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开发基于 pyrF 的基因敲除系统,用于对古菌地中海盐菌和嗜盐菌进行全基因组操作。

Development of pyrF-based gene knockout systems for genome-wide manipulation of the archaea Haloferax mediterranei and Haloarcula hispanica.

机构信息

State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

J Genet Genomics. 2011 Jun 20;38(6):261-9. doi: 10.1016/j.jgg.2011.05.003. Epub 2011 May 17.

Abstract

The haloarchaea Haloferax mediterranei and Haloarcula hispanica are both polyhydroxyalkanoate producers in the domain Archaea, and they are becoming increasingly attractive for research and biotechnology due to their unique genetic and metabolic features. To accelerate their genome-level genetic and metabolic analyses, we have developed specific and highly efficient gene knockout systems for these two haloarchaea. These gene knockout systems consist of a suicide plasmid vector with the pyrF gene as the selection marker and a uracil auxotrophic haloarchaeon (ΔpyrF) as the host. For in-frame deletion of a target gene, the suicide plasmid carrying the flanking region of the target gene was transferred into the corresponding ΔpyrF host. After positive selection of the single-crossover integration recombinants (pop-in) on AS-168SY medium without uracil and counterselection of the double-crossover pyrF-excised recombinants (pop-out) with 5-fluoroorotic acid (5-FOA), the target gene knockout mutants were confirmed by PCR and Southern blot analysis. We have demonstrated the effectiveness of these systems by knocking out the crtB gene which encodes a phytoene synthase in these haloarchaea. In conclusion, these well-developed knockout systems would greatly accelerate the functional genomic research of these halophilic archaea.

摘要

嗜盐古菌地中海盐杆菌和盐沼盐球菌都是域古菌中的多聚羟丁酸酯生产者,由于其独特的遗传和代谢特征,它们正成为研究和生物技术越来越有吸引力的对象。为了加速这两种嗜盐古菌的基于基因组水平的遗传和代谢分析,我们为这两种嗜盐古菌开发了特定的、高效的基因敲除系统。这些基因敲除系统由带有 pyrF 基因作为选择标记的自杀质粒载体和尿嘧啶营养缺陷型嗜盐古菌(ΔpyrF)作为宿主组成。对于靶基因的框内缺失,携带靶基因侧翼区域的自杀质粒被转入相应的ΔpyrF 宿主中。在没有尿嘧啶的 AS-168SY 培养基上对单交换整合重组体(pop-in)进行阳性选择,并用 5-氟乳清酸(5-FOA)对双交换 pyrF 切除重组体(pop-out)进行反选择后,通过 PCR 和 Southern blot 分析确认靶基因敲除突变体。我们通过敲除这些嗜盐古菌中的 crtB 基因(该基因编码八氢番茄红素合酶)证明了这些系统的有效性。总之,这些成熟的敲除系统将极大地加速这些嗜盐古菌的功能基因组研究。

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