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Highly efficient plant regeneration and Agrobacterium-mediated transformation of Helianthus tuberosus L.

机译:向日葵的高效植物再生和农杆菌介导的转化。

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In our current study, to develop an efficient regeneration and transformation system of Helianthus tuberosus, we verified effects of plant growth hormones, growth conditions, explant type, and transformation conditions. Leaf segments from regenerated shoots showed higher regeneration efficiency on MS basal medium containing 1.0 mg L-1 zeatin under darkness than those from maintained in vitro plant. To carry out transformation, various parameters including plant materials, Agrobacterium cell density, immersion time, and Agrobacterium strains (leaf segment, OD600-0.6, 60 min, and Agrobacterium tumefaciens LBA4404 harboring binary vector pCAMBIA1301) have been determined. The putatively transformed H. tuberosus were screened by survival rate and beta-glucuronidase (GUS) histochemical assay following two cycles of 3.0 mg L-1 hygromycin selection at callus stage. The presence of the selectable marker gene hygromycin phosphotransferase and the GUS reporter gene with intron was then confirmed by genomic PCR, Southern blot, reverse transcriptase PCR (RT-PCR) and GUS histochemical assay. The method presented here could be helpful in genetic improvement of H. tuberosus through efficient shoot regeneration and stable Agrobacterium-mediated transformation. (C) 2015 Elsevier B.V. All rights reserved.
机译:在我们当前的研究中,为开发一种高效的马铃薯块茎再生和转化系统,我们验证了植物生长激素,生长条件,外植体类型和转化条件的影响。在黑暗中,来自再生芽的叶片段在含有1.0 mg L-1玉米素的MS基础培养基上显示出比来自维持的体外植物更高的再生效率。为了进行转化,已经确定了各种参数,包括植物材料,农杆菌细胞密度,浸没时间和农杆菌菌株(叶片段,OD600-0.6、60分钟和带有二元载体pCAMBIA1301的根癌农杆菌LBA4404)。在两个愈伤组织阶段选择3.0 mg L-1潮霉素的两个周期后,通过存活率和β-葡萄糖醛酸苷酶(GUS)组织化学分析筛选推定转化的马铃薯。然后通过基因组PCR,Southern印迹,逆转录酶PCR(RT-PCR)和GUS组织化学测定法证实了选择标记基因潮霉素磷酸转移酶和带有内含子的GUS报告基因的存在。本文介绍的方法可能通过有效的枝条再生和稳定的农杆菌介导的转化,有助于马铃薯的遗传改良。 (C)2015 Elsevier B.V.保留所有权利。

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