Yoon Sun Huh, Joung Kwan Lee, Sang Young Nam, Kee Yoeup Paek, and Gang Uk Suh
Journal of Plant Biotechnology 2016; 43(1): 138-145Abstract : To find the optimal propagation condition for endangered
Yoon Sun Huh, Joung Kwan Lee, Sang Young Nam, Eui Yon Hong, Kee Yoeup Paek, and Sung Won Son
Journal of Plant Biotechnology 2016; 43(1): 132-137Abstract : The genus
Eunji Lee, and Tae-Ho Park
Journal of Plant Biotechnology 2016; 43(1): 125-131Abstract :
Trinh Ngoc Ai, Aung Htay Naing, and Chang Kil Kim
Journal of Plant Biotechnology 2016; 43(1): 119-124Abstract : Anthocyanin accumulation and plant growth were examined in petunia (NT and T2 transgenic plants) by determining the effects of different sources of light and varying light/dark cycles. Red light significantly enhanced anthocyanin content of
Chan Hoon An, Yong Wook Kim, Heung Kyu Moon, and Jae Seon Yi
Journal of Plant Biotechnology 2016; 43(1): 110-118Abstract : We compared germination efficiency for somatic embryos (SE) of
Hae-Rim Jang, Byung-Jun Park, Seung-A Park, Ok-Ja Pee, So-Young Park, and Kee-Yoeup Paek
Journal of Plant Biotechnology 2016; 43(1): 104-109Abstract :
Hojin Ryu
Journal of Plant Biotechnology 2016; 43(1): 99-103Abstract : In perennial ginseng plantations, the effective control of various diseases is one of the most critical factors for increasing yields. Enhancing the resistance to disease through induced systemic resistance (ISR) and anti-microbial activity of beneficial soil bacteria, is currently considered to be a potential promising approach to integrate pathogen management for sustainable agriculture. However, the effective
Beom-Ho Jo, Min-A Seol, Su Young Shin, II Ryong Kim, Wonkyun Choi, Soon-Jae Eum, Hae-Ryong Song, and Jung Ro Lee
Journal of Plant Biotechnology 2016; 43(1): 91-98Abstract : The growth area of living modified (LM) cotton has steadily increased every year, since its first commercialization in 1996. Development of environmental risk assessment tools and techniques for LM cotton is required for ecosystem safety. We therefore developed multiplex PCR assays for simultaneous detection of two (MON15985, MON531) and four (GHB614, LLCOTTON25, MON88913 and MON1445) LM cotton events approved in Korea, with event specific primer pairs. The PCR reactions were optimized by using event specific primers of six LM cottons at various concentrations. The reactions allows amplification of estimated amplicons of MON15985 (214 bp), MON531 (270 bp), GHB614 (119 bp), LLCOTTON25 (164 bp), MON88913 (276 bp), and MON1445 (389 bp) from multiplex PCR reactions. The multiplex PCR assay developed allowed that two annealing steps (15 cycles at 55°C and 25 cycles at 60°C) were performed for amplification of distinguished two LM cottons, and only one annealing step (50 cycles at 60°C) was necessary for tetraplex PCR. Primer extension step of all PCR reactions was skipped for time-effective amplification. Our methods suggest that two multiplex PCR assays can be cost-effective and a rapid diagnostic tool for environmental LMO monitoring of six LM cottons.
Hwan Su Hwang, and Yong Eui Choi
Journal of Plant Biotechnology 2016; 43(1): 82-90Abstract : Most Araliaceae plant species distributed in Korea are economically important because of their high medicinal values. This study was conducted to develop barcode markers from sequence analysis of chloroplast DNA in 14 taxa of Araliaceae species grown in South Korea. Sequencing of seven chloroplast DNA regions was performed to establish the DNA barcode markers, as suggested by the Consortium for the Barcode of Life (CBOL). From the sequence analysis of chloroplast DNA, we identified specific sequences and nucleotides that allowed us to discriminate among each other 14 Korean Araliaceae species. The sequence in the region of
Hak Yoon Kim, and Kyung-Min Kim
Journal of Plant Biotechnology 2016; 43(1): 76-81Abstract : We performed a molecular marker-based analysis of quantitative trait loci for traits that determine the quality of appearance of grains using 120 doubled haploid lines developed by anther culture from the F1 cross between ‘Cheongcheong’ (
Journal of
Plant BiotechnologyGenealogical diagram of the Cheongcheong/Nagdong doubled haploid population. Cheongcheong is a Tongil-type rice cultivar from an
Frequency distribution of the alkali digestion valuesin 2013 and 2014. The distribution of brown rice (A) and milled rice (B) are investigated for two years. The black bars and indicators represent 2013data while the white bars and indicators represent 2014 data. The arrows and triangles indicate Cheongcheong and Nagdong, respectively
|@|~(^,^)~|@|Genetic locations ofQTLs related to the alkali digestion of brown and milled rice. The gray quadrangles are QTLs for milled rice in 2013, while the back quadrangle and diamond are QTLs for milled rice and brown rice, respectively, in 2014
|@|~(^,^)~|@|The PCR results of 49cultivars using three markers detected from the analysis of QTL related to alkali digestion value. A: RM223, B: RM3530, C: RM18130, 1: Cheongcheong, 2: Nagdong, 3: Jogwang, 4: Dongjin 1, 5: Dunnae, 6: Keumo 3, 7: Goun, 8: Geuroo, 9: Haepyeong, 10: Hanareum, 11: Hopum, 12: Hwayoung, 13:Jeoktomi, 14: Jinbu, 15: Jinmi, 16: Joan, 17: Joun, 18: Junam, 19: Namcheon, 20: Namil, 21:Nampyeong, 22: Obong, 23: Odae, 24: Samdeog, 25: Samgang, 26: Sangju, 27: Seolgang, 28: Wangchal, 29: Yangjo, 30: U-2, 31: Akenohgshi, 32: Fukunohana, 33: Hokuriku 130, 34: Ishikari, 35: Kitaake, 36: Koganenilcari, 37: Milk Princess, 38: Milky queen, 39: Princess sari, 40: Silewah, 41: Cakmak, 42: Demir, 43: Ece, 44: Efe, 45: Gonen, 46: Karadeniz, 47: Kizilmak, 48: Ilmi, 49: Baekjinju.