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农杆菌介导的转化芦荟的研究
引用本文:何聪芬,张佳星,陈杰,叶兴国,杜丽璞,董银卯,赵华.农杆菌介导的转化芦荟的研究[J].遗传学报,2007,34(12):1053-1060.
作者姓名:何聪芬  张佳星  陈杰  叶兴国  杜丽璞  董银卯  赵华
作者单位:1. 北京工商大学化学与环境工程学院/北京市植物资源开发与利用重点实验室,北京,100037
2. 北京工商大学化学与环境工程学院/北京市植物资源开发与利用重点实验室,北京,100037;中国农业科学院作物科学研究所/国家基因资源与遗传改良重大科学工程,北京,100081
3. 中国农业科学院作物科学研究所/国家基因资源与遗传改良重大科学工程,北京,100081
摘    要:芦荟(Aloe)是美容和医疗保健工业的重要植物资源,然而基因工程途径改良芦荟鲜有报道。本实验研究了次氯酸钠、升汞不同浓度和时间对芦荟外植体的灭菌效果,比较了芦荟不同部位(叶片、叶鞘和茎段)的再生能力,利用GUS基因瞬间表达技术(X-Gluc染色)探讨了不同农杆菌对不同芦荟外植体的侵染效果,确定了G418筛选剂在芦荟转化后的最适筛选浓度,摸索了适宜于农杆菌—芦荟共培养用培养基组成和共培养条件,通过转化、筛选和移栽共获得了67棵抗性再生植株,进一步对抗性再生植株进行了PCR、Southern blotting和ELISA检测。结果表明,芦荟外植体灭菌方法为20.0%次氯酸钠溶液浸泡25min,效果优于利用0.1%升汞灭菌处理,茎部切段的再生能力高于叶片切段和叶鞘切段,适宜的共培养条件为芦荟外植体浸泡在含有农杆菌的液体共培养基中半小时后,在无菌滤纸上、24℃、10h光照共培养3天;EHA105农杆菌菌系对芦荟茎部细胞的侵染能力明显强于C58C1,EHA105侵染后GUS基因瞬时表达率达到了80.0%左右,而C58C1侵染后GUS基因瞬时表达率只有30.0%左右。G418用于筛选抗性再生芽和抗性植株的适宜浓度为10.0~25.0mg/L。PCR和Southern blotting检测证实外源基因已成功整合到芦荟基因组中,转化效率为0.9%,单拷贝整合占80.0%,2~3拷贝整合占20.0%,ELISA检测证明外源基因已在转基因芦荟中稳定表达。综上所述,初步建立了农杆菌介导转化芦荟的技术体系,为利用基因工程途径改良芦荟奠定了基础。

关 键 词:芦荟  农杆菌  遗传转化  分子检测  ELISA检测
收稿时间:2007-04-23
修稿时间:2007-07-29

Genetic Transformation of Aloe barbadensis Miller by Agrobacterium tumefaciens
Congfen He,Jiaxing Zhang,Jie Chen,Xingguo Ye,Lipu Du,Yinmao Dong,Hua Zhao.Genetic Transformation of Aloe barbadensis Miller by Agrobacterium tumefaciens[J].Journal of Genetics and Genomics,2007,34(12):1053-1060.
Authors:Congfen He  Jiaxing Zhang  Jie Chen  Xingguo Ye  Lipu Du  Yinmao Dong  Hua Zhao
Institution:College of Chemistry and Environment Engineering, Beijing Key Lab of Plant Resources Research and Development, Beijing Technology and Business University, Beijing 100037, China. hecf@th.btbu.edu.cn
Abstract:Despite the importance of aloe in cosmetic and pharmaceutical industries, improvement of aloe (Aloe barbadensis Miller) by genetic engineering was seldom reported previously. In this study, regeneration and transformation conditions, including explant selection and surface sterilization, use of different Agrobacterium strains, and co-culture processing, are optimized. The use of 20.0% sodium hypochloride (25 min) for sterilization was less detrimental to the health of explant than 0.1% mercuric chloride (10 min). Regeneration frequency from stems was much higher than that from leaves or sheaths. Explants were infected by Agrobacterium (30 min) in liquid co-cultural medium, and this was followed by three days co-culture on sterile filter papers with light for 10 h per day at 24 degrees C. Histochemical data demonstrated that the transient expression of GUS gene in the stem explants of aloe infected with Agrobacterium strains EHA105 and C58C1 was 80.0% and 30.0%, respectively, suggesting the higher sensitivity of the explants to EHA105 than to C58C1. Infected tissues were selected using G418 (10.0-25.0 mg/L) to generate transformants. Sixty-seven G418 resistant plantlets were generated from the infected explants. Southern blotting, PCR, and ELISA analyses indicated that the alien gene were successfully transferred into aloe and was expressed in the transgenic plants. This newly established transformation system could be used for the genetic improvement of aloe.
Keywords:aloe  Agrobacterium tumefaciens  transformation  molecular test  ELISA analysis
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