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Method for plantlet formation of blueberry cv. Toro, Legacy or Oregonblue using leaf explant culture
Method for plantlet formation of blueberry cv. Toro, Legacy or Oregonblue using leaf explant culture
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机译:蓝莓cv植物苗形成的方法。使用叶片外植体培养的Toro,Legacy或Oregonblue
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摘要
PURPOSE: A method for plantlet formation of blueberry cv. toro, legacy or oregonblue is provided to increase the number of plantlets during a growth culturing process since a multi-shoot formation rate is higher than a meristem-tip culture. CONSTITUTION: A blueberry leaf is taken into a medium(1) to induce an initial callus and multi-shoot. 1 to 3 mg/L of Zeatin Riboside, 30 to 60 mg/L of FeNa-EDTA, 50 to 150 mg/L of myo-inositol, 1 to 3 mg/L Thiamine HCl, 0.5 to 1.5 mg/L of Nicotinic acid, 0.5 to 1.5 mg/L of Pyridoxine HCl, 10 to 30 g/L of sucrose, and 4 to 8 g/L of agar are added to the medium and then cultured in a next medium(2) to form a plant body. In the next medium, Zeatin Riboside is added at 1/10 of the above concentration or not added, or the medium(2) is cultured in a medium added with 0.1 to 3 mg/L of IBA(Indole-3-Butyric Acid) to induce formation of rood by circulating from a culturing chamber to a greenhouse. The medium(1) includes 1 to 3 mg/L of zeatin, 30 to 60 mg/L of FeNa-EDTA, 50 to 150 mg/L of myo-inositol, 10 to 30 g/L of sucrose, and 4 to 8 g/L of agar. [Reference numerals] (AA) 14 weeks; (BB) 18 weeks; (CC) 24 weeks; (DD) 34 weeks; (EE) 3 months
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机译:目的:一种用于蓝莓简历的植株形成的方法。提供toro,legacy或oregonblue,以在生长培养过程中增加小苗的数量,因为多重芽的形成速率高于分生组织的培养速率。组成:将蓝莓叶放入培养基(1)中以诱导初始愈伤组织和多枝。 1至3 mg / L玉米蛋白核苷,30至60 mg / L FeNa-EDTA,50至150 mg / L肌醇,1至3 mg / L盐酸硫胺,0.5至1.5 mg / L烟酸将0.5至1.5 mg / L盐酸吡rid醇,10至30 g / L蔗糖和4至8 g / L琼脂添加到培养基中,然后在下一个培养基(2)中培养以形成植物体。在下一个培养基中,以上述浓度的1/10加入或不加入玉米素核糖苷,或在添加有0.1至3 mg / L IBA(吲哚-3-丁酸)的培养基中培养培养基(2)。从栽培室到温室循环以诱导成群。培养基(1)包含1至3 mg / L玉米素,30至60 mg / L FeNa-EDTA,50至150 mg / L肌醇,10至30 g / L蔗糖和4至8克/升琼脂。 [参考数字](AA)14周; (BB)18周; (CC)24周; (DD)34周; (EE)3个月
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