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作 者:刘雪梅[1] 罗雪梅[1] 王征[1] 金晓玲[1]
机构地区:[1]中南林业科技大学风景园林学院,中国长沙410004
出 处:《湖南师范大学自然科学学报》2014年第2期17-21,共5页Journal of Natural Science of Hunan Normal University
基 金:湖南省科技计划资助项目(2011NK3040);湖南省研究生科研创新基金资助项目(CX2012B329);中南林业科技大学研究生科技创新基金资助项目(CX2012B06)
摘 要:为了建立通过直接器官发生途径的榉树微繁技术体系,以当年生带芽茎段为外植体,进行了榉树不定芽的直接诱导试验.结果表明:适合不定芽诱导的培养基为MS+BA2.25—4.50μmol/L,有效芽诱导率达到76.67%;继代增殖培养的培养基为MS+BA2.25μmol/L,增殖系数为5.1;壮苗培养基为MS+BA2.25μmol/L+GA31.45μmol/L;生根培养基为1/2MS+NAA2.69μmol/L+活性炭0.1g·L^-1,生根率77.78%,生根数达4.5条.In order to establish Zelkova schneideriana regeneration system through a direct organogenesis way, the current-year stems with a bud was used as explants. Results show that it was cultured on Murashige and Skoog's (MS) medium that supplemented with 2.25 μmol/L to 4.50 μmol/L 6-benzylaminopurine (BA) to induce adventitious bud, and 76.67% of stems with a bud can form adventitious bud. Then the adventitious bud was subcul- tured on MS containing 2.25 μmol/L BA to propagate shoots, and approximately five shoots per-explants were propagation. Shoots were cuhured on MS supplemented with 2.25 ixmol/L BA and 1.45 μmol/L Gibberellin A3 ( GA3 ) could be got sound seedling. The shoots were rooted on 1/2MS containing 2.69 μmol/L naphthylene acetic acid (NAA) and 0.1 g · L^-1 activated carbon, on which 77.78% shoots developed roots with average of 4.5 roots per-shoot.
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