首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Expression of the insecticidal protein gene from Bacillus thuringiensis subsp. aizawai in Bacillus subtilis and in the thermophile Bacillus stearothermophilus by using the alpha-amylase promoter of the thermophile.
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Expression of the insecticidal protein gene from Bacillus thuringiensis subsp. aizawai in Bacillus subtilis and in the thermophile Bacillus stearothermophilus by using the alpha-amylase promoter of the thermophile.

机译:苏云金芽孢杆菌亚种杀虫蛋白基因的表达通过使用嗜热芽孢杆菌的α-淀粉酶启动子在枯草芽孢杆菌和嗜热嗜热脂肪芽孢杆菌中发现aizawai。

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摘要

Expression of the insecticidal protein gene from Bacillus thuringiensis subsp. aizawai IPL7 in B. subtilis MI113 and B. stearothermophilus SIC1 was examined. Production of the protein (130 kilodaltons [KDa]) was analyzed by its reaction with antibody against the insecticidal proteins of the parental B. thuringiensis. When the original gene containing its own promoter was subcloned in B. subtilis, only a small amount of the protein was produced. Therefore, both the promoter for the B. stearothermophilus alpha-amylase gene and the insecticidal protein gene were inserted in a repA (low-copy-number) plasmid to yield the recombinant plasmid pTBT-Pamy. B. subtilis MI113 carrying pTBT-Pamy produced more of the 130-kDa protein (about 10(4) molecules per cell) at 37 degrees C. In contrast, B. stearothermophilus SIC1 carrying pTBT-Pamy produced a small amount of 130-kDa protein (10(2) to 10(3) molecules per cell) at 55 degrees C.
机译:苏云金芽孢杆菌亚种杀虫蛋白基因的表达检查了枯草芽孢杆菌MI113和嗜热脂肪芽孢杆菌SIC1中的aizawai IPL7。通过与抗亲本苏云金芽孢杆菌的杀虫蛋白的抗体反应,分析了该蛋白的产生(130千道尔顿[KDa])。当将含有自身启动子的原始基因亚克隆到枯草芽孢杆菌中时,仅产生了少量的蛋白质。因此,将嗜热脂肪芽孢杆菌α-淀粉酶基因的启动子和杀虫蛋白基因都插入到repA(低拷贝数)质粒中,以产生重组质粒pTBT-Pamy。携带pTBT-Pamy的枯草芽孢杆菌MI113在37摄氏度下产生更多的130-kDa蛋白(每个细胞约10(4)个分子)。相反,携带pTBT-Pamy的嗜热脂肪芽孢杆菌SIC1产生少量130-kDa蛋白。蛋白质(每个细胞10(2)至10(3)个分子)在55摄氏度下。

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