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首页> 外文期刊>Journal of Plant Biochemistry and Biotechnology >A modified in planta method of Agrobacterium-mediated transformation enhances the transformation efficiency in safflower (Carthamus tinctorius L.)
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A modified in planta method of Agrobacterium-mediated transformation enhances the transformation efficiency in safflower (Carthamus tinctorius L.)

机译:农杆菌介导的转化的植物植物方法改性增强了红花(Carthamus tinctorius L)的转化效率

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摘要

Plant transformation has emerged as an important tool to integrate foreign genes in the plant genome to modify the plants for desired traits. Though many techniques of plant transformation are available; getting single copy transgenic events and cost associated remains a big challenge. Thus Agrobacterium-mediated transformation remains the method of choice due to multiple advantages. In the present work a tissue culture free protocol of Agrobacterium-mediated transformation was optimized in safflower, an oil seed crop recalcitrant to transformation. As a proof of concept we selected pCAMBIA2300 gene cassette containing Arabidopsis specific delta 15 desaturase 9FAD3) downstream to truncated seed specific promoter beta-conglycinin and optimized tissue culture free protocol of Agrobacterium-mediated transformation using embryos as explants. Addition of silwet L-77, sonication treatment, vacuum infiltration in infection medium and use of paper wicks in co-cultivation period increased the transformation efficiency to 19.3%. Further, success in transformation was confirmed via product accumulation in 21 independent transgenic events wherein oil in transformed seeds showed significant accumulation of alpha-linolenic acid 9ALA; 18: 3; n3) which is generated from linoleic acid 9LA; 18: 2; n3) in a FAD3 catalyzed reaction. The present protocol can be utilized to produce transgenic safflower with different desired characters.
机译:植物转化出现为将植物基因组中的外源基因整合到植物基因组中的重要工具以进行所需的特征。虽然有许多植物转化技术可用;获得单拷贝转基因事件和成本相关仍然是一个很大的挑战。因此,农杆菌介导的转化仍然是由于多种优点所选择的方法。在本作工作中,在红旱草中优化了农杆菌介导的转化的组织培养方案,油籽作物顽固转化。作为概念证据,我们选择含有拟南芥特异性Delta 15去饱和酶9fad3)的PCAMBIA2300基因盒在下游,以截断的种子特异性启动子β-甘氨酸和优化的组织培养自由组织培养,使用胚胎作为外植体的胚胎介导的转化。添加Silwet L-77,超声处理,感染介质的真空浸润和共培养期的纸芯的使用将转化效率提高至19.3%。此外,通过产物积聚在21种独立的转基因事件中通过产物积累证实转化的成功,其中转化的种子中的油显示出α-亚麻酸9ALA的显着积累; 18:3; N3)由亚油酸9LA产生; 18:2; N3)在FAD3催化反应中。本方案可用于生产具有不同所需特性的转基因红花。

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