摘要
本实验以大豆萌动种胚为受体,用含有CaMV35s启动子-Gus基因-ipt基因-Nos基因的融合基因根癌农杆菌LBA4404进行转化,通过对转化及对照植株苗期根的过氧化物酶同工酶及酯酶同工酶分析,结果表明酶谱有明显差异,酯酶同工酶有一条Rf为0.540的差异带,过氧化物酶同工酶有二条Rf0.514,Rf0.532的差异带;综合分析,上述三条差异带都显示的转化植株占所分析转化植株的14.4%。用此法可作为转基因植株早期筛选方法之一。
The transformation of the seed--germinating embryoes of soyhan was conduce with theAtumefactcens stlain LBA4404 cotaing CaMV 35s promoter -- Gus -- ipt -- Nos fosion gene.The analysis of the peroxidase isozymes and esterase isozymes of the seedling stage rootsof both the usnsforrned and control plants indicatalf The isozymes pattern between thethensformed and control plants presented distinct difference: The porokidase isozymes showedtwo different bands, Rf 0.514 and Rf 0.532, The esterase isozymes showed one different band:Rf 0.540. To sum up, the transformed plants shing both isozymes different bands account for14.4% of the total ones which were analysed. This can be used as one of the methods for earlyscreening of transgenic plants.
出处
《哈尔滨师范大学自然科学学报》
1996年第4期87-90,共4页
Natural Science Journal of Harbin Normal University
基金
蔡火石生物科学发展基金
省科委"八五"项目
关键词
大豆萌动种胚
IPT基因
根癌农杆菌
转化
同工酶
Seed--germinating embryoes of soybean, Ipt gene, A. tumefaciens
Transformation
Isozyme