果树学报
果樹學報
과수학보
JOURNAL OF FRUIT SCIENCE
2005年
4期
405-408
,共4页
毕静华%刘永立%Syed ASGHAR
畢靜華%劉永立%Syed ASGHAR
필정화%류영립%Syed ASGHAR
阔叶猕猴桃%愈伤组织%叶片%不定芽再生
闊葉獼猴桃%愈傷組織%葉片%不定芽再生
활협미후도%유상조직%협편%불정아재생
Actinidialatifolia%Callus%Leaf explants%Shoot regeneration
以阔叶猕猴桃(Actinidia latifolia Merr.)叶片为外植体,通过器官发生途径诱导形成不定芽,探讨了不同激素组合、暗培养时间以及不同浓度的蔗糖对叶片器官发生和植株再生的影响.结果表明,BW+0.1 μmol/LNAA+5 μmol/L Zeatin附加20g/L蔗糖,先进行21 d暗培养然后转到光下培养效果最好,6周后不定芽再生频率达91.67%,平均每个外植体再生芽数6.87个.再生芽生根良好,生根率可达100%.首次报道了阔叶猕猴桃的器官发生和植株再生,建立了叶片的高效再生体系,为今后的遗传转化研究奠定了基础.
以闊葉獼猴桃(Actinidia latifolia Merr.)葉片為外植體,通過器官髮生途徑誘導形成不定芽,探討瞭不同激素組閤、暗培養時間以及不同濃度的蔗糖對葉片器官髮生和植株再生的影響.結果錶明,BW+0.1 μmol/LNAA+5 μmol/L Zeatin附加20g/L蔗糖,先進行21 d暗培養然後轉到光下培養效果最好,6週後不定芽再生頻率達91.67%,平均每箇外植體再生芽數6.87箇.再生芽生根良好,生根率可達100%.首次報道瞭闊葉獼猴桃的器官髮生和植株再生,建立瞭葉片的高效再生體繫,為今後的遺傳轉化研究奠定瞭基礎.
이활협미후도(Actinidia latifolia Merr.)협편위외식체,통과기관발생도경유도형성불정아,탐토료불동격소조합、암배양시간이급불동농도적자당대협편기관발생화식주재생적영향.결과표명,BW+0.1 μmol/LNAA+5 μmol/L Zeatin부가20g/L자당,선진행21 d암배양연후전도광하배양효과최호,6주후불정아재생빈솔체91.67%,평균매개외식체재생아수6.87개.재생아생근량호,생근솔가체100%.수차보도료활협미후도적기관발생화식주재생,건립료협편적고효재생체계,위금후적유전전화연구전정료기출.
An efficient plant regeneration protocol for A ctinidia latifolia was achieved via organogenesis from leaf explants in vitro. In this paper, effects of different combinations of growth regulators, dark treatments and sucrose concentrations on the organogenesis from leaf explants were examined. After 6 weeks of culture maximum shoot regeneration frequency of 91.67%with 6.87 shoots per explant was obtained on BW medium containing 0.1 μmol/L α-naphthaleneacetic acid, 5 μmol/L zeatin and 20 g/L sucrose incubated in the dark for 21 days then exposured to light. When cultured in darkness no explant regenerated shoots. However, shoots appeared quickly in the following week after exposure to light in the dark treatments for 14 d, 21 d and 28 d. It is considered that light is essential for shoot regeneration from leaf explants of A. latifolia. The lower sucrose concentration (10 g/L) promoted the formation of small and stunted shoots. Higher sucrose concentrations (≥30 g/L)had a detrimental effect on shoot regeneration, and 20 g/L sucrose gave the best results. The highest rooting rate reached 100% together with the maximum roots per explant (17.53) on BW medium containing 0.1 μmoL/L 6-benzyladenine and 10μmol/L indolebutyric acid. Plantlets with good root system were successfully acclimatized to the field conditions and produced healthy plants. To our knowledge, this is the first report of an in vitro regeneration method for A. latifolia. The results of this study will facilitate the application of genetic transformation methods in A. latifolia.