Abstract：A Full-length cry1Ia gene fragment, which obtained by PCR amplification with a pair of primers designed according to cryIa-type gene sequences and DNA from Bacillus thuringiensi Btc008 as template, was introduced into expression vector pET-21b and transformed into E. coli BL21(DE3). Molecular weight of the induced express product was 81kD.The encoded protein was composed of 719 amino acid residues and the predicted MW is 81.2kD. The amino acid sequence of the Cry1Ia was very different from those of 12 known Cry1Ia-type proteins. This gene with accession number AF373207 was designated as cry1Ia8 by International Bt Insecticidal Gene Nomenclature Committee. The bioassay results indicated that the Cry1Ia toxin protein showed distinctly insecticidal activity against Ostrinia furnacalis and Plutella xylostella with LC50 of 0.268 µg/g and 2.227 µg/ml respectively, while it also had insecticidal activity against Leguminivora glycinivorella，but no activity against Pyrrhalta aenescens. The novel cry1Ia8 gene will be new resource for the construction of genetically engineered bacterium and transgenic plant for biocontrol of insect pests. It also is available for screening gene stacks to delay the resistance produce of the pests.
收稿日期: 2007-03-30
通讯作者:
宋福平
引用本文:
窦黎明 韩岚岚 张杰 何康来 赵奎军 黄大昉 宋福平. 苏云金芽孢杆菌cry1Ia基因的克隆、表达与活性研究[J]. , 2007, 15(6): 0-.
. Cloning, Expression and activity of cry1Ia Genes from Bacillus thuringiensis isolate. , 2007, 15(6): 0-.
