• Proceedings of the Korean Society of Applied Pharmacology
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• 1993.04a
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• pp.162-162
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• 1993

제 3세대 platinum complex인 SKI 2053R에 의한 Salmonella typhimurium의 복귀변이빈도, CHL세포(Chinese Hamster Lung)에 대한 염색체이상 유발율 및 ddY계 마우스에서의 골수분화세포에 대한 염색체이상유발로 기인한 소핵의 빈도수를 관찰하여 SKI 2053R의 유전독성을 평가하였다. Salmonella typhimurium를 이용한 복귀돌연변이시험에서 SKI 2053R은 매우 경미한 정도의 돌연변이 유발성을 가지는 것으로 판단되며, 균주 특이적 돌연변이 유발성으로 보아 염기쌍치환형의 돌연변이를 유발하는 것으로 사료되며 포유류배양세포를 이용한 염색체이상실험에서 대사 활성 부재 및 존재하의 모든 시험 농도에서 10％ 이상의 염색체이상을 가진 세포가 관찰되었으며 염색체 상의 종류로는 염색분체형 교환 (cse)이 가장 많이 관찰되었다. 설치류를 이용한 소헥시험에서는 ddY계 마우스 골수세포의 분화과정에서 염색체이상을 유발하며, 다염성적혈구의 정염성적혈구에 대한 출현비율이 감소하는 결과로 볼때 방추체기능의 저해를 일으키는 것으로 판단된다. 그러므로 본 시험조건데 있어서 SKI 2053R은 소핵을 유발하는 물질로 결론지었다.

• Proceedings of the Korean Society of Fisheries Technology Conference
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• 2000.05a
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• pp.165-166
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• 2000

은어는 암컷의 성장이 수컷보다 빠르고, 성숙 시 수컷의 상품가치가 크게 하락하므로 실제 양식 현장에서는 전 암컷 종묘의 생산이 절실히 요구되고 있다(방 등, 1997). 호르몬에 의한 암컷 종묘의 생산방법이 연구되었으나 암컷 유도율이 매우 낮고, 성전환된 수컷을 친어로 이용하여 단순교배에 의한 전 암컷 집단을 생산하는 유전학적 성전환 방법이 아직 확립되지 않았다(고교, 1993).유전학적 성전환을 위해 웅성호르몬 처리에 의한 phenotypic male (genetic female)을 생산하여야 하는데 본 종은 수컷으로의 성전환이 매우 어려운 종으로 알려지고 있다. 따라서 정확한 성전환 처리 방법을 구명하기 위해서 우선 성 분화 과정을 조직학적 방법으로 조사하는 것이 필요하다. (중략)

• The Korean Journal of Zoology
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• v.30 no.3
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• pp.261-271
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• 1987

계배 중추신경계의 분화에 따른 단백질 합성 양상을 SDS-PAGE와 2차원 전기영동으로 분석하였다. 약 24∼26개의 band가 densitomete떼 의해 기록되었고, 주요 band들의 분자량은 90K에서 lIft 범위에 분포하였다. 대뇌, 시엽 및 소뇌에서 가장 현저한 band는 분자량이 44.7K로 actin으로 사료되었다. 대뇌의 85.5광 및 47.9K, 시엽의 85.5K, 71.6K 및 34.9K 소뇌의 47.9K 및 34.9K band들은 부화전까지 는 증가하다가 부화후 감소하였다. 기록된 약 300개의 polypeptide중 약 9%가 분화가 진행됨에 따라 그들의 합성율에 변화를 보였으며, 대뇌의 spot 19(Mr, 63K; pl, 6.95)와 소뇌의 spot 22(Mr, 43K; pI, 6.5) 는 부화후 4일배에서 새로이 합성되었다.

• Journal of Plant Biotechnology
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• v.45 no.2
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• pp.131-139
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• 2018

We examined the effect of carbon sources on the regeneration and ex vitro acclimatization of Lycopus lucidus Turcz. ex Benth. Plantlets were regenerated on the 1/2MS medium supplemented with different concentrations (3 ~ 10%) of sucrose and glucose. The sucrose concentrations of 3% and 5% that were supplied enhanced shoot multiplication and rooting but hampered high concentration growth (including the length of the shoot and root). During ex vitro acclimatization, the tuberization of the root, the root length, the shoot length and the survival rate of Lycopus lucidus plantlets grown using 3% and 5% sucrose were found to be better than the other carbon sources and concentrations. Thus a sucrose concentration of 3% and 5% in the 1/2MS medium appeared to be better for both in vitro growth and ex vitro acclimatization of Lycopus lucidus.

• Journal of Korean Society of Forest Science
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• v.84 no.2
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• pp.145-150
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• 1995

A plant regeneration system using shoot basal callus of in vitro cultured black locust(Robinia pseudoacacia L.) was established. Shoot basal callus was induced on MS medium supplemented with BA, or NAA, and mere more proliferated on BA containing medium than NAA containing medium at both light and dark conditions. Shoot basal callus was induced during shoot multiplication procedure. Two types of callus, green colored callus and whitish-yellow colored callus, were cultured on mMS medium containing 2.0 mg/l BA and 0.5 mg/l NAA. Green colored callus showed the shoot regeneration ability while whitish-yellow callus failed to regenerate shoot and died. Regenerated shoot were rooted on hormone-free ${\frac{1}{2}}MS$ medium within 2 weeks.

• KOREAN JOURNAL OF CROP SCIENCE
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• v.42 no.3
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• pp.306-316
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• 1997

Embryogenic calli were induced from mature seed scutella of anther culture-derived rice variety Zhonghua 8. Cell suspension cultures were initiated from friable embryogenic calli and utilized as source material for protoplast isolation. Generally, the older and finer cell suspensions gave higher protoplast yields than younger suspension cultures. Protoplasts exhibited sustained cell division and formed microcalli when cultured in KPR medium supplemented with 0.5 mg $l^{-1}$ 2,4-D, 1.0 mg $l^{-1}$ NAA and 0.5 mg $l^{-1}$ zeatin using the agarose embedding procedure without feeder cells. Protoplast plating efficiencies ranged from 0.20 to 0.54％. Microcalli were transferred to MS medium supplemented with 2.0 mg $l^{-1}$ kinetin and 0.5mg $l^{-1}$ NAA for plant regeneration. The regeneration frequencies were 2 to 12％, depending on the cell suspension lines of Zhonghua 8. The plants were transferred to the glasshouse and were fertile.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.32 no.1
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• pp.117-120
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• 1999

High yields of protoplasts were obtained following enzymatic digestion of the vagetative thalli of marine green alga Monostroma nitidum. The enzyme mixtures containing $4\%$ Cellulase R-10+$3\%$ Macerozyme R-10+$3\%$ Abalone acetone power produced $4.41\times10^6$ protoplasts per 300 mg of fresh tissue. The highest yield of protoplasts was obtained by 270 minutes treatment of the thalli in enzyme solution. Freshly isolated protoplasts were spherical in shape and ranged between $13\~33\mu$m in diameter. The high efficiency of differentiation were obtained by incubating freshly isolated protoplasts in 0.4 M mannitol f/2 medium for 7 days and then transferring to 0.2 M mannitol f/2 medium. Protoplasts began to form new cell walls three days after initial culture and began to germinate after 10 days, and then form a leafy thallus after further culture in f/2 medium. The addition of antibiotics in media inhibited the differentiation of protoplasts in culture.

• Korean Journal of Plant Tissue Culture
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• v.27 no.3
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• pp.197-202
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• 2000

The effect of cultural media and growth regulators on multiple plant regeneration from leaf explants of Heloniopsis orientalis (Thunb.) Tanaka was evaluated. The highest percentage of shoot and root formation were 20 and 30% on MS medium treated at 3.0 mg $l^{-1}$ of zeatin, respectively. Also 67 and 33% of high shoot formation appeared on 1/2 MS and 5 culture medium treated at zeatin 1.0 and 3.0 mg $l^{-1}$ respectively. With MS treated at 0.5 mg $l^{-1}$ of 2,4-D 1/2 MS and B5 culture media treated at each 1.0 and 3.0 mg $l^{-1}$ of zeatin the highest ratios of plant produced were 100, 280 and 310 % respectively relative to the other treatments. Generally, there was highest possibility for multiple propagation of Heloniopsis orientalis (Thunb.) C. Tanaka with B5 culture media supplemented 3.0 mg $l^{-1}$ of zeatin.

• Horticultural Science & Technology
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• v.33 no.1
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• pp.24-30
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• 2015

This study was conducted to select proper light intensity, pot media, and fertilization level for potted Hepatica asiatica Nakai native to Korea. The plants were grown under various light intensities (shading rate, 52, 82, 90, 97%) imposed by shading net. Plants grown with 52% shading showed a low survival rate (65%). Survival rate increased as shading increased, with over 80% survival in shading above 90%. Growth indexes such as fresh weight and leaf number did not show any significant difference between shading treatments. Plants grown in a soil mixture of decomposed granite:fertilizer-amended media:Kanumatsuchi (60:10:30, v/v/v) or river sand:fertilizer-amended media:bark (50:20:30) showed over 85% survival. However, plants grown in a soil mixture of river sand:fertilizer-amended media:Kanumatsuchi (50:30:20) or upland:river sand (40:60) showed very low survival, below 60%. Leaf number and plant height were the highest in a soil mixture of decomposed granite:fertilizer-amended media:Kanumatsuchi (60:10:30) as well. To select a proper fertilization level for H. asiatica, hyponex solution diluted 1,000- or 2,000-fold were applied weekly or biweekly. The survival rate was lowest at weekly application with 1,000-fold diluted solution, and no significant difference was observed between other treatments. In conclusion, H. asiatica exhibits preferences for very low light intensity and soil with air permeability, and is adaptable to a broad range of fertilization levels.

• Korean Journal of Medicinal Crop Science
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• v.10 no.3
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• pp.217-221
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• 2002

Callus induction and embryogenesis were studied in three different genotypes of Acanthopanax senticosus, to develop a protocol for somatic embryogenesis and acclimatization. Young leaf, stem, node, petiole, peduncle, flower and root explants were collected from 3-year old trees of A. senticosus accessions (Korea, Russia and Japan). Callus was obtained from all cultured explants but showed the higher rate of callus formation in flower cultured. For the three A. senticosus accessions, callus was well formd on MS media containing 2mg/ l of 2,4-D and 2mg/ l of TDZ, 4mg/ l of 2,4-D and 1mg/ l of TDZ than other treatments. For three A. senticosus accessions, when callus transferred to MS medium with 2,4-D, embryogenic cell formed. For A. senticosus accessions Korea, embryogenic cells were obtained on callus induced from petiole, stem, node and root explants, and induction rate was lower than 3%. 200mg of embryogenic callus was transferred to MS free liquid medium and somatic embryos of heart stage were obtained after 45days of culture. When somatic embryo of germination stage were transferred to solid medium, most of the embryos were regenerated into plantlets on 1/4 MS medium. Normal plants with both shoots and roots were transferred to greenhouse soil and were successfully acclimatized.