• 한국작물학회지
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• 제38권2호
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• pp.151-158
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• 1993

참당귀(Angelica gigas Nakai)의 재배에서 크게 문제가 되는 화성억제를 위해 온도, 일장 및 광도가 화아분화와 추대에 미치는 영향을 조사했으며, 관행재배와 화성을 추제시켜 재배생산된 근의 수량을 조사하여 연근별로 비교하였다. 본 시험에서 얻어진 결과를 요약하면 다음과 같다. 1. 자연온도처리(대조구)의 경우 11월 20일 처리구의 본엽 6～8매부터 화아분화 및 추대가 시작되어 처리기간이 길어질수록 추대율이 증가하다가 익년 1월 11일 이후부터는 변화가 없었으며 본엽 2～3매 는 어떤 구에서도 추대가 전혀 없었다. 2. 인공온도처리의 경우 처리온도가 높아질수록 주온감응한계엽령이 증가하였다. 즉, 1$^{\circ}C$, 5$^{\circ}C$, 9$^{\circ}C$ 처리구 각각 3매, 5매, 6매가지는 전혀 추대가 없었으며 8주 8매구에서도 1$^{\circ}C$에서 80%, 5$^{\circ}C$에서 45%, 9$^{\circ}C$에서 5%로 추대율이 저하하였다. 3. 참당귀의 추대율은 일장이 길어질수록 증가하였고, 광도시험에 있어서는 자연광구에서 가장 높았으나 광도가 감소할수록 점차 줄었으나 차광 50%까지 유의성이 인정되지 않았다. 4. 화도를 억제시켜 재배했을 때 10a당 건근중은 3년근이 가장 많았고 1ㆍ2년근에 비해 각각 3.6배, 2.4배 증수되었으며, 관행재배보다 2년근은 73.7%, 3년근은 159.6% 증수효과가 있었다.

• Journal of Plant Biology
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• 제25권4호
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• pp.169-174
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• 1982

Using double immunodiffusion and immunoelectrophoretic techniques, attempts were made to detect any protein changes in leaf tissues of a short-day plant, Pharbitis nil Chois. variety Violet during floral induction under 8 hr light, 16 hr dark cycles. Immunoprecipitin systems shwoed at least four proteins newly appeared in the induced leaf tissues. Accumulation of the proteins were observed as the induction proceeded.

• 한국자원식물학회지
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• 제8권1호
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• pp.55-62
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• 1995

중(中) 산간지대(山間地帶)에 재배(栽培)되는 참당귀(當歸)의 화성유도(花成誘導)에 의(依)한 추밀률(抽蜜率) 감소(減少)를 위(爲)하여 1992년(年) 2월(月)부터 1994년(年) 11월(月)까지 경북농촌진흥원(慶北農村振興院) 북부시험장(北部試驗場)에서 육묘지대(育苗地帶), 육묘기간(育苗期間) 및 유기물(有機物) 시용(施用)에 따른 화성(花成) 및 품질(品質)을 비교(比較) 분석(分析)한 결과(結果)를 요약(要約)하면 다음과 같다. 1. 육묘지대(育苗地帶)에 따른 추대율(抽臺率)은 표고(標高)가 높을 수록 현저(顯著)히 낮았고, 아울러 지하부(地下部) 생육(生育) 및 수량(收量)이 200, 400m인 지대(地帶)보다 양호(良好)하여 참당귀(當歸)의 육묘적지(育苗適地)는 적어도 표고(標高) 600m 이상(以上)이 적당(適當)하다고 사료(思料)된다. 2. 중(中) 산여(山閭) 지대(地帶)에서는 육묘기간(育苗期間)이 짧아질 수록 추대율(抽臺率)이 현저(顯著)하게 낮아서 수량(收量)은 증수(增收)되었지만, extract 및 decursin 함량(含量)은 육묘기간(育苗期間)이 길어질 수록 증가(增加)하여 육묘기간(育苗期間)과 품질면(品質面)에서는 반대(反對)되는 경향(傾向)이었다. 3. 유기물(有機物) 자원별(資源別)에 따른 추대반응(抽臺反應)은 단비(單肥) 시용구(施用區)보다 유기물(有機物) 시용구(施用區)에서 추대율(抽臺率)이 낮았으며, 특(特)히 볏짚퇴비(堆肥)에서 가장 낮았고 수량(收量) 및 품질반응(品質反應)은 관행재배(慣行栽培)보다 유기물(有機物) 시용구(施用區)에서 양호(良好)하였지만 유기물(有機物) 자원간(資源間)에는 뚜렷한 차이(差異)를 보이지 않았다.

• Journal of Photoscience
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• 제12권1호
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• pp.1-9
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• 2005

The ubiquitin E3 ligase COP1 (Constitutive Photomorphogenesis 1) is a protein repressor of photomorphogenesis in Arabidopsisplants, and it found in various organisms, including animals. The COP1 protein regulates the stability of many of the light-signaling components that are involved in photomorphogenesis and in the developmental processes. To study the effect of COP1 on flowering in a short day plant, we have cloned a full-length of PnCOP1 (Pharbitis nil COP1) cDNA from Pharbitis nil Choisy cv. Violet, and we examined its transcript levels under various conditions. A full-length PnCOP1 cDNA consists of 2,280 bp nucleotidesthat contain 47 bp of 5'-UTR, 232 bp of 3'-UTR including the poly (A) tail, and 1,998 bp of the coding sequence. The deduced amino acid sequence contains 666 amino acids, giving it a theoretical molecular weight of 75 kD and a isolectric point of 6.2. The PnCOP1 contains three distinct domains, an N-terminal $Zn^2+$-binding RING-finger domain, a coiled-coil structure, and WD40 repeats at the C-terminal, implying that the protein plays a role in protein-protein interactions. The PnCOP1 transcript was detected in the cotyledon, hypocotyls and leaves, but not in root. The levels of the PnCOP1 transcript were reduced in leaves that were a farther distance away from the cotyledons. The expression level of the PnCOP1 gene was inhibited by light, while the expression was increased in the dark. During the floral inductive 16 hour-dark period for Pharbitis nil, the expression was increased and it reached its maximum at the 12th hour of the dark period. The levels of PnCOP1 mRNA were dramatically reduced upon light illumination. These results suggest that PnCOP1 may play an important function in the floral induction of Pharbitis nil.

• 한국자원식물학회지
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• 제19권3호
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• pp.427-431
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• 2006

In vitro high-frequency plant regeneration of Muscari comosum var. plumosum through somatic embryogenesis was obtained via two developmental pathways: direct embryos and multiple shoots regenerated from embryogenic callus. Flower bud with pedicel, receptacle, petal and ovary wall, floral stalk and leaf as explants were cultured in MS medium supplemented with various plant growth regulators. Embryos formed directly from pedicel, receptacle and floral stalk. Depending on explant sources, the optimal medium was MS medium supplemented with 0.2 mg/L IBA and 0.3 mg/L BA, 3.0 mg/L IBA and 3.0 mg/L BA, and MS-free medium for pedicel, receptacle, and floral stalk, respectively. Multiple shoots regenerated from embryogenic cal]i which was initiated from petal, ovary and leaf were observed in MS medium with different concentrations and combinations of hormone. The most suitable medium for each type of explant was 3.0 mg/L IBA and 3.0 mg/L BA(petal and ovary) and 5.0 mg/L IBA and 5.0 mg/L BA (leaf) Furthermore, the combination of 0.1 mg/L 2,4-D and 1.0 mg/L BA was also good for all sources of explants not only for direct embryo formation, but also, for embryogenic callus induction.

• Journal of Plant Biology
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• 제14권1호
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• pp.33-35
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• 1971

After topping, axillary buds of haploid plants derived from cultured anthers were treated with 0.4% aqueous solution of colchicine. Due to the high temperature and dry air at the time of treatment, most of the buds perished. A few months after the colchicine application, however, several shoots arose from the places where the dead buds were originally located. These shoots were mostly diploid. Induction of adventive shoots from the colchicine-treatedaxils was supposed to be rather effective method of obtaining diploid shoots from haploid plants. The diploid plants had larger floral organs than the haploid plants, and had good pollen fertility and seed setting. 24 bivalent chromosomes were observed at MI of the PMC's.

• Molecules and Cells
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• 제39권10호
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• pp.715-721
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• 2016

Plants have become physiologically adapted to a seasonally shifting environment by evolving many sensory mechanisms. Seasonal flowering is a good example of adaptation to local environmental demands and is crucial for maximizing reproductive fitness. Photoperiod and temperature are major environmental stimuli that control flowering through expression of a floral inducer, FLOWERING LOCUS T (FT) protein. Recent discoveries made using the model plant Arabidopsis thaliana have shown that the functions of photoreceptors are essential for the timing of FT gene induction, via modulation of the transcriptional activator CONSTANS (CO) at transcriptional and post-translational levels in response to seasonal variations. The activation of FT transcription by the fine-tuned CO protein enables plants to switch from vegetative growth to flowering under inductive environmental conditions. The present review briefly summarizes our current understanding of the molecular mechanisms by which the information of environmental stimuli is sensed and transduced to trigger FT induction in leaves.

• Journal of Plant Biotechnology
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• 제34권4호
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• pp.293-298
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• 2007

Robinia pseudoacacia var. umbraculifera, commonly called umbrella black locust were regenerated after co-cultivation of internode segments with Agrobacterium tumefaciens which included yeast cadmium factor 1 (YCF 1) gene. The tolerance to cadmium and lead for plants can be increased by the YCF1 gene expression. Moreover, the recent studies have shown that YCF1 gene transgenic plants increase the accumulation of cadmium and lead into plant vacuoles. The effect of plant growth regulator such as 2,4-dichlorophenoxyacetic acid (2,4-D), ${\alpha}$-naphthaleneacetic acid (NAA), 6-benzyladenine (BA), and thidiazuron (TDZ) were studied to evaluate the propagation of plants through internode explants. The efficient induction of multiple adventitious shoots and callus were observed on a medium supplemented with 0.1 mg/L TDZ + 0.2 mg/L BA. To induce shoot elongation and rooting, regenerated shoots were transferred into basal MS medium without any plant growth regulator. Successful Agrobacterium tumefaciens mediated transformation was obtained by 20 min vacuum-infiltration with $50{\mu}M$ acetosyringone on the optimal multiple shoot induction medium with 30 mg/L hygromycin and 300 mg/L cefotaxime. To confirm the integration and expression of transgene, Polymerase Chain Reaction (PCR) and Reverse Transcriptase PCR (RT-PCR) were performed with specific primers. The frequency of transformation was approximately 18.94%. This study can be used to genetic engineering of phytoremediator.

• Journal of Plant Biology
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• 제35권4호
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• pp.403-408
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• 1992

장일식물인 Lemna gibba G3의 개화유도과정에 있어서 polyamine의 관련성을 조사하였다. 이 식물의 개화는 연속광하에서 agmatine, putrescine, spermidine 및 spermine에 의해 촉진되었으며 이들의 체내 합성억제물질인 methylglyoxal-bis(guanylhydrazone)(MGBG)과 cyclohexylamine(CHA)에 의해서 억제되었다. Polyamine은 영양생장률을 거의 일정한 수준으로 유지하면서 개화를 촉진시켰으며, 억제물질에 의한 개화억제는 오히려 영양생장률의 증가를 수반하였다. 이러한 현상은 이 물질들의 개화촉진 또는 억제효과가 생장률의 일반적인 촉진 또는 억제효과에 의한 것이 아니라 선택적으로 개화과정에 작용한 결과일 것이라는 추측을 뒷받침해 준다. 배양액의 첨가된 spermidine 또는 spermine의 개화촉진 폭은 배양액에 이들의 억제물질의 함유여부와 관계없이 거의 일정한 수준으로 나타났다. 이렇듯, 외부에서 공급된 후 체내에 흡수된 spermidine과 spermine의 개화에 대한 기여도가 한정되어 있는 것으로 보아 L. gibba G3의 개화유도과정이 식물체내에서 합성되는 spermidine과 spermine에 크게 의존하고 있을 것으로 판단된다. 한편, 개화유도과정이 시작되어 점차적으로 증가한 체내의 spermidine 함량은 개화가 유도되지 않은 경우에 비하여 24시간만에 약 2배의 수준에 도달하였다. 이렇듯 체내의 spermidine량이 급격히 증가된 사실은 체내의 polyamine의 질적 및 양적 변화가 L. gibba G3의 개화유도초기과정에서 매우 중요한 역할을 하고 있을 것이라는 가정을 뒷받침하는 또 하나의 예비적 증거라 할 수 있다.

• Journal of Crop Science and Biotechnology
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• 제11권1호
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• pp.1-6
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• 2008

The covalent conjugation of SUMO(Small Ubiquitin-related MOdifier) protein to its substrates regulates numerous cellular processes, including protein stability and activity in eukaryotes as well as in plants. In this present review, we summarize biochemical aspects of SUMO conjugation and deconjugation and the functions of SUMO and sumoylation-related proteins in Arabidopsis and other plants. In particular, we provide an overview of the roles of the SUMO in widely different biological processes including the ABA response, floral induction, pathogen defense, abiotic stresses and hormone signaling. Furthermore, we explore the possible roles of SUMO in embryo and seed development.