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An efficient protocol for Agrobacterium-mediated transformation of the biofuel plant Jatropha curcas by optimizing kanamycin concentration and duration of delayed selection

机译:通过优化卡那霉素浓度和延迟选择的持续时间农杆菌介导的生物燃料植物麻风树转化的有效方案

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摘要

Jatropha curcas is considered a potential biodiesel feedstock crop. Currently, the value of J. curcas is limited because its seed yield is generally low. Transgenic modification is a promising approach to improve the seed yield of J. curcas. Although Agrobacterium-mediated genetic transformation of J. curcas has been pursued for several years, the transformation efficiency remains unsatisfying. Therefore, a highly efficient and simple Agrobacterium-mediated genetic transformation method for J. curcas should be developed. We examined and optimized several key factors that affect genetic transformation of J. curcas in this study. The results showed that the EHA105 strain was superior to the other three Agrobacterium tumefaciens strains for infecting J. curcas cotyledons, and the supplementation of 100 mM acetosyringone slightly increased the transient transformation frequency. Use of the appropriate inoculation method, optimal kanamycin concentration and appropriate duration of delayed selection also improved the efficiency of stable genetic transformation of J. curcas. The percentage of β-glucuronidase positive J. curcas shoots reached as high as 56.0 %, and 1.70 transformants per explant were obtained with this protocol. Furthermore, we optimized the root-inducing medium to achieve a rooting rate of 84.9 %. Stable integration of the T-DNA into the genomes of putative transgenic lines was confirmed by PCR and Southern blot analysis. Using this improved protocol, a large number of transgenic J. curcas plantlets can be routinely obtained within approximately 4 months. The detailed information provided here for each step of J. curcas transformation should enable successful implementation of this transgenic technology in other laboratories.Electronic supplementary materialThe online version of this article (doi:10.1007/s11816-015-0377-0) contains supplementary material, which is available to authorized users.
机译:麻疯树被认为是潜在的生物柴油原料作物。目前,麻疯树的价值有限,因为其种子产量通常较低。转基因修饰是提高麻疯树种子产量的一种有前途的方法。尽管已经进行了农杆菌介导的麻疯树的遗传转化多年,但是转化效率仍然不能令人满意。因此,应该开发一种高效,简单的农杆菌介导的麻疯树遗传转化方法。在这项研究中,我们检查并优化了影响麻疯树遗传转化的几个关键因素。结果表明,EHA105菌株在感染J. curcas子叶的过程中优于其他三株根癌农杆菌菌株,补充100 mM乙酰丁香酮会稍微增加瞬时转化频率。使用适当的接种方法,最佳卡那霉素浓度和适当的延迟选择持续时间也提高了麻疯树稳定遗传转化的效率。 β-葡萄糖醛酸苷酶阳性麻疯树芽的百分率高达56.0%,通过该方案每个外植体获得1.70个转化子。此外,我们优化了生根诱导培养基,以使生根率达到84.9%。通过PCR和Southern印迹分析证实了T-DNA稳定整合到推定的转基因品系的基因组中。使用此改进的协议,大约4个月内可以常规获得大量的转基因麻疯树幼苗。此处提供的J. curcas转化每个步骤的详细信息应能使该转基因技术在其他实验室中成功实施。电子补充材料本文的在线版本(doi:10.1007 / s11816-015-0377-0)包含补充材料,可供授权用户使用。

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