摘要
唐菖蒲种球微小茎尖在MS+6-BA 1.0~1.5 mg·L-1+NAA0.1~0.15 mg·L-1的培养基上可诱导出丛生芽,每25 d继代扩繁1次,增殖系数为3~4倍;将无根苗接种到1/2 MS+NAA 0.3 mg·L-1的培养基上,15~20 d便可形成良好的根系;继续培养3~4个月,可形成试管小球茎。经检测,供试的5个品种的组培苗均未发现感染菜豆黄花叶病毒、黄瓜花叶病毒、烟草环斑病毒和蚕豆萎焉病毒,获得无病毒植株。将无毒试管小球茎作为原原种,在隔离网内进行栽培繁殖,可为大田生产提供无毒种球。
The shoot tips of the bulbs of Gladiolus hybrids were selected as explants for tissue culture. They were cultured on MS medium containing 1 -1.5 mg L-1 BA and 0.1 -0. 15 mg L- NAA and induced to produce clustered buds. The clustered shoots were proliferated 3 to 4 times every 25 days after the clustered buds were subcuhured. Rootless plantlets formed a strong root system on the 1/2 MS culture medium supplemented with 0.3 mg L-1 NAA in 15 to 20 days, and then produced in vitro bulbs after 3 to 4 months of subculture. Virus detection showed that the in vitro bulbs of 5 varieties of G. hybrids were free of bean yellow mosaic virus (BYMV), cucumber mosaic virus (CMV), tobacco ring spot virus (TRSV) and broad bean wilt virus (BB- WV). These virus- free in vitro bulbs (initial bulbs) were cultivated in the net house for propagation of G. hy- brids. The virus-free bulbs propagated from the bulbs in the net house can be used for commercial cultivation in the field.
出处
《热带生物学报》
2013年第3期246-250,256,共6页
Journal of Tropical Biology
基金
福建省林业厅花卉种苗科技攻关项目
关键词
唐菖蒲
茎尖培养
脱毒
试管球
繁殖体系
Gladiolus hybrids
shoot-tip culture
detoxification
in vitro bulb
proliferation system