Microbiology and Molecular Biology Laboratory, Department of Biological Sciences, Indian Institute of Science Education and Research (IISER), Bhopal, India.
PLoS One. 2020 Mar 11;15(3):e0230282. doi: 10.1371/journal.pone.0230282. eCollection 2020.
Cloning and expression of a desired gene is indispensable in molecular biology studies. Expression vectors, in this regard, should offer much needed flexibility and choice of cloning strategies for both in vivo and in vitro protein expression experiments. Furthermore, availability of option to choose from various reporter tags allows one to be flexible during designing of an experiment in a more relevant manner. Thus, the need of a versatile expression system cannot be ignored. Although several different expression vectors are available for gene expression in mycobacteria, they lack the required versatility of expression and the inclusion of reporter tags. We here present the construction of a set of nine E. coli-Mycobacterium shuttle plasmids, which offer a combination of three mycobacterial promoter systems (heat shock inducible-hsp60, tetracycline-, and acetamide-inducible) along with three polypeptide tags (Green Fluorescent Protein (GFP), Glutathione S-transferase (GST) and hexa-histidine tag). These vectors offer the cloning of a target gene in all the nine given vectors in parallel, thus allowing the generation of recombinant plasmids that will express the target gene from different promoters with different tags. Here, while the hexa-histidine and GST tags can be used for protein purification and pull-down experiments, the GFP-tag can be used for protein localization within the cell. Additionally, the vectors also offer the choice of positioning of the reporter tag either at the N-terminus or at the C-terminus of the expressed protein, which is achieved by cloning of the gene at any of the two blunt-end restriction enzyme sites available in the vector. We believe that these plasmids will be extremely useful in the gene expression studies in mycobacteria by offering the choices of promoters and reporters. Our work also paves the way to developing more such plasmids with other tags and promoters that may find use in mycobacterial biology.
克隆和表达目的基因在分子生物学研究中是不可或缺的。在这方面,表达载体应该为体内和体外蛋白质表达实验提供所需的灵活性和克隆策略选择。此外,可选择各种报告标签的可用性使人们在设计实验时能够更加灵活地以更相关的方式进行。因此,需要一个多功能的表达系统。虽然有几种不同的表达载体可用于分枝杆菌中的基因表达,但它们缺乏所需的表达灵活性和报告标签的包含。我们在这里构建了一组九个大肠杆菌-分枝杆菌穿梭质粒,它们提供了三种分枝杆菌启动子系统(热休克诱导-hsp60、四环素和乙酰胺诱导)以及三种多肽标签(绿色荧光蛋白 (GFP)、谷胱甘肽 S-转移酶 (GST) 和六组氨酸标签)的组合。这些载体提供了在所有九个给定载体中平行克隆靶基因的能力,从而允许生成表达不同启动子和不同标签的靶基因的重组质粒。在这里,六组氨酸和 GST 标签可用于蛋白质纯化和下拉实验,而 GFP 标签可用于细胞内蛋白质定位。此外,载体还提供了报告标签位于表达蛋白的 N 端或 C 端的选择,这是通过在载体上可用的两个平头末端限制酶位点之一克隆基因来实现的。我们相信这些质粒将通过提供启动子和报告基因的选择,在分枝杆菌中的基因表达研究中非常有用。我们的工作也为开发具有其他标签和启动子的更多此类质粒铺平了道路,这些质粒可能在分枝杆菌生物学中得到应用。