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通过农杆菌介导法将ipt基因转化到矮牵牛中。

ipt Gene transformation in petunia by an Agrobacterium mediated method.

作者信息

Bai L J, Ye C J, Lu J Y, Yang D E, Xue H, Pan Y, Cao P X, Wang B, Liu M

机构信息

Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, P. R. China.

出版信息

J Immunoassay Immunochem. 2009;30(2):224-31. doi: 10.1080/15321810902782913.

Abstract

To prevent leaf senescence of petunia, the cytokinin biosynthetic gene isopentenyl transferase (ipt) was placed under the control of 35S promoter and introduced into petunia. PCR analysis showed an expected 0.5 Kb fragment of ipt gene in transgenic petunia. RT-PCR analysis indicated the expression of ipt gene in the transgenic lines. Leaves from transgenic plants remained green and healthy in normal culture condition, while the non-transformed plants turned to yellow. Transgenic plants showed a reduction in height and smaller leaf sizes. In transgenic lines, the internodes were shorter, and the roots grew slower than the non-transformed plants.

摘要

为防止矮牵牛叶片衰老,将细胞分裂素生物合成基因异戊烯基转移酶(ipt)置于35S启动子控制下,并导入矮牵牛。PCR分析显示转基因矮牵牛中ipt基因有预期的0.5 Kb片段。RT-PCR分析表明ipt基因在转基因株系中表达。在正常培养条件下,转基因植株的叶片保持绿色且健康,而未转化植株则变黄。转基因植株表现出高度降低和叶片尺寸变小。在转基因株系中,节间较短,根的生长比未转化植株慢。

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