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首页> 外文期刊>Acta Horticulturae >Improvement of bulb formation in micropropagated tulips by treatment with NAA and paclobutrazol or ancymidol.
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Improvement of bulb formation in micropropagated tulips by treatment with NAA and paclobutrazol or ancymidol.

机译:通过用NAA和多效唑或西咪唑处理可改善微繁郁金香中的鳞茎形成。

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Bulb formation is an essential stage in tulip micropropagation via cyclic shoot multiplication because only bulbs show high rooting ability and good field performance. The stage of bulb formation in vitro consists of three phases: (1) development of bulb primordia in shoots at the end of the last subculture prior to cooling; (2) induction of bulbing process by cooling of shoots; (3) bulb formation at 23 degrees C. Shoots of tulips 'Prominence', 'Blenda' and 'Blue Parrot' multiplied on the medium with thidiazuron (TDZ), were used for the experiments. The effects of liquid media (with or without growth regulators) added into the shoot cultures prior to cooling were examined in relation to the efficiency of bulb formation. The liquid media were added at the end of the last eight-week-multiplication subculture. 1-naphthylacetic acid (NAA) at 2 mg L-1 and inhibitors of gibberellin biosynthesis, ancymidol or paclobutrazol (1-2 mg L-1) were used. The shoots were grown on double-phase media for six weeks. The control subculture prior to cooling was prolonged to 14 weeks, but the liquid medium was not added. The shoots were then transferred onto the sucrose-rich medium without growth regulators and cooled at 5 degrees C for three months. Subsequently, they were cultured for bulb formation at 23 degrees C for 2-5 months. The application of the liquid medium containing NAA and/or ancymidol or paclobutrazol significantly enhanced the efficiency of bulb formation expressed by the ratio of the properly formed bulb to shoot numbers x 100%. For 'Prominence', it varied from 42.9% noted in control to 60.1-104.2%, for 'Blenda' - from 68.8% in control to 121.7-125.0% and in 'Blue Parrot' bulbing was sporadic in control but on double-phase ranged from 14.5% to 41.6%..
机译:由于只有鳞茎显示出高生根能力和良好的田间生长,鳞茎的形成是通过循环芽繁殖在郁金香微繁殖中必不可少的阶段。体外鳞茎形成的阶段包括三个阶段:(1)在冷却前最后一次继代培养结束时,茎中的鳞茎原基发育。 (2)通过冷却芽诱导球茎形成过程; (3)在23℃下的鳞茎形成。在培养基上用噻唑酮(TDZ)繁殖的郁金香“突出”,“ Blenda”和“蓝鹦鹉”的芽用于实验。冷却前,将液体培养基(有或没有生长调节剂)添加到枝条培养物中的效果与球茎形成效率有关。在最后八周的亚培养结束时添加液体培养基。使用浓度为2 mg L-1的1-萘乙酸(NAA)和赤霉素生物合成抑制剂ancymidol或多效唑(1-2 mg L-1)。将芽在双相培养基上生长六周。冷却前的对照传代培养延长至14周,但未添加液体培养基。然后将芽转移到没有生长调节剂的富含蔗糖的培养基上,并在5℃下冷却三个月。随后,将它们在23℃下培养2-5个月以形成球茎。含有NAA和/或ancymidol或多效唑的液体培养基的应用显着提高了球茎形成的效率,这是由正确形成的球茎与芽数之比x 100%表示的。对于“突出”,从对照中注意到的42.9%到60.1-104.2%,对于“ Blenda”-从对照中的68.8%到121.7-125.0%,在“蓝色鹦鹉”中,球茎在对照中是零星的,但在双相范围从14.5%到41.6%。

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