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苏云金杆菌δ-内毒素基因(Bt)导入苹果 被引量:8

Transfer Bt-gene to Apple
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摘要 应用携带改造过的长约1.8kb抗虫基因Bt的农杆菌LBA404对苹果品种绿袖、金矮生和长富2号的叶片外植体通过真空渗入接种、共培养和在含50mg/L卡那霉素的培养基上筛选70d,获得对卡那霉素具抗性、存活并产生愈伤组织的外植体为16.7%~373%,其中18.7%~92.9%的外植体经噻重氮苯基脲(TDZ)诱导后,即产生不定芽和形成试管绿苗营养系,营养系经过多聚酶链反应(PCR)测定表明.约有50%以上的营养系具阳性反应,证明Bt基因已被导入苹果。但是,以苹小卷叶蛾幼虫进行虫试检测,抗虫性尚不理想。 Leaf pieces from in vitro-grown shoots of 3 apple cultivars were contaminated byAgrobacterium tumefaciens strain LBA4404 containing the binary vector pBin438 or pB 48. 7 carryingmodefied about 1. 8 kb Bt-gene. The contamination has been done on condition of vaccume Aftercocultivated with the agrobacterium for 3 days and selected by kanamycin for 70 days. The rate of explantsforming callus is 16 % ~37 %. The cxplants With callus have been induced by Thidiazuron (TDZ) to formadventitious buds and to grow out new shoots. The rate of induction is about 18%~ 92% on differentcultivars. According to PCR test, over 50% of regcnerated clones perform positively. It is confirmed thatthe Bt-gene has transformed into apples. However, only a few transformed apples have weak ability ofresistance to tortrix moth (Adoxophyes congrana Walke).
出处 《西北农业学报》 CAS CSCD 1999年第1期78-81,共4页 Acta Agriculturae Boreali-occidentalis Sinica
基金 国家自然科学基金
关键词 苹果 BT基因 农杆菌 基因导入 苹小卷叶蛾 Apple Agrobacterium Genc transformation Bt-genc Tortrix month
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  • 1Gale H. McGranahan,Charles A. Leslie,Sandra L. Uratsu,Abhaya M. Dandekar. Improved efficiency of the walnut somatic embryo gene transfer system[J] 1990,Plant Cell Reports(9):512~516
  • 2David J. James,Andrew J. Passey,Derek J. Barbara,Michael Bevan. Genetic transformation of apple (Malus pumila Mill.) using a disarmed Ti-binary vector[J] 1989,Plant Cell Reports(8):658~661

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