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Rapid Propagation of Rhynchostylis retusa in Vitro
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作者 Yinkai Xi Biao Zeng Hengyu Huang 《Phyton-International Journal of Experimental Botany》 SCIE 2021年第3期987-1001,共15页
An efficient regeneration system of Rhynchostylis retusa was established to provide technical reference for the application of tissue culture tube seedlings in production.The mixtures of callus and protocorm from asep... An efficient regeneration system of Rhynchostylis retusa was established to provide technical reference for the application of tissue culture tube seedlings in production.The mixtures of callus and protocorm from aseptic germination were used as explants.The optimal media of each stage was selected for callus proliferation,protocorm occurrence and growth,rejuvenation and rooting via a single,complete combination and orthogonal experiment.The results showed that the optimal medium for callus proliferation,protocorms occurrence and growth was 1/2 Murashige and Skoog(MS)medium adding 50 g·L^(−1) banana puree,0.1 mg·L^(−1)α-naphthaleneacetic acid(NAA),1.5 mg·L^(−1)6-benzylaminopurine(6-BA)and 1.0 mg·L^(−1) kinetin(KT)with 17.33 proliferation coefficient of callus and 19.63 occurrence coefficient of buds after 90 days.Then the buds occurred from protocorm were cultured on 1/2 MS medium including 100 g·L^(−1) banana puree,1.0 mg·L^(−1) NAA,2.0 mg·L^(−1)6-BA and 0.05 mg·L^(−1) KT,in which the proliferation coefficient of callus was 10.32 and occurrence coefficient of buds reached 17.87.In the further subculture,the same medium was simultaneously used for callus proliferation,protocorm occurrence and bud growth.The plantlets developed roots in 1/2 MS medium containing 70 mL·L^(−1) coconut water and 1.5 mg·L^(−1) NAA with 100%rooting rates after 90 days.The survival rate was more than 90%after domestication and transplantation.This regeneration protocol will provide technique foundation for protecting wild resource and developing artificial cultivation. 展开更多
关键词 rhynchostylis retusa CALLUS PROTOCORM proliferation coefficient rapid propagation
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海南钻喙兰B类MADS-box基因的克隆与表达分析 被引量:9
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作者 张俊芳 李志英 徐立 《分子植物育种》 CAS CSCD 北大核心 2013年第4期570-574,共5页
为了更多的了解B类MADS-box基因对兰花花器官发育的调控机理,本研究通过设计简并引物,利用RT-PCR结合RACE技术从海南钻喙兰(Rhynchostylis gigantea)中分离得到两个B类MADS-box基因。序列分析表明,两基因分别属于B类MADS-box基因的AP3... 为了更多的了解B类MADS-box基因对兰花花器官发育的调控机理,本研究通过设计简并引物,利用RT-PCR结合RACE技术从海南钻喙兰(Rhynchostylis gigantea)中分离得到两个B类MADS-box基因。序列分析表明,两基因分别属于B类MADS-box基因的AP3和PI家族,命名为RgAP3和RgPI。RgAP3基因含有一个675bp的开放阅读框(ORF),编码225个氨基酸,RgPI基因含有一个633bp的开放阅读框,编码211个氨基酸。表达分析显示,两基因仅在生殖器官中表达,而在营养器官中没有表达,其中RgPI在花器官的各个部分均有表达,而RgAP3仅在花瓣、萼片中有表达,而在花梗和子房中没有表达。 展开更多
关键词 海南钻喙兰(rhynchostylis gigantea) MADS-BOX基因 表达模式
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