• 식물조직배양학회지
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• 제28권3호
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• pp.173-173
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• 2001

• Journal of Ginseng Research
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• 제13권1호
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• pp.79-83
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• 1989

인삼을 배배양하여 생장조절물질 IBA, GA 그리고 BA 처리에 따른 부정아 발생과 유묘 분화 그리고 화기출현 등을 조사하였던 바 결과를 요약하면 다음과 같다. 1. 부정아의 발생 및 유묘 분화는 IBA 1mg/l와 GA 5mg/l를 조합처리하였을 때 가장 양호하였다. 2. 부정아는 줄기 원기의 기능이 있어 분화하여 다량의 유직물이 되었다. 3. 부정아의 발생 형태는 배축부위에서 5~10회 정도가 윤생 또는 연속적으로 발생하였다. 4. 기내 화기 발생은 유묘가 분화되어야만 가능하였고 IBA, GA 그리고 BA를 각 3mg/l씩 조합처리하였을시 18.4%가 출현하였다.

• Journal of Forest and Environmental Science
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• 제34권6호
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• pp.435-450
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• 2018

Phenological events of four Rhododendron tree species (viz. R. arboreum, R. arboreum ssp. delavayi var. delavayi, R. barbatum and R. kesangiae) was monitored in temperate mixed broad-leaved forests of Arunachal Pradesh, India. Phenological events like flower bud formation, flowering, fruit setting, fruit maturing, seed dispersal, leaf bud formation, leaf flushing, and leaf shedding were recorded. Indices i.e., phenophase sequence index (PSI), active phenophasic period of the species (APS) and index of reproductive/vegetative activity (RVA) were also calculated. Present study revealed that bark consistency, growth form and leaf pattern of the studied species have showed variations among the species. Rhododendron species exhibited the phenological events overlapping with other phenophases. The peak flower bud formation was observed during the winter; R. arboreum ssp. delavayi var. delavayi start flowering from December, while the flowering in rest three species exhibited during February to April. Fruit setting occurred during summer to autumn while fruit maturation revealed peak during November. Leaf bud formation illustrated two peaks in April and May, leaf flushing exhibited peak in June, while leaf shedding peaked during October to November. Active phenophasic period of the species were found 12 months, which revealed that species engage in various phenophase activities throughout the year. Phenophase sequence index ranged between 0.8 to 0.9 (PSI ${\geq}0.6$), signifies that species have a sequential arrangement of phenophases. Index of reproductive/vegetative activity of the species exemplified >1, indicate that the reproductive phenophases were dominance over vegetative phenophases. The study have provided substantial insight on the life cycle events of Rhododendron species and ecological approaches for further scientific study with recent climate change and effective management and conservation.

• 식물조직배양학회지
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• 제25권1호
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• pp.63-68
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• 1998

정단 및 마디조직을 이용한 지황의 기내증식방안을 마련하기 위하여 일련의 시험을 실시하였다. 재생된 신초의 정단을 재배양하였을 경우 BA 5.0 mg/L에서 7.8개의 신초가 형성되었으며 투명화된 묘의 발생은 Gelrite 보다는 Bacto-agar 첨가구에서 감소하였다. 광도와 한천의 농도가 증가할수록 신초형성수 및 생장은 억제되었고 생체중 : 건물중의 비율도 감소하였다. 광도가 2000 lx일 때는 Bacto-agar 0.6-1.2%, 3,000 lx에서는 한천 0.4-0.6%에서 건전한 신초를 10개 이상 생산할 수 있었다. 활성탄소 0.1-0.3%첨가는 신초의 생장촉진과 뿌리형성에 촉진적으로 작용하였으며 투명화 발생률도 감소시켰으나 신초형성수는 현저히 감소시켰다. MS배지내 첨가되는 다량원소의 농도를 0.8-1.0배 하였을때 신초형성수 및 생장이 촉진되었다. 기관형성에 미치는 오옥신의 종류 및 농도별 효과를 조사한 결과 NAA나 IBA 보다는 IAA 0.3mg/L 와 BA 5.0mg/L를 혼합처리 하였을 때 증식률이 16배에 달하였다.

• 식물조직배양학회지
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• 제27권2호
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• pp.101-107
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• 2000

야콘의 절편체로부터 탈분화 조건을 규명하고, 잎의 절편체로부터 재분화 및 기내관아 형성조건을 조사하기 위하여 절편체를 배양하였다. 야콘의 잎으로부터 캘러스 형성에 MS배지가 $\frac{1}{2}$MS 및 B$_{5}$ 배지보다 효과적이었다. 잎, 엽병 및 측아 절편체로부터의 캘러스 형성률은 2,4-D 1.0, 2.0 mg/L에 kinetin 또는 BA를 0.2, 0.4 mg/L 혼용처리구가 NAA 1.0, 2.0 mg/L에 kinetin 또는 BA를 각각 0.2, 0.4 mg/L 혼용처리구보다 캘러스 형성률이 높았다. 잎으로부터 형성된 캘러스는 BA 1.0 mg/L처리에서 70%의 캘러스 증식율을 보였다. BA 1.0, 2.0 mg/L 처리 시 계대배양이 약 3~4개월 이상 지속되면서 캘러스 증식과 함께 재분율이 63% 이상 되었으나 kinetin 처리구에서는 관찰할 수 없었다. BA의 첨가에 의해 치상 후 약 3~4개월이 경과하면서 기내 소관아를 형성하기 시작하여 약 5~6개월 후에는 많은 양의 기내관아를 얻을 수 있었는데, BA를 5 mg/L 첨가한 배지에서 82.8%로써 기내소관아 형성률이 가장 높았으며, BA의 함량 증가에 따라 기내소관아 형성률도 증가하는 경향이었다. 그러나 BA의 함량이 5 mg/L이상 증가함에 따라 잎이 두꺼웠으며 줄기는 절간장이 짧고 분화 후에 생육을 지속하지 못하고 고사하였다. 한편, BA를 2 mg/L첨가하고 sucrose 첨가량을 다르게 하였을 경우, 5% sucrose를 첨가한 배지에서 소관아 형성률이 88.0% 로써 일반적으로 사용하는 3% 처리의 60.0%에 비하여 약28%증가하였다. 포장에서 수확한 관아의 액아와 기내관아의 액아의 조직학적 관찰 결과 크기에 차이가 있을 뿐 형태는 같은 것으로 관찰되었다.

• Journal of Plant Biotechnology
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• 제6권3호
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• pp.171-179
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• 2004

Hormonal requirements inducing different regeneration pathways with particular emphasis on somatic embryo-genesis in Alhagi graecorum were studied. While combination of 0.5 $\mu{M}$ 2,4-dichlorophenoxyacetic acid (2,4-D), 2.5 $\mu{M}$ 6-benzylaminopurine (BAP) and 5 $\mu{M}$ 1-naphthaleneacetic acid (NAA) in MS medium induced callus formation and callus maintenance from internodal explants, each alone or in combination with other induced distinct regeneration pathway. Adventitious bud formation was induced on MS medium supplemented with 2.5 $\mu{M}$ BAP. It was improved when 2.5 $\mu{M}$ BAP was used in combination with 5 $\mu{M}$ NAA. MS medium containing 0.5 $\mu{M}$ 2,4-D or 5 $\mu{M}$ NAA induced the formation of abnormal direct somatic embryos. While increase of 2,4-D concentration (1.125-9) resulted in the formation of viable embryogenic mass, increase of NAA did not change its effect. NAA should be used in combination with 2,4-D even at low concentration (0.5 $\mu{M}$) to form embryogenic mass. In A. gaecorum, the role of 2,4-D as trigger of somatic embryogenesis and BAP as trigger of adventitious bud formation was deduced, but for maximum yield certain auxin-cytokinin ratio should be applied. Embryogenic masses characterized by high water content, low peroxidase activity, and low number of peroxidase and glutamate oxaloacetate transaminase bands in comparison with calli obtained under conditions stimulating adventitious bud formation. The resulted differential gene expression, which could be detected by native-PAGE patterns, could be used as marker for organogenic pathway in A. graecorum.

• 원예과학기술지
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• 제32권3호
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• pp.382-389
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• 2014

Raphanus sativus L. cv. Taebaek, a efficiently microspore-derived embryo (MDE)-forming cultivar, and 'Chungwoon', a non-MDE-forming cultivar were selected as donor plants for isolated microspore culture. Radish flower bud of 2.0 (small, S), 4.0 (medium, M), and 6.0 (large, L) ${\pm}$ 0.5 mm in length were isolated to determine the temporal relationship between flower bud size and MED yield. Anatomical observations revealed no difference in the structure of the flower buds between the two cultivars. In both cultivars, the stigmas were much longer than the floral leaf in M-sized flower buds. The MDE yields for 'Taebaek' per petri dish were 6.6 and 1.3 for M- and L-sized of flower buds, respectively, but MDE formation was not induced in the S flower buds. On the other hand, 'Chungwoon' failed to form MDEs in all flower buds. The microspore density of 'Taebaek' was 1.3 times more than that of 'Chungwoon' for M sized flower buds. Of the M-sized buds from 'Taebaek' and 'Chungwoon', 92.1 and 81.6%, respectively, were in the late uninucleate microspore stage, which is characterized by the highest frequency of MDE formation. Anatomical observations of MDE formation revealed that the microspores were able to divide to form a primordium from which cell division took place continuously in the 'Teabeak' cultivar. However, the microspores of 'Chungwoon' failed to progress beyond the primodium stage, resulting in lack of MDE formation. By contrast, after the formation of the primordium, various developmental stages of embyos from microspore were observed in the 'Taebaek' cultivar. These results can be used to determine MDE forming potentials of radish cultivars.

• Journal of Plant Biotechnology
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• 제5권4호
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• pp.225-231
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• 2003

The hormonal requirement suiting micropropagation of Morus alba during any season throughout the year was studied. Sprouting frequency from axillary buds of M. alba was greatly influenced by the time of explant collection, the highest value was achieved when nodal explants were collected at the end of bud dormancy period (late in March) and cultured on Murashige and Skoog (MS) medium supplemented with low concentration (0.5 mg/L) of BAP, kinetin or IBA (85-68%). In addition, they showed higher axillary bud sprouting on growth-regulators-free medium (49%) than others collected in autumn or winter and cultured on medium supplemented with various growth regulators (47-48%). Regardless of that period, young explants with greenish buds collected in summer exhibiting high sprouting frequency (66%) on MS medium supplemented with 0.5 mg/L kinetin and 0.5 mg/L GA3. Shoot multiplication via adventitious bud formation was achieved when the nodal explants were cultured on MS medium supplemented with 2 mg/L BAP and 0.2 mg/L IBA. Further multiplication via nodal explants of in vitro grown shoots was obtained on MS medium supplemented with 0.5 mglL BAP and 0.5 mg/L GA3. While half strength MS medium supplemented with low concentration (0.5 mg/L) of IBA, IAA or 2,4-D stimulated adventitious root formation, IBA was the best. After transfer the plantlets to the soil, acclimatization for three weeks was essential prerequisite for survival in high frequency (92%). Peroxidase activity is related to break of bud dormancy where maximum enzyme activity was detected when the lateral buds were induced to commence growth under field condition (early in spring) or in vitro.

• 한국자원식물학회지
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• 제15권1호
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• pp.8-17
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• 2002

새 번식방법 개발을 위해 둥굴레 뿌리는 눈이 없어도 부정아가 발생된다는 점에 착안하여 뿌리길이와 굵기에 대한 부정아 발생에 관한 시험 연구를 한 결과는 다음과 같다. 1년차는 뿌리길이가 5cm 경우 66.5%지만 15cm에서는 113% 부정아 발생되었고, 뿌리의 굵기 5mm이하는 98.3%지만 10mm이상은 113.3%로 46.7% 차이를 보였다. 2년차는 부정아 생성률은 15cm에서는 1년차의 3배, 시험구 설치 당시 전혀 눈이 없는 상태에서 4배의 증식을 보였다. 용토는 일반토양 2.6배 보다 모래나 펄라이트가 3.1~3.3배 증식 되었다. 대량번식을 위한 가장 좋은 방법은 10mm 둥굴레 뿌리를 5cm로 절단하여 모래에 식재하는 방법으로 판단된다.

• 한국동물학회지
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• 제4권2호
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• pp.13-19
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• 1961

Free amino acids at five different developemntal stages (Gastrulation-Hatching -out stage) of Hynobius leechi BOULENGER were analyzed qualitatively by the use of paper paitition chromatography. It was found that the number of free amino acids increased as the development proceeded. The free amino acids identified at each stages are as follows : Gastrulation stage : Alaninie, Aspartic acid, Glutamin acid, Histidine, Methionine. Neural plate formation stage : Alanine , Aspartic acid, Glutamic acid, Glycine, Histidine, MEthionine, Phenylalanine, Proline, Serine, Trypotophan. Middle tail-bud stage : Alanine, Arginine, Asparagine,Aspartic acid, Citrulline, Glutamic acid, Glycine, Histidie,Hydroxyproline, Proline, Leucine, Methionine, Ornithine, Phenylalanine, Serine, Threonine, Tryptophan. Late tail-bud stage : Alanine, Arginine, Asparagine, Aspartic acid, Citrulline, Glutamic acid. Glycine, Histidine, Hydroxyproline, Leucine, Methionine, Ornithine, Phenylalanine, Proline, Serine, Threonine, Tryptophan, Valine. Hatching -out stage : the same with the late tail-bud stage. It seems probable that the metabolic systems of amino acids before and after the middle tail-bud stage are quite different from each other. Before the middle tail=-bud stage, the reaction system of amino acids is thought not to be completed while after that stage the system has been completed , because in the former period of the development , the number of freeamino acids increased rapidly with the development , and after that stage, there is practically no change in the number of free amino acids.