首页> 外文期刊>Plant molecular biology reporter >Expression of Maize Gene Encoding C-4-Pyruvate Orthophosphate Dikinase (PPDK) and C-4-Phosphoenolpyruvate Carboxylase (PEPC) in Transgenic Arabidopsis
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Expression of Maize Gene Encoding C-4-Pyruvate Orthophosphate Dikinase (PPDK) and C-4-Phosphoenolpyruvate Carboxylase (PEPC) in Transgenic Arabidopsis

机译:编码C-4-丙酮酸正磷酸二激酶(PPDK)和C-4-磷酸烯醇丙酮酸羧化酶(PEPC)的玉米基因在转基因拟南芥中的表达

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摘要

To improve the efficiency of CO2 fixation in C3 photosynthesis, C4-cycle genes were overexpressed in Arabidopsis plants. In this study, a full-length cDNA for pyruvate orthophosphate dikinase (PPDK) with 971 amino acids was isolated from Zea mays using LA-PCR. The PPDK gene (GenBank accession number GU363532) and the phosphoenolpyruvate carboxylase (PEPC) gene (GenBank accession number: FJ415327) derived from a previous study were introduced into wild-type Arabidopsis both individually and in combination. The vector pCAMBIA3301 (p3301) was introduced into Arabidopsis as a control using an Agrobacterium-mediated system. The integration, transcription, and translation of the PPDK and the PEPC genes were confirmed by Southern blot, quantitative real-time PCR, and Western blot analysis. The average enzyme activity of C4-PPDK and C4-PEPC peaked at 4.63- and 5.81-fold compared to that of controls, respectively. The insertion of PPDK was found to increase the activity of PEPCase and vice versa. The photosynthetic rates of C4-PPDK, C4-PEPC, and C4-PKC(PPDK+PEPC) transgenic lines increased to 123.3, 136.4, and 146.6 % compared to that of controls, respectively.
机译:为了提高在C3光合作用中固定CO2的效率,在拟南芥植物中过表达了C4循环基因。在这项研究中,使用LA-PCR从玉米中分离出具有971个氨基酸的丙酮酸正磷酸二激酶(PPDK)的全长cDNA。将先前研究衍生的PPDK基因(GenBank登录号GU363532)和磷酸烯醇丙酮酸羧化酶(PEPC)基因(GenBank登录号:FJ415327)单独或组合引入野生型拟南芥中。使用农杆菌介导的系统将载体pCAMBIA3301(p3301)引入到拟南芥中作为对照。 PPDK和PEPC基因的整合,转录和翻译已通过Southern印迹,定量实时PCR和Western印迹分析得到了证实。与对照相比,C4-PPDK和C4-PEPC的平均酶活性分别达到4.63和5.81倍的峰值。发现插入PPDK可增加PEPCase的活性,反之亦然。与对照相比,C4-PPDK,C4-PEPC和C4-PKC(PPDK + PEPC)转基因株系的光合速率分别提高到123.3%,136.4和146.6%。

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