Eady C C, Weld R J, Lister C E
New Zealand Institute for Crop & Food Research Ltd, Private Bag 4704, Christchurch, New Zealand e-mail:
Plant Cell Rep. 2000 Mar;19(4):376-381. doi: 10.1007/s002990050743.
An Agrobacterium tumefaciens-mediated transformation method has been developed for onions (Allium cepa L.) using immature embryos as the explant source. Transgenic plants were recovered from the open-pollinated onion cultivar Canterbury Longkeeper at a maximum transformation frequency from immature embryos of 2.7%. The method takes between 3-5 months from explant to primary regenerant entering the glasshouse. Multiple-shoot formation from primary transgenic material made possible the clonal multiplication of transformants. The binary vector used carried the nptII antibiotic resistance gene and the m-gfp5-ER reporter gene. Transgenic cultures were initially screened for their ability to fluoresce and to grow in the presence of geneticin (5-25 mg/l). The transgenic nature of individual plants was confirmed by Southern blot analysis.
已开发出一种根癌农杆菌介导的转化方法,以未成熟胚作为外植体来源用于洋葱(Allium cepa L.)。从开放授粉的洋葱品种坎特伯雷长 keeper 的未成熟胚中获得了转基因植株,最高转化频率为 2.7%。该方法从外植体到初级再生植株进入温室需要 3 - 5 个月。初级转基因材料的多芽形成使得转化体能够进行克隆繁殖。所使用的二元载体携带 nptII 抗生素抗性基因和 m-gfp5-ER 报告基因。最初通过检测转基因培养物的荧光能力以及在遗传霉素(5 - 25mg/l)存在下的生长能力来进行筛选。通过 Southern 杂交分析确认了单株植物的转基因性质。