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茎用芥菜细胞质雄性不育系子叶原生质体培养和高效植株再生(英文)
引用本文:陈利萍,张明方,平田豊,曹家树,陈竹君.茎用芥菜细胞质雄性不育系子叶原生质体培养和高效植株再生(英文)[J].植物生理与分子生物学学报,2001,27(5):437-440.
作者姓名:陈利萍  张明方  平田豊  曹家树  陈竹君
作者单位:陈利萍(浙江大学农业与生物技术学院园艺系,杭州 310029)       张明方(浙江大学农业与生物技术学院园艺系,杭州 310029)       平田(日本东京农工大学农学部研究生院,东京 183-8509)       曹家树(浙江大学农业与生物技术学院园艺系,杭州 310029)       陈竹君(浙江大学农业与生物技术学院园艺系,杭州 310029)
基金项目:This work was supported by the Natural Science Foundation of Zhejiang (J39832).
摘    要:利用茎用芥菜细胞质雄性不育系原生质体培养获得了再生植株,并研究了影响原生质体培养的因素.结果表明,子叶是茎用芥菜原生质体培养最佳的外植体,10 d苗龄的子叶原生质体在改良MS培养基上培养3 d后发生第1次细胞分裂,6 d后发生第2次分裂,3周后形成细胞团,5周后形成肉眼可见的小愈伤.培养基中缺少NAA或2,4-D都会降低愈伤组织的再生能力.在含一定浓度的NAA(0.25 mg/L)和2,4-D(0.25 mg/L)培养基上诱导的愈伤组织质地致密且有光泽,芽的分化能力高;在MS+BA l mg/L+NAA 0.2 mg/L的培养基上芽的分化频率高达近29%,再生芽在1/2MS+NAA0.1 mg/L培养基上生根,形成完整植株.

关 键 词:茎用芥菜  细胞质雄性不育系  原生质体培养  植株再生
修稿时间:2000年2月28日

Efficient Plant Regeneration from Cotyledon-derived Protoplasts of Cytoplasmic Male-sterile Tuber Mustard (Brassica juncea Coss. var. tumida Tsen et Lee)
Abstract.Efficient Plant Regeneration from Cotyledon-derived Protoplasts of Cytoplasmic Male-sterile Tuber Mustard (Brassica juncea Coss. var. tumida Tsen et Lee)[J].Journal Of Plant Physiology and Molecular Biology,2001,27(5):437-440.
Authors:Abstract
Abstract:Plants of cytoplasmic male sterile (CMS) tuber mustard were regenerated from cotyledon derived protoplasts. The factors affecting protoplast culture and plant regeneration were studied. Protoplasts isolated from 10 day old seedlings of CMS tuber mustard showed cell division upon culture on modified MS medium, and microcalli were produced at a high plating efficiency of nearly 16% after a 5 week culture. Various combinations and concentrations of growth regulators were added to the medium for the proliferation of microcalli, and to obtain regenerants from the calli. The results showed that NAA or 2,4 D was necessary for callus proliferation. The absence of NAA and 2,4 D resulted in production of the callus with low regenerative potential, and in the presence of NAA ( 0.25 mg/L) and 2,4 D(0.25 mg/L), compact and bright calli were produced with high reproductive potential. Regenerated shoots were obtained at a frequency of nearly 29% when the compact and bright calli were selected and transferred at an early stage to the medium containing BA (1 mg/L) and NAA( 0.2 mg/L). All the regenerated shoots were rooted on 1/2 MS medium with NAA 0.1 mg/L added.
Keywords:tuber mustard  cytoplasmic male  sterile line    protoplast culture  regeneration  
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