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TRANSGENIC PERENNIAL RYEGRASS (LOLIUM PERENNE) PLANTS FROM MICROPROJECTILE BOMBARDMENT OF EMBRYOGENIC SUSPENSION CELLS

机译:微弹轰击胚性悬浮细胞的转基因多年生黑麦草(萝橙)

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Transgenic forage-type perennial ryegrass (Lolium perenne L.) plants have been obtained by microprojectile bombardment of embryogenic suspension cells using a chimeric hygromycin phosphotransferase (hph)gene construct driven by rice Act1 5' regulatory sequences. Parameters for the bombardment of embryogenic suspension cultures with the particle inflow gun were partially optimized using transient expression assays of a chimeric beta-glucuronidase (gusA) gene driven by the CaMV 35S promoter. For the recovery of stably transformed clones, hygromycin selection using liquid and solidified media was tested. Initial selection in liquid culture medium allowed for a higher, compared with continuous plate selection using solid medium, recovery efficiency of transformed hygromycin resistant clones. Plants were regenerated from 23% of the hygromycin resistant calli obtained. The transgenic nature of the regenerated plants was demonstrated by Southern hybridization analysis. Expression of the transgene in transformed adult perennial ryegrass plants was confirmed by Northern analysis and a hygromycin phosphotransferase enzyme assay. [References: 34]
机译:通过使用水稻Act1 5'调控序列驱动的嵌合潮霉素磷酸转移酶(hph)基因构建体,通过微粒轰击胚胎悬浮细胞,获得了转基因牧草型多年生黑麦草(黑麦草)。使用由CaMV 35S启动子驱动的嵌合β-葡糖醛酸糖苷酶(gusA)基因的瞬时表达测定,部分优化了使用粒子流入枪轰击胚胎发生的悬浮培养物的参数。为了回收稳定转化的克隆,测试了使用液体和固化培养基对潮霉素的选择。与使用固体培养基的连续平板选择相比,在液体培养基中的初始选择允许更高的转化潮霉素抗性克隆的回收效率。从获得的潮霉素抗性愈伤组织的23%再生植物。通过Southern杂交分析证实了再生植物的转基因性质。通过Northern分析和潮霉素磷酸转移酶测定法证实了转化的成年多年生黑麦草植物中转基因的表达。 [参考:34]

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