Agrobacterium을 이용한 Saccharomyces cerevisiae Acid Phosphatse 유전자 (PHO5) 의 식물체로의 도입

Agrobacterium-Mediated Transformation on a Plant with Saccharomyces cerevisiae Acid Phosphatse Gene(PHO5)

Agronacterium tumefaciens(strain LBA4404)를 매개로 한 외래 유전자의 식물체로의 도입에 관한 실험을 하여 아래와 가은 결과를 얻었다. 모델 식물로는 담배(Nivotuana tabacum c.v. samsun)를 사용하였으며, 외래 유전자는 효모 유래의 Acid phosphatase 유전자인 PH05를 사용하였다. pVC727G에서 PH05를 잘라내어 전기영동 및 graphical estimation법으로 확인한 결과, PH05의 크기는 1.5kb였다. pVC727G와 광역plasmid인 qBI121을 이용하여 식물체 형질전환을 위한 vector인 pBKJ I을 만들었다. pBKJ I을 Agronacterium LBA4404에 subcloninggksgn 담배의 leaf dise를 Agronacterium LBA4404과 공배양하여 형질전환을 유도하였다. kanamycindmf 첨가한 MS-n/B음지에서 형질전환된 shoots를 얻었으며, 이들의 재분화를 실시하여 형질전환된 식물체를 얻었다. 형질전환된 식물체의 genomic DNA를 PH05로서 southern hybridization하여 형질전환을 확인하였으며, 식물체의 잎, 줄기 및 뿌리의 Apase(PH05)활성을 측정하여 도입한 PH05가 발현됨을 확인하였다.

This study was conducted to obtain the transformed tobacco plants with S. cerevisiae Acid phosphatase gene(PH05) using Agrobacterium tumefaciens and th confirm plant transformation and gene expression. the results obtained were summarized as follows: APase activity of Saccharomyces cereviase NA 87-11A was remarkably showed up as deep red color when assayed by Tohe and Oshima(1974). PH05 fragment, Apase gene, was obtained from pVC727G and the graphically estimated size was about 1.5kb by agarose gel electrophoresis. The sequencing results of 5'end and 3'end of PH05 using dideoxy chain termination method were coinsided with the full length nucleotide already. pBKJ I vector was constructed by isolation of PH05 fragment from pVC727-1 and pBKSI-1 digesred with Sma I and Xba I. Isolated plasmid from transformed A. tumefaciens with constructed pBKJ I when it was electrophoresed with agarose gel. The dosc of tobacco leaf was cocultivated 재소 transformed Agronacterium tumefaciens. Transformed shoots were selected on kanamtcin-containing MS-n/B medium and they were regenerated. The transgenic tobacco plants were elucidated by isolation of genomic DNA and genomic southern hybridization using ${\alpha}-^{32}P$ labelled PH05 fragments. The PH05 in transformed tobacco plants was expressed in leaf, stem and root, and its APase activity was estimated as deep red color by Tohe method.