• Title/Summary/Keyword: Korean horticulture

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Touch-induced gene (IbTCH1) from sweet potato [Ipomoea batatas (L.) Lam.]: molecular cloning and functional analysis

  • Seo, Sang-Gyu;Kim, Ji-Seong;Kang, Seung-Won;Shin, Mi-Rae;Yang, You-Sun;Lee, Gung-Pyo;Hong, Jin-Sung;Kim, Sun-Hyung
    • Plant Biotechnology Reports
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    • v.2 no.4
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    • pp.253-258
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    • 2008
  • The cDNA of the touch-induced genes (TCH) of the sweet potato [Ipomoea batatas (L.) Lam.] has been cloned and analyzed. IbTCH1, which exists as at least two-copy genes in the genome of the sweet potato, encodes for 148-amino acid polypeptides, and harbors four conversed $Ca^{2+}-binding$ motif EF-hands. IbTCH1 was shown to be expressed in the flower, leaf, thick pigmented root, and particularly in the white fibrous root, but expressed only weakly in the petiole. IbTCH1 is upregulated upon exposure to environmental stresses, dehydration, and jasmonic acid. Furthermore, IbTCH1 is developmentally regulated in the leaf and root. These results strongly indicate that the gene performs functions in both plant development and in defense/stress-signaling pathways.

Growth and Yield of Tomato and Cucumber Plants in Polycarbonate or Glass Greenhouses

  • Kwon, Joon Kook;Khoshimkhujaev, Bekhzod;Lee, Jae Han;Yu, In Ho;Park, Kyoung Sub;Choi, Hyo Gil
    • Horticultural Science & Technology
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    • v.35 no.1
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    • pp.79-87
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    • 2017
  • We examined the effect of two greenhouse covering materials (glass or solid polycarbonate sheets) on the light environment and growth of tomato and cucumber plants. Spectral analysis showed that polycarbonate sheets entirely blocked radiation in both the UV - B (300 - 320 nm) and UV - A (320 - 400 nm) ranges, whereas glass transmitted UV - A and was only opaque to UV - B. The transmittance of photosynthetically active radiation (400 - 700 nm) and near infrared radiation (700 - 1100 nm) was higher in polycarbonate than glass. Air and soil temperatures were not significantly different between greenhouses covered with either material. The growth of cucumber plants was slightly affected by covering materials, whereas no significant changes in growth parameters were observed for tomato plants. The color parameters of tomato fruits were affected by the cover material, whereas cucumber fruits showed similar coloration in both glass and polycarbonate greenhouses.

Evolutionary Rates and Phylogeographical Analysis of Odontoglossum Ringspot Virus Based on the 166 Coat Protein Gene Sequences

  • He, Zhen;Dong, Tingting;Wu, Weiwen;Chen, Wen;Liu, Xian;Li, Liangjun
    • The Plant Pathology Journal
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    • v.35 no.5
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    • pp.498-507
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    • 2019
  • Odontoglossum ringspot virus (ORSV) is a member of the genus Tobamovirus. It is one of the most prevalent viruses infecting orchids worldwide. Earlier studies reported the genetic variability of ORSV isolates from Korea and China. However, the evolutionary rate, timescale, and phylogeographical analyses of ORSV were unclear. Twenty-one coat protein (CP) gene sequences of ORSV were determined in this study, and used them together with 145 CP sequences obtained from GenBank to infer the genetic diversities, evolutionary rate, timescale and migration of ORSV populations. Evolutionary rate of ORSV populations was $1.25{\times}10^{-3}nucleotides/site/y$. The most recent common ancestors came from 30 year ago (95% confidence intervals, 26-40). Based on CP gene, ORSV migrated from mainland China and South Korea to Taiwan island, Germany, Australia, Singapore, and Indonesia, and it also circulated within east Asia. Our study is the first attempt to evaluate the evolutionary rates, timescales and migration dynamics of ORSV.

Overview of CRISPR/Cas9: a chronicle of the CRISPR system and application to ornamental crops

  • Lee, Hyunbae;Subburaj, Saminathan;Tu, Luhua;Lee, Ka-Yeon;Park, Gwangsu;Lee, Geung-Joo
    • Korean Journal of Agricultural Science
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    • v.47 no.4
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    • pp.903-920
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    • 2020
  • Since its first demonstration as a practical genome editing tool in the early 2010s, the use of clustered regularly interspaced short palindromic repeat (CRISPR) along with the endonuclease Cas9 (CRISPR/Cas9) has become an essential choice for generating targeted mutations. Due to its relative simplicity and cost-effectiveness compared to other molecular scissors, i.e., zinc finger nuclease (ZFN) and transcription activator-like effector nuclease (TALEN), the CRISPR/Cas9 system has been shown to have a massive influence on genetic studies regardless of the biological kingdom. Although the system is in the process of being established, numerous protocols have already been released for the system and there have been various topics of CRISPR related papers published each year in ever-increasing manner. Here, we will briefly introduce CRISPR/Cas9 system and discuss the variants of the CRISPR system. Also, their applications to crop improvement will be dealt with mainly ornamental crops among horticultural crops other than Arabidopsis as a model plant. Finally, some issues on the barriers restraining the use of CRISPR system on floricultural crops, the prospect of CRISPR system as a DNA-free genome editing tool with efficient facilitators and finally, the future perspectives on the CRISPR system will be described.

Plant regeneration of Korean wild ginseng (Panax ginseng Meyer) mutant lines induced by ${\gamma}$-irradiation ($^{60}Co$) of adventitious roots

  • Zhang, Jun-Ying;Sun, Hyeon-Jin;Song, In-Ja;Bae, Tae-Woong;Kang, Hong-Gyu;Ko, Suk-Min;Kwon, Yong-Ik;Kim, Il-Woung;Lee, Jaechun;Park, Shin-Young;Lim, Pyung-Ok;Kim, Yong Hwan;Lee, Hyo-Yeon
    • Journal of Ginseng Research
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    • v.38 no.3
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    • pp.220-225
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    • 2014
  • An efficient in vitro protocol has been established for somatic embryogenesis and plantlet conversion of Korean wild ginseng (Panax ginseng Meyer). Wild-type and mutant adventitious roots derived from the ginseng produced calluses on Murashige and Skoog (MS) medium supplemented with 0.5 mg/L 2,4-dichlorophenoxyacetic acid and 0.3 mg/L kinetin; 53.3% of the explants formed callus. Embryogenic callus proliferation and somatic embryo induction occurred on MS medium containing 0.5 mg/L 2,4-dichlorophenoxyacetic acid. The induced somatic embryos further developed to maturity on MS medium with 5 mg/L gibberellic acid, and 85% of them germinated. The germinated embryos were developed to shoots and elongated on MS medium with 5 mg/L gibberellic acid. The shoots developed into plants with well-developed taproots on one-third strength Schenk and Hildebrandt basal medium supplemented with 0.25 mg/L 1-naphthaleneacetic acid. When the plants were transferred to soil, about 30% of the regenerated plants developed into normal plants.

Screening of melon genotypes identifies gummy stem blight resistance associated with Gsb1 resistant loci

  • Hassan, Md Zahid;Robin, Arif Hasan Khan;Rahim, Md Abdur;Natarajan, Sathishkumar;Kim, Hoy-Taek;Park, Jong-In;Nou, Ill-Sup
    • Journal of Plant Biotechnology
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    • v.45 no.3
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    • pp.217-227
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    • 2018
  • Gummy stem blight (GSB) is one of the most destructive and economically important, soil borne diseases of melon caused by the ascomycete fungus, Didymella bryoniae throughout the world. In Korea, however, no GSB resistant genotype has been reported yet. The study aimed to identify GSB resistant melon germplasm. We screened a total of 60 genotypes including 16 lines and 44 melon cultivars collected from USA and Korea. Among the 16 melon lines, four lines including 'PI482399', 'PI140471', 'PI136170' and 'PI420145', and two Korean cultivars viz. 'Asia Papaya' and 'Supra' showed complete resistance. We were aware that both genotypic and environmental variations could influence the phenotypic screening of resistance and susceptibility. We therefore, further assessed all genotypes using 20 SSR markers. The SSR marker 'CMCT505' linked to Gsb1 in chromosome 1 perfectly grouped resistant and susceptible lines indicating that resistance is probably due to the presence of Gsb1 gene. Cloning and sequencing of resistant and susceptible Gsb1 amplicons showed that there were 32-bp deletions in resistant line and 39-bp deletions in resistant cultivar compared to susceptible one. Thus, the resistant melon lines and cultivars identified in this study could be recommended for the melon breeding program. Furthermore, the SSR marker 'CMCT505' which is tightly linked with Gsb1 could be used for molecular screening of melon germplasm.