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Shoot-Tip Culture of Acerola (Malpighia glabra L.)

机译:Acerola的射击剧培养(Malpighia Glabra L.)

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Culture conditions for shoot tips excised from cutting propagated plants of aceraia (Malpighia glabra L.) were investigated to develop a shoot-tip culture system. Shoot tips of aceraia "Sanmikei (Hosoba) " were grown on a medium, consisting of MS basal components with 3% sucrose. The addition of 0.1 ppm 6-benzylaminopurin (BA), 0.05 ppm BA + 0.05 ppm zeatin or 0.1 ppm BA + 0.1 ppm zeatin was effective for the proliferation of shoots. Those that had grown two to three cm from the subculture, were examined further for rooting, which had been stimulated when the shoots were immersed in 250 ppm indole-3-butyric acid (IBA) for 15 seconds. Ten to eleven days of dark treatment enhanced this. All plantlets were recovered after acclimatization. Sequence-related amplified polymorphism (SRAP) was conducted to validate the genetic homogeneity of the regenerated plants. In SRAP analysis, using 13 primer combinations, no polymorphisms among the regenerated and original plants were detected.
机译:研究了从切割植物(Malpighia Glabra L.)切割繁殖植物中切除的射击提示的培养条件开发射精培养系统。 Aceraia的射击尖端“Sanmikei(Hosoba)”在培养基中生长,由蔗糖3%的蔗糖组成。 添加0.1ppm 6-苄基氨基嘌呤(Ba),0.05ppm Ba + 0.05ppm Zeepin或0.1ppm Ba + 0.1ppm Zeepin对于芽的增殖是有效的。 从途中生长两到三厘米的那些,进一步研究了生根,当枝条浸入250ppm吲哚-3-丁酸(IBA)时被刺激了15秒。 十到十一天的黑暗处理增强了这一点。 均在适应后恢复所有植株。 进行序列相关的扩增多态性(SRAP)以验证再生植物的遗传均匀性。 在SRAP分析中,使用13个引物组合,未检测到再生和原始植物中的多态性。

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