• 제목/요약/키워드: plant cultured cells

검색결과 271건 처리시간 0.025초

주목 세포배양에 의한 Taxoll 생산 1.주목 부위 및 서식 고도별 Taxol 함량 및 세포주 유도에 관한 연구 (Taxol Production in Taxus sap. Cell Cultures 1. Studies on Taxol Content in Yew Trees and Cultured Plant Cells)

  • 강인선;전정욱
    • KSBB Journal
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    • 제9권3호
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    • pp.299-305
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    • 1994
  • 15년생 주목의 부위별 단위 질량당 taxal 함량은 줄기수피, 뿌리수피, 잎 그리고 종자의 순으로 높았 고, 종자에서는 종피 (seed caa t), 배 (embrya) 그리 고 배유(endasperm)의 순으로 taxal 함량이 높게 측정되었다. 15년생 주목 1그루로부터 이론적으로 얻을 수 있는 taxal의 양은 1.68g이었는데 잎, 줄기 수피, 뿌리수피, 종자로부터 각각 48.0, 23.8, 27.9 빛 0.4%씩 얻을 수 있었다. 주목의 taxal 함량은 서식 고도에 따라 차이가 있었다. 해발 1000m 이상 의 높은 고도에서 서식하는 주목의 taxal 함량이 낮은 고도(600-800m)에서 서식하는 주목보다 높았다. 주목 세포배양 결과 callus 및 현탁배양 세포에 셔 taxal이 검출되었으며 함량은 서l포의 상태 및 주 목의 종류에 따라 서로 차이가 있었다. 이라한 결과로 주목 세포배양에 의한 taxal 생산의 가능성을 확 인할 수 있었다.

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Filter membrane과 feeder세포를 이용한 벼의 원형질체 배양 (The Filter Membrane Culture Procedure with Feeder Cells in Rice Protoplast Culture)

  • LEE, Sung-Ho;SHON, Young Geol;Lee, Soo In;DAVEY Micheal R.;COCKING Edward C.;CHO, Moo Je
    • 식물조직배양학회지
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    • 제24권5호
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    • pp.295-303
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    • 1997
  • Japonica 벼 품종 Taipei 309 성숙 종자의 배반에서 유도된 캘러스로부터 유기 시킨 세포 현탁 배양체에서 원형질체를 분리하여 filter membrane과 feeder 세포를 이용한 여러가지 조건에서 배양하였다. 이러한 조건들은 gelling agents, feeder 세포와 원형질체 밀도, feeder 세포의 종류 및 heat shock 처리 등이며 이들이 filter membrane 배양 방법에서 원형질체 평판 효율에 미치는 효과들을 조사하였다. 원형질체 평판 효율은, Lolium multiflorum을 feeder 세포로 사용하고 (10 mL의 원형질체 배양 배지당 0.5 mL pcv) 원형질체를 mL 당 $5\;\times\;10^{5}$개로 하여 Sea Plague agarose 배지에 원형질체를 배양 했을때 최고치를 얻었다. 원형질체에 heat shock 처리를 했을 때 원형질체 평판 효율은 변화가 없었다. carbohydrate source로서 sucrose로서 sucrose 대신에 maltose를 사용했을 때 식물체 재분화율이 높았으며 원형질체로부터 재분화된 이들 식물체들은 임성을 나타내었다.

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Chlorella의 생리적, 생화학적 제활성에 미치는${\gamma}$-선의 영향

  • 이영록
    • Journal of Plant Biology
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    • 제7권3호
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    • pp.9-14
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    • 1964
  • The sensitivities of Chlorella ellipsoidea to ${\gamma}$-ray from Cobalt-60 were determined by measuring the photosynthetic and respiratory activities and the changes in phosphate contents in various fractions of the irradited cells, which were further grown in a standard medium after irradiation, were compared to those of non-irradiated normal cells. The photosynthetic and repiratory activities of the cells were almost inversely proportional to the dose of ${\gamma}$-ray irradiated and the photosynthetic activity was more sensitive than the respiratory activity of the cells. The most sensitive to ${\gamma}$-ray was growth activity, followed by photosynthesis, exogenous and endogenous respirations of the cells in decreasing order. Chlorella cells were so resistant to ${\gamma}$-ray comapred with other organisms that about 280,000 r dose of ${\gamma}$-ray irradiaton was necessary to reduce as much as half the subsequent photosynthetic activity. When the irradiated algae were further cultured in a standard medium, the phosphate contents in the fraction of DNA, RNA and phosphoprotein decreased considerably compared with those of non-irradiated normal cells, while the phosphate contents in the fraction of polyphosphates increased than those of control. Therefore, it was deduced that ${\gamma}$-ray inhibited the synthesis of DNA from polyphosphates, that the growth of Chlorella cells were consequently retarded.

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콩 원형질체내로의 담배 엽록체 이입 (Incorporation of Tobacco Chloroplasts into Soybean Protoplasts)

  • 차현철
    • Journal of Plant Biology
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    • 제25권4호
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    • pp.181-188
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    • 1982
  • Chloroplasts isolated from tobacco (Nicotiana tabacum L. cv. Virginia 115) leaves have been transferred into protoplasts of soybean (Glycine max Merr. cv. Jangyeop) suspension-cultured cells with the help of polyethylene glycol (PEG). The increased yield in protoplasts of chloroplast uptake was depended upon the concentration of both PEG 4,000 and PEG 6,000. The highest yield(36%) occurred at 50% of both PEG, and the yield was decreased above this concentration. The rate of uptake with the incubation time was highest at one hour, then decreased. The process of the chloroplast uptake into the protoplasts was similar with that of a protoplast fusion, except forming invagination during uptake.

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건조, 염분 및 탕의 처리가 쇠비름(Portulaca oleracea L.) 배양세포의 재분화에 미치는 영향 (Effects of Dessication, Sucrose and Salt Stress on the Regeneration of Portulaca oleracea Cultured Cells)

  • 권순태;오세명
    • 식물조직배양학회지
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    • 제21권2호
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    • pp.117-121
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    • 1994
  • 쇠비름(portuaaca oleracea L.)의 줄기절편체로부터 캘러스유도를 위한 적정배지는 BAP 0.1 + 2,4-D 1.0 mg/L., 30g/L sucrose 및 10 g/L agar를 첨가한 MS배지로 나타났으며, 액체배양에 의한 세포의 증식에는 BAP 0.1 + 2,4-D 0.5mg/L가 함유된 MS배지가 효과적이었다. 장시간 건조처리는 세포는 활력과 재생 및 재분화율이 강하게 억제되나, 1시간 및 2시간동안의 단시간 건조처리한 세포의 재분화율은 각각 83및 80%로 나타나나 무처리 61%에 비해 높았다. 0.6% NaCl의 2일간 전처리는 세포의 재분화율에는 영향을 미치지 않으나, 세포활력 및 재생률에는 억제작용을 나타내었다. Sucrose 70및 100 g/L를 전처리한 쇠비름세포의 재분화율은 각각 80및 81%로 무처리에 비해 높았다.

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토마토(Lycopersicon esculentum Mill) 현탁배양세포에서 Superoxide Dismutase 활성 (Superoxide Dismutase Activity in Suspension Cultured Cells of Tomato (Lycopersicon esculentum Mill))

  • 유순희;허경혜;권석윤;이행순;방재욱;곽상수
    • 식물조직배양학회지
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    • 제24권1호
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    • pp.57-61
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    • 1997
  • Superoxide dismutase (SOD) 고생산세포주로 선발된 토마토(Lycopersicun esculentum) 배양세포를 사용하여 현탁배양에 따른 SOD 활성과 isoenzyme변화를 조사하고 토마토 식물체의 것과 비교하였다. 현탁배양은 세포생중량 2 g을 1 mg/L 2,4-D, 30 g/L sucrose를 함유한 MS 배지 50 mL과 함께 mL flask에서 $25^{\circ}C$암상태로 배양(100 rpm)하였다. 세포생장은 계대배양후 20일에 최고점에 도달한 후, 급격히 감소하며 배양 후 23일부터 세포가 검게 변하였다. 세포 단위무게당 SOD활성(unit/g dry cell wt)은 배양 후 23일부터 증가하여 28일째에 최고활성(52,400 unit)을 나타낸 후 급격히 감소하였다. 세포 밖으로 분비되는 extracellular SOD활성은 배양 후 25일에 최고치(27,800 unit/so mL medium)를 나타낸 후 감소하였다. Flask 전체의 SOD활성은 배양 후 25일에 최대치(35,700 unit)를 나타내었으며 extracellular SOD 활성이 약 75%을 차지하였다. 토마토 배양세포에는 4개의 SOD isoenzyme이 존재하며, isoenzyme의 패턴변화는 세포생장에 따른 효소활성의 변화와 일치하였다. 토마토 식물체는 배양세포에 없는 CuZnSOD가 존재하며 배양세포와 식물체 조직사이에는 서로 다른 isoenzyme 패턴이 존재함을 알 수 있었다.

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Variation of Ginkgolides and Bilobalide Contents in Leaves and Cell Cultures of Ginkgo biloba L.

  • Park, Young-Goo;Kim, Su-Jung;Jung, Hee-Young;Kang, Young-Min;Kang, Seung-Mi;D. Theertha Prasad;Kim, Sun-Won;Park, Myung-Suk
    • Biotechnology and Bioprocess Engineering:BBE
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    • 제9권1호
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    • pp.35-40
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    • 2004
  • Ginkgolides (GK) and bilobalide are valuable compounds that belong to the lactone terpene. The contents of these metabolites were determined by HPLC from female and male tree of Ginkgo biloba L. The productivity of G. biloba cells was also compared with the corresponding individual trees. High variations in the ginkgolides and bilobalide were observed from different individuals, plant parts, and cultured cells. The ginkgolides and bilobalide contents were different depending on the plant parts. Callus was obtained from various plant tissues, and NAA was better at callogenesis than 2,4-D in both the female and male trees. The plants and their corresponding cells showed considerable variation in their ginkgolides and bilobalide concentrations. The ginkgolides and bilobalide contents were not correlated with the production between dominant trees and their corresponding cells. Light irradiation enhanced the production of GK-A and GK-B, however, the concentration of bilobalide decreased under dark conditions.

애기장대 줄기 조직배양에 있어서 식물생장조절제가 캘러스 형성과 기관분화에 미치는 영향 (Effect of Plant Growth Regulators on Calls Initiation and Organogenesis from Tissue Culture of Arabidopsis thaliana Stem)

  • 박정안;박종범
    • Journal of Plant Biotechnology
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    • 제30권3호
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    • pp.257-261
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    • 2003
  • This experiment was carried out to investigate the effects of plant growth regulators on the organogenesis from the tissue culture of Arabidopsis thaliana stem, and the origin of the callus development. When the stem segments were cultured on medium with 2mg/L IAA or NAA, adventitious roots and trichomes were differentiated after 11 days of culture. Callus vigorously formed on medium with 2/L2,4 after 7 days of culture, but adventitious roots and trichomes were not differentiated from callus after 10 days of culture. This results suggesting that picloram is very effective auxin for the callus formation and organogenesis. Callus weakly formed on 0.05mg/L kinetin, and formed on combination of auxins(2mg/L) with 0.05mg/L kinetin. But the effect of combination of auxins and kinetin the callus formation was less than 2,4-D or picloram alone. A histological examination of callus formed on picloram showed that phloram showed that phloem parenchyma cells were divided and enlarged after 2 days of culture. Cortex parenchyma cells were divided and meristematic nodules were developed from these cells after 4 days of culture. Finally, callus formed on outside of cortex and epidermis by division of meristematic nodules after 7 days of culture.

개 유선종양세포에 대한 자연살해세포 독성 (Cytotoxicity of natural killer cells on canine mammary carcinoma cells)

  • 정다운;변정수;구나연;정문희;김은희;김형석;조인수;송재영;현방훈;이지현
    • 대한수의학회지
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    • 제60권1호
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    • pp.25-32
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    • 2020
  • Natural killer (NK) cells play have a crucial role in the early phase of immune responses against various pathogens. We compared characteristics of canine NK cells against two canine mammary carcinoma cell lines, REM134 and CF41.Mg. REM134 showed higher expression of progesterone receptor, proliferative cell nuclear antigen, Ki67, multiple drug resistance, Bmi-1, c-myc, E-cadherin, and human epidermal growth factor receptor type-2 than that of CF41.Mg. For specific expansion and activation of NK cells, we isolated CD5 negative cells from canine peripheral blood mononuclear cells and co-cultured K562 cells in the presence of interleukin (IL)-2, IL-15, and IL-21 for 21 days. As a result, we found that expression markers of activated NK cells such as NKp30, NKp44, NKp46, NKG2D, CD244, perforin, granzyme B, and tumor necrosis factor alpha were highly upregulated. In addition, we found there was upregulated production of interferon gamma of activated NK cells against target cells such as REM134 and CF41.Mg. Specifically, we observed that cytotoxicity of NK cells against target cells was more sensitively reacted to CF41.Mg than REM134. Based on the results of this study, we recommend the development of an experimental application of CF41Mg, which has not been reported in canine mammary carcinoma research.