Hammelmann M, Soppa Jörg
Institute for Molecular Biosciences, Biocentre, Goethe-University, D-60438 Frankfurt, Germany.
J Microbiol Methods. 2008 Oct;75(2):201-4. doi: 10.1016/j.mimet.2008.05.029. Epub 2008 Jun 8.
A method for the construction of in frame deletions in chromosomal genes of the archaeon Haloferax volcanii has been described recently (Allers et al. (2004), Appl. Environ. Microbiol. 70:943-953). Two steps of the procedure for deletion vector construction were optimized. First, the deletion version of the gene of interest was generated by fusion of two PCR products, which were comprised of the upstream and downstream regions of the gene, respectively, using a third PCR reaction. Second, the fusion PCR product was ligated with the optimized vector pMH101 in the presence of one of four possible restriction enzymes ("restriction selection cloning"). Taken together, the optimized procedure omits one cloning step and enhances both speed and efficiency of deletion vector construction considerably.
最近已经描述了一种构建嗜盐嗜热栖热菌染色体基因框内缺失的方法(Allers等人,(2004年),《应用与环境微生物学》70:943 - 953)。优化了缺失载体构建过程的两个步骤。首先,使用第三个PCR反应,通过融合分别由基因的上游和下游区域组成的两个PCR产物,生成感兴趣基因的缺失版本。其次,在四种可能的限制酶之一存在的情况下,将融合PCR产物与优化载体pMH101连接(“限制酶选择克隆”)。总体而言,优化后的程序省略了一个克隆步骤,并显著提高了缺失载体构建的速度和效率。