• Journal of Photoscience
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• v.12 no.3
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• pp.163-169
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• 2005

Recent reports suggest that floral organs such as sepals, petals, stamens, and carpels are specified by quaternary MADS protein complexes with different combinations. The formation of quaternary complexes of ABCDE MADS proteins may be the molecular basis of ABCDE model for the floral organ development. The MADS complexes involved in each floral organ development seem to be conserved in at least dicot species although detailed molecular mechanism is slightly different depending on species. Even in monocot, at least rice, MADS complexes similar to those in dicot exist, suggesting that the floral organ specification by MADS protein complexes may be conserved in most of plants. The MADS protein complexes may have more specific recognition of target genes or more transcription activation ability than monomers or dimers, resulting in finely regulated floral organ development.

• Journal of Plant Biotechnology
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• v.4 no.4
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• pp.171-178
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• 2002

Chlorophyll (Chl) fluorescence imaging was used to investigate the effectiveness of in vivo incorporation methods for two chemicals, 3-(3',4'-dichlorophenyl)-1,1-dimethylurea (DCMU) and methyl viologen (MV) in rice, a monocot, and cucumber, a dicot, leaves. four different methods (vacuum infiltration, floating, transpiration-aided incorporation through petiole and spraying) were compared, and $F_i$ and $F_v$/$F_m$ were chosen for the imaging of the DCMU- and MV-treated leaves, respectively. The effects of the chemicals in plants were generally heterogeneous over the whole leaf area. Moreover, the effectiveness of the treatment of a chemical in plant leaves was dependent on chemical species, plant species, concentration of the chemical, the treatment method, the duration of the treatment, the existence of light and detergent, etc. In conclusion, we suggest that to achieve the proposed effects of chemicals in plants for an actual experiment, these factors must be considered before the chemical treatment, and the best method for the treatment of the chemicals tested was floating and vacuum infiltration in the dicot and the monocot leaves, respectively, as drawn from Chl fluorescence imaging analysis.

• Proceedings of the Korean Society of Potoscience Conference
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• 2002.06a
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• pp.67-67
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• 2002

• Journal of environmental and Sanitary engineering
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• v.5 no.2
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• pp.89-99
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• 1990

Morphology, anatomy and diurnal acid fluctuations were investigated monthly for the succulent C4 dicot Portulaca grandiflora Hook. growing under natural environmental conditions. Modified Kranz-Type sturcture and typical CAM-like cells were shown in leaves and stems, respectively. Values of indices of mesophyll succulence inleaves stems were 5.62 and 16.68, respectively. The number of stomata were 1476$\textrm{cm}^{-2}$ in leaves while the stomata in stems were not observed through growing seasons from spring to summer. However, on Sep. 16, 1981 in defoliate autumn season, stomata were begun to be produced for the first time in stems and the number were increased gradually to 216$\textrm{cm}^{-2}$ on Oct. 29. This feature can be interpreted as a seasonal plant dimorphism. P. grandiflora exhibited a diurnal fluctuation of titratable acidity in leaves and stems. Seasonal amplitudes of acid fluctuation in stems were as follows: 27 $\mu$eq./g.f.wt. on Sep. 21; 57$\mu$eq/g.f.wt. on Oct. 3; 80$\mu$eq./g.f.wt. on Oct. 21. Such the results in seasonal amplitude were able to consider due to decrease of light period and cool night air temperature according to change of season. Also, the naturally defoliated stems which had already stomata exhibited usual diurnal acid fluctuation, on the other hand the treated stems which possessed artificially closed stomata showed a few of acid fluctuation. Especially, stomata in stems are developed by seasonal dimorphism and activated stomata participate in CAM behavior of stems.

• Molecules and Cells
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• v.40 no.11
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• pp.828-836
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• 2017

Eukaryotic cells consist of a complex network of thousands of proteins present in different organelles where organelle-specific cellular processes occur. Identification of the subcellular localization of a protein is important for understanding its potential biochemical functions. In the post-genomic era, localization of unknown proteins is achieved using multiple tools including a fluorescent-tagged protein approach. Several fluorescent-tagged protein organelle markers have been introduced into dicot plants, but its use is still limited in monocot plants. Here, we generated a set of multicolored organelle markers (fluorescent-tagged proteins) based on well-established targeting sequences. We used a series of pGWBs binary vectors to ameliorate localization and co-localization experiments using monocot plants. We constructed different fluorescent-tagged markers to visualize rice cell organelles, i.e., nucleus, plastids, mitochondria, peroxisomes, golgi body, endoplasmic reticulum, plasma membrane, and tonoplast, with four different fluorescent proteins (FPs) (G3GFP, mRFP, YFP, and CFP). Visualization of FP-tagged markers in their respective compartments has been reported for dicot and monocot plants. The comparative localization of the nucleus marker with a nucleus localizing sequence, and the similar, characteristic morphology of mCherry-tagged Arabidopsis organelle markers and our generated organelle markers in onion cells, provide further evidence for the correct subcellular localization of the Oryza sativa (rice) organelle marker. The set of eight different rice organelle markers with four different FPs provides a valuable resource for determining the subcellular localization of newly identified proteins, conducting co-localization assays, and generating stable transgenic localization in monocot plants.

• Journal of Plant Biotechnology
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• v.2 no.3
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• pp.115-121
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• 2000

A cDNA clone encoding chloroplast triosephosphate isomerase (TPI-cp) was isolated from strawberry fruit cDNA library. Sequence analyses indicated that the cDNA contains an open reading frame of 314 amino acids (33.5 kDa) composed of a transit peptide (59 amino acids) in amino terminal region and mature protein (255 amino acids). The existence of transit peptide in the deduced amino acid sequence implies that it encodes a chloroplast isoform. The protein sequence is more similar to other plant chloroplast isoforms than cytosolic isoforms. RNA blot analysis indicated that its expression is ubiquitous in examined five tissues, flowers, leaves, petioles, roots and fruits, and shows differential pattern according to fruit ripening. Genomic DNA blot analysis showed that TPI-cp is encoded by multiple genes in strawberry. Through sequence comparison and phylogenetic tree construction, TPI-cp is distinctively grouped into dicot and chloroplast isoforms.

• Journal of Plant Biotechnology
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• v.5 no.3
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• pp.149-155
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• 2003

Metabolic engineering for production of isoflavones in nonlegume plants could distribute the health benefits of these phytoestrogens in more widely-consumed grains. Series of investigation to check the ability of the heterologous isoflavone synthase enzyme to interact with the endogenous phenylpropanoid pathway have been conducted. Overall, results provide possibility of production of isoflavonoids in several plant tissue systems including soybean and nonlegumes. In tissue that undergoes naturally enhanced synthesis of anthocyanins, genistein production was enhanced. In a monocot cell system, introduced expression of a transcription factor regulating genes of the anthocyanin pathway was effective in conferring the ability to produce genistein in the presence of the isoflavone synthase gene. However, in this case the intermediate accumulated to high levels indicating an inefficiency in its conversion. Introduction of a third gene, chalcone reductase, provided the ability to synthesize an additional substrate of isoflavone synthase resulting in production of the isoflavone daidzein. These research efforts provide insight into requirements for metabolic engineering for isoflavone production in nonlegume dicot and monocot tissues.

• Proceedings of the Korean Society of Plant Biotechnology Conference
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• 2003.04a
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• pp.77-84
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• 2003

Metabolic engineering for production of isoflavones in non-legume plants could distribute the health benefits of these phytoe-strogens in more widely-consumed grains. We investigate the ability of the heterologous isoflavone synthase enzyme to interact with the endogenous phenylpropanoid pathway. Overall, results provide possibility of production of isoflavonoids in several plant tissue systems including soybean and non-legumes. In tissue that undergoes naturally enhanced synthesis of anthocyanins, genistein production was enhanced. In a monocot cell system, introduced expression of a transcription factor regulating genes of the antho-cyanin pathway was effective in conferring the ability produce genistein in the presence of the isoflavone synthase gene. However, in this case the intermediate accumulated to high levels indicating an inefficiency in its conversion. Introduction of a third gene, chalcone reductase, provided the ability to synthesize an additional substrate of isoflavone synthase resulting in production of the isoflavone daidzein. These research efforts provide insight into requirements for metabolic engineering for isoflavone production in non-legume dicot and monocot tissues.

• Journal of Plant Biology
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• v.39 no.1
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• pp.9-13
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• 1996

A clone, LCM1, which encodes calmodulin (CaM) was isolated and characterized from monocot lily (Lilium longiflorum Thunb.) plants. The clone is 681 bps and contains the 447 bp coding region, 8 bp leader sequence, 210 bp 3'-untraslated region, and a poly(A) tail. The coding region of 149 amino acids encodes a protein of predicted Mr 17 kD. Comparison of the LCM1 amino acid sequence with other CaMs revealed that the protein is highly conserved among various living organisms. The expression level of calmodulin gene in lily was studied by RNA blot analysis. The LCM1 mRNA was present in all tissues tested. However, a higher level of calmodulin was observed in anther and floral bud. The level of calmodulin mRNA in anther was about 10 times higher than that in anther was about 10 times higher than that in vegetative tissues. The anther preferential expression of CaM in lily is currently investigated in dicot plants.

• Korean Journal of Weed Science
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• v.17 no.3
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• pp.256-261
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• 1997

Effect of a new postemergence herbicide carfentrazone-ethyl on controlling weeds in pear orchards was examined and compared with that of glyphosate and glufosinate. Herbicides tested were applied in mid June when weeds had reached at an average height of 15 to 20cm. The experimented orchards were infested mainly by dicots of Artemisia princeps, Chenopodium album, Polygonum hydropiper, Erigeron canadensis, Commelina cummunis, Calystegia japonica, and Amaranthus ascenders, and monocots of Echinochlor crus-galli, Digitaria sangunalis, Setaria viridis, and several sedges, Carfentrazone-ethyl alone effectively controlled dicot weeds in the orchards, but not monocot weeds. Especially, sedges were not adequately controlled by carfentrazone-ethyl alone at any application rates examined. Glyphosate or glufosinate was more effective to control monocot weeds than carfentrazone-ethyl, whereas carfentrazone-ethyl exhibited higher effect on dicot weeds than glyphosate or glufosinate. Carfentrazone-ethyl mixed with glyphosate of the half recommended rate exhibited a higher degree of weed control, especially of E. crus-galli, as compared to the herbicide mixture of carfentrazone-ethyl with glufosinate of the half recommended rate. However, no phytotocixity of the herbicides to pear trees was observed. Our results demonstrate that catfentrazone-ethyl is useful to reduce the application rates and to accelerate the weed controlling effect of glyphosate or glufosinate. Thus, carfentrazone-ethyl in combination with glyphosate or glufosinate can successfully be used to control the most important weeds in orchards.