首页> 外文期刊>Plant Science: An International Journal of Experimental Plant Biology >Production of transgenic Hypericum perforatum plants via particle bombardment-mediated transformation of novel organogenic cell suspension cultures
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Production of transgenic Hypericum perforatum plants via particle bombardment-mediated transformation of novel organogenic cell suspension cultures

机译:通过粒子轰击介导的新型器官发生细胞悬浮培养物转化生产转基因贯叶连翘植物

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摘要

We have developed particle bombard ment-medi ated transformation procedure for Hypericum perforatum L. (St. John's wort), an important medicinal species that remains highly recalcitrant towards Agrobacterium-mediated transformation. Among the major transformation techniques evaluated in the present study (Agrobacterium? tumefaciens-, A. rhizogenes- and biolistics-mediated), particle-bombardment-mediated gene transfer was found to be the most successful one. GUS positive cells were obtained from organogenic nodules bombarded with the plasmid vector pCAMBIA1301 encoding an intron-containing beta-glucuronidase (gusA) and hygromycin phosphotransferase (hpt) genes. After 3 months of continuous selection of bombarded nodules with 20 mg1(-1) hygromycin, transgenic hygromycin-resistant callus cultures and subsequently transgenic plants were produced. PCR analysis of DNA isolated from GUS positive plants showed the presence of both gusA and hpt genes. Southern blot analysis confirmed the transgene integration and revealed diverse copy numbers and insertion sites. The data presented here demonstrate for the first time H. perforatum can be efficiently transformed via particle bombardment of organogenic cell suspension. Our results open the possibility of using particle bombardment-mediated transformation to elucidate biosynthetic pathways and to improve secondary metabolite production in H. perforatum. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
机译:我们已经开发了贯叶连翘(圣约翰草)的粒子轰击介导的转化程序,这是一种对农杆菌介导的转化仍然高度顽固的重要药用物种。在本研究评估的主要转化技术中(根癌农杆菌,发根农杆菌和生物弹药介导的),发现粒子轰击介导的基因转移是最成功的技术。 GUS阳性细胞是从被质粒载体pCAMBIA1301轰击的器官发生结节中获得的,该质粒载体编码含有内含子的β-葡萄糖醛酸苷酶(gusA)和潮霉素磷酸转移酶(hpt)基因。经过连续3个月选择含有20 mg1(-1)潮霉素的轰击结节后,产生了转基因潮霉素抗性愈伤组织培养物,并随后生产了转基因植物。从GUS阳性植物中分离的DNA的PCR分析表明gusA和hpt基因均存在。 Southern印迹分析证实了转基因整合并揭示了不同的拷贝数和插入位点。此处提供的数据首次证明了穿孔穿梭菌可以通过对器官发生细胞悬浮液的轰击来有效转化。我们的研究结果开辟了使用粒子轰击介导的转化阐明生物合成途径并提高穿孔贯线虫次生代谢产物生产的可能性。 (C)2007 Elsevier Ireland Ltd.保留所有权利。

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