摘要
本研究利用农杆菌介导的方法将高亲和NH4+转运因子融合基因转入甜菜子叶节外植体。遗传转化过程主要包括子叶节预培养、侵染转化、共培养、洗菌、抑菌培养、潮霉素筛选分化培养、抗性苗生根移栽。实验获得抗性苗140株,抗性芽分化率为8.14%,随机抽取24株抗性苗进行PCR检测,获得转基因植株10株。
In this study, high-affinity NH4+ transporter fusion gene was successfully transformed into the cotyledon node explants of sugar beet by using Agrobacterium-mediated transformation methord. Genetic transformation process includes cotyledon node pre-culture, infection transformation, co-culture, washed bacteria, bacteriostatic culture, differentiation culture of hygromycin selection, and resistance seedlings to root transplanting. As the experimental result, 140 resistant seedlings were obtained and its differentiation rate was 8.14%, 24 resistant seedlings were selected randomly to PCR detecte, and PCR assaying of plant DNA confirmed 10 transgenic plants.
出处
《分子植物育种》
CAS
CSCD
2010年第2期287-292,共6页
Molecular Plant Breeding
基金
现代农业产业技术体系建设专项资金(nycytx-25-04)资助
关键词
甜菜
农杆菌介导
高亲和NH4+转运因子
遗传转化
融合基因
Sugar beet (Beta Vulgaris) Agrobacterium-mediated High-affinity NH4+ transporter Genetic transformation Fusion gene