Pharmacophore

(1) Background: Peptides are good candidates for anticancer drugs due to their natural existence in the body and lack of secondary effects. (KLAKLAK)₂ is an antimicrobial peptide that also shows good anticancer properties. (2) Methods: The Solid Phase Peptide Synthesis (Fmoc-strategy) was used for the synthesis of target molecules, analogs of (KLAKLAK)₂-NH₂. The purity of all compounds was monitored by HPLC, and their structures were proven using mass spectrometry. Cytotoxicity and antiproliferative effects were studied using 3T3 NRU and MTT tests, respectively. For determination of antimicrobial activity, the disc-diffusion method was used. Hydrolytic stability at three pH values, which mimic the physiological pH in the body, was investigated by means of the HPLC technique. (3) Results: A good selective index against MCF-7 tumor cell lines, combined with good cytotoxicity and antiproliferative properties, was revealed for conjugates NphtG-(KLAKLAK)₂-NH₂ and Caf-(KLAKLAK)₂-NH₂. The same compounds showed very good antifungal properties and complete hydrolytic stability for 72 h. The compound Caf-(KLβ-AKLβ-AK)₂-NH₂ containing β-Ala in its structures exhibited good antimicrobial activity against Escherichia coli K12 407 and Bacillus subtilis 3562, in combination with very good antiproliferative and cytotoxic properties, as well as hydrolytic stability. (4) Conclusions: The obtained results reveal that all synthesized conjugates could be useful for medical practice as anticancer or antimicrobial agents.     

Exploring the synthetic potency of the first furanothioglycoligase through original remote activation

Thioglycosidic bonds are of utmost importance in biomolecules as their incorporation led to more stable glycomimetics with potential drug activities. Until now only chemical methods were available for their incorporation into glycofuranosyl conjugates. Herein, we wish to describe the use of the first furanothioglycoligase for the preparation of a great variety of thioaryl derivatives with moderate to excellent yields. Of great interest, a stable 1-thioimidoyl arabinofuranose, classically used in chemical glycosylation, was able to efficiently act as a donor through an original enzymatic remote activation mechanism. Study of the chemical structure as well as the nucleophilicity of the thiol allowed us to optimize this biocatalyzed process. As a consequence, this mutated enzyme constitutes an original, mild and eco-friendly method of thioligation.     

Characterization of New Titanium Oxide Polymer Hybrid Membranes for Biofilm Formation

Abstract

Presently, there is great need to create new matrices for diverse applications particularly in the fields of biotechnology and food industry. Here, we report on the synthesis of new matrices based on a mixture of polymer cellulose acetate butyrate/copolymer polyacrylonitrile acrylamide/TiO₂. The characterization of the new matrices was performed using IR spectroscopy, QCM technology, and SEM. The tests revealed that when we use our polymers as carriers, there is a limit for the concentration of titanium of 5%. Further increasing of Ti concentration leads to precipitation processes. The QCM analyses show that a low concentration of Ti(OBu)₄ does not influence the viscosity of the matrices obtained, but their elasticity changes significantly. The membranes obtained were successfully applied for biofilm formation of Yeast strain Saccharomyces cerevisiae.     

Optical and selected thermal properties of samarium-doped fluorochlorozirconate (FCZ) glass-ceramics: Formation and growth of BaCl2 nanocrystals in FCZ glass-ceramics

Photoluminescence (PL) and conventional and modulated temperature differential scanning calorimetry (DSC and MDSC) experiments have been carried out on a typical fluorochlorozirconate glass and glass-ceramics doped with Sm³⁺ and Sm²⁺ introduced by the addition of SmF₃ and a reducing agent, NaBH₄, into the initial mixture of constituents. The nominal FCZ composition was 53% ZrF₄, 20% NaF, 3% AlF₃, 3% LaF₃, 1% SmF₃, 1% BaF₂, 19% BaCl₂ (molar percentages). Prior to DSC and PL measurements, some of the glasses have been heat treated (annealed at an elevated temperature) under different conditions, which has resulted in glass-ceramics containing BaCl₂ nanocrystals with a hexagonal and/or orthorhombic crystal structure, depending on the heat treatment conditions. Hexagonal nanocrystals may be obtained by a simple one step annealing process while the formation of orthorhombic crystallites requires sequential multistep annealing treatments. Long duration, low temperature annealing, required for the formation of orthorhombic BaCl₂ nanocrystals, leads to the appearance of an endothermic enthalpy peak at around 250 °C on the conventional DSC thermogram. Temperature modulated DSC experiments identify a clear glass transformation in this regions; and the endothermic peak has been attributed to the structural relaxation enthalpy in the host glass which is usually obscured by the thermal effects associated with the formation of BaCl₂ nanocrystals. The observed thermodynamic effects correlate with the suppression of the broad PL band around 900 nm, which is most likely due to Sm²⁺ ions near or in the “shell-region” of the glass surrounding the nanocrystals.     

Acylhydrazone Subunits as a Proton Cargo Delivery System in 7-Hydroxyquinoline

The reimagined concept of long-range tautomeric proton transfer using crane subunits is shown by designing and synthesising two new acylhydrazones containing a 7-hydroxyquinoline (7-OHQ) platform. The acylhydrazone subunits attached to the 7-OHQ at the 8th position act as crane arms for delivering proton cargo to the quinoline nitrogen. Light-induced tautomerization to their keto forms leads to Z/E isomerization of the C=C axle bond, followed by proton delivery to the quinoline nitrogen by the formation of covalent or hydrogen bonds. The axle‘s being either an imine or ketimine bond is the structural difference between the studied compounds. The −CH₃ group in the latter provides steric strain, resulting in different proton transport pathways. Both compounds show long thermal stability in the switched state, which creates a tuneable action of bidirectional proton cargo transport by using different wavelengths of irradiation. Upon the addition of acid, the quinoline nitrogen is protonated; this results in E/Z configuration switching of the acylhydrazone subunits. This was proven by single-crystal X-ray structure analysis and NMR spectroscopy.     

Titan Based Hybrid Organic-Inorganic Gels Comprising Carbohydrate Moiety

Abstract

A series of titanium based gels comprising carbohydrate moieties was synthesized. The sugars used include a specific hydrazide group as complex forming agent. Additionally, this group forms stable hydrates which allow further slow water release. As a result, the compounds used in this study form transparent and stable gels with titanium alkoxide without addition of external water. Interpretation of the IR-spectra reveals that some compounds form monodentate ligands and other bidentate ligands. Further Tian-Calvet calorimetric measurements confirmed our IR-based conclusions. This strategy of synthesis gives a new opportunity to obtain hybrid materials by addition of natural chelating ligands to slow down the hydrolysis/condensation reactions that occur during the sol-gel process. Therefore, carbohydrate moieties have been incorporated in the gels obtained and different type of Ti coordination was proposed based on the IR spectroscopy studies. SEM investigations show the influence of the ligand on the morphology of the xerogel.

GRAPHICAL ABSTRACT