عنوان مقاله :
تراريختي چغندرقند با ژن cry1Ab به كمك آگروباكتريوم و ايجاد گياهان تراريخته مقاوم به آفت پرودنيا (Spodoptera littoralis)
عنوان به زبان ديگر :
Transformation of cry1Ab gene to sugar beet (Beta vulgaris L.) by
Agrobacterium and development of resistant plants against Spodoptera
littoralis
پديد آورندگان :
جعفري ، نويسنده Jafari, M. , وليزاده ، مصطفي نويسنده گروه زراعت و اصلاح نباتات- دانشكده كشاورزي- دانشگاه تبريز Valizadeh, M , قره ياضي، بهزاد نويسنده موسسه تحقيقات بيوتكنولوژي كشاورزي كرج Ghareh Yazi, B. , محمدي، ابوالقاسم نويسنده دانشكده كشاورزي-دانشگاه تبريز Mohammadi, A. , نوروزي، پيمان نويسنده مؤسسه تحقيقات چغندرقند- كرج Norouzi, P , ملبوبي، محمدعلي نويسنده مركز ملي مهندسي ژنتيك و بيوتكنولوژي Melboobi, M.A.
اطلاعات موجودي :
دوفصلنامه سال 1387
رتبه نشريه :
فاقد درجه علمي
كليدواژه :
sugar beet , epidopteran pests , Spodoptera littoralis , Agrobacterium tumefaciens , آفات پروانهاي , cry1Ab gene , چغندرقند , ransformation , تراريختي , ژن
چكيده لاتين :
Lepidoteran pests of sugar beet (Beta vulgaris L.) cause a severe yield reduction in the most
sugar beet growing areas of the world as well as in Iran. Due to limited genetic resources of
resistance to insect pest and polygenic inhertance, improvement of pest resistance in beet by
conventional breeding is a difficult task. Biotechnological enhancement by introducing insect
resistance genes such as Bt genes provides a complementary/alternative strategy to control
insect pest of sugar beet. Two sugar beet diploid genotypes were used for transformation by
Agrobacterium tumefaciens strain GV3101 harboring pBI35Scry construct containing synthetic
cry1Ab gene under the control of CaMV 35S promoter and nptII gene as selectable marker. Leaf
blades including shoot bases were used as explants for tranformation. Putative transformants
were screened on medium containing different concentrations of kanamycin. PCR analysis
using cry1Ab-specific primers showed the presence of the transgene in a relatively higher than
50% of regenerated kanamycin-resistant plants. Integration of at least one copy of cry1Ab gene
into the genome of putative transgenic was confirmed by Dot blot analysis. Western blot
analysis using anti-cry1Ab polyclonal antibody revealed the presence of Cry1Ab protein with
the expected size of 67 kDa in transgenic sugar beet lines. Based on bioassay results with
Spodoptera littoralis, T0 plants were exhibited an enhancement of resistance, ranging 37 to 70%
mortality of the pest within 1 week of infestation.
اطلاعات موجودي :
دوفصلنامه با شماره پیاپی سال 1387
كلمات كليدي :
#تست#آزمون###امتحان