首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >Establishment of an Agrobacteriuim-mediated cotyledon disc transformation method for Jatropha curcas
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Establishment of an Agrobacteriuim-mediated cotyledon disc transformation method for Jatropha curcas

机译:农杆菌介导的麻疯树子叶盘转化方法的建立

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Jatropha curcas contains high amounts of oil in its seed and has been considered for bio-diesel production. A transformation procedure for J. curcas has been established for the first time via Agrobacterium tumefaciens infection of cotyledon disc explants. The results indicated that the efficiency of transformation using the strain LBA4404 and phosphinothricin for selection was an improvement over that with the strain EHA105 and hygromycin. About 55% of the cotyledon explants produced phosphinothricin-resistant calluses on Murashige and Skoog (MS) medium supplemented with 1.5 mg 1(-1) benzyladenine (BA), 0.05 mg 1(-1) 3-indolebutyric acid (IBA), 1 mg 1(-1) phosphinothricin and 500 mg 1(-1) cefotaxime after 4 weeks. Shoots were regenerated following transfer of the resistant calli to shoot induction medium containing 1.5 mg 1(-1) BA, 0.05 mg 1(-1) IBA, 0.5 mg 1(-1) gibberellic acid (GA3), 1 mg 1(-1) phosphinothricin and 250 mg 1(-1) cefotaxime, and about 33% of the resistant calli differentiated into shoots. Finally, the resistant shoots were rooted on 1/2 MS media supplemented with 0.3 mg 1(-1) IBA at a rate of 78%. The transgenic nature of the transformants was demonstrated by the detection of beta-glucuronidase activity in the primary transformants and by PCR and Southern hybridization analysis. 13% of the total inoculated explants produced transgenic plants after approximately 4 months. The procedure described will be useful for both, the introduction of desired genes into J. curcas and the molecular analysis of gene function.
机译:麻疯树的种子中含有大量的油,已被考虑用于生物柴油的生产。首次通过根癌土壤杆菌感染子叶盘外植体建立了麻疯树的转化方法。结果表明,与菌株EHA105和潮霉素相比,使用菌株LBA4404和膦丝菌素进行选择的转化效率有所提高。约55%的子叶外植体在补充了1.5 mg 1(-1)苄腺嘌呤(BA),0.05 mg 1(-1)3-吲哚丁酸(IBA),1的Murashige和Skoog(MS)培养基上产生了耐草丁膦的老茧4周后注射1 mg膦丝菌素和500 mg 1(-1)头孢噻肟。将抗性愈伤组织转移至含有1.5 mg 1(-1)BA,0.05 mg 1(-1)IBA,0.5 mg 1(-1)赤霉素(GA3),1 mg 1(- 1)膦丝菌素和250 mg 1(-1)头孢噻肟,约33%的抗性愈伤组织分化为芽。最后,将抗性枝条生根于补充有0.3 mg 1(-1)IBA的1/2 MS培养基上,比率为78%。通过检测初级转化体中的β-葡萄糖醛酸苷酶活性以及通过PCR和Southern杂交分析证明了转化体的转基因性质。大约4个月后,总接种外植体的13%产生了转基因植物。所描述的程序对于将所需基因引入麻疯树和基因功能的分子分析都是有用的。

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