Murphy R C, Stevens S E
Department of Biology, Memphis State University, Memphis, Tennessee 38152.
Appl Environ Microbiol. 1992 May;58(5):1650-5. doi: 10.1128/aem.58.5.1650-1655.1992.
A mosquitocidal cyanobacterium has been developed by introducing the mosquito-toxic cryIVD gene from Bacillus thuringiensis subsp. israelensis into the unicellular cyanobacterium Agmenellum quadruplicatum PR-6 (Synechococcus sp. strain PCC 7002). The cryIVD gene was introduced into the cyanobacterium on a derivative of the PR-6 expression vector pAQE19 delta Sal in which the cryIVD gene was translationally fused to the initial coding sequence of the highly expressed PR-6 cpcB gene. Coomassie blue staining and immunoblot analysis of gel-fractionated cell extract polypeptides indicate that the cpcB-cryIVD gene fusion is expressed at high levels in the cyanobacterial cells, with little or no apparent degradation of the cryIVD gene product. Larvicidal assays revealed that freshly hatched Culex pipiens mosquito larvae readily ingested the transformed cyanobacteria and that the cells proved to be toxic to the larvae.
通过将来自苏云金芽孢杆菌以色列亚种的杀蚊cryIVD基因导入单细胞蓝细菌四聚体阿格门氏菌PR - 6(聚球藻属菌株PCC 7002),已培育出一种杀蚊蓝细菌。cryIVD基因通过PR - 6表达载体pAQE19 delta Sal的衍生物导入蓝细菌,其中cryIVD基因与高表达的PR - 6 cpcB基因的起始编码序列进行了翻译融合。考马斯亮蓝染色和凝胶分离细胞提取物多肽的免疫印迹分析表明,cpcB - cryIVD基因融合体在蓝细菌细胞中高水平表达,cryIVD基因产物几乎没有明显降解。幼虫毒性试验表明,刚孵化的致倦库蚊幼虫很容易摄取转化后的蓝细菌,且这些细胞对幼虫有毒性。