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铁皮石斛无菌播种产业化繁育技术研究
引用本文:付传明,赵志国,黄宁珍,何金祥,唐凤鸾,石云平. 铁皮石斛无菌播种产业化繁育技术研究[J]. 广西植物, 2012, 32(2): 238-242
作者姓名:付传明  赵志国  黄宁珍  何金祥  唐凤鸾  石云平
作者单位:付传明 (广西壮族自治区中国科学院,广西植物研究所,广西,桂林,541006) ; 赵志国 (广西壮族自治区中国科学院,广西植物研究所,广西,桂林,541006) ; 黄宁珍 (广西壮族自治区中国科学院,广西植物研究所,广西,桂林,541006) ; 何金祥 (广西壮族自治区中国科学院,广西植物研究所,广西,桂林,541006) ; 唐凤鸾 (广西壮族自治区中国科学院,广西植物研究所,广西,桂林,541006) ; 石云平 (广西壮族自治区中国科学院,广西植物研究所,广西,桂林,541006) ;
基金项目:广西科技攻关项目,广西林业厅项目,桂林市科学研究与技术开发计划项目,广西植物研究所基本业务费项目
摘    要:以铁皮石斛的蒴果为外植体,采用种子→原球茎→完整植株→移栽的途径快速成苗进行工厂化生产,对各阶段培养基进行筛选,以及其他一些影响因子进行比较研究。结果表明:人工授粉后生长60~180d的铁皮石斛种子在离体条件下均能萌发,其中授粉150~180d种子的萌发效果最好,萌发率为87.2%~94.4%,适宜的萌发培养基为MS+6-BA 1.0mg/L+NAA 0.1mg/L+马铃薯汁200g/L+AC 1.0g/L;原球茎增殖的最佳培养基为MS+6-BA 1.5mg/L+NAA 0.1mg/L+香蕉汁100g/L+AC 1.0g/L,繁殖系数约为20倍/50d;原球茎在MS+6-BA 1.0mg/L+NAA 0.1mg/L+马铃薯汁200g/L+AC 1.0g/L培养基上进行分化培养,分化的同时还能进行一定的增殖;将已分化的芽苗转接到壮苗培养MS+6-BA 0.5mg/L+NAA 0.2mg/L+香蕉汁100g/L+AC 1.0g/L上培养1代后,转接到生根培养基1/2MS+NAA 0.8mg/L+无机盐A 0.2~0.5mg/L+香蕉汁100g/L+AC 1.0g/L上,培养50~70d后,生根率100%,无机盐A可以有效地控制愈伤或原球茎的形成,明显提高生根苗的数量和质量。在桂林地区,生根苗以3~5月和9~10为最佳移栽期,以通过高温处理并堆沤腐熟的松树皮为基质,移栽成活率可达90%。

关 键 词:铁皮石斛  无菌播种  原球茎  产业化

Study on technology of aseptic sowing and rapid propagation of Demdrobium officinale
FU Chuan-Ming,ZHAO Zhi-Guo,HUANG Ning-Zhen,HE Jin-Xiang,TANG Feng-Luan,SHI Yun-Ping. Study on technology of aseptic sowing and rapid propagation of Demdrobium officinale[J]. Guihaia, 2012, 32(2): 238-242
Authors:FU Chuan-Ming  ZHAO Zhi-Guo  HUANG Ning-Zhen  HE Jin-Xiang  TANG Feng-Luan  SHI Yun-Ping
Affiliation:(Guangxi Institute of Botany,Guangxi Zhuang Autonomous Region and the Chinese Academy of Sciences,Guilin 541006,China)
Abstract:Seeds of Demdrobium officinale could be used as explants to rapid propagate by the way of seed→protocorm→the whole plant→transplant,and medium in each culture stage and some other factors were studied comparatively.The results showed that all seeds of D.officinale which were 60-180 d,especially 150-180 d after pollination could germinate,with a germination rate of 87.2%-94.4%.The suitable medium for seed germination was MS+6-BA 1.0 mg/L+NAA 0.1 mg/L+potato 200 g/L+active carbon 1.0 g/L.The best medium for the formation and multiplication of protocorm was MS+6-BA 1.5 mg/L+NAA 0.1 mg/L+banana mud 100 g/L+active carbon 1.0 g/L,the propagation coefficient was about 20 times/50 d.And the protocorm differentiated on MS+6-BA 1.0 mg/L+NAA 0.1 mg/L+potato 200 g/L+active carbon 1.0 g/L medium,which could have some multiplication in the meantime.After being cultured on MS+6-BA 0.5 mg/L+NAA 0.2 mg/L+banana mud 100 g/L+active carbon 1.0 g/L for a generation,the vigorous plantlets were transferred to rooting medium which was 1/2MS +NAA 0.8 mg/L+mineral salt A 0.2-0.5 mg/L +banana mud 100 g/L+active carbon 1.0 g/L and were cultured for 50-70 d,with 100% rooting rate.Mineral salt A could effectively control the formation of callus or protocorm,and obviously improve the quality and quantity of root regeneration plants.The best time for the transplantation of root regeneration plants was March-May and September-October in Guilin area.The plantlets were transplanted into rotten pine bark handled with high temperature in seedbed of greenhouse resulted in more than 90%survival rates.
Keywords:Demdrobium officinale  aseptic sowing  protocorm  industrialization
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