고준위폐기물 심지층 처분장 설계시 주요한 고려인자는 완충재의 건전성 유지를 위하여 폐기물로부터 발생되는 열로 인하여 완충재의 온도가 100'C를 넘지 않도록 하는 것이다. 본 연구에서는 이러한 요건을 만족하는 고준위폐기물 심지층 처분장 배치를 위하여 처분터널 및 처분공 간격에 대한 분석을 수행하였다. 이를 위하여, 기준 처분개념을 바탕으로 사용후핵연료의 냉각기간 및 처분터널/처분공 간격을 다양하게 설정하여, 처분시스템에서의 열적 안정성 해석 및 결과를 비교분석하였다. 분석결과, 처분장 열적 요건을 만족하는 배치는 처분터널의 간격 보다는 처분공 간격을 조절하여 배치하는 것이 유리한 것으로 판단되었다. 본 연구의 결과는 심지층 처분시설 설계시 활용될 것이다. 향후, 정확한 부지특성 자료를 통한 상세한 분석이 수행되면, 분석결과의 불확실성을 줄일 것이다.

한국형처분시스템에 이용될 가압경수로형 사용후핵연료를 위한 KDC-1 처분용기를 개발하였다. 처분용기 안전성 평가의 일환으로서 처분용기에 대한 구조적 안전성을 평가하였다. 처분용기의 구조적 안전성은 처분조건과 취급조건 2가지로 구분하여 평가하였다. 처분조건에서는 3가지 하중 조건, 정상하중 조건, 비정상 하중 조건, 암반의 움직임을 고려하였다. 처분조건에서 평가 결과 3가지 조건에 대해 모두 안전계수가 설계기준보다 컸다. 취급조건에서는 처분용기 취급 중 구조해석과 처분용기 낙하 사고시 구조해석을 수행하였다. 취급장비 고장 시나리오 평가결과 1개 혹은 2개의 취급 장치가 고장을 일으켰을 때도 취급장비를 계속 운전하는 것이 가능하였다. 처분용기 낙하 시나리오에서는 계산결과 최대 응력은 0.762 MPa 이었으며, 이 값은 주철의 항복응력과 비교하면 거의 무시할 수 있는 값이었다. 본 논문에서 제안한 KDC-1 처분용기에 대한 처분조건 및 취급조건에서의 구조해석 결과, 한국형처분시스템에서 고려하고 있는 조건에서 그 구조적 안전성을 확인하였다.

The yields of the n-hexane-soluble, ethyl acetate-soluble, methanol-soluble and methanol-insoluble fractions from the powdered water extracts were 8.2%, 10.6%, 32.0% and 49.2%, respectively (Table 1). The antifungal activities of water extracts, n-hexane-soluble fraction, ethyl acetate-soluble fraction, methanol-soluble fraction and methanol-insoluble fraction against L. edodes were 23.5%, 26.2%, 41.5%, 25.4% and 2.5%, respectively, at 1000ppm (Figure3). The ethyl acetate-soluble fraction showed much higher antifungal activity than the other fractions. The antifungal activity of the ethyl acetate-soluble fraction against L. edodes at 1000 ppm showed a statistically significant difference in the fractions of n-hexane-soluble, ethyl acetate-soluble, methanol-soluble and methanol-insolub

The yields of the fractions of n-hexane-soluble, ethyl acetate-soluble and methanol-soluble from the P. densiflora sawdust were obtained 1.36%, 2.21% and 4.03% using organic solvents, respectively (Table 1). The antifungal activity of the n-hexane extracts against L. edodes at concentrations 125, 250, 500, 750 and 1000 ppm were 36.5%, 41.2%, 43.1%, 45.4% and 47.6%, respectively (Table 2). The percent of antifungal activity against L. edodes was the greatest for the n-hexane extracts, ranging from 36.5% to 47.6% at a concentrations of 125 ppm to 1000ppm, with the values for all concentrations significantly different from one another. In this experiment, the antifungal activity by the n-hexane extracts was the highest. This result supposed that the n-hexane extracts have not only many more inhibitory compounds against L. edodes than the ethyl acetate and methanol extracts but also the inhibitory compound may be more easily dissolved by n-hexane than by ethyl acetate or methanol.

본 연구에서는 사전연구로부터 사용후핵연료의 처분용기 원형모델로 제안된 처분용기의 전체 크기와 배열을 평가하기 위하여 일련의 공학적 분석을 수행하였다. 그러한 노력의 결과 용기 내부 저장통의 배열형태와 외곽쉘과 상하부 뚜껑의 두께와 같은 새로운 설계변수를 도출하였다. 공학적 분석 작업에는 처분용기의 기계구조 해석 결과를 근거로 도출된 용기의 규격자료에 대한 방사선 안전성 측면에서의 타당성을 검토하기 위하여 방사선차폐 해석과 핵 임계 해석 등이 수행되었다. 처분용기 내부 삽입체의 직경 변화에 따른 구조안정성 해석 결과에 따르면, 직경 102cm 일 때 극한 외압조건은 물론 정상적인 외압조건 하에서도 최대 Von Mises 응력이 안전계수 2.0을 만족하는 것으로 나타났다. 이 경우에서도 핵 임계 및 방사선차폐 해석 결과 안전기준치를 만족시키며, 무게는 20톤 가량 줄어드는 효과가 있는 것으로 나타났다.

1. Antifungal activity of water extracts The antifungal activity of the water extracts against L. edodes was proportional to the concentration of the water extracts. The antifungal activity of the water extracts at 1000 ppm was the highest among the tested concentration against L. edodes mycelia. The antifungal activity were significantly different from each concentration of the water extracts. Therefore, it can be concluded that the water extracts of the P. densiflora sawdust have inhibitory compounds to the growth of L. edodes mycelia. 2. Yield and antifungal activity of fractions from water extracts The powdered water extracts was further treated serially using organic solvents in order to separate the water extracts into the fractions of n-hexane-soluble, ethyl acetate-soluble, methanol-soluble and methanol-insoluble. The ethyl acetate-soluble fraction showed much higher antifungal activity than the other fractions. The antifungal activity of the ethyl acetate-soluble fraction against L. edodes at 1000 ppm showed a statistically significant difference in the fractions of n-hexane-soluble, ethyl acetate-soluble, methanol-soluble and methanol-insoluble. And, there was not significantly difference between the antifungal activities of the n-hexane-soluble and methanol-soluble fractions at 1000 ppm. 3. Antivungal activity of fractions of organic solvent extracts The fractions were isolated from each organic solvent by the silica-gel column chromatography and then the fractions were confirmed and divided on the values of Rf by the thin-layer chromatography. The fractions were produced six band of the n-hexane, nine band of the ethyl acetate and eight band of the methanol extracts. The HIII fraction from the n-hexane extracts showed the highest growth inhibition against L. edodes mycelium.

After having inoculated the mycelium of L. edodes on the block medium, the P. densiflora sawdust of the B and C groups were the slowest of their respective groups on day 169.4 and day 169.9 harvesting times. The first harvest of the fruiting body from the Q. variabilis sawdust of the control medium was obtained on day 162.9

유방촬영장치(mammography equipment, ME)을 이용한 유방검사(mammography, MG)의 경우 유방암의 조기진단을 위해 가장 일반적으로 시행되고 있는 검사방법으로 유방 내 섬유화 조직, 미소석회화 및 종양덩어리의 발견과 진단은 유방촬영장치의 품질관리(quality management, QM)에 의해 크게 영향을 받게 된다. 특히, 유방검사에서 품질관리란 장치와 연관된 문제점들이 임상영상에서 영상의 질(image quality, IQ) 저하로 진단영역 축소를 초래할 수 있는 발생가능한 모든 문제점을 사전에 파악하여 교정함으로써 항상 일정 수준의 영상의 질을 유지하고 영상을 획득할 수 있게 하는 행위를 의미한다. 이에 본 연구진은 유방촬영장치를 이용한 유방검사의 품질관리에 대한 일반적인 내용을 요약하여 보고 한다.

Mungbean (Vigna radiata) is a fast-growing, warm-season legume crop that is primarily cultivated in developing countries of Asia. We constructed a draft genome sequence of mungbean to facilitate genome research into the subgenus Ceratotropis and to enable a better understanding of the evolution of leguminous species. The draft genome sequence covers 80% of the estimated genome, of which 50.1% consists of repetitive sequences. In total, 22,427 high confidence protein-coding genes were predicted. Based on the de novo assembly of additional wild mungbean species, the divergence of what was eventually domesticated and the sampled wild mungbean species appears to have predated domestication. Moreover, the de novo assembly of a tetraploid Vigna species (Vigna reflexo-pilosa var. glabra) provided genomic evidence of a recent allopolyploid event. To further study speciation, we compared de novo RNA-seq assemblies of 22 accessions of 18 Vigna species and protein sets of Glycine max and Cajanus cajan. The species tree was constructed by a Bayesian Markov chain Monte Carlo method using highly confident orthologs shared by all 24 accessions. The present assembly of V. radiata var. radiata will facilitate genome research and accelerate molecular breeding of the subgenus Ceratotropis.

Arabidopsis atDjC53 and atDjC32 gene DnaJ-like protein homologous to DnaJ-like protein was characterized for the functional analysis of DnaJ-like protein. It was shown that atDjC53 and atDjC32 RNA expression is induced by heat shock stress and atDjC53- and atDjC32-GFP was targeted to the nucleus of protoplasts. The atDjC53 and atDjC32 promoter (1 kb) was isolated and fused to the GUS reporter gene to investigate gene regulation of atDjC53 and atDjC32 specific to heat shock stress or to developmental organ in the transgenic lines. RNAi and overexpression construct was employed to generate atDjC53 and atDjC32 knock-out plants for the study of their function. Molecular function of atDjC53 and atDjC32 is discussed in relation to heat shock and also developmental stages in Arabidopsis.

Heat shock transcription factors (HSFs) are the major heat shock factors regulating the heat stress response. They participate in regulating the expression of heat shock proteins (HSPs), which are critical in the protection against stress damage and many other important biological processes. In this study, a genome-wide analysis was carried out to identify all HSFs soybean genes. Twenty six nonredundant HSF genes (GmHsf) were identified in the latest soybean genome sequence. Chromosomal location, protein domain and motif organization of GmHsfs were analyzed in soybean genome. The phylogenetic relationships, gene duplications and expression profiles of GmHsf genes were also presented in this study. According to their structural features, the predicted members were divided into the previously defined classes A–C, as described in Arabidopsis. Using RT-PCR, the expression patterns of 26 GmHsf genes were investigated under heat stress. The data revealed that these genes presented different expression levels in response to heat stress conditions. Real-time (q)RT-PCR was performed to investigate transcript levels of five GmHsfs in response to multiple abiotic stresses. Differential expression of five GmHsfs implies their role during abiotic stresses. Subcellular localization using GFP-fusion protein demonstrated that GmHsf12 and GmHsf34 were restricted to the nucleus and GmHsf28 was localized in the nucleus and cytoplasm in plant. The results provide a fundamental clue for understanding of the complexity of the soybean HSF gene family and cloning specific function genes in further studies and applications.

Salinity stress severely affects plant growth and development causing crop loss worldwide. Suaeda asparagoides is a salt-marsh euhalophyte widely distributed in southwestern foreshore of Korea. To isolate salt tolerance genes from S. asparagoides, we constructed a cDNA library from leaf tissues of S. asparagoides that was treated with 200 mM NaCl. A total of 1,056 clones were randomly selected for EST sequencing, and 932 of them produced readable sequence. By sequence analysis, we identified 538 unigenes and registered each in National Center for Biotechnology Information. The 80 salt stress related genes were selected to study their differential expression. Reverse Transcriptase-PCR and Northern blot analysis revealed that 23 genes were differentially expressed under the high salinity stress conditions in S. asparagoides. They are functionally diverse including transport, signal transduction, transcription factor, metabolism and stress associated protein, and unknown function. Among them dehydrin (SaDhn) and RNA binding protein (SaRBP1) were examined for their abiotic stress tolerance in yeast (Saccharomyces cerevisiae). Yeast overexpressing SaDhn and SaRBP1 showed enhanced tolerance to osmotic, freezing and heat shock stresses. This study provides the evidence that SaRBP1 and SaDhn from S.asparagoides exert abiotic stress tolerance in yeast. Information of salt stress related genes from S. asparagoides will contribute for the accumulating genetic resources to improve osmotic tolerance in plants.

We have isolated wound-inducible genes from soybean using suppression subtractive hybridization (SSH) method and were able to obtain the full-length clone of GmDjp1 gene encoding DnaJ-like protein. The full-length cDNA of GmDjp1 is 689 bp with an open reading frame (ORF) consisting of 163 amino acid (aa). Genomic southern blot confirmed that soybean genome has two copies of GmDjp1 gene. Northern blot analysis showed that the RNA expression of GmDjp1 gene is specifically induced by heat, NaCl, wounding and drought stresses. It was demonstrated that GmDjp1-GFP was targeted to the nucleus in tobacco cell. GmDjp1 overexpression plants showed more susceptible to salt and heat stress compared to WT. RNA expression level of Hsp18.2 and Hsp25.3-P was lower than that of WT during recovery after heat hock in plants. This indicates that GmDjp1 may play a negative regulator to stress responses in plants.

A low temperature-inducible cDNA designated as VrUBC1 from mungbean (Vigna radiata) was isolated by subtractive hybridization method. By rapid amplification of cDNA end technique, the full-length cDNA of VrUBC1 was obtained. The full-length cDNA of VrUBC1 contains an open reading frame of 444 nucleotides in length and capable of specifying a 16.5-kDa protein of 148 amino acids (aa) with an isoelectric point of 7.72. VrUBC1 mRNA was induced by NaCl and ABA, but not by wounding and low temperature stress. It was shown that VrUBC1-GFP was localized to the cytoplasm in tobacco cell. To examine the function of VrUBC1, VrUBC1 was expressed in Escherichia coli as His-fusion protein. Purified VrUBC1-His recombinant protein was shown to have ubiquitination activity in vitro. For the in vivo functional analysis of VrUBC1, VrUBC1 was expressed in yeast ubc4/5 double mutant. Stress tolerance was tested in the VrUBC1 overexpressing Arabidopsis transgenic plants. We propose that VrUBC1 play an important role in protein degradation processes during abiotic stress in plants.

R genes are a key component of genetic interactions between plants and biotrophic bacteria and are known to regulate resistance against bacterial invasion. The most common R proteins contain a nucleotide-binding site and a leucine-rich repeat (NBS-LRR) domain. Some soybean NBS-LRR genes have also been reported to function in disease resistance. A total of 319 genes were determined to be putative NBS-LRR genes in the soybean genome. The number of NBS-LRR genes on each chromosome was highly correlated with the number of disease resistance QTL in the 2-Mb flanking regions of NBS-LRR genes. In addition, the recently duplicated regions contained duplicated NBS-LRR genes and duplicated disease resistance QTL, and possessed either an uneven or even number of NBS-LRR genes on each side. The significant difference in NBS-LRR gene expression between a resistant near-isogenic line (NIL) and a susceptible NIL after inoculation of Xanthomonas axonopodis pv. glycines supports the conjecture that NBS-LRR genes have disease resistance functions in the soybean genome. The number of NBS-LRR genes and disease resistance QTL in the 2-Mb flanking regions of each chromosome was significantly correlated, and several recently duplicated regions that contain NBS-LRR genes harbored disease resistance QTL for both sides. In addition, NBS-LRR gene expression was significantly different between the BLP-resistant NIL and the BLP-susceptible NIL in response to bacterial infection. From these observations, NBS-LRR genes are suggested to contribute to disease resistance in soybean. Moreover, we propose models for how NBS-LRR genes were duplicated, and apply Ks values for each NBS-LRR gene cluster.