Tounsi Slim, Jaoua Samir
Laboratoire des Biopesticides, Centre de Biotechnologie de Sfax, P.O. Box 'K', 3038, Sfax, Tunisia.
Biotechnol Lett. 2003 Aug;25(15):1219-23. doi: 10.1023/a:1025016221891.
A 4 kb BamHI-HindIlI fragment, corresponding to the cry2A operon of Bacillus thuringiensis subsp. kurstaki strain BNS3, was cloned. The sequencing of the corresponding cry2Aa-type gene, termed crybns3-4, revealed an open reading frame of 1902 bp, encoding a protein of 633 amino-acid residues. Both nucleotide and amino-acid sequences similarity analysis revealed that crybns3-4 is a new cry2Aa-type gene which has several differences from the reported cry2Aa-type genes. The transfer of the cloned operon to an acrystalliferous mutant of BNS3, revealed an expression of the new cry2Aa-type gene and a production of parasporal crystal inclusions in the transformants.
克隆了一个4 kb的BamHI-HindIII片段,其对应于苏云金芽孢杆菌库斯塔克亚种BNS3菌株的cry2A操纵子。对相应的cry2Aa型基因(命名为crybns3-4)进行测序,发现一个1902 bp的开放阅读框,编码一个由633个氨基酸残基组成的蛋白质。核苷酸和氨基酸序列相似性分析均表明,crybns3-4是一个新的cry2Aa型基因,与已报道的cry2Aa型基因存在若干差异。将克隆的操纵子转移至BNS3的无晶体突变体中,结果显示新的cry2Aa型基因在转化体中得以表达,并产生了伴孢晶体包涵体。