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蔗糖對花生花藥癒合組織誘導及分化的影響

Effects of Sucrose on Callus Induction and Differentiation from Anther Culture in Arachis hypogaea L.

摘要


以栽培種花生(Arachis hypogaea L.)台南11號(TN11)及台農5號(TN5)二品種之單核期花藥為培植體,利用MS配方為基礎培養基,添加2 mg/l 2, 4-D及0.5 mg/l kinetin,再各分別添加30、60、90 g/l蔗糖,及8 g/l agar等三種培養基(代號分別為D30、D60、D90):TN11及TN5二品種在3種培養基癒合組織之誘導率均佳。TN11癒合組織之形成率隨蔗糖濃度增加而降低(92.2%,92.1%及83.2%),而TN5卻隨蔗糖濃度增加而增加(76.7%,89.3%及94.6%),但二品種均以60 g/l蔗糖時有最大的生長指數。TN11及TN5於含60 g/l蔗糖之D60培養基培養30天後,可產生體胚,其誘導率僅為2.0%,切片顯示體胚已發育至魚雷形期。而2品種在3種培養基均可形成白色突起,切片顯示白色突起為分化之根,內部已有維管束組織的分化。

關鍵字

花生 花藥培養 體細胞胚 體胚形成 分化

並列摘要


Anthers at uninucleate stage of two cultivars, Tainan No. 11 (TN11) and Tainong No. 5 (TN5) cultured on MS basal medium containing 2 mg/l 2, 4-D and 0.5 mg/l kinetin with addition of 30, 60, or 90 g/l sucrose , respectively.All the three media gave successful induction of callia, and showed that, when the level of sucrose increased, the callus induction rate decreased (92.2%, 92.1% and 83.2%) in TN11, while the rate increased (76.7%, 89.3% and 94.6%) in TN5. Both TN11 and TN5 had the heightest growth index of callus in D60 medium. After thirty days, both TN11 and TN5 cultured on D60 medium obtained the 2.0% of somatic embryo induction rate. When anthers of TN11 on D60 and D90 media, or TN5 on D30, D60 or D90 media, there produced the white protrusions. Observation by parraffin section showed that the somatic embryo stage had developed to torpedo stage and the white protrusions were the differentiated roots with vascular system inside.

被引用紀錄


鄭伊婷(2012)。蘭花花粉塊組織培養下小孢子發育的研究〔碩士論文,國立臺灣大學〕。華藝線上圖書館。https://doi.org/10.6342/NTU.2012.01102

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