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논문 기본 정보

자료유형
학술저널
저자정보
저널정보
한국육종학회 한국육종학회지 한국육종학회지 제46권 제4호
발행연도
2014.1
수록면
372 - 380 (9page)

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We tried to develop the protocol for embryogenesis and plant regeneration from anther culture of carrot (Daucus carotaL.) genotype ‘S&P2342’. Anthers were cultured on MS medium with B5 vitamins containing different combinations of 2,4-Dand NAA for 18 weeks in the dark. The best induction of callus and embryo was obtained in the medium containing 0.1 mg/L2,4-D and 0.1 mg/L NAA, on which 22.0% callus and 2.0% embryo were induced. When primary embryos induced directly fromanther culture were transferred to the regeneration medium, secondary embryos were initiated from primary embryos after 4weeks of culture and 62.5% converted into plantlets after 8 weeks of culture. The plantlets with true leaves were obtained after12 weeks of culture. When the calli derived from anther culture were transferred to the regeneration medium, 38.8% of the calliproduced primary embryos and plantlets after 8 weeks of culture. The plantlets with 2 or more leaves cultured on the regenerationunder the different light intensity for the growth of in vitro plantlets. The plantlets cultured at 100 μmol・m-2・s-1 showed thehighest growth rate. For the acclimatization, the in vitro plantlets with 4 or more leaves cultivated under the different lightintensity and temperature, respectively. The survival rate and growth of plantlets was best at 15℃ and 100 μmol・m-2・s-1,respectively. The plants were successfully acclimatized and had a normal phenotype. The anther culture system could be usedto prepare the doubled haploid lines as an appropriate breeding material for F1 hybrid breeding program.

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