摘要
以刚果12号桉授粉13-16d的胚珠为外植体,消毒处理后对胚珠进行离体培养。结果表明:最佳诱导愈伤组织的培养基为MS+1.5mg·L^-1 6-BA+1.0mg·L^-1 IAA,诱导频率32.5%;将红色紧密的愈伤组织转至MS+1.0mg·L^-1 6-BA+1.0mg·L^-1 NAA的培养基上,经连续继代后形成不定芽,根据多倍体的形态特征,对再生植株进行分离培养,生根后取根尖染色体显微观察,染色体数目均为33。
Taking ovules pollinated 13- 16 d of eucalyptus 12ABL as materials, the endosperm development was at vigorous stage, suitable for culture in vitro at this moment. The experiments showed that endosperm inoculated on MS medium supplemented with 1.5 mg · L^-1 6-BA and 1.0 mg·L^-1 IAA, gave the highest callus induction rate (32.5 %). Endesperm callus cultured in medium MS containing 1.0 mgL^-1 6- BA and 1.0 mg · L^-1 , could regenerate more shoots than those in any other media. Many endosperm-derived plantlets were obtained and were proved to be triploid plants by observing the chromosomes under microscope.
出处
《西北林学院学报》
CSCD
北大核心
2008年第3期101-104,113,共5页
Journal of Northwest Forestry University
基金
华南热带农业大学科技基金
海南省教育厅高校科研资助项目(HjKj200625)
华南热带农业大学大学生创新基金项目
关键词
刚果12号桉
胚乳培养
植株再生
Eucalyptus 12ABL
endosperm culture
plant regeneration