dc.contributor.advisor | Jae-Hoon Kim | |
dc.contributor.author | Bachchu, Md. Adnan Al | |
dc.date.accessioned | 2022-04-24T06:20:59Z | |
dc.date.available | 2022-04-24T06:20:59Z | |
dc.date.issued | 2011-02 | |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/754 | |
dc.description | Citrus fruits are economically valuable crops throughout the world due to their high
nutritional value, large volume of production, and use in diverse processed products
(Chaturvedi ef al., 2001). Miyagawa Wase, a common cultivar of the Satsuma mandarin
(Citrus unshiu Marc.), is grown in Korea, China, and Japan. Unlike most fruit species,
Satsuma mandarins are difficult to breed using conventional breeding methods due to long
juvenility, high heterozygosity, and several unique reproductive characteristics such as
polyembryony, generative sterility, and parthenocarpy (Grosser and Gmitter, 1990). As a
result, most cultivars of the Satsuma mandarin have arisen from bud mutations or clonal
selections despite efforts to develop new cultivars by sexual hybridization (Moore et al.,
2005). | en_US |
dc.description.abstract | Miyagawa Wase, a common cultivar of the Satsuma mandarin (Citrus unshiu Marc.), is
characterized by its tender peel and seedless nature. In this study, Agrobacterium-mediated
transformation of Miyagawa Wase was performd using embryogenic calluses from
unfertilized ovules. Agrobacterium tumefaciens strain EHA105 harboring the binary vector
pCAMBIA1300 that contained the miraculin gene (a taste-modifying protein) and
hygromycin as a selection marker were used. After 5 days of co-culture in a medium
containing 100 pM acetosyringone, calluses were transferred to the liquid half EME medium
with 15 mg/L hygromycin and 250 mg/L cefotaxime and then cultured for 2 weeks.
Subsequently, the calluses were grown on a solid selection medium with 20 mg/L
hygromycin for 4 weeks, followed by selection with 25 mg/L hygromycin for 4 more weeks.
Total 168 resistant embryos were selected and transferred to the embryo maturation medium.
After 3 weeks of culture, the heart-shaped embryos were transferred to MT medium
containing 1 mg/L GA3, 20 ml/L coconut water, 20 pg/L NAA, and 14.6 pg/L coumarin for
embryo germination. Finally, 135 germinated embryos were cultured on MT medium
containing 30 g/L sucrose and 8 g/L agar and recovered 115 normal plants. This
transformation procedure yielded 37 trangenic plants containing miraculin genes as verified
by PCR amplification. Southern blot analyse of 5 randomly selected plants further confirmed
the miraculin transgene was stably integrated into the Miyagawa Wase genome. | en_US |
dc.language.iso | en | en_US |
dc.publisher | JEJU NATIONAL UNIVERSITY | en_US |
dc.subject | three novel citrus ERF genes | en_US |
dc.subject | Phenotype analysis of the transgenic plants | en_US |
dc.subject | Cloning and sequencing of CuERF gene. | en_US |
dc.title | Functional expression of miraculin, a taste modifying protein, in Citrus unshiu Marc. and characterization of three novel citrus ERF genes | en_US |
dc.type | Thesis | en_US |