390 research outputs found

    OHS: OH-airglow Suppressor for the Subaru Telescope

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    This paper describes an OH-airglow Suppressor (OHS) for the infrared Nasmyth focus of the Subaru telescope. OHS has the capability of eliminating 224 airglow-lines in the JJ- and HH-bands, which are major sources of background radiation at near-infrared wavelengths up to 2 μ\mum. Specifically, it is a pre-optics system installed between the telescope and an infrared camera/spectrograph (CISCO). The suppressor reduces sky background emissions to 1/25 and its throughput is 40%. As a result, the S/N gain achieved with OHS is more than 1 mag compared to the typical spectroscopic approach. The limiting magnitude measured during a test observing run was found to be HH = 21.1 mag (λ/Δλ\lambda/\Delta\lambda = 210, S/N = 5) in the standard 4000 s exposure sequence.Comment: 6 pages, 9 figures. Accepted for publication in PASJ(2001

    JHK Spectra of the z=2.39 Radio Galaxy 53W002

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    We present low-resolution, near-IR JHK spectra of the weak z=2.39 radio galaxy 53W002, obtained with the OH-airglow Suppressor spectrograph (OHS) and Cooled Infrared Spectrograph and Camera for OHS (CISCO) on the Subaru Telescope. They cover rest-frame wavelengths of 3400-7200 A, and the emission lines of [O II]3727, Hb, [O III]4959, 5007, Ha, [N II]6548, 6583 and [S II]6716, 6731 were detected. Using the Ha/Hb line ratio, we find an extinction of E(B-V)=0.14. The emission-line ratios are reproduced by a cloud of electron density n_e=1x10^{3-4}(/cm3) with solar metallicity, ionized by an alpha=-0.7 power-law continuum with ionizing parameter U=1x10^-3. In addition to these emission lines, we make the first spectroscopic confirmation of the Balmer discontinuity in a high-z radio galaxy. Together with rest-frame UV photometry from the literature, we show that at least 1/3 of the present stellar mass was formed in the current starburst. The stellar mass was estimated to be (1-1.4)x10^11 M_sol by one-component model fitting, which is smaller than that of typical z~1 B2/6C radio galaxies. We suggest that 53W002 is currently assembling a large part of its stellar mass through merger events with the surrounding sub-galactic clumps, some of which can be identified with the Lya emitters detected in narrow-band imaging. After a few such events over the next few Gyr, 53W002 will evolve into a massive elliptical galaxy.Comment: 10 pages, including 11 figures. Accepted for publication in PASJ(2001). Revised 5/15/200

    Coexistence of two- and three-dimensional Shubnikov-de Haas oscillations in Ar^+ -irradiated KTaO_3

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    We report the electron doping in the surface vicinity of KTaO_3 by inducing oxygen-vacancies via Ar^+ -irradiation. The doped electrons have high mobility (> 10^4 cm^2/Vs) at low temperatures, and exhibit Shubnikov-de Haas oscillations with both two- and three-dimensional components. A disparity of the extracted in-plane effective mass, compared to the bulk values, suggests mixing of the orbital characters. Our observations demonstrate that Ar^+ -irradiation serves as a flexible tool to study low dimensional quantum transport in 5d semiconducting oxides

    CISCO: Cooled Infrared Spectrograph and Camera for OHS on the Subaru Telescope

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    This paper describes a Cooled Infrared Spectrograph and Camera for OHS (CISCO), mounted on the Nasmyth focus of the Subaru telescope. It is primarily designed as a back-end camera of the OH-Airglow Suppressor (OHS), and is also used as an independent, general-purpose near-infrared camera/spectrograph. CISCO is based on a single 1024x1024 format HgCdTe HAWAII array detector, and is capable of either wide-field imaging of 1.8'x1.8' field-of-view or low-resolution spectroscopy from 0.9 to 2.4 um. The limiting magnitudes measured during test observations were found to be J=23.5mag and K'=22.4mag (imaging, 1" aperture, S/N=5, 1 hr exposure).Comment: 14 pages, 15 figures, accepted by PASJ. Figures with higher resolution are available at http://www.ioa.s.u-tokyo.ac.jp/~kmotohara/CISCO/ciscopap.tar.g

    Microleakage of composite resin restorations in cervical cavities prepared by Er,Cr: YSGG laser radiation

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    Background: Evaluation of microleakage is important for assessing the success of new methods for surface preparation and new adhesive restorative materials. The aim of this laboratory study was to assess microleakage at the margins of composite restorations in Er,Cr:YSGG laser prepared cavities on the cervical aspects of teeth by means of dye penetration, and compare this with conventionally prepared and conditioned cavities. Methods: Class V cavities were produced on sound extracted human teeth, which had been assigned randomly to one of three groups (N = 10 each), as follows: Group 1 – prepared using a diamond cylindrical bur and then treated with 37% phosphoric acid; Group 2 – irradiated with an Er,Cr:YSGG laser (Biolase Waterlase) and then treated with 37% phosphoric acid; Group 3 – irradiated only with the laser. After application of bonding agent (Excite, Ivoclar Vivadent), all cavities were restored with composite resin (Heliomolar). After polishing the restorations, the teeth were thermocycled from 5–50°C for 500 cycles. Dye leakage was assessed after immersion in methylene blue, by examining longitudinal sections in a stereomicroscope at ×30 magnification. Results: The extent of dye penetration was lowest in the laser only group (Group 3). Penetration of dye to dentine and axial walls occurred in 80 per cent of conventionally prepared (bur + acid) specimens, but in the laser group, dye penetration to the axial wall occurred in only 30 per cent of cases. There was a strong statistical association between treatment group and the distribution of microleakage scores (Chi-square, P = 0.0023). Conclusions: For Class V cavities, with the adhesive materials employed, higher microleakage occurs with phosphoric acid etching of bur- or laser-cut surfaces, than with the surface created by use of the laser alone without additional conditioning

    Integration of Global Signaling Pathways, cAMP-PKA, MAPK and TOR in the Regulation of FLO11

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    The budding yeast, Saccharomyces cerevisiae, responds to various environmental cues by invoking specific adaptive mechanisms for their survival. Under nitrogen limitation, S. cerevisiae undergoes a dimorphic filamentous transition called pseudohyphae, which helps the cell to forage for nutrients and reach an environment conducive for growth. This transition is governed by a complex network of signaling pathways, namely cAMP-PKA, MAPK and TOR, which controls the transcriptional activation of FLO11, a flocculin gene that encodes a cell wall protein. However, little is known about how these pathways co-ordinate to govern the conversion of nutritional availability into gene expression. Here, we have analyzed an integrative network comprised of cAMP-PKA, MAPK and TOR pathways with respect to the availability of nitrogen source using experimental and steady state modeling approach. Our experiments demonstrate that the steady state expression of FLO11 was bistable over a range of inducing ammonium sulphate concentration based on the preculturing condition. We also show that yeast switched from FLO11 expression to accumulation of trehalose, a STRE response controlled by a transcriptional activator Msn2/4, with decrease in the inducing concentration to complete starvation. Steady state analysis of the integrative network revealed the relationship between the environment, signaling cascades and the expression of FLO11. We demonstrate that the double negative feedback loop in TOR pathway can elicit a bistable response, to differentiate between vegetative growth, filamentous growth and STRE response. Negative feedback on TOR pathway function to restrict the expression of FLO11 under nitrogen starved condition and also with re-addition of nitrogen to starved cells. In general, we show that these global signaling pathways respond with specific sensitivity to regulate the expression of FLO11 under nitrogen limitation. The holistic steady state modeling approach of the integrative network revealed how the global signaling pathways could differentiate between multiple phenotypes

    The role of the RACK1 ortholog Cpc2p in modulating pheromone-induced cell cycle arrest in fission yeast

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    The detection and amplification of extracellular signals requires the involvement of multiple protein components. In mammalian cells the receptor of activated C kinase (RACK1) is an important scaffolding protein for signal transduction networks. Further, it also performs a critical function in regulating the cell cycle by modulating the G1/S transition. Many eukaryotic cells express RACK1 orthologs, with one example being Cpc2p in the fission yeast Schizosaccharomyces pombe. In contrast to RACK1, Cpc2p has been described to positively regulate, at the ribosomal level, cells entry into M phase. In addition, Cpc2p controls the stress response pathways through an interaction with Msa2p, and sexual development by modulating Ran1p/Pat1p. Here we describe investigations into the role, which Cpc2p performs in controlling the G protein-mediated mating response pathway. Despite structural similarity to Gβ-like subunits, Cpc2p appears not to function at the G protein level. However, upon pheromone stimulation, cells overexpressing Cpc2p display substantial cell morphology defects, disorientation of septum formation and a significantly protracted G1 arrest. Cpc2p has the potential to function at multiple positions within the pheromone response pathway. We provide a mechanistic interpretation of this novel data by linking Cpc2p function, during the mating response, with its previous described interactions with Ran1p/Pat1p. We suggest that overexpressing Cpc2p prolongs the stimulated state of pheromone-induced cells by increasing ste11 gene expression. These data indicate that Cpc2p regulates the pheromone-induced cell cycle arrest in fission yeast by delaying cells entry into S phase

    Nutrient Control of Yeast PKA Activity Involves Opposing Effects on Phosphorylation of the Bcy1 Regulatory Subunit

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    Kelch repeat proteins Gpb1 and Gpb2 control yeast PKA activity in response to nutrients by stimulating phosphorylation of the Bcy1 regulatory subunit. Gpb1 and Gpb2 function by blocking inhibition of Bcy1 phosphorylation by PKA catalytic subunits. Phosphorylated Bcy1 is more stable and is a more effective inhibitor of PKA activity

    Identification of Lck-derived peptides applicable to anti-cancer vaccine for patients with human leukocyte antigen-A3 supertype alleles

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    The identification of peptide vaccine candidates to date has been focused on human leukocyte antigen (HLA)-A2 and -A24 alleles. In this study, we attempted to identify cytotoxic T lymphocyte (CTL)-directed Lck-derived peptides applicable to HLA-A11+, -A31+, or -A33+ cancer patients, because these HLA-A alleles share binding motifs, designated HLA-A3 supertype alleles, and because the Lck is preferentially expressed in metastatic cancer. Twenty-one Lck-derived peptides were prepared based on the binding motif to the HLA-A3 supertype alleles. They were first screened for their recognisability by immunoglobulin G (IgG) in the plasma of prostate cancer patients, and the selected candidates were subsequently tested for their potential to induce peptide-specific CTLs from peripheral blood mononuclear cells of HLA-A3 supertype+ cancer patients. As a result, four Lck peptides were frequently recognised by IgGs, and three of them – Lck90−99, Lck449−458, and Lck450−458 – efficiently induced peptide-specific and cancer-reactive CTLs. Their cytotoxicity towards cancer cells was mainly ascribed to HLA class I-restricted and peptide-specific CD8+ T cells. These results indicate that these three Lck peptides are applicable to HLA-A3 supertype+ cancer patients, especially those with metastasis. This information could facilitate the development of peptide-based anti-cancer vaccine for patients with alleles other than HLA-A2 and -A24

    Whole-Genome Sequencing of Sake Yeast Saccharomyces cerevisiae Kyokai no. 7

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    The term ‘sake yeast’ is generally used to indicate the Saccharomyces cerevisiae strains that possess characteristics distinct from others including the laboratory strain S288C and are well suited for sake brewery. Here, we report the draft whole-genome shotgun sequence of a commonly used diploid sake yeast strain, Kyokai no. 7 (K7). The assembled sequence of K7 was nearly identical to that of the S288C, except for several subtelomeric polymorphisms and two large inversions in K7. A survey of heterozygous bases between the homologous chromosomes revealed the presence of mosaic-like uneven distribution of heterozygosity in K7. The distribution patterns appeared to have resulted from repeated losses of heterozygosity in the ancestral lineage of K7. Analysis of genes revealed the presence of both K7-acquired and K7-lost genes, in addition to numerous others with segmentations and terminal discrepancies in comparison with those of S288C. The distribution of Ty element also largely differed in the two strains. Interestingly, two regions in chromosomes I and VII of S288C have apparently been replaced by Ty elements in K7. Sequence comparisons suggest that these gene conversions were caused by cDNA-mediated recombination of Ty elements. The present study advances our understanding of the functional and evolutionary genomics of the sake yeast
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