Abstract
To improve transformation efficiency, the callus of Lilium lancifolium Thunb. were bombarded by particles coated with pIG 121 Hm which include NPT II and GUS genes, and then cocultivated with Agrobacterium tumefaciens EHA101 which contain pIG121Hm binary vector, carrying neomycin phosphotransferase (NPT II) and $\beta$-Glucuronidase (GUS) genes. Three days after cocultivation with Agrobacterium tumefaciens and particle bombardment, the callus clusters were transferred to MS medium containing 1mg/L 2,4-D, 0.1mg/L BAP, 100mg/L kanamycin and 200mg/L carbenicillin. Four weeks after transfer to the selection medium, GUS expression was detected and PCR analysis revealed the presence of NPT II fragment of the expected size (700 bp) in the transformed callus. The GUS expression from Agrobacterium-mediated transformants after particle bombardment increased to over 3-folds compared with that of callus cocultivated with Agrobacterium tumefaciens without particle bombardment. The callus clusters containing kanamycin resistant gene were transferred to MS medium containing 1mg/L NAA and 1mg/L BAP. Somatic embryos were developed in four weeks and microbulbs expressing GUS were formed.
형질전환 효율을 높이기 위하여, NPTII와 GUS유전자를 포함하고 있는 pIG121Hm을 미세 입자에 코팅하여 particle bombardment를 수행한 후 pIG121Hm가 도입된 Agrobacterium tumefaciens EHA101와 3일간 공동 배양하였다. 그 후 캘러스를 1mg/L 2,4-D, 0.1mg/L BAP, 100mg/L kanamycin, 그리고 200mg/L carbenicillin이 포함된 MS배지로 옮겨 4주간 성장시킨 후 kanamycin저항성 캘러스를 선발하여 GUS 발현을 관찰하였고, PCR 분석을 통하여 700 bp의 NPT II 유전자가 도입된 것을 확인하였다. Particle bombardment 후 Agrobacterium과 공동배양 한 처리구가 Agrobacterium과 공동배양만 한 처리구보다 GUS발현 분석에 의한 형질전환 효율이 3배정도 더 높았다 형질전환 된 재분화 식물체를 얻기위해 다시 선발된 kanamycin저항성 캘러스는 1mg/L NAA와 1mg/L BAP가 포함된 재분화 배지에 옮겨져 4주 후 형질전환 된 소인경을 형성하였다.
