河北省科技攻关计划项目(No.042401116D-1);转基因生物新品种培育重大专项子课题(No.2008ZX08004-002-1-5;2009ZX08004-001B)
本研究以GUS基因在子叶节区的瞬时表达为依据,通过探讨影响农杆菌转化效率的因素,优化了大豆子叶节非组织培养遗传转化体系;利用该体系对冀豆16号进行Bar基因的遗传转化,并使用针刺法对转基因植株进行草铵膦筛选。结果表明,侵染液中附加3%蔗糖、OD6OO=0.6、以脱脂棉作为菌液附着介质同时不添加表面活性剂Silwet L-77、侵染1次的GUS阳性率最高达到62.13%。草铵膦抗性植株经PCR检测获得T0代阳性植株10个,转化率为2.5%。经PCR和RT-PCR鉴定共获得3株T1代阳性植株,初步证明目的基因已整合到大豆基因组中。
By investigating the factors influencing the transformation efficiency of Agrobacterium, a genetic transformation system of soybean cotyledonary node with non tissue-culture was optimized according to the transient expression of GUS in the region of cotyledonary node; The gene Bar was transformed into soybean jidou16, and the transgenic plants were screened by glufosinate injected on leaves. The results indicated that infection medium contains 3% sugar and none Silwet L-77、OD6OO=0.6、with the absorbent cotton as attached media、infect one time have the highest percentage of GUS positive, was 62.13%. We obtained 10 positive plants in T0 generation after detected the transgenic plants resistant to glufosinate by PCR, the transformation efficiency was 2.5%. 3 positive plants of T1 generation were obtained by detection of PCR and RT-PCR, preliminary demonstrated that the target gene was integrated into the soybean genome.
李丹丹,张 洁,刘 娜,等.农杆菌介导的大豆子叶节非组织培养遗传转化体系优化[J].植物遗传资源学报,2012,13(5):789-797.
复制