期刊文献+

枸杞胚乳愈伤组织细胞的悬浮培养及无丝分裂的活体观察 被引量:5

SUSPENSION CULTURE OF ENDOSPERM CALLUS CELL AND AMITOSIS IN VITRO
在线阅读 下载PDF
导出
摘要 The endosperm calli were induced on MS basic medium supplemented with lppm 2,4-D,0.5ppm KT and 5% sucrose.The medium which contained lppm BAP,0.1ppm NAA and 2%sucrose was used for cell suspension culture.In suspension cell culture,amitosis of cleavagedivision of nucleus have been observed after 5 days of culture.First the nuclear membraneand nucleolus disappeared.The crevice appeared in the center of the nucleus,and the nucleusdivided into two daughter nuclei of similar size and each with a nucleolus.The daughter nu-cleus resembled an eye in shape.FoIlowing;the emergence of cell wall,the two new unequalcells were produced.Such amitotic division proceeded repeatedly until the callus developedand eventually plantlet regenerated, The endosperm calli were induced on MS basic medium supplemented with lppm 2,4-D, 0.5ppm KT and 5% sucrose.The medium which contained lppm BAP,0.1ppm NAA and 2% sucrose was used for cell suspension culture.In suspension cell culture,amitosis of cleavage division of nucleus have been observed after 5 days of culture.First the nuclear membrane and nucleolus disappeared.The crevice appeared in the center of the nucleus,and the nucleus divided into two daughter nuclei of similar size and each with a nucleolus.The daughter nu- cleus resembled an eye in shape.FoIlowing;the emergence of cell wall,the two new unequal cells were produced.Such amitotic division proceeded repeatedly until the callus developed and eventually plantlet regenerated,
出处 《Acta Botanica Sinica》 CSCD 1991年第6期478-481,共4页 Acta Botanica Sinica(植物学报:英文版)
基金 中国科学院科学基金资助课题
关键词 枸杞 胚乳 愈伤组织 细胞悬浮培养 Lycium Endosperm callus Cell suspension culture Amitosis of cleavage division Plantlets regeneration
  • 相关文献

参考文献7

  • 1桂耀林,武汉植物学研究,1986年,4卷,13页
  • 2王莉,遗传学报,1985年,12卷,433页
  • 3顾淑荣,植物学报,1985年,27卷,106页
  • 4孙敬三,实验生物学报,1984年,17卷,281页
  • 5陆文梁,中国科学.B,1983年,4期,321页
  • 6陆文梁,科学通报,1981年,12期,753页
  • 7顾淑荣,植物学报,1981年,23卷,246页

同被引文献158

引证文献5

二级引证文献42

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部