园艺与种苗
園藝與種苗
완예여충묘
Rain Fed Crops
2011年
4期
104-107
,共4页
邢桂梅%吴海红%徐兴伟%王茹
邢桂梅%吳海紅%徐興偉%王茹
형계매%오해홍%서흥위%왕여
君子兰%叶片%组织培养
君子蘭%葉片%組織培養
군자란%협편%조직배양
Clivia miniata Regel%Leaf%Tissue culture
[目的]筛选适宜君子兰叶片离体的条件。[方法]选取君子(Clivia miniata Regel)品种“油匠”的叶片为外植体进行离体培养,在MS培养基中附加不同浓度的2,4~D、BA、NAA和KT,对外植体采用不用时间的低温预处理,并对接种后的外植体分别进行不同时长的暗培养,研究不同培养条件对外植体愈伤组织诱导和分化的影响。[结果]叶片诱导分化的最佳培养基为MS+BA2.0mg/L+NAA3.0mg/L+KT1.0mg/L+蔗糖3.0%,诱导与分化率分别为59.2%和55.2%;暗培养10d后外植体诱导与分化率较高,为l3.8%和25.0%。[结论]培养基中加入活性炭对叶片诱导与分化不利;接种前低温预处理1d,叶片诱导与分化率较高,分别为3313%和25.0%、
[目的]篩選適宜君子蘭葉片離體的條件。[方法]選取君子(Clivia miniata Regel)品種“油匠”的葉片為外植體進行離體培養,在MS培養基中附加不同濃度的2,4~D、BA、NAA和KT,對外植體採用不用時間的低溫預處理,併對接種後的外植體分彆進行不同時長的暗培養,研究不同培養條件對外植體愈傷組織誘導和分化的影響。[結果]葉片誘導分化的最佳培養基為MS+BA2.0mg/L+NAA3.0mg/L+KT1.0mg/L+蔗糖3.0%,誘導與分化率分彆為59.2%和55.2%;暗培養10d後外植體誘導與分化率較高,為l3.8%和25.0%。[結論]培養基中加入活性炭對葉片誘導與分化不利;接種前低溫預處理1d,葉片誘導與分化率較高,分彆為3313%和25.0%、
[목적]사선괄의군자란협편리체적조건。[방법]선취군자(Clivia miniata Regel)품충“유장”적협편위외식체진행리체배양,재MS배양기중부가불동농도적2,4~D、BA、NAA화KT,대외식체채용불용시간적저온예처리,병대접충후적외식체분별진행불동시장적암배양,연구불동배양조건대외식체유상조직유도화분화적영향。[결과]협편유도분화적최가배양기위MS+BA2.0mg/L+NAA3.0mg/L+KT1.0mg/L+자당3.0%,유도여분화솔분별위59.2%화55.2%;암배양10d후외식체유도여분화솔교고,위l3.8%화25.0%。[결론]배양기중가입활성탄대협편유도여분화불리;접충전저온예처리1d,협편유도여분화솔교고,분별위3313%화25.0%、
[Objective] Selected the best medium for vitro cuhure. [Method] The leaf of Clivia miniata Regel. 'Youjiang' was used as explants for in vitro culture. The explants were cultured on MS medium supplemented with different concentration of 2,4-D,BA,NAA,KT and were treated with low temperature pretreatment. The inoculation explants were treated with dark culture. The influence of callus induction and differentiation were studied. [Result] The results showed that the best optimum medium was MS+BA2.0 mg/L+NAA3.0 mg/L+KT1.0 mg/L sucrose with induction and differentiation rates of 59.2 and 55.2 percentages; The induction rate were higher is 13.8 and 25.0 percentages after clark culturing for 10 day, [Conelusionl The active carbon was harmful to the callus induction and differentiation of leaf because of enhancing the browning of explants. The rates of induction and differentiation were higher after dark culturing forld and treating in 4 ℃ before inoculation with rates of 33.3 and 25.0 percentages respectively.