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New Strategy for Isolating Novel Nematicidal Crystal Protein Genes from Bacillus thuringiensis Strain YBT-1518▿

机译:苏云金芽孢杆菌YBT-1518菌株中新的杀线虫晶体蛋白基因新分离策略

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摘要

We have developed a strategy for isolating cry genes from Bacillus thuringiensis. The key steps are the construction of a DNA library in an acrystalliferous B. thuringiensis host strain and screening for the formation of crystal through optical microscopy observation and sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analyses. By this method, three cry genes—cry55Aa1, cry6Aa2, and cry5Ba2—were cloned from rice-shaped crystals, producing B. thuringiensis YBT-1518, which consists of 54- and 45-kDa crystal proteins. cry55Aa1 encoded a 45-kDa protein, cry6Aa2 encoded a 54-kDa protein, and cry5Ba2 remained cryptic in strain YBT-1518, as shown by SDS-PAGE or microscopic observation. Proteins encoded by these three genes are all toxic to the root knot nematode Meloidogyne hapla. The two genes cry55Aa1 and cry6Aa2 were found to be located on a plasmid with a rather small size of 17.7 kb, designated pBMB0228.
机译:我们已经开发了一种从苏云金芽孢杆菌中分离cry基因的策略。关键步骤是在无结晶苏云金芽孢杆菌宿主菌株中构建DNA库,并通过光学显微镜观察和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分析筛选晶体的形成。通过这种方法,从稻米状晶体中克隆了三个cry基因cry55Aa1,cry6Aa2和cry5Ba2,从而产生了苏云金芽孢杆菌YBT-1518,它由54-和45-kDa的晶体蛋白组成。如SDS-PAGE或显微镜观察所示,cry55Aa1编码一个45 kDa的蛋白质,cry6Aa2编码一个54 kDa的蛋白质,而cry5Ba2在YBT-1518菌株中仍然是隐秘的。这三个基因编码的蛋白质对根结线虫Meloidogyne hapla均具有毒性。发现两个基因cry55Aa1和cry6Aa2位于质粒上,其大小很小,只有17.7 kb,称为pBMB0228。

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