Old and New Fields on Super Riemann Surfaces

The ``new fields" or ``superconformal functions" on $N=1$ super Riemann surfaces introduced recently by Rogers and Langer are shown to coincide with the Abelian differentials (plus constants), viewed as a subset of the functions on the associated $N=2$ super Riemann surface. We confirm that, as originally defined, they do not form a super vector space.Comment: 9 pages, LaTex. Published version: minor changes for clarity, two new reference

Chemistry for Sustainable Development 15 (2007) 305-312 Primary Toxicological Parameters of Fluorine-Containing Organic Compounds of Practical Significance

Abstract Primary toxicological parameters of fluorine-containing alcohols, dialkyl ethers, acetales, acrylates, esters of carboxylic and dicarboxylic aliphatic acids, epoxides and olefins used as the materials and intermediate products of organofluoric synthesis are considered. The regularities of the effect of fluorine atoms on the toxicity of the compounds are revealed. All the investigated compounds belong to the III and IV class of danger and are safe for developing fluorinated materials on their basis. Some examples of the application of these classes of compounds are discussed

Static and resonant properties of decorated square kagome lattice compound KCu7_7(TeO4_4)(SO4_4)5_5Cl

The magnetic subsystem of nabokoite, KCu$_7$(TeO$_4$)(SO$_4$)$_5$Cl, is constituted by buckled square kagome lattice of copper decorated by quasi-isolated Cu$^{2+}$ ions. This combination determines peculiar physical properties of this compound evidenced in electron spin resonance (ESR) spectroscopy, dielectric permittivity $\varepsilon$, magnetization $M$ and specific heat $C_p$ measurements. At lowering temperature, the magnetic susceptibility $\chi = M/H$ passes through broad hump at about 150 K inherent for low-dimensional magnetic systems and evidences sharp peak at antiferromagnetic phase transition at $T_N = 3.2$K. The $C_p(T)$ curve also exhibits sharp peak at $T_N$ readily suppressed by magnetic field and additional peak-like anomaly at $T_\textrm{peak}= 5.7$ K robust to magnetic field. The latter can be ascribed to low-lying singlet excitations filling the singlet-triplet gap in magnetic excitation spectrum of the square kagome lattice [J.Richter, O.Derzhko and J.Schnack, Phys. Rev. B 105, 144427 (2022)]. According to position of $T_\textrm{peak}$, the leading exchange interaction parameter $J$ in nabokoite is estimated to be about 60K. ESR spectroscopy provides indications that antiferromagnetic structure below $T_N$ is non-collinear. These complex thermodynamic and resonant properties signal the presence of two weakly coupled magnetic subsystems in nabokoite, namely spin-liquid with large singlet-triplet gap and antiferromagnet represented by decorating ions. Separate issue is the observation of antiferroelectric-type behavior in $\varepsilon$ at low temperatures, which tentatively reduces the symmetry and partially lifts frustration of magnetic interactions of decorating copper ions with buckled square kagome lattice.Comment: 13 pages, 13 figure

Detection of some genes encoding pathogenicity factors in the typical isolates of Escherichia coli

Using polymerase chain reaction 316 strains of E. coli (strains with normal enzymatic activity, strains with weak enzymatic activity and strains with hemolytic activity) were examined for the presence of pathogenicity genes. They were isolatedfrom healthy children and children with functional disorders of the gastro-intestinal tract. The studies have shown that strains of Escherichia coli have pathogenic potential, as evidenced by the presence of genetic pathogenicity markers in them

Interplay of rare-earth and transition-metal subsystems in Cu<inf>3</inf>Yb(SeO<inf>3</inf>)<inf>2</inf>O<inf>2</inf>Cl

©2017 American Physical Society We present the synthesis and the experimental and theoretical study of the new member of the francisite family, Cu 3 Yb(SeO 3 ) 2 O 2 Cl. The compound reaches an antiferromagnetic order at T N = 36.7 K and experiences first-order spin-reorientation transition to weakly ferromagnetic phase at T R = 8.7 K evidenced in specific heat C p and magnetic susceptibility χ measurements. Distinctly different magnetization loops in T < T R and T R < T < T N temperature ranges reflect the interplay of rare-earth and transition-metal subsystems. At low temperatures, the saturation magnetization M s ∼ 5.2 μ B is reached in pulsed magnetic-field measurements. The electron spin resonance data reveal the complicated character of the absorption line attributed to response from both copper and ytterbium ions. Critical broadening of the linewidth at the phase transitions points to quasi-two-dimensional character of the magnetic correlations. The spectroscopy of Yb 3+ ions evidences splitting of the lowest-energy Kramers doublet of 2 F 5 / 2 excited multiplet at T R < T < T N while the ground Kramers doublet splits only at T < T R . We describe the magnetic properties both above and below the spin-reorientation transition in the framework of a unified approach based on the mean-field approximation and crystal-field calculations

Applications of Site-Specific Labeling to Study HAMLET, a Tumoricidal Complex of α-Lactalbumin and Oleic Acid

umor cells), and its tumoricidal activity has been well established.-acetylgalactosaminyltransferase II (ppGalNAc-T2) and further conjugated with aminooxy-derivatives of fluoroprobe or biotin molecules.We found that the molten globule form of hLA and αD-hLA proteins, with or without C-terminal extension, and with and without the conjugated fluoroprobe or biotin molecule, readily form a complex with OA and exhibits tumoricidal activity similar to HAMLET made with full-length hLA protein. The confocal microscopy studies with fluoroprobe-labeled samples show that these proteins are internalized into the cells and found even in the nucleus only when they are complexed with OA. The HAMLET conjugated with a single biotin molecule will be a useful tool to identify the cellular components that are involved with it in the tumoricidal activity

Microsporidia::Why Make Nucleotides if You Can Steal Them?

Microsporidia are strict obligate intracellular parasites that infect a wide range of eukaryotes including humans and economically important fish and insects. Surviving and flourishing inside another eukaryotic cell is a very specialised lifestyle that requires evolutionary innovation. Genome sequence analyses show that microsporidia have lost most of the genes needed for making primary metabolites, such as amino acids and nucleotides, and also that they have only a limited capacity for making adenosine triphosphate (ATP). Since microsporidia cannot grow and replicate without the enormous amounts of energy and nucleotide building blocks needed for protein, DNA, and RNA biosynthesis, they must have evolved ways of stealing these substrates from the infected host cell. Providing they can do this, genome analyses suggest that microsporidia have the enzyme repertoire needed to use and regenerate the imported nucleotides efficiently. Recent functional studies suggest that a critical innovation for adapting to intracellular life was the acquisition by lateral gene transfer of nucleotide transport (NTT) proteins that are now present in multiple copies in all microsporidian genomes. These proteins are expressed on the parasite surface and allow microsporidia to steal ATP and other purine nucleotides for energy and biosynthesis from their host. However, it remains unclear how other essential metabolites, such as pyrimidine nucleotides, are acquired. Transcriptomic and experimental studies suggest that microsporidia might manipulate host cell metabolism and cell biological processes to promote nucleotide synthesis and to maximise the potential for ATP and nucleotide import. In this review, we summarise recent genomic and functional data relating to how microsporidia exploit their hosts for energy and building blocks needed for growth and nucleic acid metabolism and we identify some remaining outstanding questions

ROS-Induced DNA Damage Associates with Abundance of Mitochondrial DNA in White Blood Cells of the Untreated Schizophrenic Patients

Objective. The aim of this study was (1) to examine the leukocyte mtDNA copy number (CN) in unmedicated (SZ (m−)) and medicated (SZ (m+)) male patients with paranoid schizophrenia (SZ) in comparison with the healthy male controls (HC) and (2) to compare the leukocyte mtDNA CN with the content of an oxidation marker 8-oxodG in lymphocytes of the SZ (m−) patients. Methods. We evaluated leukocyte mtDNA CN of 110 subjects with SZ in comparison with 60 male HC by the method qPCR (ratio mtDNA/nDNA (gene B2M) was detected). SZ patients were divided into two subgroups. The patients of the subgroups SZ (m+) (N=55) were treated with standard antipsychotic medications in the hospital. The patients of the subgroup SZ (m−) (N=55) were not treated before venous blood was sampled. To evaluate oxidative DNA damage, we quantified the levels of 8-oxodG in lymphocytes (flow cytometry) of SZ (m−) patients (N=55) and HC (N=30). Results. The leukocyte mtDNA CN showed no significant difference in SZ (m+) patients and HC. The mtDNA CN in the unmedicated subgroup SZ (m−) was significantly higher than that in the SZ (m+) subgroup or in HC group. The level of 8-oxodG in the subgroup SZ (m−) was significantly higher than that in HC group. Conclusion. The leukocytes of the unmedicated SZ male patients with acute psychosis contain more mtDNA than the leukocytes of the male SZ patients treated with antipsychotic medications or the healthy controls. MtDNA content positively correlates with the level of 8-oxodG in the unmedicated SZ patients