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Expression of the staphylococcal protein A gene in Bacillus subtilis by gene fusions utilizing the promoter from a Bacillus amyloliquefaciens alpha-amylase gene.

机译:利用来自解淀粉芽孢杆菌α-淀粉酶基因的启动子的基因融合,在枯草芽孢杆菌中表达葡萄球菌蛋白A基因。

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摘要

Gene fusions of DNA sequences encoding protein A from Staphylococcus aureus (spa) with expression elements from an alpha-amylase gene from Bacillus amyloliquefaciens (amyEBamP) directed the synthesis and efficient secretion of protein A in Bacillus subtilis. The fusions were established on multicopy pUB110-based plasmid vectors, in contrast to the intact spa gene, which could not be stably established on plasmids in B. subtilis. Some of the resulting B. subtilis strains secreted protein A at levels in excess of 1 g/liter, demonstrating that a foreign protein encoded by an engineered gene can be secreted by B. subtilis at levels comparable to endogenous exoproteins.
机译:编码金黄色葡萄球菌(spa)的蛋白A与来自解淀粉芽孢杆菌(amyEBamP)的α-淀粉酶基因表达元件的DNA序列的基因融合,指导枯草芽孢杆菌中蛋白A的合成和有效分泌。与完整的spa基因相比,融合蛋白是在基于多拷贝pUB110的质粒载体上建立的,而完整的spa基因无法在枯草芽孢杆菌的质粒上稳定建立。一些所得的枯草芽孢杆菌菌株以超过1 g /升的水平分泌蛋白A,这表明枯草芽孢杆菌可以分泌与内源性外蛋白相当的水平的工程基因编码的外源蛋白。

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