Jia Hongge, Liao Mingjun, Verbelen Jean-Pierre, Vissenberg Kris
Department of Biology, University of Antwerp, Groenenborgerlaan 171, 2020 Antwerp, Belgium.
Plant Cell Rep. 2007 Nov;26(11):1961-5. doi: 10.1007/s00299-007-0403-y. Epub 2007 Jul 19.
Agroinfiltration is employed as a fast way to directly create marker-free transgenic tobacco plants. As an example for the efficiency of the method, Agrobacterium cells harboring a marker-free vector coding for beta-glucuronidase (GUS) were infiltrated into the leaf discs of Nicotiana tabacum, which were then used as explants for marker-free plant regeneration by tissue culture. Through GUS staining, a large number of small calli were shown to be stably transformed on the treated leaf discs at 17 days after agroinfiltration. Most importantly, after continuous culture of the leaf discs until shoot regeneration, about 15% of the regenerants were proven to be transformants by polymerase chain reaction (PCR) analysis.
农杆菌浸润法被用作一种直接创建无标记转基因烟草植株的快速方法。作为该方法效率的一个例子,将携带编码β-葡萄糖醛酸酶(GUS)的无标记载体的农杆菌细胞浸润到烟草叶片圆片中,然后将这些叶片圆片用作通过组织培养进行无标记植株再生的外植体。通过GUS染色,在农杆菌浸润后17天,大量小愈伤组织在处理过的叶片圆片上被证明是稳定转化的。最重要的是,在将叶片圆片持续培养直至芽再生后,通过聚合酶链反应(PCR)分析,约15%的再生植株被证明是转化体。