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根癌农杆菌介导的百脉根遗传转化体系的优化研究
引用本文:孙艳香,杨红梅,耿云红,朱晔荣,王宁宁,王勇.根癌农杆菌介导的百脉根遗传转化体系的优化研究[J].南开大学学报,2006,39(2):51-57.
作者姓名:孙艳香  杨红梅  耿云红  朱晔荣  王宁宁  王勇
作者单位:南开大学生命科学学院,南开大学生命科学学院,南开大学生命科学学院,南开大学生命科学学院,南开大学生命科学学院,南开大学生命科学学院 天津300071,河北廊坊师范学院生物系,河北廊坊060051,天津300071,天津300071,天津300071,天津300071,天津300071,天津市农业生物技术研究中心,天津300192
基金项目:天津市农业生物技术研究中心资助项目;天津市科委资助项目
摘    要:百脉根(L otus corn icu la tus L.)是世界著名的多年生优良豆科牧草之一,也是常见的庭院观赏植物.本文通过比较不同根癌农杆菌转化百脉根的效率和优化百脉根子叶遗传转化的条件,建立了一套有效的遗传转化体系.实验结果表明,EHA 105作为宿主菌对百脉根进行转化较LBA 4404和GV 3101具有更高的转化率;5 d苗龄的子叶最适合作为转化的外植体;浸染过程中0.05 M Pa负压处理5 m im以及在共培养培养基中添加20 m g/L的乙酰丁香酮均可提高转化效率.卡那霉素抗性植株经3次选择继代培养后,PCR检测全部为阳性.对部分PCR阳性植株进行PCR-Sou thern杂交,证实PCR产物真实可靠,表明外源基因已整合进入百脉根基因组中.

关 键 词:百脉根  根癌农杆菌  遗传转化  苗龄  负压处理
文章编号:0465-7942(2006)02-0051-07
收稿时间:07 5 2005 12:00AM
修稿时间:2005年7月5日

Optimization of A. tumefaciens-mediated Transformation Procedure for Lotus Corniculatus
Sun Yanxiang,Yang Hongmei,Geng Yunhong,Zhu Yerong,Wang Ningning,Wang Yong.Optimization of A. tumefaciens-mediated Transformation Procedure for Lotus Corniculatus[J].Acta Scientiarum Naturalium University Nankaiensis,2006,39(2):51-57.
Authors:Sun Yanxiang  Yang Hongmei  Geng Yunhong  Zhu Yerong  Wang Ningning  Wang Yong
Institution:1. College of Life Sciences, Nankai University, Tianjin 300071, China; 2. Department of Biology, Teachers College of Langfang, Langfang 065001, China; 3. Agriculture Biotechnique Research Center of Tianjin, Tianjin 300192, China
Abstract:Lotus corniculatus L.is one of wellknown leguminous forages around the world and also often used as ornamentals to decorate houses.In this study,a reproducible and efficient Lotus corniculatus transgenic system was established through comparing transformation efficiency of different Agrobacterium strains and optimizing factors affecting the transformation.The results show that strain EHA105 is more efficient than strans LBA4404 and GV3101 in performing transfer of foreign genes into Lotus corniculatus.Cotyledons of 5-day-old seedlings were found to be most suitable for infecting L.corniculatus with A.tumefaciens.And transformation efficiency was improved either by subjecting cotyledons to-0.05 MPa pressure for 5 min while they were being infected or by adding AS at 20 mg/L into co-culture medium.After a 3-round selection of kan-resistance,selected kan-resistant plants were further identified by PCR and PCR based Southern blot analysis.The results demonstrate that all the kan-resistant plants are transgenic ones and that the exogenous target gene,the AVP1 gene,has been integrated into the genomic DNA of all transformants obtained.
Keywords:AS
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