期刊文献+

黄姜组培快繁技术试验研究 被引量:6

Studies on Tissue Culture and Rapid Propagation of Dioscorea Zingi Berensis C.H.Wright
下载PDF
导出
摘要 分别以黄姜茎段、叶片、块根为外植体,进行无菌系建立、芽分化、生根等试验,探讨黄姜组培快繁技术.结果表明:(1)茎段在①MS+BA1.0mg.L-1+NAA0.2mg.L-1(单位下同);③MS+BA2.0+NAA0.2;⑤B5+BA1.0+NAA0.2;⑦B5+BA2.0+NAA0.2四个培养基上培养,均能诱导出愈伤组织,但尤以⑦号培养基长势最佳;而在这四个培养基上接种的叶片因为全被污染,无愈伤组织形成.(2)块根在②MS+BA1.0+NAA0.5;④MS+BA2.0+NAA0.5;⑥B5+BA1.0+NAA0.5;⑧B5+BA2.0+NAA0.5四个培养基上均不能诱导成愈伤组织.(3)愈伤组织在①~⑧号共八个培养基上均能分化出芽,但分化率不一,以③号最高(达100%),④号最低(25.0%).(4)当丛生芽长至高约3~4cm时,转接到以MS或1/2MS为基本培养基、附加有不同浓度NAA和IBA的培养基中,进行生根培养.生长素NAA与IBA配合均能诱导生根,NAA的浓度增高对根的诱导有抑制作用,而且使苗的生长受阻,出现叶片卷曲现象,用1/2MS与用MS相比,用1/2MS生根更粗壮.(5)将经过炼苗的生根试管苗移栽到混有河沙和砻糠灰(体积比为1:2)的复合基质中,移栽后35d成活率达到87%以上. Taking stem sections, tender leaves, roots of Dioscorea Zingi berensis C.H. Wright for explants respectively, experiments such as callus formation, buds differentiation, rooting were conducted. The results showed as follows: The first, stem sections were taken explants, callus could be produced in the following 4 mediums including ①MS + BA1.0 mg. L - 1 + NAA0.2 mg. L - 1 ( the unit was the same below) ,③MS + BA2.0 + NAA0.2,⑤B5 + BA1.0 + NAA0.2,⑦B5 + BA2.0 + NAA0.2 among which ⑦B5 + BA2.0 + NAA0. 2 was the best; The second, roots were taken explants, callus couldn, t be produced in the following 4 mediums including ②MS + BA1.0 + NAA 0.5 ;④MS + BA2.0 + NAA0.5 ;⑥B5 + BA1.0 + NAA0.5 ;⑧B5 + BA2.0 + NAA0.5. The third, sprouts could be differentiated from callus in the mediums from No. ① to No. ⑧ among which No.③ ,s differentiation rate was the highest( 100 % ) and No. ④ , s differentiation rate was the lowest (25.0 % ). The forth, when sprouts length amounted to 3 - 4 cm, rooting was conducted in MS or 1/2MS medium supplemented with different concentrations NAA and IBA, NAA matching with IBA could induce roots production and high NAA concentration inhibited roots production; roots were more robust in 1/2MS as compared to in MS. The fifth, 35 d after being transplanted, tube -seedlings grew well and the transplantation living rate amounted to up to 87.0 % on the compound substrate composed of fiver sand and long kang'ash (1:2 by volume) .
作者 梁称福 易诚
出处 《湖南环境生物职业技术学院学报》 CAS 2006年第2期135-138,共4页 JOurnal of Hunan Environment Biological Polytechnic
基金 湖南省教育厅资助项目(编号:04C027)
关键词 黄姜 组织培养 快速繁殖 Dioscorea Zingiberensis C.H. Wright tissue culture rapid propagation
  • 相关文献

参考文献2

二级参考文献15

  • 1莫成凡,Richard R Williams.影响培养基pH值变化的因素[J].Acta Botanica Sinica,1997,39(4):347-352. 被引量:4
  • 2许智宏.植物原生质体培养的进展[M].北京:科学出版社,1986..
  • 3Joan L. John,William H. Courtney,Dennis R. Decoteau. The influence of plant growth regulators and light on microtuber induction and formation in Dioscorea alata L. cultures[J] 1993,Plant Cell, Tissue and Organ Culture(3):245~252
  • 4D. Lauzer,G. Laublin,G. Vincent,M. Cappadocia. In vitro propagation and cytology of wild yams, Dioscorea abyssinica Hoch. and D. mangenotiana Miège[J] 1992,Plant Cell, Tissue and Organ Culture(2):215~223
  • 5Martine Jean,Mario Cappadocia. In vitro tuberization in Dioscorea alata L. ‘Brazo fuerte’ and ‘Florido’ and D. abyssinica Hoch[J] 1991,Plant Cell, Tissue and Organ Culture(3):147~152
  • 6Sinclair H. Mantell,Sarah A. Hugo. Effects of photoperiod, mineral medium strength, inorganic ammonium, sucrose and cytokinin on root, shoot and microtuber development in shoot cultures of Dioscorea alata L. and D. bulbifera L. yams[J] 1989,Plant Cell, Tissue and Organ Culture(1):23~37
  • 7Ana Maria Viana,Sinclair H. Mantell. Callus induction and plant regeneration from excised zygotic embryos of the seed-propagated yams Dioscorea composita Hemsl. and D. cayenensis Lam.[J] 1989,Plant Cell, Tissue and Organ Culture(2):113~122
  • 8Shou Yong Choy Ng. In vitro tuberization in white yam (Dioscorea rotundata Poir)[J] 1988,Plant Cell, Tissue and Organ Culture(2):121~128
  • 9Jayanti Sengupta,G. C. Mitra,A. K. Sharma. Organogenesis and tuberization in cultures of Dioscorea floribunda[J] 1984,Plant Cell, Tissue and Organ Culture(4):325~331
  • 10李宪章,李明福,侯林林.马铃薯无病毒苗的获得与病毒检测[J].植物学通报,1997,14(2):52-54. 被引量:3

共引文献34

同被引文献62

引证文献6

二级引证文献28

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