Rouis Souad, Chakroun Maissa, Jaoua Samir
Laboratory of Biopesticides, Centre of Biotechnology of Sfax, P.O. Box "K" 3038, Sfax, Tunisia.
Mol Biotechnol. 2008 Mar;38(3):233-9. doi: 10.1007/s12033-007-9021-8. Epub 2007 Nov 27.
A comparative study of different steps in the mode of action of the individual Bacillus thuringiensis kurstaki BNS3 Cry1Aa and Cry1Ac delta-endotoxins on E. kuehniella larvae was performed in order to investigate the origin of the difference in the response of this larvae to each of the latter. Proteolytic activation was shown to be one of the main steps impaired in E. kuehniella tolerance to Cry1Aa. The absence of two proteinase activities as well as an altered activity level observed in the case of Cry1Aa would be the consequence of proteinase-mediated tolerance of E. kuehniella to this toxin. In situ binding and histopathological effect analyses allowed concluding that the binding of the toxin to BBMV receptors is the key step in E. kuehniella tolerance to Cry1Aa toxin. The latter was slightly bound to apical membranes of epithelial cells that remained intact, whereas Cry1Ac was tightly bound to completely damaged cells basal membranes.
为了研究库氏粉斑螟幼虫对苏云金芽孢杆菌kurstaki BNS3的Cry1Aa和Cry1Ac δ-内毒素各自反应差异的来源,对这两种毒素作用模式的不同步骤进行了比较研究。结果表明,蛋白水解激活是库氏粉斑螟对Cry1Aa耐受性受损的主要步骤之一。库氏粉斑螟对Cry1Aa的耐受性由蛋白酶介导,这表现为两种蛋白酶活性的缺失以及Cry1Aa情况下观察到的活性水平改变。原位结合和组织病理学效应分析表明,毒素与刷状缘膜囊泡(BBMV)受体的结合是库氏粉斑螟对Cry1Aa毒素耐受性的关键步骤。Cry1Aa与保持完整的上皮细胞顶端膜轻微结合,而Cry1Ac则与完全受损细胞的基底膜紧密结合。