Men S, Ming X, Wang Y, Liu R, Wei C, Li Y
Peking-Yale Joint Center for Plant Molecular Genetics and Agrobiotechnology, The National Laboratory of Protein Engineering and Plant Genetic Engineering, Department of Biotechnology, College of Life Sciences, Peking University, 100871 Beijing, China.
Plant Cell Rep. 2003 Feb;21(6):592-8. doi: 10.1007/s00299-002-0559-4. Epub 2002 Dec 19.
We report here the transformation of two species of orchid, Dendrobium phalaenopsis and D. nobile,by biolistic bombardment. Calli or protocorm-like bodies (PLBs) were used as target explants. Gold particles (1.0 microm) coated with plasmid DNA (pCAMBIA1301) encoding an intron-containing beta-glucuronidase gene (gus-int) and a hygromycin phosphotransferase (hpt) gene were introduced into the PLBs or calli using the Bio-Rad PDS-1000/He Biolistic Particle Delivery System. Calli and PLBs were then chopped up and pre-cultured in 1/2-strength MS medium supplemented with 0.4 M mannitol for a 1-h osmoticum treatment before bombardment. Immediately after bombardment, the calli and PLBs were transferred to 1/2-strength MS medium without mannitol for recovery. Putatively transformed plantlets were obtained by selection and regeneration on medium supplemented with 30 mg/l hygromycin. The highest efficiency of transformation was obtained when selection was conducted at 2 days post-bombardment. For D. phalaenopsis and D. nobile, respectively, about 12% and 2% of the bombarded calli or PLBs produced independent transgenic plants. Integration and expression of the transgenes were confirmed by Southern hybridization and Northern hybridization. No nontransformed plants were regenerated, indicating a tight selection scheme. However, separate incorporation of the gus gene and the hpt gene was observed, and in one transgenic line the gus gene was integrated into the genome of the transgenic plant, but not expressed.
我们在此报告通过生物弹轰击对两种兰花,即蝴蝶石斛和金钗石斛进行转化的情况。愈伤组织或原球茎状小体(PLBs)用作靶外植体。使用Bio-Rad PDS-1000/He生物弹粒子递送系统,将包被有编码含内含子的β-葡萄糖醛酸酶基因(gus-int)和潮霉素磷酸转移酶(hpt)基因的质粒DNA(pCAMBIA1301)的金粒子(1.0微米)导入PLBs或愈伤组织。然后将愈伤组织和PLBs切碎,并在添加有0.4M甘露醇的1/2强度MS培养基中预培养1小时进行渗透处理,然后再进行轰击。轰击后立即将愈伤组织和PLBs转移至不含甘露醇的1/2强度MS培养基中进行恢复。通过在添加有30mg/l潮霉素的培养基上进行选择和再生获得推定转化的小植株。在轰击后2天进行选择时获得了最高的转化效率。对于蝴蝶石斛和金钗石斛,分别约有12%和2%的被轰击愈伤组织或PLBs产生了独立的转基因植株。通过Southern杂交和Northern杂交证实了转基因的整合和表达。没有再生出未转化的植株,表明选择方案严格。然而,观察到gus基因和hpt基因是分别整合的,并且在一个转基因株系中,gus基因整合到了转基因植物的基因组中,但未表达。