• Molecular & Cellular Toxicology
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• v.3 no.sup4
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• pp.38-38
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• 2007

• Journal of Life Science
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• v.3 no.1
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• pp.18-24
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• 1993

毒에는 비소, 수은처럼 無機毒과 식물, 동물성의 有機毒이 있으며, 有機毒에는 알카로이드, 배당체, 단백毒 등이 있다. 식물의 알카로이드毒을 중심으로 이것이 어떻게 藥物로서 이용되어 왔는지에 관해 다루었다. Morphine의 발견을 계기로 여러 종류의 식물 알카로이드가 계속 분리되었으며, 藥의 탐구의 새로운 길을 열었다. Morphine은 우수한 진통의 효과를 가졌지만, 흡수억제 및 습관성의 결점을 가지고 있다. 또, Areca catechu L. 의 종자(빈낭자)에는arecoline, arecaidine 등의 piperidine系의 알카로이드를 함유하고 있다. Arecoline은 副交感神經 흥분작용이 있고, 침분비 촉진, 比瀉 등으로 사용되어 왔지만, 지금은 그 용도가 적어졌다. 그리고 화살독이 되는 毒을 약물로 사용한 것은 Acontium屬 식물이 유일한 것이다. 중국에서는 이를 身體四肢關節의 마비, 疼痛의 회복, 대사기능실조의 회복 등의 목적으로 사용해 왔다.

• Journal of Life Science
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• v.4 no.2
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• pp.60-63
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• 1994

Protein A는 Jensen법에 의하여 Staphylococcus aureus Cowan type 1 (SCI)주의 가열균 체에서 추출한 단백으로서 최근에는 lysostaphin-chromatography 방법으로 순수분리할 수 있는 natural protein이다. Protein A를 다량 함유한 SCI은 혈청중의 IgG를 흡착하므로 혈청 중에 IgG를 제거할 목적으로 사용할 수 있다. 본고에서는 protein A가 면양적혈구로 면역한 가토혈청의 적혈구 응집소가 및 용혈소가에 미치는 영향을 기술하였다.

• Journal of Sericultural and Entomological Science
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• v.52 no.1
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• pp.25-32
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• 2014

We produced the transgenic silkworm that expressed the enhanced blue fluorescent protein (EBFP) in the cocoon of silkworms. The EBFP fusion protein, each with N- and C-terminal sequences of the fibroin H-chain, was designed to be secreted into the lumen of the posterior silk glands. The expression of the EBFP/H-chain fusion gene was regulated by the fibroin H-chain promoter. The use of the $3{\times}P3$-driven DsRed2 cDNA as a marker allowed us to rapidly distinguish transgenic silkworm. A mixture of the donor and helper vector was micro-injected into 300 eggs of silkworms, Baegokjam. We obtained 5 broods. The cocoon displayed blue fluorescence, proving that the fusion protein was present in the cocoon. Also, the presence of fusion proteins in cocoons was demonstrated by SDS-PAGE and western blot analysis. Accordingly, we suggest that the EBFP fluorescence silk will enable the production of the silk-based biomaterials.

• Proceedings of the Korean Society of Applied Pharmacology
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• 1994.04a
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• pp.204-204
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• 1994

Ganoderma lucidum의 균사체로 부터 얻어진 G009의 이화학적 특성을 규명하였다. G009는 넓은 범위의 분자량 분포를 가지고 있는 다당체로 분자량 9.4kD의 물질이 주성분이었다 G009의 당의 함량은 약 70%이었고 단백질은 약 2.4%인 것으로 나타났다. G009의 주요 구성당은 glucose, xylose, mannose, galactose 등이었고, glycine, leucine, alanine, valine, isoleucine, proline 등 17종의 아미노산이 확인되었다. 유기원소 분석 결과 G009는 탄소 약 40%, 수소 5.7%, 질소 1.8%의 구성비를 보였으며, 무기원소 분석결과 Ca, Mg, Zn 등이 확인되었다. 이상의 결과로 부터 G009는 9.4 kD의 분자량을 갖는 단백다당체를 주성분으로 하는 당화합물로 추정된다.

• Proceedings of the Korean Society of Applied Pharmacology
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• 1992.05a
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• pp.24-24
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• 1992

담자균류인 말징버섯 Calvatia craniformis의 성분을 연구하기 위하여 그 균사체를 액내 배양하여 열수 추출한 후 ethanol로 침전시켜 단백 결합 다당체를 분리하였다. 이 성분을 DEAE-cellulose ion exchange, Sepharose CL-4B gel filtration 그리고 Concanavalin A Sepharose 4B affinity chromatography를 실시하여 총 6가지 분획(Fr. A~F)으로 정제하였다. 이들을 각각 10또는 20mg/kg/day의 용량으로 마우스의 복강에 투여하였을때, 육종 180 고형암에 디하여 41.7~74.1%의 종양억제율을 나타내었고 $\beta$-형 다당체인 Fr. F가 종양 억제율이 가장 높았다. 화학 분석에 의해, 이 성분은 4기의 단당 mannose, xylose, galactose, glucose로 구성된 87.2% polysaccharide와 1.9%의 Protein 및 1.3%의 hexosamine 함유하고 있고 이 성분의 분자량은 5.5 $\times$ $10^4$ dalton이었다. 이 성분을 calvatan이라 명명 하였다.

• Tuberculosis and Respiratory Diseases
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• v.39 no.3
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• pp.242-247
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• 1992

Background: The ability to precisely measure specific mRNA levels by hybridization to complementary DNA probes is an important tool for analyzing the regulation of gene expression. Surfactant proteins have important roles in regulating surfactant metabolism as well as in determing its physical properties. Method: The complete coding regions for rat surfactant protein complementary DNA of surfactant protein B were subcloned into pGem 3Z or 4Z such that either antisense or sense transcripts were obtained by using SP 6 RNA polymerase. Surfactant protein B mRNA was measured by filter hybridization. Results: Equation of standard curve between counts per minute (Y) and surfactant protein B mRNA transcript input (X) was Y=2034.9 X+159.1. Correlation coefficient was 1.0. Couclusions: Filter hybridization assay is suited to situation when rapid, accurate quantitation of multiple samples is required.

• Journal of Food Hygiene and Safety
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• v.4 no.2
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• pp.109-118
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• 1989

To find antitumor components in the cultured mycelia of Lepiota procera, the proteinpolysaccharide obtained from the mycelia was subjected to DEAE - Sephadex A-50 column chromatography and Sepharose-4B gel filtration. Of the fractions, the purified Fraction C1 was named lepiotan and examined for antitumor activity against the solid form of sarcoma 180 in ICR mice. The inhibition ratio of lepiotan was 64% at the dose of 10 mg/kg/day for 10days. The chemical analysis of lepiotan showed 60% polysaccharide and 21 % protein. The polysaccharide moiety was found to be a heteromannoglucan which consisted of 46.3% glucose, 40.2% mannose and 11.0% fucose. When the antitumor component, Fraction A, was examined for immunopotentiation activity, it was found to increase the number of plaques in hemolytic plaque assay and to restore the immunity in the tumor-bearing mice up to 89.7% of the normal level. Also the antitumor acitivity was suppressed by the treatment with carrageenan, an antimacrophage agent. These results indicate that the antitumor activity was exerted through immunopotentiation, but not through direct cytotoxicity against the tumor.

• Journal of Plant Biology
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• v.35 no.3
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• pp.219-227
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• 1992

Formation, cellular distribution and structural changes of storage lipid, and active site and cellular localization of lipase in endosperms and cotyledons of lipid-rich seeds such as Helianthus annuus, Ricinus communis and Pinus koraiensis, and in those of starch-rich seeds such as Pisum sativum and Zea mays were investigated in relation to the seed development by cytochemical methods. In endosperms and storage cotyledons of lipid- and starch-rich seeds after seed-gathering, there were widely distributed storage material which was composed of spherical protein bodies, spherosomes, and starch granules. But cellular organelles were hardly observed in the cytoplasm. Staining pattern of vesicles released from SER, and of low electron dense membraneous granules, which were perhaps at an early stage of spherosomes, were the same as in the spherosome. Electrondense granules released from RER were observed in the vicinity of plasma membrane. As a result of lipid staining, the spherosomes were more electron dense and were uniform as compared with the protein matrix within the protein body and cytoplasmic proteinaceous granules. The major component of the spherosome was determinated to be lipid. Spherosomes and vesicles containing SER-released materials showed the same as in the electron density. Lipase activity was especially strong in the inner region and on the surface of decomposed spherosomes and near the plasma membrane.mbrane.

• The Korean Journal of Mycology
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• v.24 no.2 s.77
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• pp.142-148
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• 1996

To find compounds of immunomodulating and anti-allergic function, effects of protein-bound polysaccharides extracted from Phellinus igniarius (PI), Fomitella fraxinea (FF) and Agrocybe cylindracea (AC) on hemagglutinin titer (HA), hemolysin titer (HY), plaque forming cell (PFC), rosette forming cell (RFC) and phagocytosis were investigated in BALB/C mice. The oral administration of the protein-bound polysaccharides of PI, FF and AC for 10 days resulted in the enhanced phagocytic activity of peritoneal exudate cells (PEC), spleen cells (SC) and blood lymphocyte cells (BLC). Moreover, PI showed the activating effect on the phagocytosis of PEC and AC in SC. In the experiment of PFC and RFC, the results of the experimental group which was given each samples as compared to the control group, showed the enhanced level of activity such as PI 130%, FF 90% and AC 70%. Generally, HY and HA showed from ten to hundred times of level in each sample groups, as compared to the control group.