• Korean Journal of Medicinal Crop Science
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• v.11 no.4
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• pp.274-278
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• 2003

The various plant organs of fennel (Foeniculum vulgare Mill.) were investigated to identify their volatile components using Dynamic Headspace (purge & trap). They showed slight differences concerning the volatile components both qualitatively and quantitatively. Results revealed that trans-anethole (12.65%) was the major compound in the leaf. The highest compound was ${\alpha}-pinene$ (28.78%), and trans-anethole (7.90%) was highly detected in the stem. The maximum values were 5.64, 4.59, 1.58, 1.51, and 1.04% for ${\alpha}-pinene,\;{\gamma}-terpinene,\;{\beta}-pinene$, 1,8-cineol and fenchone, respectively in the flower. However, very little trans-anethole was detected (0.27%) in the flower. From these results, it was suggested that the major components were different depending on the plant organs. However it was demonstrated that the related plant organs like flower-fruit and leaf-stem contained the similar components.

• Journal of Environmental Science International
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• v.17 no.9
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• pp.1015-1021
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• 2008

This study was performed to examine the accumulated concentrations (conc.) of cadmium (Cd) in the organs of Arabidopsis thaliana grown in the soil with different conc. of Cd. The official standard conc. of Cd of pollutant exhaust notified by the Korean ministry of environment (0.1 mg/L) and ten times higher (1 mg/L) and fifty times higher (5 mg/L) conc. and no Cd in the soil as control were used for this investigation. The results showed that accumulated conc. of Cd in the stems of plant grown in the soil with different conc. (0.1, 1 and 5 mg/L) were increased 9%, 24% and 286% respectively, compared with normal plant stem. The accumulated conc. of Cd in the leafs of plant gown in the soil with official standard conc. and conc. ten times higher and conc. fifty times higher were increased 3%, 22% and 453%, respectively, compared with normal plant leaf. The accumulated conc. of Cd in the root of plant grown in the soil with 0.1 and 1 mg/L conc. of Cd were increased 6%, 19%, respectively, compared with normal plant root. However, it was observed about 84% of increased accumulation of the Cd in the root of plant, when highest (5 mg/L) conc. was used. The accumulated conc. of Cd in the different organs of Arabidopsis thaliana were increased according to increase of Cd conc. in the soil. When official standard conc. and ten times higher conc. of Cd were used, the accumulated conc. of Cd increased average 6%, 21%, respectively, compared with normal plant organ, and the accumulated conc. of Cd between leaf, stem and root were not significant. However, the accumulated conc. of Cd in the plant organs gown in the conc. fifty times higher were increased about 285%, compared with normal plant. In addition, the accumulated conc. of Cd in different organs of Arabidopsis thaliana exhibited wide differences between organs, that is, stem was increased 118% than root, leaf was increased 256%, 64% than root and stem, respectively. These results show that accumulated conc. of Cd in Arabidopsis thaliana with highest (5 mg/L) conc. of Cd in soil, were much higher in the leaf than the stem or root in proportion to the conc. of Cd contaminated within the soil.

• Journal of Ginseng Research
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• v.11 no.2
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• pp.111-117
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• 1987

The phase and times on the development of dormancy bud in seedling, and those of flower organs in 2-year-old ginseng are different to those of over 2-,3-year-old plant, respectively. The growing aspects of dormancy bud in seedling were investigated from rooting stage (April, 8) to Mid-June, and those of flower organs in 2-year-old plant had done once in two days late in April after compound leaves were unfolded. Firstly, the formation of dormancy bud in seedling was begun on Mid-late in March. This is early about one month compare with those of over 2-year-old plant. Fine bud in seedling was formed between cotyledons, at W spot under young shoot. Secondly, development of flower organs in 2-year-old plant was completed from late of April to early of May after compound leaves of transplanted plant were unfolded. In tare, this is very different characteristics because plants of any other ages form the flower organs one year ago. Thirdly, flower organs of ginseng plant, over 3-year-old plant, always develop in the rhizome formed one year ago, but those of 2-year-old plant develop in apical shoot meristem.

• Journal of Plant Biotechnology
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• v.5 no.3
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• pp.137-142
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• 2003

The morphology of the leaves and the flowers of angiosperms exhibit remarkable diversity. One of the factors showing the greatest variability of leaf organs is the leaf index, namely, the ratio of leaf length to leaf width. In some cases, different varieties of a single species or closely related species can be distinguished by differences in leaf index. To some extent, the leaf index reflects the morphological adaptation of leaves to a particular environment. In addition, the growth of leaf organs is dependent on the extent of the expansion of leaf cells and on cell proliferation in the cellular level. The rates of the division and enlargement of leaf cells at each stage contribute to the final shape of the leaf, and play important roles throughout leaf development. Thus, the control of leaf shape is related to the control of the shape of cells and the size of cells within the leaf. The shape of flower also reflects the shape of leaf, since floral organs are thought to be a derivative of leaf organs. No good tools have been available for studies of the mechanisms that underlie such biodiversity. However, we have recently obtained some information about molecular mechanisms of leaf morphogenesis as a result of studies of leaves of the model plant, Arabidopsis thaliana. For example, the ANGUSTIFOLIA (AN) gene, a homolog of animal CtBP genes, controls leaf width. AN appears to regulate the polar elongation of leaf cells via control of the arrangement of cortical microtubules. By contrast, the ROTUNDIFOLIA3 (ROT3) gene controls leaf length via the biosynthesis of steroid(s). We provide here an overview of the biodiversity exhibited by the leaf index of angiosperms. Taken together, we can discuss on the possibility of the control of the shapes and size of plant organs by transgenic approaches with the results from basic researches. For example, transgenic plants that overexpressed a wildtype ROT3 gene had longer leaves than parent plants, without any changes in leaf width. Thus, The genes for leaf growth and development, such as ROT3 gene, should be useful tools for the biodesign of plant organs.

• Proceedings of the Korean Society of Plant Biotechnology Conference
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• 2003.04a
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• pp.49-55
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• 2003

The morphology of the leaves and the flowers of angiosperms exhibit remarkable diversity. One of the factors showing the greatest variability of leaf organs is the leaf index, namely, the ratio of leaf length to leaf width. In some cases, different varieties of a single species or closely related species can be distinguished by differences in leaf index. To some extent, the leaf index reflects the morphological adaptation of leaves to a particular environment. In addition, the growth of leaf organs is dependent on the extent of the expansion of leaf cells and on cell proliferation in the cellular level. The rates of the division and enlargement of leaf cells at each stage contribute to the final shape of the leaf, and play important roles throughout leaf development. Thus, the control of leaf shape is related to the control of the shape of cells and the size of cells within the leaf. The shape of flower also reflects the shape of leaf, since floral organs are thought to be a derivative of leaf organs. No good tools have been available for studies of the mechanisms that underlie such biodiversity. However, we have recently obtained some information about molecular mechanisms of leaf morphogenesis as a result of studies of leaves of the model plant, Arabidopsis thaliana. For example, the ANGUSTIFOLIA (AN) gene, a homolog of animal CtBP genes, controls leaf width. AN appears to regulate the polar elongation of leaf cells via control of the arrangement of cortical microtubules. By contrast, the ROTUNDIFOLIA3 (ROT3) gene controls leaf length via the biosynthesis of steroid(s). We provide here an overview of the biodiversity exhibited by the leaf index of angiosperms. Taken together, we can discuss on the possibility of the control of the shapes and size of plant organs by transgenic approaches with the results from basic researches. For example, transgenic plants that overexpressed a wild-type ROT3 gene had longer leaves than parent plants, without any changes in leaf width. Thus, The genes for leaf growth and development, such as ROT3 gene, should be useful tools for the biodesign of plant organs.

• Proceedings of the Plant Resources Society of Korea Conference
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• 2002.11b
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• pp.15-15
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• 2002

In higher dicotyledonous plants, the floral organs are arranged in four different whorls, containing sepals, petals, stamens and carpels. petals, stamens and carpels. The specification of floral organ identity is explained by the ABC model (Weigel and Meyerowitz 1994). Expression of an A-function gene specifies sepal formation in whorl 1. the combination of A-and B-function genes specifies the formation of petals in whorl 2, B-and C-function genes spesify stamen formation in whorl 3, and expression of the C-function alone determines the formation of carpels in whorl 4. A-. B-, C-function genes have been isolated from many plant species and most of them belong to the family of MADS-box genes encoding transcription factor. In contrast to the flower of higher dicots, the perianths of genseng plants have three whorls of almost identical petaloid organs. van Tunen et al. (1993) proposed a modified ABC model, exemplified with tulip. In this model, B-function genes are expressed in whorl 1 as well as whorl 2 and 3, theefore the organs of whorl 1 and whorl 2 have the same petaloid structure. They proposed this model with the molphological data of wild type and mutant flowers of tulip, however, there are no molecular data.(중략)

• Proceedings of the Plant Resources Society of Korea Conference
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• 2002.11a
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• pp.98-98
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• 2002

In higher dicotyledonous plants, the floral organs are arranged in four different whorls, containing sepals, stamens and carpels. petals, stamens and carpels. The specification of floral organ identity is explained by the ABC model (Weigel and Meyerowitz 1994). expression of an A-function gene specifies sepal formation in whorl 1. the combination of A-and B-function genes specifies the formation of petals in whorl 2, B-and C-function genes spesify stamen formation in whorl 3, and expression of the C-function alone determines the formation of carpels in whorl 1. A-, B-, C-function genes have been isolated from many plant species and most of them belong to the family of MADS-box genes encoding transcription factor. In contrast to the flower of higher dicots, the perianths of genseng plants have three whorls of almost identical petaloid organs. van Tunen et al. (1993) proposed a modified ABC model, exemplified with tulip. In this model, B-function genes are expressed in whorl 1 as well as whorl 2 and 3, theefore the organs of whorl 1 and whorl 2 have the same petaloid structure. They proposed this model with the molphological data of wild type and mutant flowers of tulip, however, there are no molecular data. To date, B-function genes were isolated several grass plants, rice, wheat and maize. However, grass plants have highly derived flowers, without well-developed perianths. To find out how the ABC model has to be modified for the Genseng plants, we have cloned and characterized orthologs of A-, B-, C-function genes from genseng.

• Korean Journal of Medicinal Crop Science
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• v.10 no.4
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• pp.298-302
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• 2002

The essential oils were isolated by hydrodistillation and their composition determined capillary GC method with standards. The essential oil content showed significant differences between the two populations on the vegetative organs. The essential oil level of the leaves and roots was considerably higher in the Korean population at full flowering and waxy ripening stage but essential oil content of the roots was significantly higher in the Hungarian taxon at leaf rosette stage. We observed the essential oil accumulation tendency was mianly dependent on plant organs and intra-specific taxon during the vegeation period. Butylidene-phthalide was proved to be the main component of the oil in both population roots (50.9-73.3%), while dimethyl-acetate was showed as a major compound on the over-ground parts (56.7-62.0%). The qualitative composition of the essential oil in the reproductive organs concerning the identified compounds was the same as the vegetative parts with the main component ${\alpha}-phellandrene$ (4.8-28.1%) and butylidene-phtalide (9.7-16.1%), The quantitative composition showed some changes during the ontogenesis phases. Most characteristic ones are the decreasing proportion of dimethyl-acetate (from 7.3% to 1.1%) and the appearance of ${\alpha}-pinene$ (from 0.5% to 1.5%) only after fruit setting in both population.

• Korean Journal of Medicinal Crop Science
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• v.8 no.4
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• pp.312-318
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• 2000

To obtain the basic information for commercial process and high quality production of Saururus chinensis, useful components were determined at different growth stages and organs. The contents of quercetin, quercitrin and tannin at different growth stages were decreased before flowering time but slightly increased after flowering. The contents of quercetin, quercitrin and tannin collected on July 26 were 5.72, 5.45g/kg and 1.5%, respectively. The contents of quercetin, quercitrin and tannin were the highest in white leaf, leaf and flower, respectively.

• BMB Reports
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• v.42 no.9
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• pp.611-616
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• 2009

We investigated the expression pattern of dehydration responsive element-binding protein-3 in tomato under different abiotic stresses. Full length LeDREB3 cDNA was isolated from tomato plant, followed by phylogenetic analysis based on deduced amino acid sequences that revealed significant sequence similarity to DREB proteins belonging to diverse families of plant species. Southern blot analysis showed duplicate copies of LeDREB3 in the tomato genome while organ-specific expression profiling indicated constitutive expression of LeDREB3 in all tested organs, which was particularly strong in flower. LeDREB3 expression was significantly induced by Nacl, drought, low temperature and $H_2O_2$. Moreover, LeDREB3 was slightly regulated by treatment with ABA and MV. These observations suggest that the LeDREB3 gene may be involved in the response of the tomato plant to stress.