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首页> 外文期刊>Enzyme and Microbial Technology >Enhanced stability of the cloned Bacillus subtilis alkaline protease gene in alginate-immobilized B. subtilis cells
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Enhanced stability of the cloned Bacillus subtilis alkaline protease gene in alginate-immobilized B. subtilis cells

机译:在藻酸盐固定的枯草芽孢杆菌细胞中克隆的枯草芽孢杆菌碱性蛋白酶基因的稳定性增强

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摘要

Expression and stability of the cloned Bacillus ubtilis alkaline protease (aprE)gene was monitored throughout the growth of free and alginate-immobilized B. subtilis cells. The time as well as the level of expression of the aprE gene in alginate-immobilized cells was found to be close to that of free cells. The multicopy plasmid that carries the aprE gene was stably maintained in alginate-immobilized cells. Plasmid stability was greatly enhanced, it reached 83% and 8% after ten growth cycles for alginate-immoblized and free cells in the absence of stress, respectively. Data presented demonstrate that immobilization of B. subtilis recombinant cells would partially solve the problem of plasmid instability in B. subtilis.
机译:在游离和藻酸盐固定的枯草芽孢杆菌细胞的整个生长过程中,监测克隆的枯草芽孢杆菌碱性蛋白酶(aprE)基因的表达和稳定性。发现在藻酸盐固定的细胞中aprE基因的时间和表达水平与游离细胞接近。携带aprE基因的多拷贝质粒被稳定地固定在藻酸盐固定的细胞中。质粒的稳定性大大增强,在没有压力的情况下,经过十个生长周期的藻酸盐固定化和游离细胞,质粒稳定性分别达到83%和8%。所提供的数据表明,枯草芽孢杆菌重组细胞的固定化将部分解决枯草芽孢杆菌中质粒不稳定的问题。

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