The safety degree of navigation for collision avoidance is closely related with the combination between mariner's behavior and navigational environment. The condition of navigational environment is mainly decided by navigable waters, ship traffic, rule of road, sea state, weather and so on. Especially, the condition of navigable waters and ship traffic in navigational environment are ones of the important factors to attain safe navigation when mariners are underway and crossing, head on or overtaking situation. Thus this paper is to analyze the characteristics of mariner's behavior for collision avoidance caused by ship traffic and navigable waters by analyzing the contents of questionnaire and the results of international collaborative research. As a result, it can be concluded that the density of ship traffic and the area of navigable waters affect mariner's ship handling for collision avoidance.

Ammonia (NH3 ) volatilization from a silty clay loam paddy soil applied with non, straight urea, and coated urea, respectively, under transplanting in Milyang, Korea from 2002 and 2003 was simulated by a Water and Nitrogen Management Model (WNMM). Based on the data from the in-situ measurements, NH3 volatilization during the rice growth was 6.04% and 1.46% of the applied nitrogen (N) from straight urea and coated urea, respectively. The bulk aerodynamic approach in WNMM satisfactorily predicted the difference in NH3 loss during the given rice growing seasons from the two urea fertilizers. R2 for the correlation between the predicted and observed NH3 loss during the calibration year (2002) was 0.53 less than 0.68 of the application year (2003). This difference could be due to the weather condition such as heavy rainfall and temperature during the calibration year.

A narrow loop noise bandwidth method is desirable to reduce the error of raw measurements due to the thermal noise. However, it degrades the performance of GPS initial synchronization such as mean acquisition time. And it restricts the loop noise bandwidth to a fixed value determined by the lower bound of the allowable range of carrier-to-noise power ratio, so that it is difficult to optimally track GPS signal. In order to make up for the weak points of the fixed-type narrow loop noise bandwidth method and simultaneously minimize the error of code and carrier measurements, this paper proposes a stepwise-type adaptive bandwidth algorithm for DGPS reference receivers. In this paper, it is shown that the proposed adaptive bandwidth algorithm can provide more accurate measurements than those of the fixed-type narrow loop noise bandwidth method, in view of analyzing the simulation results between two signal tracking algorithms. This paper also carries out sensitivity analysis of the proposed adaptive bandwidth algorithm due to the estimation uncertainty of carrier-to-noise power ratio. Finally the analysis results are verified by the experiment using GPS simulator.

A new cultivar of Dianthus caryophyllus "Deneb" was selected from the progenies of a cross "Mantovani" and "Deborah" in 1996 at the National Horticultural Research Institute, Rural Development Administration. It was finally selected in 2001 after the investigation of the characteristics for five years (1996-2001). "Deneb" was developed for a cut flower with a spray type. It has white with red edge flower color. The flower color is particularly clean and beautiful in indoor. It has a long flower stem and a long vase life. It is grown over 8℃ at night and under 25℃ at day. The cultivar was applied for a variety protection 2001 and was released to the growers and commercialized in 2002.

A new cultivar of Dianthus caryophyllus "Phoenix" was selected from the progenies of a cross "Rossini" and "Charlotte" in 1997 at the National Horticultural Research Institute, Rural Development Administration. It was finally selected in 2001 after the investigation of the characteristics for four years (1997-2001). "Phoenix" was developed for a cut flower with a spray type. It has red flower color and lots of petals. It was moderately resistant against Fusarium oxysporum. Its flower looks like a rose when the outer petals bloom. It is grown over 8℃ at night and under 25℃ at day. The cultivar was applied for a variety protection 2001 and was released to the growers and commercialized in 2002.

Lunasin is small subunit peptide of coded from Gm2S-1 gene in soybean. It has been previously demonstrated that lunasin is a novel and promising cancer preventive peptide. Lunasin peptide is found only in the seed and not other tissues. And lunasin peptide starts to appear at 5 weeks after flowering and remains in the mature seed. We report here firstly lunasin peptide identified from soybean callus induced by the tissue culture and demonstrate its anticancer properties. The lunasin was identified and purified from soybean callus aged for 6 months. The callus lunasin(1μm) inhibited the acetylation of histone H3 and H4 by 58.8% and 56.5%, respectively. And it fully inhibited foci formation compared to the values of the positive control(no lunasin) and negative control(no MCA). Purified lunasin was able to internalize into the cell and localized in the nucleus.

Introduction The ginseng saponin (ginsenoside) is one of the most important secondary metabolites in ginseng and hasvarious pharmacological activities. To date about 38 kinds of ginsenosides have been isolated and identified from Panax ginseng C. A. Meyer. Among these ginsenosides, Rg3 is a precursor for ginsenoside Rh2, which has a very strong antitumor effect. and has many pharmaceutical activities. However, Rg3 is extremely low in normal ginseng. Thus production of ginsenoside Rg3 would be very important and many studies have aimed to convert major ginsenosides to the more active minor ginsenoside Rg3. The enzymatic conversion through sugar hydrolysis at a specific position is desirable for the production of active minor ginsenoside Rg3. Material and Method The isolation of β-glucosidase-producing microorganisms was performed according to a previously published method. Each microbialsuspension cultured in nutrient broth was added to the same volume of 1 mM ginsenoside Rb1 solution and then incubated on a rotary shaker at 30°C for 48 h. The reaction mixture was extracted with butanol saturated with H2O and then analyzed by thin layer chromatography (TLC). 8 μl of the ginseng extract solution was spotted on a TLC plate and developed to 5.5 cm distance in a chamber with chloroform/methanol/water as the mobile phase. Bands on the TLC plates were detected by spraying 10% H2SO4, followed by heating. Result and Discussion Ginseng(the root of Panax ginseng C. A. Meyer, Araliaceae) is frequently used as a crude substance taken orally in Korea, China and Japan, as well as other Asian countries, as a traditional medicine. Ginsenosides are the principal components having pharmacological and biological activities. More than 38 different ginsenosides so far have been isolated and identified from ginseng saponins. Among them, deglycosylated ginsenosides are known to be more effective in vivo physiological action and to act as active compounds. A lactic acid bacteria, which have β-glucosidase activity, were isolated from soil and kimchi using a MRS-Esculin agar. These strains were identified on the basis of phylogenetic inference based on 16S rDNA sequences. TLC and HPLC were used to analysis transformed ginsenosides. Ginsenosides are main pharmacoactive component in ginseng. When ginseng was orally administered, the absorption of ginsenosides from the gastrointestinal tract are extremely low. In order to improve oral bioavailability, transforming major ginsenosides into more active minor ginsenoside is very important. Caulobacter leidyia GP45 and Micro- bacterium esteraromaticum GS514 were isolated from ginseng field for converting major ginsenosides into minor ginsenosides. In the co-culture of strain GP45 and GS514 with ginsenoside Rb1, produced compound K and ginsenoside Rg3 individually. The transformation pathway of ginsenoside Rb1 were confirmed Rb1⟶Rd⟶F2⟶compound K and Rb1⟶Rd⟶Rg3.

Ginseng (Panax ginseng C. A. Meyer), a perennial herb in the Araliaceae family, is one of the most commonly utilized medicinal plants in the world. Because whole genome sequence of the ginseng plant is not analyzed, the expressed sequence tags (ESTs) from a ginseng plant was studied by constructing cDNA libraries. Almost 20,000 ESTs were collected and BLAST comparisons of the cDNAs in GenBank’s non-redundant databases revealed that many cDNAs (89.1%) exhibited a high degree of sequence homology to genes from other organisms. The majority of the identified transcripts were found to be genes related with energy, metabolism, subcellular localization, and protein synthesis. Many cDNA clones containing fructose-1,6-bisphosphate aldolase, dehydrin, catalase, and glutathion-S-transferase etc. were analyzed to study their characteristics. The expressions of the genes in different organs were analyzed using reverse transcriptase (RT)-PCR. In addition, the expressions of the genes under different abiotic stresses were analyzed at different time points. Ginseng Genetic Resource Bank (GGRB) in Kyung Hee University is the center constructed for ginseng genomic and genetic information. GGRB collects genetic resources of ginseng cultivars with systematic management system for effective conservation and application of the resources. GGRB supplies researchers new ginseng cultivars, specific markers, ginseng DNA and RNA for scientific researches.

The object of this study was to use genomic information obtained from wheat-rice sequence to develop genome-specific PCR primer for Agp-L gene involved in starch biosynthesis. Intron locations in wheat were inferred through alignment of wheat cDNA sequence of Agp-L with rice genomic sequence. Exon-anchored primer which amplify across introns allowed sequencing of introns from the three genomes provided the basis for genome-specific primer design. The single nucleotide polymorphism (SNP) was identified and this SNP could be converted into cleaved amplified polymorphism sequence (CAPS).

Photoperiod sensitive genetic male sterile (PGMS) rice is sterile mutant controlled by photoperiod. A PGMS mutant 920S was sterile grown under long-day (LD) photoperiod (14 h light/10 h dark) but fertile grown under short-day (SD) photoperiod (10 h light/14 h dark). Proteome analysis revealed that 12 protein spots were differentially expressed in the spikelets of 920S plants either treated with LD or SD photoperiod. Among these proteins, three proteins including chlorophyll a/b binding protein, vacuolar ATPase β-subunit,~;α-tubulin and an unknown protein were more than three-fold abundant in the spikelet of the SD-treated plants than those of the LD-treated plants. On the other hand, eight proteins including acetyl transferase, 2, 3- biphosphoglycerate, aminopeptidase N, pyruvate decarboxylase, 60S acidic ribosomal protein and three unknown protein spots were more abundant in the spikelets of the LD-treated plants than those of the SD-treated plants. The results suggest that the observed proteins may be involved in sterile or fertile pollen development under LD or SD photoperiod respectively in the PGMS mutant rice.