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        검색결과 12

        2.
        2013.09 구독 인증기관 무료, 개인회원 유료
        The karyotype of Korean short-hair cat was presented using the G-, C- and NOR- banding techniques. For chromosomes preparation, the fetus skin fibroblast cells were cultured and metaphases were obtained. In results, the Korean short-hair cat had 38 chromosomes with XX or XY, which consisted of 5 pairs of metacentric chromosomes(Group A and C), 3 pairs of submetacentric chromosomes (Group B), 6 pairs of medium metacentric chromosomes except for 1 pair of medium submetacentric D2 chromosomes (Group D, E), 2 pairs of acrocentric chromosomes(Group F) and metacentric X and Y sex chromosomes. In G-banding analysis, the Korean short-hair cat exhibited a typical and identical G-banding pattern in each homologous chromosome. Total number of bands and landmarks on the G-banded chromosomes of Korean short-hair cat well correspond to those of international standardization of karyotype of domestic cat. The heterochromatins of Korean short-hair cat chromosomes distributed at terminal and/or centromere regions on almost chromosomes by C-banding analysis. In addition, the C-banding pattern showed greatly heteromorphic in some chromosomes. Using the AgNOR-staining, we found the nucleolar organizer regions(NORs) of Korean short-hair cat located at chromosomes 1p12 site in E group. The quantity and number of NORs were constant among cells.
        4,000원
        3.
        2006.12 구독 인증기관 무료, 개인회원 유료
        The Chinese Hamster Ovarian cells CHOK1 are one of the most extensively used cells for the evaluation of gene expression and toxicology. However, these cells are frequently used for biomedical research without consideration of their cytogenetic characteristics. Therefore, we carried out to investigate the karyologic profiles, the frequency and type of chromosome aberration, and the distribution of telomeric DNA on chromosomes of the CHOK1 cells. The GTGbanding and fluorescence in situ hybridization on CHOK1 cells were performed to characterize the karyotype and the distribution of telomeric DNA. The present study revealed that the chromosome modal number of CHOK1 cells was 2n=20; eight chromosomes appeared to be identical with those of the normal Chinese hamster, whereas the remaining 12 chromosomes were shown to be translocated, deleted, inversed, or rearranged from Chinese hamster chromosomes. The telomeric DNA on CHOK1 chromosomes was intensively distributed at the centromeres rather than the ends of chromosomes. In addition, three chromosomes had interstitial telomeres and one marker chromosome entirely consisted of telomeric DNAs. The frequency and type of chromosome aberrations in CHOK1 cells were examined. Of the 822 metaphase spreads, 68 (8.3%) cells resulted in chromosome aberrations of which the chromosome breakage was the most frequently occurred.
        4,000원
        5.
        1999.04 KCI 등재 구독 인증기관 무료, 개인회원 유료
        동치미액은 전통적으로 냉면국물로 이용되어왔다. 냉면국물의 미생물 오염문제를 해결하기 위하여 항균활성이 높은 김치 젖산균 Lactobacillus homohiochii B21과 Leuconostoc mesenteroides subsp. mesenteroides C16을 스타터로 혼합사용하여 동치미액을 제조하고, 이를 냉면국물에 100%, 50%, 10% 및 0% 첨가하여 20℃ 및 10℃에서 보관할 때에 동치미액의 항균력으로 인하여 의도적으로 첨가한 Listeria monocytogenes와 Escherichia coli O157:H7의 증식이 억제되는 정도를 조사하였다. 동치미액 100%인 냉면국물은 20℃에서 보관할 때에 Listeria monocytogenes는 8시간만에, Escherichia coli O157:H7는 40시간만이 10^6CFU/ml에서 10^0CFU/ml로 각각 급격히 사멸하였고, 10℃에서 보관할 때에도 시간경과에 따라 생균수가 급격히 감소하였으나 감소속도는 20℃에서 보관할 때보다 느렸다. 동치미액을 50% 첨가한 육수에서도 Listeria monocytogenes와 Escherichia coli O157:H7는 시간경과에 따라 급격히 감소하였으며, 감소속도는 동치미액 100%일 경우보다 느렸다. 동치미액을 10% 첨가한 육수는 20℃에서 보관할 때는 초기에 Listeria monocytogenes 및 Escherichia coli O157:H7의 균수증가가 약간 있었으나 동치미액 무첨가에 비하여 현저히 억제되었으며, 16시간 이후부터는 균수가 서서히 감소하였다. 동치미액을 첨가하지 않은 육수는 20℃에서 보관할 때는 초기부터 Listeria monocytogenes 및 Escherichia coli O157:H7의 균수증가가 급격히 이루어졌으며, 10℃에서 보관할 때는 24시간 이후부터 서서히 증가하였다. Listeria monocytogenes 및 Escherichia coli O157:H7에 대한 본 동치미액의 항균활성은 후자의 미생물보다 전자에 대하여 더욱 강하게 나타났다. 본 연구의 동치미액을 육수에 50% 첨가하여 냉면국물을 제조한다면 보관중의 미생물 오염문제 해결에 큰 도움이 될 것으로 판단된다.
        4,000원
        6.
        1999.04 KCI 등재 구독 인증기관 무료, 개인회원 유료
        Solid phase micro extraction(SPME)법의 최적조건 실험 및 SPME로 추출된 산초(Zanthoxylum schinifolium)의 휘발성 성분을 GC/MSD로 확인하였다. 휘발성 성분 추출에 자주 이용되는 동시증류추출(SDE)법으로 산초의 휘발성분을 분석하여 SP-ME 법에서 확인된 휘발성 성분과 조성비를 비교하였다. SPME 최적조건 시험에서 분자량이 적고 비점이 낮은 성분은 온도가 증가할수록 화이버에 흡착되는 양은 적게 나타났으며, 분자량이 크고 비점이 높은 성분은 추출시간이 증가할수록 흡착되는 양은 증가하였다. SPME 최적조건인 추출시간 30분과 50℃에서 분리된 휘발성 성분에서는 limonene(14.65%), geranyl acetate(11.07%), β-phellandrene(7.42%), 및 phellandral(3.08%) 등의 monoterpenoids 화합물과 caproic acid(11.99%), caprylic acid(8.01%), heptanoic acid(3.49%) 등의 지방산 화합물이 주요 성분으로 확인되었고, SDE법으로 추출된 휘발성 성분에서는 geranyl acetate(13.31%), limonene(12.81%) β-phellandrene(8.86%), trans-geraniol(5.22%) 및 caprylic acid(3.03%) 등의 화합물이 주요 성분으로 확인되었다. 지방산 성분들은 SPME법에서 높게 나타난 반면에 알코올 성분들은 SDE법보다 낮았다. SPME법은 적은 양의 시료로도 매우 신속하고 간단하게 전처리 할 수 있기 때문에 기존의 휘발성분 분석시 주로 사용한 SDE법에 비해 편리하며 경제적인 것으로 생각된다.
        4,000원
        7.
        1999.04 KCI 등재 구독 인증기관 무료, 개인회원 유료
        냉동 검은밀복어 10개체를 반 해동상태에서 근육, 껍질, 간장 및 내장으로 분리하여 독성검사와 총지질량을 구하였고 TLC로 조성을 조사하였다. Silicic column chromatography에 의하여 간유로부터 중성지질, 인지질 및 당지질을 분리하였으며 중성지질중의 DHA 및 EPA함량을 gas chromatography로 분석하였다. 검은밀복어의 총지질 함량은 간장 29.34∼36.54, 내장 4.95∼6.11, 껍질 1.12∼1.60 및 근육 0.23∼0.38%로 나타났고, TLC 분석 결과 다양한 지질성분으로 구성되었다. 그 중에서 triglyceride가 가장 많았다. 지질 함량이 가장 높은 간장 부위의 총지질의 지방산은 주로 palmitic acid(16:0), palmitoleic acid(16:1), stearic acid(18:0), oleic acid(18:1), EPA(20:6) 및 DHA(22:1)이었다. 포화지방산에 대한 고도 불포화 지방산의 비율(0.84)은 높았고, DHA와 EPA의 함량은 각각 15.99와 3.04%였다. 간유 중의 중성지질 95.46, 당지질 1.45 및 인지질 3.09%의 함량인데, 이 중 가장 함량이 높은 것으로 나타난 중성지질을 분리하여 분석한 결과 주요 지방산은 palmitic acid(16:0), stearic acid(18:0), oleic acid(18:1), EPA(20:5) 및 DHA(22:6)로 나타났다. 그 중의 DHA와 EPA함량 비율은 각각 16.62와 2.41%로 나타났다. 한편, 간장내의 지질 추출 전과 후에 대한 독성치는 모두 무독한 것으로 판명되었다.
        4,000원
        8.
        2015.09 서비스 종료(열람 제한)
        Telomeres at the end of the eukaryotic chromosomes consist of tandem repeats of (TTAGGG)n DNA sequence and shelter in protein complex. Telomeres have the essential functions in chromosome stability and genome integrity and are hence related to cell senescence and cancer. Stripped, Black and White Cattle (Endangered Korean Native Cattle) characterized by their coat color, live in the Korean peninsula. However, they are endangered, with very small populations remaining. To investigate the karyotypic pattern of chromosome and also to quantify the amount of telomeric DNA was carried out from the traditional Korean beef cattle species, HanWoo and endangered cattle bull. We quantified the amount of telomeric DNA by the Quantitative-Fluorescence in situ Hybridization (Q-FISH) technique using the telomeric DNA probe and chromosome analysis of lymphocytes was carried out using GTG-banding in 9 bull at age of 18 months. In results, we found that the normal (60, XY) male karyotype were detected in metaphase chromosomes from korean native cattle including Hanwoo, Stripped, Black and White cattle, respectively. In addition, there were no significant differences in the relative amount of telomeric DNA among the korean cattle bull. However, the relative amount of telomeric DNA of Hanwoo was slightly higher than that of White cattle. In conclusion, this study reported karytype and the amount of telomeric DNA which could serve as baseline information for comparison in conditions of physiological and health status of endangered Korean native cattle. Although we have no definitive explanations as to why this occurs, further investigations are needed to continue investigation of these animals throughout their life spans.
        10.
        2009.12 KCI 등재 서비스 종료(열람 제한)
        A resveratrol synthase (RS) gene was isolated from peanut (Arachis hypogaea, L. cv. Jinpoong) plants. This gene was placed under the control of the cauliflower mosaic virus 35S promoter (CaMV35S) and introduced into two Korean varieties of potato (Solanum tuberosum L. cvs. Jasim and Jowon) plants by Agrobacterium-mediated gene transfer. Putative transformants were screened by PCR with primers designed from CaMV 35S promoter, NOS terminator and RS gene. Most of selected transgenic potato plants showed the amplification of expected fragments by PCR of genomic DNA with gene-specific primers, while they were absent in untransformed control plants. Expression of the resveratrol synthase gene was also examined by northern blot analysis. The transformants showed a band which was lacking in the control plant, confirming that the introduced gene is transcribed into mRNA in the transformants. The strength of the band, which reflected the level of mRNA expression, differed among the individual transformants. Among the transformants obtained, the highest trans-resveratrol content in the transgenic young leaves of purple-fleshed "Jashim" was 2.11 μgg-1 fresh weight and that in the microtubers in vitro of purple fleshed "Jashim" was 8.31 μgg-1 fresh weight. This amount of resveratrol may have a positive biological effect on human health.
        11.
        2007.06 KCI 등재 서비스 종료(열람 제한)
        We performed field trials to assess levels of changes in intrinsic properties and resistance against soft rot of the potato cultivar ‘Irish Cobbler’ upon the introduction of the Shiva-1 gene. Each five lines, transformed with Shiva-1 gene controlled by the PAL5 promoter (P) and by the CaMV 35S promoter (E) were evaluated in the field. In based on evaluation of 10 defined morphological characteristics, all the transgenic clones of both lines proved to be true to type. When five agronomic characteristics were taken into account as well, all the transgenic lines except E8 were considered to be true to type. According to the result of northern blot analysis, seven (P1, P3, P4, P6, E10, E12, and E16) transgenic clones could be distinguished clearly from corresponding untransformed clones. But in three lines (P8, E5, and E8), no hybridization signal was detected. There seems to be positive correlation between the levels of resistance to soft rot and the transgenic expression at mRNA levels in P lines. But in the case of E lines, however, there doesn’t seem to be any correlation between the levels of disease resistance and mRNA expression