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  • 學位論文

千年桐之組織培養

Tissue culture of Aleurites montana

指導教授 : 王亞男

摘要


本研究以千年桐的未成熟、成熟種子,經過1%次氯酸鈉消毒10分鐘,置於MS培養基,在25℃光照16小時、光度28μEm-2s-1下,可100%發芽成無菌苗。將無菌苗之莖段切成0.5~1.0cm,置入MS添加4mg/l BA中4週,可誘得綠色癒合組織,再將其切取0.5cm3放入MS添加4mg/L BA與0.1mg/L IBA,光照16小時,8週後可誘得97%多芽體。   切取無菌苗之根,置於MS添加4mg/L BA,光照16小時,4週後,每一培殖體可誘導48.2個體胚;如繼代於同樣培養基,在相同培養下,可產生二次體胚;將體胚置於添加0.1mg/l IBA培養基中,可促進體胚成熟及轉換率。   另取2.0mg/l綠色硬實的癒合組織,置入含50ml液態培養基中,每7天以舊液:新液=1:5進行繼代,1個月後增殖為3.3mg/L ,且有細胞質濃密之細胞團出現。

關鍵字

千年桐 癒合組織 多芽體 體胚 懸浮培養

並列摘要


The Mature and non-mature seeds of Aleurites montana were used in this study, after arterialized with 1% sodium hypochlorite solution for 10 minutes. The seeds were cultured in MS culture medium, treated at 25℃ with a photoperiod of 16 hours and a light intensity of 28μEm-2s-1,which would result in 100% aseptic seedling. Cutting the stem of aseptic seedling into a length of 0.5~1.0 cm, cultured the samples in MS culture medium with 4mg/IBA for 4 weeks, which could induce the green callus, then taking 0.5cm3 sample from the green callus, cultured the sample in MS culture medium with 4mg/IBA, treated with a photoperiod of 16 hours, which could induce 97% multi-buds after 8 weeks. Cutting roots from the aseptic seedlings, the roots were cultured in MS culture medium with 4mg/IBA, treated with a photoperiod of 16 hours, after 4 weeks, each explants could induce 48.2 somatic embryos, if sub-cultured in the same culture medium and with the same treatment, which could produce secondary somatic embryo; putting somatic embryo in the culture medium with 0.1mg/IBA, which would promote the maturation of somatic embryo and conversion ratio. Taking 2.0mg/l green and tight callus, putting in 50ml liquid culture medium, in every 7 days, it was sub-cultured under the conditions of old liquid : new liquid = 1:5, which would increase to 3.3mg/l, and appear the formation of cell with dense cytoplasm.

參考文獻


陳冠燁 (2008) 無患子體胚誘導之研究,國立台灣大學森林研究所碩士論文。
Tsay, H. S., P. C. Lai and L. J.Chen (1982) Organ differentiation from callus deived from anther, stem and tuber of sweet potato. J. Agric. Res. China. 31:191-198.
Ashok-Kummar, H. G., H. N. Murthy and K. Y. Peak (2002) Somatic embryogenesis and plant regeneration in Gymnema Sylvestre. Plant Cell Tiss. Org. Cult. 71: 85-88.
Attree, S. M., S. Budimir and L. C. Fowke (1990) Somatic embrogenesis and regeneration from cultured shoots and cotyledons of seedlings from stored seeds of black and white spurce (Picea mariana and picea glauca). Can. J. Bot. 68: 30-34.
Attree, S. and Fowke, L. C (1993) Embryogeny of gymnosperms:advances in sybthetic seed technology of conifers Plant Cell Tiss. Org. Cult. 35:1-35.cultures of Eucalyptus. Plant Sci. Lett. 14: 63-65.

被引用紀錄


周沁澐(2017)。薄葉嘉賜木微體繁殖之研究〔碩士論文,國立臺灣大學〕。華藝線上圖書館。https://doi.org/10.6342/NTU201700521

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