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Tetracycline-Dependent Conditional Gene Knockout in Bacillus subtilis

机译:枯草芽孢杆菌中四环素依赖性条件基因敲除。

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摘要

Reversible tetracycline-dependent gene regulation allows induction of expression with the tetracycline repressor (TetR) or gene silencing with the newly developed reverse mutant revTetR. We report here the implementation of both approaches with full regulatory range in gram-positive bacteria as exemplified in Bacillus subtilis. A chromosomally located gene is controlled by one or two tet operators. The precise adjustment of regulatory windows is accomplished by adjusting tetR or revtetR expression via different promoters. The most efficient induction was 300-fold in the presence of 0.4 μM anhydrotetracycline obtained with a Pr-xylA-tetR fusion. Reversible 500-fold gene knockouts were obtained in B. subtilis after adjusting expression of revTetR by synthetically designed promoters. We anticipate that these tools will also be useful in many other gram-positive bacteria.
机译:可逆的四环素依赖性基因调节允许通过四环素阻遏物(TetR)诱导表达,或使用新开发的反向突变体revTetR沉默基因。我们在这里报告了这两种方法在革兰氏阳性细菌中具有完全调节范围的实施,例如在枯草芽孢杆菌中。染色体定位的基因由一个或两个tet操纵子控制。调节窗的精确调节是通过不同启动子调节tetR或revtetR表达来实现的。在通过Pr-xylA-tetR融合获得的0.4μM脱水四环素存在下,最有效的诱导是300倍。通过合成设计的启动子调节revTetR的表达后,在枯草芽孢杆菌中获得了可逆的500倍基因敲除。我们预计这些工具还将在许多其他革兰氏阳性细菌中有用。

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