费乌瑞它马铃薯茎尖分化成苗的培养基筛选与病毒的RT-PCR检测  

Screening the Culture Medium of Favorita Potato Meristem Differentiation Seedlings and RT-PCR Detection of Virus

作　　者：冯光惠[1] 杜虎平[1] 李夏隆[1] 亢福仁[1] 

机构地区：[1]榆林学院生命科学学院,陕西榆林719000

出　　处：《湖北农业科学》2014年第20期4988-4991,共4页Hubei Agricultural Sciences

基　　金：陕西省教育厅项目(08JK508;08JK509)

摘　　要：以分别携带3种病毒(PVX、PVY、PLRV)和纺锤块茎类病毒(PSTVd)的费乌瑞它(Favorita)马铃薯(Solanum tuberosum)无菌苗为材料,38℃、4 h热处理4周,剥离带1个叶原基的茎尖,接种至不同浓度激素组合的24种MS固体培养基上,24℃、16 h培养15 d后统计茎尖的愈伤组织诱导率和分化成苗率;反转录PCR(RT-PCR)检测茎尖分化再生苗的脱毒率。结果表明,最适宜费乌瑞它马铃薯茎尖分化成苗的培养基为MS+0.075 mg/L 6-BA+0.05 mg/L NAA+0.10 mg/L GA3,愈伤组织诱导率为75%,分化成苗率为47.5%;再生苗3种病毒PVX、PVY和PLRV的脱毒率分别为65%、90%和100%,纺锤块茎类病毒PSTVd的脱毒率为10%。Aseptic seedlings of Favorita potato carrying three kinds of potato viruses（PVX,PVY,PLRV） and potato spindle tuber viroid （PSTVd） were treated with 38 ℃,4 hours for 4 weeks,stripped with oneleaf primordia of potato meristem,inoculated with 24 kinds of MS solid media of different hormone combinations.The callus induction rate of meristem and differentiation seedling rate after cultured by 24 ℃,16 hours for 15 days were determined statistically.Reverse transcription PCR （RT-PCR） was used to detect the virus-free rate of meristem regeneration.The results showed that the best meristem differentiation medium was MS＋0.075 mg/L 6-BA ＋0.05 mg/L NAA＋0.10 mg/L GA3 with the callus inductionrate of 75％ and differentiation seedling rate of 47.5％.The rate of detoxification of regenerated plantlets of three potato virus PVX,PVY and PLRV were 65％,90％ and 100％.The virus-free rate of potato spindle tuber viroid was 10％.

关 键 词：费乌瑞它马铃薯(Solanum tuberosum) 茎尖 分化成苗 培养基 RT-PCR检测 

分 类 号：S532[农业科学—作物学]