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表达苏云金芽孢杆菌δ-内毒素基因的转基因烟草植株的抗虫性

Insect resistance of transgenic tobacco plants expressing delta-endotoxin gene of Bacillus thuringiensis.

作者信息

Tian Y C, Qin X F, Xu B Y, Li T Y, Fang R X, Mang K Q, Li W G, Fu W J, Li Y P, Zhang S F

机构信息

Institute of Microbiology, Chinese Academy of Sciences, Beijing.

出版信息

Chin J Biotechnol. 1991;7(1):1-13.

PMID:1663400
Abstract

The initiative B.thuringiensis delta-endotoxin (Bt toxin) gene clones TH12 and TH48 contain two different classes of homologous genes, the 5.3 kb class and 6.6 kb class, respectively. Bt toxin genes of both classes, modified at the 5'-end and truncated at the 3'-end, can still be expressed to produce the insecticidal, truncated toxin proteins in E. coli. The modified Bt toxin genes were inserted into the plant binary expression vector pBin 437 (a derivative plasmid of pBin 19) and were transferred into tobacco by Ti plasmid-mediated gene transfer system. Southern blot and DNA slot blot analysis indicate that the Bt toxin genes have been integrated into tobacco genome at a copy number of 1 to 5. Northern blot analysis of polyA+ RNAs from progeny of the transgenic plants revealed that Bt toxin genes of both 5.3 kb and 6.6 kb classes were expressed in transgenic plants, though the transcripts were degraded to RNAs of lower molecular weights. In insecticidal test, 5 plants from the progeny of 5.3 kb class gene-transformed SR1 tobacco plants and 3 plants from those of 6.6 kb class gene-transformed plants were found to be toxic to the testing larvea of H.assulta. In comparison with the control, mortality of the insects fed on transgenic plants reached 40-50% and the growth of the survived insects was remarkably inhibited. These results indicate that the modified Bt genes of the 5.3 kb and 6.6 kb classes were expressed in transgenic plants and could confer on the transgenic plants a new character of insect resistance.

摘要

起始的苏云金芽孢杆菌δ-内毒素(Bt毒素)基因克隆TH12和TH48分别包含两类不同的同源基因,即5.3 kb类和6.6 kb类。两类Bt毒素基因在5′端进行了修饰,在3′端进行了截短,仍能在大肠杆菌中表达产生具有杀虫活性的截短毒素蛋白。将修饰后的Bt毒素基因插入植物双元表达载体pBin 437(pBin 19的衍生质粒),并通过Ti质粒介导的基因转移系统导入烟草。Southern杂交和DNA斑点杂交分析表明,Bt毒素基因已以1至5的拷贝数整合到烟草基因组中。对转基因植物后代的多聚腺苷酸+RNA进行Northern杂交分析表明,5.3 kb和6.6 kb两类Bt毒素基因均在转基因植物中表达,尽管转录本被降解为分子量较低的RNA。在杀虫试验中,发现5.3 kb类基因转化的SR1烟草植株后代中的5株和6.6 kb类基因转化的植株后代中的3株对烟青虫的测试幼虫有毒性。与对照相比,取食转基因植物的昆虫死亡率达到40%至50%,存活昆虫的生长受到显著抑制。这些结果表明,5.3 kb和6.6 kb两类修饰后的Bt基因在转基因植物中表达,并能赋予转基因植物新的抗虫特性。

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