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改良且通用的转化系统,可对嗜热古菌柯达嗜热栖热菌进行多种基因操作。

Improved and versatile transformation system allowing multiple genetic manipulations of the hyperthermophilic archaeon Thermococcus kodakaraensis.

作者信息

Sato Takaaki, Fukui Toshiaki, Atomi Haruyuki, Imanaka Tadayuki

机构信息

Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto 615-8510, Japan.

出版信息

Appl Environ Microbiol. 2005 Jul;71(7):3889-99. doi: 10.1128/AEM.71.7.3889-3899.2005.

Abstract

We have recently developed a gene disruption system for the hyperthermophilic archaeon Thermococcus kodakaraensis by utilizing a pyrF-deficient mutant, KU25, as a host strain and the pyrF gene as a selectable marker. To achieve multiple genetic manipulations for more advanced functional analyses of genes in vivo, it is necessary to establish multiple host-marker systems or to develop a system in which repeated utilization of one marker gene is possible. In this study, we first constructed a new host strain, KU216 (DeltapyrF), by specific and almost complete deletion of endogenous pyrF through homologous recombination. In this refined host, there is no need to consider unknown mutations caused by random mutagenesis, and unlike in the previous host, KU25, there is little, if any, possibility that unintended recombination between the marker gene and the chromosomal allele occurs. Furthermore, a new host-marker combination of a trpE deletant, KW128 (DeltapyrF DeltatrpE::pyrF), and the trpE gene was developed. This system made it possible to isolate transformants through a more simple selection procedure as well as to deduce the transformation efficiency, overcoming practical disadvantages of the first system. The effects of the transformation conditions were also investigated using this system. Finally, we have also established a system in which repeated utilization of the counterselectable pyrF marker is possible through its excision by pop-out recombination. Both endogenous and exogenous sequences could be applied as tandem repeats flanking the marker pyrF for pop-out recombination. A double deletion mutant, KUW1 (DeltapyrF DeltatrpE), constructed with the pop-out strategy, was demonstrated to be a useful host for the dual markers pyrF and trpE. Likewise, a triple deletion mutant, KUWH1 (DeltapyrF DeltatrpE DeltahisD), could also be constructed. The transformation systems developed here now provide the means for extensive genetic studies in this hyperthermophilic archaeon.

摘要

我们最近通过利用嗜热古菌柯达热栖热球菌(Thermococcus kodakaraensis)的pyrF缺陷型突变体KU25作为宿主菌株,并将pyrF基因作为选择标记,开发了一种基因破坏系统。为了在体内对基因进行更深入的功能分析而实现多重基因操作,有必要建立多个宿主 - 标记系统,或者开发一种能够重复利用一个标记基因的系统。在本研究中,我们首先通过同源重组特异性地几乎完全删除内源性pyrF,构建了一个新的宿主菌株KU216(ΔpyrF)。在这个优化的宿主中,无需考虑随机诱变引起的未知突变,并且与先前的宿主KU25不同,标记基因与染色体等位基因之间发生意外重组的可能性很小(如果有的话)。此外,还开发了一种新的宿主 - 标记组合,即色氨酸合成酶E缺失突变体KW128(ΔpyrF ΔtrpE::pyrF)和trpE基因。该系统不仅能够通过更简单的筛选程序分离转化体,还能推断转化效率,克服了第一个系统的实际缺点。我们还使用该系统研究了转化条件的影响。最后,我们还建立了一个系统,通过弹出式重组切除可反向选择的pyrF标记,从而实现其重复利用。内源性和外源性序列均可作为标记pyrF两侧的串联重复序列用于弹出式重组。用弹出策略构建的双缺失突变体KUW1(ΔpyrF ΔtrpE)被证明是pyrF和trpE双标记的有用宿主。同样,也可以构建三缺失突变体KUWH1(ΔpyrF ΔtrpE ΔhisD)。这里开发的转化系统现在为这种嗜热古菌的广泛遗传研究提供了手段。

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