热带农业科学
熱帶農業科學
열대농업과학
CHINESE JOURNAL OF TROPICAL AGRICULTURE
2015年
7期
22-26,35
,共6页
陆顺教%易双双%任羽%冷青云%黄少华
陸順教%易雙雙%任羽%冷青雲%黃少華
륙순교%역쌍쌍%임우%랭청운%황소화
蝴蝶兰%叶片%不定芽%TDZ%暗培养
蝴蝶蘭%葉片%不定芽%TDZ%暗培養
호접란%협편%불정아%TDZ%암배양
Phalaenopsis%leaf%adventitious bud%TDZ%dark culture
以蝴蝶兰幼嫩花梗诱导的无菌苗叶片为外植体,以MS为基本培养基,研究不同暗培养时间和TDZ浓度对蝴蝶兰叶片诱导不定芽的影响。结果表明:暗培养和TDZ对接种的蝴蝶兰叶片的成活率均具有显著影响,暗培养60 d时,叶片的存活率在90%以上,而在同一暗培养时间条件下,叶片的存活率随着TDZ浓度的增加而上升;在TDZ浓度为3.0 mg/L,暗培养60 d时,蝴蝶兰存活叶片不定芽的诱导率最高,达到93.45%;诱导的不定芽数最多,平均每个外植体诱导的不定芽数为13.22个。综合考虑外植体的成活率、不定芽诱导率和诱导的不定芽数,蝴蝶兰叶片诱导不定芽的最佳条件为: MS+TDZ 3.0 mg/L,暗培养60 d。
以蝴蝶蘭幼嫩花梗誘導的無菌苗葉片為外植體,以MS為基本培養基,研究不同暗培養時間和TDZ濃度對蝴蝶蘭葉片誘導不定芽的影響。結果錶明:暗培養和TDZ對接種的蝴蝶蘭葉片的成活率均具有顯著影響,暗培養60 d時,葉片的存活率在90%以上,而在同一暗培養時間條件下,葉片的存活率隨著TDZ濃度的增加而上升;在TDZ濃度為3.0 mg/L,暗培養60 d時,蝴蝶蘭存活葉片不定芽的誘導率最高,達到93.45%;誘導的不定芽數最多,平均每箇外植體誘導的不定芽數為13.22箇。綜閤攷慮外植體的成活率、不定芽誘導率和誘導的不定芽數,蝴蝶蘭葉片誘導不定芽的最佳條件為: MS+TDZ 3.0 mg/L,暗培養60 d。
이호접란유눈화경유도적무균묘협편위외식체,이MS위기본배양기,연구불동암배양시간화TDZ농도대호접란협편유도불정아적영향。결과표명:암배양화TDZ대접충적호접란협편적성활솔균구유현저영향,암배양60 d시,협편적존활솔재90%이상,이재동일암배양시간조건하,협편적존활솔수착TDZ농도적증가이상승;재TDZ농도위3.0 mg/L,암배양60 d시,호접란존활협편불정아적유도솔최고,체도93.45%;유도적불정아수최다,평균매개외식체유도적불정아수위13.22개。종합고필외식체적성활솔、불정아유도솔화유도적불정아수,호접란협편유도불정아적최가조건위: MS+TDZ 3.0 mg/L,암배양60 d。
Used leaves of in vitro plantlets which induced from young pedicels of Phalaenopsis as explants and the MS as basal medium, the effect of dark culture phase and TDZ on adventitious shoot induction from leaves of Phalaenopsis were investigated. The result showed that: dark culture and TDZ had a significant impact on survival rate of inoculated leaves, and the survival rate was more than 90%when the dark culture phase was 60 d, the survival rate increased with the increase of TDZ concentrations under same dark culture phase; The highest inductivity of 93.45% and maximum average number of adventitious shoots were obtained on the MS medium supplemented with 3.0 mg/L TDZ and under 60 d dark culture. Considering of survival rate, regeneration rate and adventitious shoot number, the optimum culture condition for adventitious shoots induction from leaf explants of Phalaenopsis was MS appended with 3.0 mg/L TDZ and 60 d dark culture treatment.