利用iptg诱导的枯草芽孢杆菌pspace启动子制备无诱导剂表达质粒

Phuong Thi Mai Chu, H. Phan, H. Nguyen, T. Phan
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引用次数: 2

摘要

枯草芽孢杆菌(Bacillus subtilis)低表达水平的无诱导剂表达载体是基础研究的必要条件。在这项研究中,我们通过去除一部分lacI基因,构建了携带iptg诱导启动子P空间的无诱导剂表达质粒。然后,我们分析了目标基因bgaB和gfp +在枯草芽孢杆菌中的表达。Western blot实验表明,带P空间的无诱导剂质粒可以在枯草芽孢杆菌菌株中低水平产生报告基因,并且在1 mM IPTG的诱导下与相应的可诱导构建体相当。报告子活性表明,P空间启动子的无诱导剂表达量显著低于先前报道的具有强启动子P grac 01和P grac 100的无诱导剂质粒,分别为BgaB的16.2 ~ 20.3倍和GFP +的24.7 ~ 34.3倍。综上所述,携带P空间启动子的无诱导剂表达载体可以在枯草芽孢杆菌中低水平地组成表达外源重组蛋白。
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Development of inducer-free expression plasmidsusing IPTG-inducible Pspac promoter for Bacillus subtilis
: An inducer-free expression vector for the low expression levels in Bacillus subtilis (B. subtilis) is necessary for fundamental research. In this study, we constructed inducer-free expression plasmids carrying P spac , a well-known IPTG-inducible promoter, by removing a part of the lacI gene. Then, we analysed the expression of the target genes bgaB and gfp + in B. subtilis. Western blot experiments demonstrated that the reporters from the inducer-free plasmids with P spac could be produced at low levels in B. subtilis strains and were equivalent to their corresponding inducible constructs with 1 mM IPTG. The reporter activities showed that inducer-free expression from the P spac promoter was dramatically less than that of the inducer-free plasmids with the strong promoters P grac 01 and P grac 100 reported previously, about 16.2 to 20.3 times for BgaB and 24.7 to 34.3 times for GFP + , respectively. In conclusion, the inducer-free expression vectors carrying P spac promoters allow the constitutive expression of heterologous recombinant proteins at low levels in B. subtilis .
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