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  • 學位論文

青脆枝的微體繁殖

The Micropropagation of Nothapodytes nimmoniana

指導教授 : 王亞男

摘要


以七月份採收未成熟的青脆枝種子,洗淨後以1%次氯酸鈉溶液超音波震盪處理10分鐘進行表面消毒,無汙染率84%。 青脆枝種子胚經無菌播種於MS培養基誘導無菌苗。再以無菌苗頂芽和莖段作為培殖體,置於MS培養基添加0.3mg/L TDZ,以頂芽誘導之多芽體發生率90%、莖段為83%。 多芽體切成1cm長的片段進行芽體抽長,以MS培養基添加0.2mg/L BA及0.1mg/L IBA促進芽體抽長,芽體抽長率87%,平均芽體長度4.2cm,之後以1/4MS培養基添加0.5mg/L IBA及1mg/L IAA誘導芽體發根,發根率達87%,平均發根數為每個培植體3根,平均根長4.6cm。 發根的芽體可用於馴化,馴化60天的成活率為55%。

關鍵字

青脆枝 微體繁殖 多芽體 TDZ 馴化

並列摘要


The Immature Nothapodyes nimmoniana seeds were harvested in July. The seeds were sterilized sonicated for 10 min with 1% sodium hypochlorite aqueous solution after washing, the sterilization rate was 84%. The zygotic embryos were sown on MS medium in aseptic environment for cultivating aseptic seedlings. The apical buds and stem segment of Nothapodyes nimmoniana aseptic seedling were used as explants for multiple buds inducing test. The optimal formula for multiple buds inducting test was MS medium and 0.3mg/L PGR TDZ. The induting rate on apical buds and stem segment were 90% and 83% respectively. Multiple buds were cut into 1cm segment for shoot elongation. The optimal formula for shoot elongation was MS medium, 0.2mg/L BA and 0.1mg/L IBA. Elongated shoots were used as explants for roots induction. The optimal formula for root induction was 1/4MS, 0.5mg/L IBA and 1mg/L IAA. Shoots with root were used in adaptation. The survival rate was 55%.

參考文獻


朱建鏞、馮莉真。2003。聖誕紅「光輝」之微體繁殖。植物種苗 5(2):48-60.
何政坤、張淑華。2007。利用青脆枝優良種苗枝葉生產喜樹鹼。林學研究專訊,14(1):35。
袁秋英、張育修、蔡巨才。2005。利用AFLP分子標誌技術探討台灣原生種青脆枝族群之遺傳變異。中國園藝,51(3):283-293。
陳冠燁。2008。無患子體胚誘導之研究。國立台灣大學森林環境暨資源學系碩士論文。
黃筱瑋。2008。粗肋草花序培養、不定芽再生繁殖及瓶內馴化。國立台灣大學生物資源暨農學院園藝系碩士論文。

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