烟草SOC1基因的克隆和表达分析

被引:5
作者
石永春
杨永银
刘卫群
机构
[1] 河南农业大学生命科学学院
关键词
烟草; SOC1; 转基因; 光合; 抗坏血酸;
D O I
暂无
中图分类号
S572 [烟草(菸草)];
学科分类号
摘要
为明确SOC1基因在叶片中的生理作用,克隆到烟草中SOC1基因的完整开放阅读框,全长806 bp。农杆菌介导转化烟草后,获得26棵转基因植株,其中23棵鉴定为阳性植株,转化率为88.46%。与野生型烟草K326相比,获得的SOC1过表达烟株开花提前,株高增加,叶片宽大。半定量RT-PCR结果显示,SOC1过表达不影响叶片中Rubisco大亚基、蔗糖磷酸合成酶和蔗糖合成酶基因的表达水平,但提高了抗坏血酸氧化酶的表达水平;提高了碳酸酐酶活性、蔗糖含量和还原性抗坏血酸含量,并降低了抗坏血酸过氧化物酶活性。表明SOC1可能通过影响氧化还原状态而提高碳酸酐酶活性和光合速率。
引用
收藏
页码:99 / 103
页数:5
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