Show simple item record

dc.contributor.advisorJae-Hoon Kim
dc.contributor.authorBachchu, Md. Adnan Al
dc.date.accessioned2022-04-24T06:20:59Z
dc.date.available2022-04-24T06:20:59Z
dc.date.issued2011-02
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/754
dc.descriptionCitrus 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.abstractMiyagawa 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.isoenen_US
dc.publisherJEJU NATIONAL UNIVERSITYen_US
dc.subjectthree novel citrus ERF genesen_US
dc.subjectPhenotype analysis of the transgenic plantsen_US
dc.subjectCloning and sequencing of CuERF gene.en_US
dc.titleFunctional expression of miraculin, a taste modifying protein, in Citrus unshiu Marc. and characterization of three novel citrus ERF genesen_US
dc.typeThesisen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record