摘要
报道了金边瑞香顶芽在MS+0,05mg/L6-BA+0.1mg/LNAA培养基中预培养20d,再在34℃(11h)+23℃(13h)的昼夜温度交替下处理30d后,剥离0.2-0.3mm大小的茎尖在MS+0,1mg/L6-BA+0.1mg/LNAA培养基中的诱导成活率为80.0%,并获得脱毒苗。继代和增殖培养基为MS+0.5-1.0mg/L6-BA+0.1mg/LNAA,增殖系数4,1。试管苗在适宜培养条件下平均生根率为82.6%,在珍珠岩:泥炭=2:1基质中生根苗移栽成活率达到96.46%。
The following experimental results have been obtained:the terminal buds of Daphne odora var. naginata Mak were fires cultured on MS + 0.05 mg/L 6 - BA + 0.1 mg/L NAA for 20 days then in the condition of day and night with 34 ℃ (11 h) + 23 ℃ (13 h) For 30 days. The surviral radio with shoot - tip of 0.2 -0.3 mm was 80.0% on MS +0.1 mg/L6 - BA +0. lmgLNAA . The virus -free seedlings were obtained. The terminal buds diffevertiated a numbers of young buds on MS medium containing 6 - BA0.5 - 1.0 mg/L and NAA 0.1 mg/L. On this medium shoot multiplication occurred at a 4.1 - fold rate. The average ratio of rooting of the high - quali tyseeding was 82.6% in the suitable condition of culture. The survival ratio of transplanting reached 96.5% in the medium ( pearlite : peaty soil = 2 : 1 ).
出处
《南昌大学学报(理科版)》
CAS
北大核心
2008年第1期59-61,65,共4页
Journal of Nanchang University(Natural Science)
基金
国家科技部农业转化资金资助项目(05EFN213600143)
江西省农业重点资助项目(赣科鉴字[2005]16号)
关键词
金边瑞香
茎尖脱毒
快速繁殖
组织培养
Daphne odora var. naginata Mak
virus - free by shoot - tip
invitro propagation
tissue culture