• The Journal of the Acoustical Society of Korea
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• v.16 no.1
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• pp.81-87
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• 1997

In this paper, a new pre-processing method for the recognition of single vowels by use of spectrum envelope is presented. We use new extraction method of a spectrum envelope using the diffusion filter bank. By dividing analysis band of a diffusion filter bank into subbands, we decreased the number of diffusion process. And, by increasing the number of difference, we got higher selectivity. As a result of them, we reduced the total processing time, and got higher enhancement of discrimination. By getting 88.3% of average recognition rate for single vowels of natural voice through computer simulation. We confirmed it to be useful for speech recognition which use spectrum analysis of the voice signal to have many frequency components.

• The Bulletin of The Korean Astronomical Society
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• v.45 no.1
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• pp.70.1-70.1
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• 2020

A type IIb supernova (SN IIb) is the result of core-collapse of a massive star which lost most of its hydrogen-rich envelope during its evolution. The pre-SN progenitor properties, such as the total radius and the mass of the hydrogen-rich envelope, can widely vary due to the mass-loss history of the progenitors. Optical light curves of SNe IIb are dominated by energy released by the hydrogen recombination and the radioactive decay of 56Ni in the early and late epochs respectively. This may result in distinctive double peaked light curves like the one observed in SN 1993J. The first peak, caused by the hydrogen recombination, can be modelled with numerical simulations providing information on the pre-SN progenitor properties. We compare two radiation-hydrodynamics codes, STELLA and SNEC, that are frequently used in SNe modelling, and investigate the effect of opacity treatment on the temporal evolution of the color temperature of SNe and eventually on the optical light curves. We find that with a proper treatment of the scattering opacity, SNe IIb models exploded from the progenitor models evolved with latest stellar evolution model hardly match the observational data. We also discuss the smaller scale features found in the models during hydrogen recombination phase.

• The Bulletin of The Korean Astronomical Society
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• v.44 no.2
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• pp.48.3-48.3
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• 2019

In the early stages of star formation, a protostar is deeply embedded in an optically thick envelope such that it is not directly observable. Variations in the protostellar accretion rate, however, will cause luminosity changes that are reprocessed by the surrounding envelope and are observable at submillimeter wavelengths. We searched for submillimeter flux variability toward 12 Planck Galactic Cold Clumps detected by the James Clerk Maxwell Telescope (JCMT)-SCUBA-2 Continuum Observations of Pre-protostellar Evolution (SCOPE) survey. These observations were conducted at 850 ㎛ using the JCMT/SCUBA-2. Each field was observed three times over about 14 months between 2016 April and 2017 June. We applied a relative flux calibration and achieved a calibration uncertainty of ~3.6% on average. We identified 136 clumps across 12 fields and detected four sources with flux variations of ~30%. For three of these sources, the variations appear to be primarily due to large-scale contamination, leaving one plausible candidate.

• BMB Reports
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• v.29 no.2
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• pp.180-182
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• 1996

One of the essential functions of virus surface proteins is the recognition of specific receptors on target cell membranes, and cellular receptors play an important role in viral pathogenesis. But the earliest steps of hepatitis B virus (HBV) infection, such as hepatocyte receptor interaction with the virus, are poorly understood. Previous work has suggested an important role of the preS1 region of HBV envelope protein in mediating viral binding to hepatocytes. Although hepatitis B virus (HBV) infection appears to be initiated by specific binding of virions to cell membrane structures via one or potentially several viral surface proteins, data showing the identification or isolation of the HBV receptor (s) are not yet available. The receptor-like proteins on the plasma membrane surface of HepG2 cells that bind to PreS1 were separated and identified using affinity chromatography, and the amino-terminal amino acid sequences of the receptor-like proteins were determined.

• BMB Reports
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• v.29 no.2
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• pp.175-179
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• 1996

Viral surface proteins are known to play an essential role in attachment of the virus particle to the host cell membrane. In case of the hepatitis B virus (HBV) several reports have described potential receptors on the target cell side, but no definite receptor protein has been isolated yet. As for the viral side, it has been suggested that the preS region of the envelope protein, especially the preS1 region, is involved in binding of HBV to the host cell. In this study, preS1 region was recombinantly expressed in the form of a maltose binding protein (MBP) fusion protein and used to identify and visualize the expression of putative HBV receptor(s) on the host cell. Using laser scanned confocal microscopy and by FACS analysis, MBP-preS1 proteins were shown to bind to the human hepatoma cell line HepG2 in a receptor-ligand specific manner. The binding kinetic of MBP-preS1 to its cellular receptor was shown to be temperature and time dependent. In cells permeabilized with Triton X-100 and treated with the fusion protein, a specific staining of the nuclear membrane could be observed. To determine the precise location of the receptor binding site within the preS1 region, several short overlapping peptides from this region were synthesized and used in a competition assay. In this way the receptor binding epitope in preS1 was revealed to be amino acid residues 27 to 51, which is in agreement with previous reports. These results confirm the significance of the preS1 region in virus attachment in general, and suggest an internalization pathway mediated by direct attachment of the viral particle to the target cell membrane.

• Bulletin of the Korean Mathematical Society
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• v.50 no.1
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• pp.11-24
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• 2013

Let m and n be fixed positive integers and M a right R-module. Recall that M is said to be ($m$, $n$)-injective if $Ext^1$(P, M) = 0 for any ($m$, $n$)-presented right R-module P; M is said to be ($m$, $n$)-flat if $Tor_1$(N, P) = 0 for any ($m$, $n$)-presented left R-module P. In terms of some derived functors, relative injective or relative flat resolutions and dimensions are investigated. As applications, some new characterizations of von Neumann regular rings and p.p. rings are given.

• Journal of Astronomy and Space Sciences
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• v.19 no.4
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• pp.255-262
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• 2002

We present the infrared spectra of Herbig Ae/Be stars including the Infrared Space Ob-servatory (ISO) data. To investigate the overall properties of their circumstellar dust envelope and/or disk, we combine the IR spectra with photometric data ranging from the UV through the optical into the sub-mm region. We study the general characteristics of the spectral energy distributions using simple analysis. We plot the positions on the HR-diagram to compare with the theoretical pre-main-sequence evolution tracks.

• Biotechnology and Bioprocess Engineering:BBE
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• v.11 no.2
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• pp.173-177
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• 2006

In this study, a novel strategy was developed for the highly selective immobilization of proteins, using the polyhydroxyalkanoate (PHA) depolymerase substrate binding domain (SBD) as an active binding domain. In order to determine the appropriacy of this method for immunodiagnostic assays, the single-chain antibody (ScFv) against the hepatitis B virus (HBV) preS2 surface protein and the severe acute respiratory syndrome coronavirus (SARS-CoV) envelope protein (SCVe) were fused to the SBD, then directly immobilized on PH A-coated slides via microspotting. The fluorescence-labeled HBV antigen and the antibody against SCVe were then utilized to examine specific interactions on the PHA-coated surfaces. Fluorescence signals were detected only at the spotted positions, thereby indicating a high degree of affinity and selectivity for their corresponding antigens/antibodies. Furthermore, we detected small amounts of ScFv-SBD (2.7 ng/mL) and SCVe-SBD fusion proteins (0.6ng/mL). Therefore, this microarray platform technology, using PHA and SBD, appears generally appropriate for immunodiagnosis, with no special requirements with regard to synthetic or chemical modification of the biomolecules or the solid surface.

• Journal of Microbiology
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• v.45 no.5
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• pp.431-440
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• 2007

A silkworm (Bombyx mori L.) extract known to contain naturally occurring iminosugars, including 1-deoxynojirimycin (1-DNJ) derived from the mulberry tree (Morus alba L.), was evaluated in surrogate HCV and HBV in vitro assays. Antiviral activity of the silkworm extract and one of its purified constituents, 1-DNJ, was demonstrated against bovine viral diarrhea virus (BVDV) and GB virus-B (GBV-B), both members of the Flaviviridae family, and against woodchuck hepatitis virus (WHV) and hepatitis B virus (HBV), both members of the Hepadnaviridae family of viruses. The silkworm extract exhibited a 1,300 fold greater antiviral effect against BVDV in comparison to purified 1-DNJ. Glycoprotein processing of BVDV envelope proteins was disrupted upon treatment with the naturally derived components. The glycosylation of the WHV envelope proteins was affected largely by treatment with the silkworm extract than with purified 1-DNJ as well. The mechanism of action for this therapy may lie in the generation of defective particles that are unable to initiate the next cycle of infection as demonstrated by inhibition of GBV-B in vitro. We postulate that the five constituent iminosugars present in the silkworm extract contribute, in a synergistic manner, toward the antiviral effects observed for the inhibition of intact maturation of hepatitis viral particles and may complement conventional therapies. These results indicate that pre-clinical testing of the natural silkworm extract with regards to the efficacy of treatment against viral hepatitis infections can be evaluated in the respective animal models, in preparation for clinical trials in humans.

• Korean Journal of Microbiology
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• v.28 no.1
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• pp.13-18
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• 1990

A DNA sequence encoding the adr subtype preS2 region of hepatitis B virus envelope protein was fused to 5' end of lacZ gene yielding a plasmid pTSZ, in order to produce a preS2-$\beta$-galactosidase fusion protein. Serial deletions from 3' and 5' end of preS2 were constructed in plasmids, which were expressed and their antigenicities were examined with the monoclonal antibody H8. Deletions from amino and carboxy terminal to certain points did not affect the antigenicity, but the longer deletions destroyed the antigenicity. End points of deleted preS2 sequence were determined by DNA sequencing. As a result, each end of preS2 epitope was located in the region of amino acid residue 130-132 and 140-142, respectively. Residue 143 may be supplementary for antigenic epitope since the deletion from carboxy terminal to residue 143 revealed partial defect of antigenicity. In the interval of antigenic epitope the amino acid differences between adr and adw2 subtype occurred ar residue 130, 132, and 141. This result indicated that one or more of the three residues are responsible for the binding specificity of monoclonal antibody H8 to adr subtype preS2 fusion protein.