摘要
以萱草的根茎为材料,进行愈伤组织诱导和分化,试管苗的生根、移栽和移植的研究,建立萱草再生体系技术。结果证明:MS+BA0.4mg/L+NAA0.1mg/L+2,4-D0.1mg/L是愈伤组织诱导培养的理想培养基;MS+NH_4H_2PO_450mg/L+BA1.0mg/L+NAA0.1mg/L是愈伤组织增殖继代培养的理想培养基;MS+AgNO_30.5mg/L+GA_30.5mg/L+BA0.5mg/L+NAA0.1mg/L是愈伤组织分化培养的理想培养基;1/2MS+NAA0.1mg/L+IAA0.2mg/L是不定芽生根培养的理想培养基。在河沙中试管苗易移栽成活;移植到花坛中的试管苗根系发达、生长旺盛。
The study was mainly to probe an efficient way through tissues culture and rapid propagation of Hemerocallis fulva. The rhizome was taken as explants.The main results are as follows:The optimum medium was MS+BA0.4mg/L+NAA0.1mg/L+2,4-D0.1mg/L for inducing callus; the optimum culture medium of proliferating callus was MS+NH4H2PO450mg/L+BA1.0mg/L+NAA0.1mg/L; the optimum culture medium of differentiating callus was MS+AgNO30.5mg/L+GA30.5mg/L+BA 0.5mg/L+NAA 0.1mg/L; the optimum culture medium for rooting was 1/2MS+NAA0.1mg/L+IAA0.2mg/L.The transplant medium with riversand is optimal for Hemerocallis fulva. Seedling transferred from test tubes grew well.
出处
《中国园艺文摘》
2010年第3期8-10,共3页
Chinese Horticulture Abstracts
关键词
萱草
组织培养
再生体系
Hemerocallis fulva
tissue culture
regeneration system