High electronic-optical conversion efficiency in avertical-to-surface transmission electro-photonic device with a verticalcavity

Electronic-optical conversion efficiency of 11.4% in a vertical-to-surface-transmission electrophotonic device with a vertical cavity is reported. Reduction of the electrical resistance by the double mesa structure, efficient confinement of carriers in the active region by the proton implanted structure, and photon recycling by sidewall reflectors lead to this high conversion efficiency. Efficiency over 10% is achieved for the first time in surface-emitting devices     

Effects of vesnarinone on the bone marrow stromal cell-dependent proliferation and differentiation of HL60 cells in vitro

There is no simple and efficient method for assaying phage isolated from libraries without having to resort to PEG purification of the phage, or to the biotinylation or other labelling of the target molecule. We report here a method for producing 'bifunctional' phage that express two types of peptide; one peptide, fused to pVIII, will bind to immobilized fibrinogen, allowing capture of the phage out of culture supernatants; this allows the other peptide, fused to pIII or pVIII to be assayed by simple ELISA. This system has also been developed for the capture of phage bearing a streptavidin-binding peptide. The bifunctional phage are produced by bacterial cells bearing a plasmid that expresses pVIII fused either to the fibrinogen-binding peptide or to the streptavidin-binding one. Thus, when these cells are infected with a phage clone or pool to be assayed, phage will be produced whose 'capture-peptide' is produced from the plasmid and whose 'assay-peptide' is produced from the phage genome. We show here that, by this method, bifunctional phage can be produced that will bind to immobilized streptavidin or fibrinogen.     

Reversible MR findings of hemolytic uremic syndrome with mild encephalopathy

We report the reversible MR findings in a 7-year-old girl with hemolytic uremic syndrome and mild encephalopathy. The splenium of the corpus callosum showed isointense to low signal intensity on T1-weighted images and high signal intensity on T2-weighted images, representing local edema. These findings returned to near normal on MR images obtained 1 week later. The patient recovered without CNS impairment.     

Relationship between platinum wire temperature and catalytic heat release rate on platinum in unsteady‐state hydrogen–air mixture

The authors have proposed a hydrogen concentration probe using a catalytic reaction on the surface of a platinum wire. To use this probe for detecting the concentration change in a supersonic mixing layer, the response of the catalytic heat release rate must depend only on the change of concentration around the probe. The catalytic heat release rate on the surface of the platinum wire in an unsteady state was measured by a constant‐temperature hot‐wire anemometer and a shock tube to investigate the relationship between the response of the catalytic heat release rate and the temperature of the platinum wire. The catalytic heat release rate began increasing upon the introduction of the shock wave. The rate of increase of catalytic heat release depended on the temperature of the platinum wire when the temperature of the hot wire was low. However, the dependence was very weak when the temperature of the hot wire was above 400°C. This shows that it is not the catalytic reaction but rather molecular transfer from the flow to the surface of the platinum wire is the controlling step when the temperature of the platinum wire is high. In conclusion, the temperature of the platinum wire must be above 400°C to use the hydrogen concentration probe in a supersonic mixing layer. © 2003 Wiley Periodicals, Inc. Heat Trans Asian Res, 33(1): 1–11, 2004; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/htj.10129     

Measurements of thermal conductivity of 1‐butyl‐3‐methylimidazolium tetrafluoroborate at high pressure

Ionic liquids are salts that are liquid at room temperature. They have attracted considerable attention as new materials. In this study, a transient short‐hot‐wire apparatus was prepared, and the thermal conductivity of 1‐butyl‐3‐methylimidazolium tetrafluoroborate ([bmim] [BF₄]) was measured. The experimental temperatures were from 294 to 334 K, and the pressures were from 0.1 to 20 MPa. It was found that the thermal conductivity of an ionic liquid has a very small temperature and pressure dependence. © 2007 Wiley Periodicals, Inc. Heat Trans Asian Res, 36(6): 361–372, 2007; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/htj.20166     

Reconstitution and function of Tetragenococcus halophila chaperonin 60 tetradecamer

Tetragenococcus halophila originally isolated from soy sauce is a halophilic lactic acid bacterium which can grow under 4 M sodium chloride. T. halophila chaperonin composed of a core moiety of chaperonin 60 (cpn60) and a lid moiety of chaperonin 10 (cpn10), is thought to contribute to host halotolerant capability. In this report, we reconstituted and characterized the core complex of T. halophila chaperonin by using a recombinant T. halophila cpn60 (Tcpn60) overexpressed in Escherichia coli. The reconstitution of Tcpn60 was performed in the presence of 10 mM MgCl2, 2 mM ATP and 0.8 M (NH4)2SO4 and the resultant oligomer was purified by gel filtration chromatography. Electron microscopy of the reconstituted Tcpn60 revealed a double toroidal tetradecameric structure that is characteristic of bacterial cpn60. The T. halophila tetradecamer cpn60 exhibited an ATPase activity and a refolding activity of both chemically and thermally denatured enolases under wide range of salt concentrations. Furthermore, we demonstrated that heterologous expression of Tcpn60 allowed the normal growth of host Escherichia coli cells under salt stress conditions and this effect was further enhanced by co-expression with Tcpn10. These results suggested that Tcpn60 contributes to the halotolerance property of T. halophila cell as a tetradecamer complex, probably associated with the Tcpn10 complex.