期刊文献+

金钱树的组织培养 被引量:5

Tissue Culture of Zamioculcas zamiifolia (Loddiges) Engler
在线阅读 下载PDF
导出
摘要 以金钱树[Zamioculcaszamiifolia(Loddiges)Engler]的幼嫩小叶为外植体,采用幼叶→愈伤组织→丛生芽→完整植株的途径进行繁殖。结果表明:叶片在MS+BA2mg/L+2,4-D1.0mg/L+PVP0.5mg/L+活性炭0.5mg/L+蔗糖30g/L培养基上暗培养30d,可诱导形成愈伤组织;愈伤组织在MS+BA4mg/L+KT0.5mg/L+蔗糖30g/L培养基上光照培养25d,可诱导形成丛生芽(丛生芽在继代培养过程中每20~25d可增殖3~5倍);丛生芽接种于MS+BA3mg/L+NAA0.2mg/L+蔗糖30g/L培养基上壮苗培养4周后,再转入1/2MS+BA2mg/L+NAA0.5mg/L+蔗糖30g/L培养基上培养30d,可诱导形成完整的根系。 Leaf explants of Zamioculcas zamiifolia (Loddiges) Engler were inoculated on MS medium containing 2 mg/L BA (6-benzylaminopurine), 2,4-D (2,4-dichlorophenoxya-cetic acid) 1.0 mg/L, PVP (Polyvinylpyrolidone) 0.5 mg/L, AC (Active carbon) 0.5 mg/L, 30 g/L Suc for inducing callus. After being cultured in darkness for 25 days, calli were formed. They were then transferred onto the MS medium supplemented with 4 mg/L BA, 0.5 mg/L KT and 30 g/L Suc for inducing clustered buds. The clustered buds were formed after being cultured for 25 days (they were multiplied 3-5 times every 20-25 days of subculture). After cultured on the MS medium containing 0.2 mg/L NAA, 3 mg/L BA and 20 g/L Suc for about 4 weeks, the clustered buds were transferred onto the 1/2 MS medium containing 0.5 mg/L NAA, 2 mg/L BA and 30 g/L Suc for roofing. This cultural system is very useful for commercial proliferation of Z. zamiifolia.
出处 《热带农业科学》 2006年第2期19-21,32,共4页 Chinese Journal of Tropical Agriculture
关键词 金钱树 观赏植物 组织培养 愈伤组织 丛生芽 Zamioculcas zamiifolia (Loddiges) Engler tissue culture
  • 相关文献

参考文献5

二级参考文献25

  • 1李永红,谢利娟.外源激素对一品红扦插效应初探[J].深圳职业技术学院学报,2002,1(2):21-24. 被引量:2
  • 2张育松,赖明志,陈华冠,陈井木.5种外源物质对台湾种茉莉扦插生根的效应[J].福建农业大学学报,1997,26(1):44-47. 被引量:22
  • 3[1]Metha U, IVR Rao , H Y Mohan Ram. Somatic embryogenesis in bamboo. In: Proc. V. International Congress of Plant Tissue & Cell Culture. 1982:109~110
  • 4[3]Huang L C , T Murashige. Tissue culture investigation of bamboo. I. callus cultures of bambusa, Phyllostachys, and Sasa. Bot. Bull. Academia Sninca, 1983, 24:31~52
  • 5[4]Rao I U, IVR Rao, V Narang. Somatic embryogenesis and regeneration of plants in the bamboo. Plant Cell Reports, 1985, 4:191~194
  • 6[5]Yeh M L, W C Chang. Somatic embryogenesis and subsequent plant regeneration from inflorescence of bambusa beecheyana Munro vqr. Beecheyana. Plant Cell Reports,1986, 5:409~411
  • 7[6]Yeh M L,W C Chang. Plant regeneration through somatic embryogenesis in callus culture of green bamboo(Bambusa oldhamii Munro). Theor Appl Grnet, 1986,73:161~163
  • 8[7]Yeh M L,W C Chang. Plant regeneration via somatic embryogenesis in mature embryo-de-rived callus culture of Sinocalamus Iatiflora (Munro) McClure. Plant Science, 1987, 51:93~96
  • 9[8]Huang L C, W L Chen,B L Huang. Tissue culture investigations of bamboo II. Liquid suspension cultures of bambusa, Phyllostachys and Sasa cells. Bot . bull. Academia Sinica, 1988, 29:177~182
  • 10[9]Huang L C, W L Chen , B L Huang. Tissue culture investigations of bamboo III. A method for viable protoplast isolation from Bambusa celis of liquid suspension culture. Bot. Bot . bull. Academia Sinica, 1989,30:49~57

共引文献40

同被引文献29

引证文献5

二级引证文献5

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