CAJ | 학술논문

本研究通过对秦薯4号微茎尖剥离加变温处理的措施，诱导再生植株，获得脱毒原株，再通过优化培养基中植物生长调节剂的配比，建立脱毒试管苗快速繁殖繁的技术参数。结果表明：①添加有6-BA0.5mg/L和0.1 mg/LNAA的MS培养基较适用于秦薯4号脱毒单株快繁。于MS培养基和MB培养基对甘薯试管苗的增殖作用比B5和N6好。
본연구통과대진서4호미경첨박리가변온처리적조시，유도재생식주，획득탈독원주，재통과우화배양기중식물생장조절제적배비，건립탈독시관묘쾌속번식번적기술삼수。결과표명：①첨가유6-BA0.5mg/L화0.1 mg/LNAA적MS배양기교괄용우진서4호탈독단주쾌번。우MS배양기화MB배양기대감서시관묘적증식작용비B5화N6호。
This research through stripping and variable temperature measures for Qinshu 4 micro shoot tip to induce regeneration plants, obtain virus-free original strains, then through optimizing composition of plant growth regulators in culture medium to establish technical parameters of rapid propagation of virus-free plantlets. The results show that: ①MS medium with 6-BA 0.5mg/L and 0.1 mg/LNAA is suitable for Qinshu 4 virus-free plant rapid propagation. ②The proliferative effects of MS medium and MB medium for sweet potato vitro plantlets is better than B5 and N6 medium.