Please use this identifier to cite or link to this item:
Transfer of the Insecticidal Crystal Protein Gene of Bacillus thuringiensis into Cabbage (Brassica oleracea L. var. capitata L.)
|關鍵字:||Gene transfer;蘇力菌;Bacillus thuringiensis;cry1A(b);蘇力菌殺蟲晶體蛋白基因;基因轉移||Project:||興大園藝, Volume 22, Issue 1, Page(s) 61-73.
Horticulture NCHU, Volume 22, Issue 1, Page(s) 61-73.
本試驗將攜帶有 Cauliflower Mosaic Virus 35S(CaMV 35S)及rubisco small subunit(rbcS)啟動子的轉殖載體，以蘇力菌殺蟲晶體蛋白基因(crylA(b))，利用農桿菌基因轉移法將其轉移到甘藍(新豐、初秋)的子葉或下胚軸。本實驗之目的在建立甘藍基因轉移及植株再生系統，研究不同啟動子對表現此基因的影響，並探討培育成抗蟲之蔬菜的可行性。
The research focuses on the use of cruciferous vegetables as a model system to establish the gene transfer technology, and to study the possibility for improvement of cruciferous vegetable with insect resistance, through the art of genetic engineering.
The δ-toxin gene of Bacillus thuringiensis (cryl A(b)) was transfer into hypocotyl and cotyledon of cabbage (New top, K-Y cross) via Agrobacterium mediated transformation. Regenerated plants were obtained after transformation with two kinds of plasmids. The regeneration rate of transformation was 2.1% to 3.6%. The transformed plants were examined by PCR, Southern and Northern blot hybridization. The results indicated that the expression of constructed genes was a little higher in transgenic plants transferred with rbcS as promoter than CaMV 35S promoter. Insecticidal effects on Plutella xylostellac was demonstrated in cryl A(b)-transformed cabbage plants.
|Appears in Collections:||園藝學系|
Show full item record
Files in This Item:
TAIR Related Article
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.