Preparation of conducting In-based copper oxide by annealing under high pressure

By annealing InBa_2CuO_4.44 in oxygen at a pressure of 60MPa, a new conducting cuprate InBa_2CuO_4.54 with having a- and c-axis lengths of 4.190A and 8.363A was formed. Its crystal structure was refined by the X-ray Rietveld analysis method. The factors R_wp, R_e, and S were 9.11%, 9.12%, and 1.0, respectively, indicating that the refined structure is an appropriate one. There were four distinct differences between InBa_2CuO_4.44 and InBa_2CuO_4.54. The first was an increase in the oxygen occupancy in the CuO_2 plane; the oxygen occupancy in the CuO_2 plane increased from 26.5% to 27%. The second was a drastic increase in the c-axis length from 8.09A to 8.36A . The third was the inter-substitution of In and Cu. About 35% of In and Cu atoms were substituted each other in the InBa_2CuO_4.54. The fourth was a drastic decrease in the electrical resistivity; the resistivity at room temperature decreased from 28.8MΩcm to 90.3kΩcm. These differences are discussed in connection with the oxygen content in the InBa_2CuO_y.　PACS 74.72.Jt　　key words: CuO_2 layer, Cu valence, high pressure synthesis, nBa_2CuO_y, oxygen content, tetragonal phase, orthorhombic phase

Anomalous Change of y\u27 and z in Na_x(H?O)_zCoO?・y\u27H?O at x ? 0.33

Abstract: We prepared some Nax(H?O)zC0O?・yH?O with BLH single phase and examined the Na content (x), H?O content (z)and H?O content (y). Nax(H?O)zC0O?・yH?O with BLH single phase and 0.28≦x≦0.36 were prepared by changing the amount of Br? used. The drastical changes in the c-axis length and z, Co valence, y around x=0.33 were observed, strongly suggesting that there exists a phase transition here

Avian myeloblastosis virus-induced lymphosarcoma producing erythroblastic leucosis in chicks

Acute myeloblastosis and several forms of tumor, including one case of lymphosarcoma occurred when avian myeloblastosis virus (BAI-A strain) was inoculated into newly hatched chicks (SPF). The homogenate of lymphosarcoma inoculated intraperitoneally into other newly hatched chicks induced a high incidence of erythroblastic leucosis. Electron microscopy did not reveal the presence of C-type virus particles in the tumor tissue. The relationship between avian myeloblastosis virus, lymphosarcoma and erythroblastic leucosis is discussed.</p

Deep Knot Structure for Construction of Active Site and Cofactor Binding Site of tRNA Modification Enzyme

AbstractThe tRNA(Gm18) methyltransferase (TrmH) catalyzes the 2′-O methylation of guanosine 18 (Gua18) of tRNA. We solved the crystal structure of Thermus thermophilus TrmH complexed with S-adenosyl-L-methionine at 1.85 Å resolution. The catalytic domain contains a deep trefoil knot, which mutational analyses revealed to be crucial for the formation of the catalytic site and the cofactor binding pocket. The tRNA dihydrouridine(D)-arm can be docked onto the dimeric TrmH, so that the tRNA D-stem is clamped by the N- and C-terminal helices from one subunit while the Gua18 is modified by the other subunit. Arg41 from the other subunit enters the catalytic site and forms a hydrogen bond with a bound sulfate ion, an RNA main chain phosphate analog, thus activating its nucleophilic state. Based on Gua18 modeling onto the active site, we propose that once Gua18 binds, the phosphate group activates Arg41, which then deprotonates the 2′-OH group for methylation

Inhibitory effects on HAV IRES-mediated translation and replication by a combination of amantadine and interferon-alpha

Hepatitis A virus (HAV) causes acute hepatitis and sometimes leads to fulminant hepatitis. Amantadine is a tricyclic symmetric amine that inhibits the replication of many DNA and RNA viruses. Amantadine was reported to suppress HAV replication, and the efficacy of amantadine was exhibited in its inhibition of the internal ribosomal entry site (IRES) activities of HAV. Interferon (IFN) also has an antiviral effect through the induction of IFN stimulated genes (ISG) and the degradation of viral RNA. To explore the mechanism of the suppression of HAV replication, we examined the effects of the combination of amantadine and IFN-alpha on HAV IRES-mediated translation, HAV replicon replication in human hepatoma cell lines, and HAV KRM003 genotype IIIB strain replication in African green monkey kidney cell GL37. IFN-alpha seems to have no additive effect on HAV IRES-mediated translation inhibition by amantadine. However, suppressions of HAV replicon and HAV replication were stronger with the combination than with amantadine alone. In conclusion, amantadine, in combination of IFN-alpha, might have a beneficial effect in some patients with acute hepatitis A

The Non-Canonical Hydroxylase Structure of YfcM Reveals a Metal Ion-Coordination Motif Required for EF-P Hydroxylation

EF-P is a bacterial tRNA-mimic protein, which accelerates the ribosome-catalyzed polymerization of poly-prolines. In Escherichia coli, EF-P is post-translationally modified on a conserved lysine residue. The post-translational modification is performed in a two-step reaction involving the addition of a β-lysine moiety and the subsequent hydroxylation, catalyzed by PoxA and YfcM, respectively. The β-lysine moiety was previously shown to enhance the rate of poly-proline synthesis, but the role of the hydroxylation is poorly understood. We solved the crystal structure of YfcM and performed functional analyses to determine the hydroxylation mechanism. In addition, YfcM appears to be structurally distinct from any other hydroxylase structures reported so far. The structure of YfcM is similar to that of the ribonuclease YbeY, even though they do not share sequence homology. Furthermore, YfcM has a metal ion-coordinating motif, similar to YbeY. The metal ion-coordinating motif of YfcM resembles a 2-His-1-carboxylate motif, which coordinates an Fe(II) ion and forms the catalytic site of non-heme iron enzymes. Our findings showed that the metal ion-coordinating motif of YfcM plays an essential role in the hydroxylation of the β-lysylated lysine residue of EF-P. Taken together, our results suggested the potential catalytic mechanism of hydroxylation by YfcM

A Sillén Oxyhalide SrBi₃O₄Cl₃ as a Promising Photocatalyst for Water Splitting: Impact of the Asymmetric Structure on Light Absorption and Charge Carrier Dynamics

Bismuth-based oxyhalides with layered Sillén(–Aurivillius) structures have attracted significant attention as photocatalysts. Recent studies have unveiled a part of the structure–property relationship of the materials; however, it has not been fully understood. In the present study, we investigated a Sillén-type oxyhalide SrBi₃O₄Cl₃ with single and double halogen layers. Interestingly, SrBi₃O₄Cl₃ showed a visible light response up to ∼460 nm, whereas SrBiO₂Cl and BiOCl with single and double halogen layers, respectively, did not. Rietveld refinement and STEM-EDX mapping determined the asymmetric Bi occupation in the fluorite [Sr₀.₅Bi₁.₅O₂] layer of SrBi₃O₄Cl₃, which was derived from the coexistence of the halogen layers. DFT calculations and Madelung potential calculations showed that the asymmetric Bi occupation affords both the Bi–Bi interaction across the single halogen layer and the electrostatic destabilization of Cl in the double halogen layer, probably leading to the narrow bandgap of SrBi₃O₄Cl₃. Another merit of possessing the two different halogen layers was revealed by time-resolved microwave conductivity measurements as well as DFT calculations; the spatial separation of the conduction band minimum and valence band maximum based on the coexistence of the halogen layers would promote charge carrier separation. Visible-light-driven Z-scheme water splitting was accomplished using a RuO₂-loaded SrBi₃O₄Cl₃ sample as an O₂-evolving photocatalyst. This study provides another option for engineering band structures and promoting the charge carrier separation of layered oxyhalides for efficient water splitting under visible light

Diagnostic utility of C-reactive Protein combined with brain natriuretic peptide in acute pulmonary edema: a cross sectional study

Introduction Discriminating acute lung injury (ALI) or acute respiratory distress syndrome (ARDS) from cardiogenic pulmonary edema (CPE) using the plasma level of brain natriuretic peptide (BNP) alone remains controversial. The aim of this study was to determine the diagnostic utility of combination measurements of BNP and C-reactive protein (CRP) in critically ill patients with pulmonary edema

Human Desmocollin 1 (Dsc1) Is an Autoantigen for the Subcorneal Pustular Dermatosis Type of IgA Pemphigus

IgA pemphigus showing IgA anti-keratinocyte cell surface autoantibodies is divided into subcorneal pustular dermatosis (SPD) and intraepidermal neutrophilic IgA dermatosis (IEN) types. We previously showed by immunoblotting that IgA from some IgA pemphigus patients reacted with bovine desmocollins (Dsc), but not human Dsc. To determine the antigen for IgA pemphigus, we focused on conformation-dependent epitopes of Dsc, because sera of patients with classical pemphigus recognize conformation-sensitive epitopes of desmogleins. We constructed mammalian expression vectors containing the entire coding sequences of human Dsc1, Dsc2, and Dsc3 and transiently transfected them into COS7 cells by lipofection. Immunofluorescence of COS7 cells transfected with single human Dscs showed that IgA antibodies of all six SPD-type IgA pemphigus cases reacted with the surface of cells expressing Dsc1, but not with cells expressing Dsc2 or Dsc3. In contrast, none of seven IEN-type IgA pemphigus cases reacted with cells transfected with any Dscs. These results convincingly indicate that human Dsc1 is an autoantigen for SPD-type IgA pemphigus, suggesting the possibility of an important role for Dsc1 in the pathogenesis of this disease. This study shows that a Dsc can be an autoimmune target in human skin disease