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首页> 外文期刊>Current Microbiology: An International Journal >Cloning and characterization of two novel genes, cry24B and s1orf2, from a mosquitocidal strain of Bacillus thuringiensis serovar sotto
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Cloning and characterization of two novel genes, cry24B and s1orf2, from a mosquitocidal strain of Bacillus thuringiensis serovar sotto

机译:苏云金芽孢杆菌血清毒杀蚊灭蚊菌株两个新基因cry24B和s1orf2的克隆和鉴定

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Two new crystal protein genes, cry24B and s1orf2, were cloned from a mosquitocidal Bacillus thuringiensis serovar sotto strain. The cry24B and s1orf2 genes encoded a 76-kDa and 62-kDa protein, respectively. The Cry24B protein retained five conserved regions commonly found in the existing Cry proteins. The amino acid sequence of the S1ORF2 had a high homology to that of the ORF2 protein of B. thuringiensis serovar jegathesan. Southern hybridization experiments with a cry24B gene-specific probe revealed that these genes are located on two large plasmids of > 100 kb. When the two genes, cry24B and s1orf2, were expressed in an acrystalliferous B. thuringiensis host, the proteins were synthesized and accumulated as inclusions. These inclusions exhibited no larvicidal activities against three mosquito species: Aedes aegypti, Anopheles stephensi, and Culex pipiens molestus. Likewise, the inclusions contained no cytocidal activity against HeLa cells.
机译:从一个灭​​蚊的苏云金芽孢杆菌血清型sotto菌株中克隆了两个新的晶体蛋白基因cry24B和s1orf2。 cry24B和s1orf2基因分别编码一个76 kDa和62 kDa的蛋白质。 Cry24B蛋白保留了现有Cry蛋白中常见的五个保守区。 S1ORF2的氨基酸序列与苏云金芽孢杆菌血清杰加特桑的ORF2蛋白具有高度同源性。使用cry24B基因特异性探针进行的Southern杂交实验表明,这些基因位于两个大于100 kb的大质粒上。当两个基因cry24B和s1orf2在无结晶苏云金芽孢杆菌宿主中表达时,这些蛋白质被合成并作为包涵体积累。这些包裹体没有表现出对三种蚊子的杀幼虫活性:埃及伊蚊,埃及按蚊和淡色库蚊。同样,内含物也没有针对HeLa细胞的杀细胞活性。

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