둥굴레 ‘건강백세’의 기내 대량번식

In Vitro Micropropagation of Polygonatum odoratum cv. Gungangbeaksea

경상남도 농업기술원에서 육성된 둥굴레 ‘건강백세(Polygonatumodoratum cv. Gungangbeaksea)’를 분양받아 배양하였다. 둥굴레 지하경 절편체를 MS 배지에 BA 3.0 ㎎/L가 첨가된 배지에서 배양하면서 증식된 부정신초괴를 실험재료로 사용하였다. 배양 8주후, 신초의 증식은 TDZ 3.0 ㎎/L 첨가배지에서 2.8개로 가장 많았으며 생체중도 절편체당 2.32 g으로 가장 높게 나타났다. TDZ와 NAA가 첨가된 배지에서는 신초 및 부정신초괴의 증식이 다소 증가하였다. TDZ 3.0 ㎎/L와 NAA 5.0 ㎎/L 첨가배지, TDZ 5.0 ㎎/L와 NAA 3.0 ㎎/L 첨가배지에서 신초수3.7개, 생체중 2.9 g으로 다소 증가하였다. MS 염류농도가 높아질수록 신초 및 부정신초괴의 증식은 저조하였다. 그러나sucrose 농도가 3%에서 7%로 증가함에 따라 신초수, 생체중 및부정신초괴의 형성이 증가하였다. 뿐 만 아니라 둥굴레 부정신초절편체에서 신초 및 부정신초괴의 증식은 MS 배지에 TDZ와 NAA3.0～5.0 ㎎/L와 sucrose 7%가 첨가된 배지가 적합하였다. 발근율은 IBA 3.0 ㎎/L 또는 NAA 2.0 ㎎/L 첨가배지에서 80% 이상으로 높았으며, 발근된 식물체의 순화는 vermiculite 단용 또는 perlite,vermiculite 1:1 혼용처리에서 순화율 100%로 적합하였다

The Polygonatum odoratum cv. Gungangbeaksea, bred in Gyeongsangnam-Do Agricutural Research & Extension Service, was cultured in vitro for micropropagate rapidly through the culture of rhizome explants (5 × 5 ㎜). The 7 × 7 ㎜ explants of adventitious multi-bud clusters (AMC), obtained through the culture of rhizome explants (MS + 3.0 ㎎/L BA) were cultured on MS media with BA and TDZ. The shoot multiplication was favorable on the MS medium containing 3.0 ㎎/L TDZ with 2.8 in shoot number. But the formation of AMC was low in all media tested. The explants of AMC were cultured on MS media containing 1.0～5.0 ㎎/L TDZ and NAA to multiplicate AMC more. The formation of AMC was a little more stimulated on combined MS media of TDZ and NAA, than that with TDZ alone. The multiplication of shoots and AMC was favorable on MS media with 3.0 ㎎/L TDZ and 5.0 ㎎/L NAA, and 5.0 ㎎/L TDZ and 3.0 ㎎/L NAA. As the concentration of MS salts increased, the formation of AMC was decreased. But the formation of AMC was more stimulated, as the concentration of sucrose increased to 7%. Therefore, the multiplication of shoots and AMC was suitable on media containing 3.0～5.0 ㎎/L TDZ and NAA, and 7% of sucrose. The explants of AMC were rooted on media with 3.0 ㎎/L IBA, or 2.0 ㎎/L NAA with more than 80% in rooting ratio. The plantlets were treated at 5 ℃ for 8 weeks, and cultured ex vitro for 8 weeks. The survival ratio of plantlets were 100% in vermiculite, and the mixed soil with perlite 1 volumn and vermiculite 1 volumn.3