• Proceedings of the Korean Society of Plant Pathology Conference
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• 2003.10a
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• pp.138.2-139
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• 2003

Grapevine leafroll-associated 1 virus (GLRaV-1) and Grapevine leafroll-associated 3 virus (GLRaV-3), member of the genus Ampelovirus, are important viral disease of grapevine in the world. these viruses transmitted only dicotyledonous host by vectors such as mealybugs and there is no suitable herbaceous host for virus. The diseased leaves turn yellowish or reddish depending on cultivars and viruses. Viruses are existed at low concentration and ununiformly distribution in grapevine. Using small-scale double-stranded RNA (dsRNA) extraction method, reverse transcription and polymerase chain reaction (RT-PCR) product of 1Kb long which encoded of coat protein (CP) gene for both viruses was successfully amplified with a specific primers. The RT-PCR product was cloned into the plasmid vector and its nucleotide sequences were determined from selected recombinant cDNA clones. Sequence analysis revealed that the CP of GLRaV-1 consisted of 969 nucleotide, which encoded 323 amino acid residues and CP of GLRaV-3 consisted of 942 nucleotide, which encoded 314 amino acid residues. The CP of GLRaV-1 and GLRaV-3 has 93.8％ and 98.7％ amino acid sequence identities, respectively.

• Microbiology and Biotechnology Letters
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• v.23 no.3
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• pp.275-281
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• 1995

From the plasmid pYA300 carring a CMCase of Rhizobium fredii USDA193 plasmid was subcloned into pBluescript II KS(+)/pBluescript II SK(+) vectors and designated pYA500 and pYA600, respectively. Escherchia coli cells transformed with pYA500 porduced the CMCase more than with pYA600. The orientation of the cloned fragment in pBluescript vector had the effect on gene expression in E. coli background. When the 1.7 kb CMCase gene fragment of R. fredii USDA193 was hybridized to EcoRI-digested total DNA from R. meliloti and R. fredii USDA 191 the unique bands hybridized respectively, indicating that some genetic diversity exists in the EcoRI restriction enzyme site for CMCase gene in Rhizobium strains. The optimum pH of enzyme activity was 7 and the optimum temperature of that was nearly 37$\circ$C. The cellulase-minus derivatives of pYA500 were constructed by Tn5 insertional mutation. Among 6000 transconjugants, two mutant plasmids (designated pYA500::Tn5a and pYA500::Tn5b) were detected from the cellulase- negative transconjugants. The product of CMCase gene was analyzed by one dimensional SDS- PAGE of the cell extracts. About 45 kDa protein was considered to be a product of CMCase gene.

• YAKHAK HOEJI
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• v.35 no.1
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• pp.1-6
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• 1991

Fast Hartley transform(FHT) was used for the identification of derivative UV spectra of pharmaceuticals, with the advantages of relatively shorter computing time of FHT and more precise results. The arccosine value of dot product of two vectors of normalized FHT coefficients calculated from two compared derivative spectra was a reasonable parameter for the spectral identification. Using this parameter, the similar patterns of derivative spectra of 13 penicillins can be differenciated from each other. The concentration difference and the minor contamination did not interfere the results of identification procedures. All these procedures of identification were accomplished successfully by the computer program, [SPECMAN PLUS] version 1.30, which was developed for this article.

• Journal of applied mathematics & informatics
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• v.18 no.1_2
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• pp.247-259
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• 2005

Necessary and sufficient conditions, under which there exists (at least) a sequence of vectors of real numbers for which the distribution function (d.f.) of any vector of extreme order statistics converges to a non-degenerate limit, are derived. The interesting thing is that these conditions solely depend on the univariate marginals. Moreover, the limit splits into the product of the limit univariate marginals if all the bivariate marginals of the trivariate d.f., from which the sample is drawn, is of negative quadrant dependent random variables (r.v.'s). Finally, all these results are stated for the multivariate extremes with arbitrary dimensions.

• Journal of Microbiology and Biotechnology
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• v.14 no.1
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• pp.1-14
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• 2004

More than twenty years have passed since the approval of the first recombinant DNA product for therapeutic use (recombinant human insulin, 1982). However, the biotechnology industry is still facing a shortage of manufacturing capacity due to the increasing demand of therapeutic proteins. This demand has prompted the search for a growing number of biological production systems but, nevertheless, the Gram-negative bacterium Escherichia coli remains one of the most attractive production hosts. This review highlights the most important features and developments of plasmid vector design, emphasizing the different reported strategies for improving the expression and secretion of heterologous proteins using the cellular machinery of E. coli.

• Applied Biological Chemistry
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• v.31 no.3
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• pp.267-273
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• 1988

Transformed, hybrid strains of the yeast Saccharomyces capable of simultaneous secretion of both glucoamylase and ${\alpha}-amylase$ have been produced. These strains can carry out direct, one-step assimilation of starch with conversion efficiency greater than 93% during a 5 day growth period. One of the transformants converts 92.8% of available starch into reducing sugars in only 2 days. Glucoamylase secretion by these strains results from expression of one or more chromosomal STA genes derived from Saccharomyces diastaticus. The strains were transformed by a plasmid(pMS12) containing mouse salivary ${\alpha}-amylase$ cDNA in an expression vector containing yeast alcohol dehydrogenase promoter and a segment of yeast $2{\mu}$ plasmid. The major starch hydrolysis product produced by crude amylases found in culture broths is glucose, indicating that ${\alpha}-amylase$ and glucoamylase act cooperatively.

• KSBB Journal
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• v.5 no.3
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• pp.293-298
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• 1990

Alpha-interferon was produced by using recombinant Escherichia coli strains, which carry cloned alpha-interferon gene in plasmid vectors, pIF-III-B and pIF-III-C. With the aid of signal sequence of E. coli lipoprotein, which is placed right in front of the upstream of the cloned alpha-interferon gene of the plasmids, about 50% of alpha-interferon produced was excreted or secreted. Meanwhile, there was no extracellular production of alpha-interferon from the recombinant strain carrying the plasmid Hif-2h that lacks the signal sequence of lipoprotein.

• Journal of information and communication convergence engineering
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• v.20 no.1
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• pp.1-7
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• 2022

Herein, a new space-time block coding technique is proposed for a MIMO 2 × 2 multiple-input multiple output (MIMO) system to minimize the bit error rate (BER) in Rayleigh fading channels with reduced decoding complexity using ZF and MMSE linear detection techniques. The main objective is to improve the service quality of wireless communication systems and optimize the number of antennas used in base stations and terminals. The idea is to exploit the correlation product technique between both information symbols to transmit per space-time block code and their own orthogonal Walsh-Hadamard sequences to ensure orthogonality between both symbol vectors and create a full-rate orthogonal STBC code. Using 16 quadrature amplitude modulation and the quasi-static Rayleigh channel model in the MATLAB environment, the simulation results show that the proposed space-time block code performs better than the Alamouti code in terms of BER performance in the 2 × 2 MIMO system for both cases of linear decoding ZF and MMSE.

• Mycobiology
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• v.31 no.1
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• pp.42-45
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• 2003

For transformation of Pleurotus ostreatus, two novel vectors, pPhKM1 and pPhKM2, were constructed, using the regulatory sequences of the P. sajor-caju $\beta$-tubulin gene(TUB1) and the ble gene encoding phleomycin binding protein. pPhKM1 contains ble fused to the TUB1 promoter and the Schizophyllum commune GPD terminator. pPhKM2 contains ble fused to the promoter and terminator regions of P. sajor-caju TUB1. To confirm phleomycin-resistance activity, each vector was cotrans-formed with pTRura3-2 into the P. ostreatus homokaryotic $ura^-$ strain. The transforming DNA was stably integrated into the genomic DNA. Subsequently, phleomycin resistance was conferred on wild-type dikaryotic P. ostreatus by transformation with pPhKM1 or pPhKM2. This transformation system generated stable phleomycin-resistant transformants.

• Proceedings of the KSRS Conference
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• 2005.10a
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• pp.52-53
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• 2005

Time series of gridded surface wind and wind-stress vectors over the world ocean have been constructed by satellite scatterometer data. The products are derived from the ERS-l,2 covering 9 years during 1992-2000 and the Sea Winds on board QuikSCAT (Qscat) which has been operating up to the present since June 1999, so they allows us to analyze variabilities with various time scales. In this study, we focus on interannual variability of the wind stress in the mid- and high-latitude region of North Pacific. These are compared with those by numerical weather prediction(NWP) ones (NCEP Reanalysis). We also examine variability in the wind-stress curl field that is an important factor for ocean dynamics and focus its time and spatial characters in the northwestern Pacific around Japan. It is found that the vorticity field in the lower atmosphere tends to increase gradually with time, suggesting the enhancement of the North Pacific subtropical gyre.