Podwyszyńska Małgorzata, Sochacki Dariusz
Research Institute of Pomology and Floriculture, Skierniewice, Poland.
Methods Mol Biol. 2010;589:243-56. doi: 10.1007/978-1-60327-114-1_23.
We describe here a new tulip micropropagation method based on the cyclic shoot multiplication in presence of the thidiazuron (TDZ), which enables the production of virus-free stock plants, speeds up breeding, and provides new genotypes for the market. In our novel protocol, cyclic shoot multiplication can be performed for 2-3 years by using TDZ instead of other cytokinins, as 6-benzylaminopurine (BAP) and N(6)-(-isopentyl)adenine (2iP). It makes possible to produce 500-2,000 microbulbs from one healthy plant. There are six main stages of tulip micropropagation. Stage 0 is the selection of true-to-type and virus-free plants, confirmed by ELISA. Fragments of flower stems isolated from bulbs are used as initial explants. Shoot multiplication is based on the regeneration of adventitious shoots, which are sub-cultured every 8 weeks. In the Stage 3, the specially prepared shoots are induced by low temperature treatment to form bulbs which finally develop on a sucrose-rich medium at 20 degrees C. Bulbs are then dried for 6 weeks and rooted in vivo. The number of multiplication subcultures should be limited to 5-10 cycles in order to lower the risk of mutation. Virus indexing should be repeated 3-4 times, at the initial stage and then during shoot multiplication. Genetic stability of micropropagated shoots can be confirmed using molecular markers.
我们在此描述一种基于在噻苯隆(TDZ)存在下进行循环芽增殖的郁金香微繁殖新方法,该方法能够生产无病毒的母株,加速育种,并为市场提供新的基因型。在我们的新方案中,使用TDZ而非其他细胞分裂素(如6-苄基腺嘌呤(BAP)和N⁶-(-异戊烯基)腺嘌呤(2iP))可进行2至3年的循环芽增殖。这使得从一株健康植株能够生产500至2000个微型鳞茎成为可能。郁金香微繁殖有六个主要阶段。阶段0是通过酶联免疫吸附测定(ELISA)确认选择典型且无病毒的植株。从鳞茎分离的花茎片段用作初始外植体。芽增殖基于不定芽的再生,不定芽每8周继代培养一次。在阶段3,经过特殊处理的芽通过低温处理诱导形成鳞茎,这些鳞茎最终在富含蔗糖的培养基上于20℃下发育。然后将鳞茎干燥6周并在体内生根。增殖继代培养的次数应限制在5至10个周期,以降低突变风险。病毒检测应在初始阶段以及芽增殖期间重复进行3至4次。可使用分子标记确认微繁殖芽的遗传稳定性。