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西洋参叶肉原生质体的游离与培养
引用本文:高利.西洋参叶肉原生质体的游离与培养[J].安徽农业科学,2007,35(23):7194-7195.
作者姓名:高利
作者单位:辽东学院农学院,辽宁丹东,118003
摘    要:目的]为了探讨西洋参叶肉原生质体游离和培养的最佳条件。方法]以5年生西洋参为材料,研究了纤维素酶的种类,酶的浓度和渗透压对西洋参叶肉原生质体游离的影响,并探讨了西洋参叶肉原生质体在KM8P、MS基本培养基中的分裂情况。结果]在混合酶液其他组分相同的情况下,日本产R-10纤维素酶的游离效果最好。酶浓度为4%时,3 h后大部分叶片都被解离成原生质体。幼嫩叶片的原生质体产量最高,为4.8×105个/g。KM8P培养基适合于西洋参叶肉原生质体的培养,较高的2,4-D浓度可以促进分裂。结论]用混合酶系统处理,能够获得大量(4.8×105个/g)有活性的原生质体。游离原生质体的酶浓度以1%~2%为宜。KM8P+2,4-D(2.0 mg/L)+6-BA(2.0 mg/L)+KT(0.7 mg/L)培养基适宜培养西洋参叶肉原生质体。

关 键 词:西洋参  原生质体  游离    培养基
文章编号:0517-6611(2007)23-07194-02
修稿时间:2007-04-15

Primary Discussion on Leaf Protoplast Dissociation and Culture of America Ginseng
GAO Li.Primary Discussion on Leaf Protoplast Dissociation and Culture of America Ginseng[J].Journal of Anhui Agricultural Sciences,2007,35(23):7194-7195.
Authors:GAO Li
Institution:College of Agronomy, Liaodong University, Dandong, Liaoning 118003
Abstract:Objective] The study aimed to discuss the optimum conditions of leaf protoplast dissociation and culture of America ginseng.Method] With 5-year-old America ginseng as material,the effects of cellulase species,enzyme concentrations and osmotic pressure on leaf protoplast of America ginseng were studied and the dissociation of America ginseng leaf protoplast on KM8P and MS basic medium wasdiscussed.Result] When the other components of mixed enzyme liquid was same,the dissociation effect of R-10 cellulase made in Japan was best.When the enzyme concentration was 4%,most leaves were dissociated into protoplasts after 3 h.The protoplast output of young leaves was highest,being 4.8×105 per gram.KM8P medium was proper to cultivate America ginseng leaf protoplast and 2,4-D with higher concentration could promote the dissociation.Conclusion] A lot of activated protoplasts(4.8×105 /g) were got through mixed enzyme system treatment.The enzyme concentration for dissociatingprotoplast should be 1 %~2 % and mediumfor cultivatingAmerica ginsengleafprotoplast should be KM8P + 2,4-D(2.0)+ 6-BA(2.0)+ KT(0.7).
Keywords:America ginseng  Protoplast  Dissociation  Enzyme  Culture medium
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