• 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.

• Journal of Plant Biology
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• 제33권1호
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• pp.49-54
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• 1990

Chlorella cells were cultured with M4N media treated with glucose (5 mM) sucrose (10 mM) and raffinose (30 mM). Phospholipids and their fatty acid compositions were analyzed in the chloroplast isolated from cultured Chlorella cells. Growth rate was prominently raised in the treatment with raffinose. Glucose was the most excellent carbon source in the biosynthesis of total lipid, phosphatidylcholine(PC), phosphatidylethanolamine(PE), phosphatidylinositol(PI) of the chloroplast. Also, the major fatty acids were palmitic, linoleic and linolenic acid during the biosynthesis of phospholipid in the control and in the treatment with carbon sources.

• 식물조직배양학회지
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• 제25권1호
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• pp.7-11
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• 1998

Streptanthus 조직 배양 세포를 사용하여 사부를 순수분리 시키고, 분리된 사부에서 사부 하적에 대한 기작을 규명하기 위해 다음 연구를 하였다. 유조직 세포는 0.2% macerase 와 0.03% cellulase의 가수분해 효소로 처리하여 원형질체를 얻었고, 분화된 세포에서는 0.03% cellulase + 0.02% pectinase + 0.2% macerase + 0.025% rohamet PC로 가수분해시켜서 순수한 사부 세포와 사부 원형질체와 반세포의 원형질체를 분리하였다. 분리된 유조직 세포와 반세포의 원형질체에서는 단당류인 포도당을 수송시키나, 설탕은 수송시키지 못했다. 반면 분리된 사부 세포는 설탕을 능동수송 시키나 포도당은 수송시키지 못했다. 이는 설탕의 사부 하적은 반세포 없이도 가능하며, 반세포는 설탕 운반체가 없어서 설탕을 직접 수송할 수 있는 능력이 없다는 것을 보여주는 것이다. 그리고 사부 세포에서 설탕의 수송은 에너지대사에 의존하는 능동수송으로 나타났다.

• 한국식물병리학회:학술대회논문집
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• 한국식물병리학회 2005년도 한국식물병리학회 임시총회 및 춘계학술발표회
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• pp.92.1-92.1
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• 2005

• 한국식물생명공학회:학술대회논문집
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• 한국식물생명공학회 2002년도 춘계학술대회
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• pp.146-146
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• 2002

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2001년도 추계정기 학술발표회 초록집
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• pp.71-71
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• 2001

• Journal of Plant Biotechnology
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• 제1권1호
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• pp.61-68
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• 1999

Rapid accumulation of reactive oxygen species (ROS) and their toxic reaction products with lipids and proteins significantly contributes to the damage of crop plants under biotic and abiotic stresses. We have identified several stress activated alfalfa genes, including the gene of the alfalfa ferritin and a novel NADPH-dependent aldose/aldehyde reductase enzyme. Transgenic tobacco plants that synthesize alfalfa ferritin in vegetative tissues-either in its processed form in chloroplast or in the cytoplasmic non-processed form-retained photosynthetic function upon free radical toxicity generated by paraquat treatment and exhibited tolerance to necrotic damage caused by viral and fungal infections. We propose that by sequestering intracellular iron involved in generation of the very reactive hydroxyl radicals through a Fenton reaction, ferritin protects plant cells from oxidative damage. Our preliminary results with the other stress-inducable alfalfa gene (a NADPH-dependent aldo-keto reductase) indicate, that the encoded enzyme may play role in the stress response of the plant cells. These studies reveal new pathways in plants that can contribute to the increased stress resistance with a potential use in crop improvement.

• Journal of Plant Biology
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• 제39권2호
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• pp.107-112
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• 1996

To study the compensatory aspect of putrescine biosynthetic enzyme n tobacco suspension cultured cells, we examined the contents of the cellular polyamines and the activities of arginine decarboxylase (ADC, EC 4.1.1.19) and ornithine decarboxylase (ODC, EC 4.1.1.17) in the tobacco suspension cells treated with $\alpha$-difluoromethyl arginine (DFMA) or $\alpha$-difluoromethyl ornithine (DFMO). In the untreated cells, the content of the cellular putrescine was decreased during the first 3 hours and then subsequently increased. However, the content of the cellular spermidine and spermine remained constant during the incubation time. While ADC activity increased after 6 hours, ODC activity decreased following the rapid increase until 6 hours. DFMA induced the decrease in the contents of putrescine and spermidine, and the increase in that of spermine. It also caused the inhibition of ADC and ODC activities throughout the incubation time. DFMO produced the stimulation of ADC activity about 2 times of untreated cells and the decrease in the content of putrescine about 50% of them at 12 hour. The application of putrescine or cycloheximide prevented the increase of ADC activity by DFMO but that of actinomycin-D did not show any detectable effect. The stimulation of ADC activity by DFMO in tobacco suspension cultured cells was probably due to the enhancement of de novo synthesis for ADC protein, which might be regulated in the translation step by the content of the cellular putrescine.

• Journal of Plant Biology
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• 제35권4호
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• pp.359-364
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• 1992

은행나무 유식물에서 유관속형성층은 성숙한 잎을 포함하여 5장의 잎이 자라고 있을 때 제일 먼저 자엽절에서 발생되고, 이어서 지하기관인 배축-뿌리로 그리고 지상부의 줄기로 즉, 양쪽 방향으로 분화되었다. 접선면 관찰에서 자엽절의 유관속형성층 발생유형은 줄기와 같고 뿌리와는 다르다. 자엽절에서 초기의 전형성층은 동일형의 세포로 구성된 균일구조를 이루고, 발생이 진행됨에 따라 신장생장을 하는 일부세포와 횡단분열을 하는 나머지 세포의 두 종류 세포로 된 비균의 구조로 전환된다. 신장을 하는 긴 세포로부터 유관속형성층의 방추형 시원세포가 그리고 횡단분열을 하는 짧은 세포로부터 방사조직 시원세포가 기원된다. 그러므로 방추된 시원세포는 심한 관입생장을 거쳐서 발생된다.

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2018년도 춘계학술발표회
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• pp.92-92
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• 2018

Solanum nigrum L. (SNL), generally known as black nightshade, is traditionally used as medicine to reduce inflammation caused by several diseases like asthma, chronic bronchitis and liver cirrhosis. In this study, anti-inflammatory effects of SNL extract were examined and possible molecular mechanisms of the anti-inflammatory effects were investigated. The inhibitory effects of SNL extract on nitric oxide (NO), pro-inflammatory cytokines ($TNF-{\alpha}$, IL-6) and Matrix metallopeptidase 9 (MMP-9) productions were dissected using lipopolysaccharide (LPS) stimulated murine macrophage-like cell line Raw264.7 cells and human microglial cell line BV2 cells. We further investigated whether SNL extract could suppress the phosphorylation of ERK1/2, JNK, and p38 and the nuclear expression of nuclear factor $NF-{\kappa}B$ p65 in LPS-stimulated Raw264.7 cells and BV2 cells. As a result, we showed that the SNL extract significantly decreased the production of pro-inflammatory cytokines, NO, and MMP-9. In addition, the SNL strongly inhibited the phosphorylation of ERK1/2, JNK, p38 and nuclear translocation of $NF-{\kappa}B$ p65 in activated cells. We confirmed that the extracts of SNL effectively inhibits the anti-inflammatory and may be used as a therapeutic to various inflammatory diseases.