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Abstract
Cultivated bananas are vegetatively propagating herbs, which are difficult to breed because of widespread male and female sterility. As a complementary gene transfer method in banana, the described Agrobacterium protocol relies on highly regenerable embryogenic cell cultures. Embryogenic cells are infected and co-cultivated in the presence of acetosyringone with Agrobacterium tumefaciens harboring a binary plasmid vector to obtain a mixed population of transformed and untransformed plant cells. Transformed plant cells are promoted to grow for 2 to 3 mo on a cell colony induction medium containing the antibiotics geneticin or hygromycin as selective agents, while agrobacteria are counterselected by timentin. The whole procedure, including plant regeneration, takes approx 6 mo and results in an average frequency of 25 to 50 independent transgenic plants per plate, which equals 50 mg of embryogenic cells. This method has been applied to a wide range of cultivars and to generate large populations of transgenic colonies and plants for tagging genes and promoters in banana.
Affiliation(s): (3) Departamento de Fruticultura Tropical, Instituto Canario de Investigaciones Agrarias, Apartado 60, 38200 La Laguna, Santa Cruz de Tenerife, Spain
(4) Laboratory of Tropical Crop Improvement, Katholieke Universiteit Leuven, Kasteelpark Arenberg 13, B-3001 Leuven, Belgium
Series: Methods in Molecular Biology  |  Volume: 344  |  Pub. Date: Sep-01-2006  |  Page Range: 167-175  |  DOI: 10.1385/1-59745-131-2:167
Subject:  Plant Sciences
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