Synthesis,Anticancer Potential and Comprehensive Toxicity Studies of Novel Brominated Derivatives of Bacterial Biopigment Prodigiosin from Serratia marcescens ATCC 27117

Prodigiosins (prodiginines) are a class of bacterial secondary metabolites with remarkable biological activities and color. In this study, optimized production, purification, and characterization of prodigiosin (PG) from easily accessible Serratia marcescens ATCC 27117 strain has been achieved to levels of 14 mg/L of culture within 24 h. Furthermore, environmentally friendly bromination of produced PG was used to afford both novel mono- and dibrominated derivatives of PG. PG and its Br derivatives showed anticancer potential with IC₅₀ values range 0.62–17.00 µg/mL for all tested cancer cell lines and induction of apoptosis but low selectivity against healthy cell lines. All compounds did not affect Caenorhabditis elegans at concentrations up to 50 µg/mL. However, an improved toxicity profile of Br derivatives in comparison to parent PG was observed in vivo using zebrafish (Danio rerio) model system, when 10 µg/mL applied at 6 h post fertilization caused death rate of 100%, 30% and 0% by PG, PG-Br, and PG-Br_2, respectively, which is a significant finding for further structural optimizations of bacterial prodigiosins. The drug-likeness of PG and its Br derivatives was examined, and the novel Br derivatives obey the Lipinski’s “rule of five”, with an exemption of being more lipophilic than PG, which still makes them good targets for further structural optimization.     

Lower bounds for the first eigenvalue of the magnetic Laplacian

We consider a Riemannian cylinder Ω endowed with a closed potential 1-form A and study the magnetic Laplacian ${\mathrm{\Delta }}_A$ with magnetic Neumann boundary conditions associated with those data. We establish a sharp lower bound for the first eigenvalue and show that the equality characterizes the situation where the metric is a product. We then look at the case of a planar domain bounded by two closed curves and obtain an explicit lower bound in terms of the geometry of the domain. We finally discuss sharpness of this last estimate.     

On the first eigenvalue of the Dirichlet-to-Neumann operator on forms

We study a Dirichlet-to-Neumann eigenvalue problem for differential forms on a compact Riemannian manifold with smooth boundary. This problem is a natural generalization of the classical Dirichlet-to-Neumann (or Steklov) problem on functions. We derive a number of upper and lower bounds for the first eigenvalue in several contexts: many of these estimates will be sharp, and for some of them we characterize equality. We also relate these new eigenvalues with those of other operators, like the Hodge Laplacian or the biharmonic Steklov operator.     

A Reilly Formula and Eigenvalue Estimates for Differential Forms

We derive a Reilly-type formula for differential p-forms on a compact manifold with boundary and apply it to give a sharp lower bound of the spectrum of the Hodge Laplacian acting on differential forms of an embedded hypersurface of a Riemannian manifold. The equality case of our inequality gives rise to a number of rigidity results, when the geometry of the boundary has special properties and the domain is non-negatively curved. Finally, we also obtain, as a byproduct of our calculations, an upper bound of the first eigenvalue of the Hodge Laplacian when the ambient manifold supports non-trivial parallel forms.     

Laser induced breakdown spectroscopy on soils and rocks: Influence of the sample temperature,moisture and roughness

ExoMars, ESA's next mission to Mars, will include a combined Raman/LIBS instrument for the comprehensive in-situ mineralogical and elemental analyses of Martian rocks and soils. It is inferred that water exists in the upper Martian surface as ice layers, “crystal” water or adsorbed pore water. Thus, we studied Laser Induced Breakdown Spectroscopy (LIBS) on wet and dry rocks under Martian environmental conditions in the temperature range − 60 °C to + 20 °C and in two pressure regimes, above and below the water triple point. Above this point, the LIBS signals from the rock forming elements have local minima that are accompanied by hydrogen (water) emission maxima at certain temperatures that we associate with phase transitions of free or confined water/ice. At these sample temperatures, the plasma electron density and its temperature are slightly lowered. In contrast to powder samples, a general increase of the electron density upon cooling was observed on rock samples. By comparing the LIBS signal behavior from the same rock with different grades of polishing, and different rocks with the same surface treatment, it was possible to distinguish between the influence of surface roughness and the bulk material structure (pores and grains). Below the triple point of water, the LIBS signal from the major sample elements is almost independent of the sample temperature. However, at both considered pressures we observed a hydrogen emission peak close to − 50 °C, which is attributed to a phase transition of supercooled water trapped inside bulk pores.     

A parametric study of the lensing properties of dodecagonal photonic quasicrystals

We present a study of the lensing properties of two-dimensional (2-D) photonic quasicrystal (PQC) slabs made of dielectric cylinders arranged according to a 12-fold-symmetric square-triangle aperiodic tiling. Our full-wave numerical analysis confirms the results recently emerged in the technical literature and, in particular, the possibility of achieving focusing effects within several frequency regions. However, contrary to the original interpretation, such focusing effects turn out to be critically associated to local symmetry points in the PQC slab, and strongly dependent on its thickness and termination. Nevertheless, our study reveals the presence of some peculiar properties, like the ability to focus the light even for slabs with a reduced lateral width, or beaming effects, which render PQC slabs potentially interesting and worth of deeper investigation.     

n-Si/SiGe quantum cascade structures for THz emission

In this work we report on modeling the electron transport in n-Si/SiGe structures. The electronic structure is calculated within the effective-mass complex-energy framework, separately for perpendicular (X_z) and in-plane (X_xy) valleys, the degeneracy of which is lifted by strain, and additionally by size quantization. The transport is described via scattering between quantized states, using the rate equations approach and tight-binding expansion, taking the coupling with two nearest-neighbour periods. The acoustic phonon, optical phonon, alloy and interface roughness scattering are taken in the model. The calculated U/I dependence and gain profiles are presented for a couple of QC structures.     

Monoclinic structure and nonstoichiometry of `KAlSiO4‐O1'

Crystals of KAlSiO₄‐O1 (potassium aluminium silicate) were synthesized using a flux method and analysed utilizing single‐crystal X‐ray diffraction and electron microprobe analysis. Both methods confirm that the crystals are nonstoichiometric according to K_1−xAl_1−xSi_1+xO₄ with x = 0.04 (1). KAlSiO₄‐O1 is closely related to the stuffed derivatives of tridymite, although the topology of the Si/Al‐ordered framework is different. Six‐membered rings of UUDDUD and UUUDDD (U = up and D = down; ratio 2:1) configurations are present in layers parallel to the ab plane. In contrast, the framework of tridymite exhibits UDUDUD rings. The crystals are affected by inversion, pseudo‐orthorhombic and pseudo‐hexagonal twinning.     

Visualizing chemical reactions in solution by picosecond x-ray diffraction

We present a time-resolved x-ray diffraction study to monitor the recombination of laser-dissociated iodine molecules dissolved in CCl4. The change in structure of iodine is followed during the whole recombination process. The deexcitation of solute molecules produces a heating of the solvent and induces tiny changes in its structure. The variations in the distance between pairs of chlorine atoms in adjacent CCl4 molecules are probed on the mA length scale. However, the most striking outcome of the present work is the experimental determination of temporally varying atom-atom pair distribution functions. Variations of the mean density of the solution during thermal expansion are also followed in real time. One concludes that not only time-resolved optical spectroscopy but also time-resolved x-ray diffraction can be used to monitor atomic motions in liquids.