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Improved and Versatile Transformation System Allowing Multiple Genetic Manipulations of the Hyperthermophilic Archaeon Thermococcus kodakaraensis

机译:改进和多功能的转换系统允许对超嗜热古生热球菌kodakaraensis进行多种遗传操作。

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摘要

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 (ΔpyrF), 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 (ΔpyrF ΔtrpE::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 (ΔpyrF ΔtrpE), 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 (ΔpyrF ΔtrpE ΔhisD), could also be constructed. The transformation systems developed here now provide the means for extensive genetic studies in this hyperthermophilic archaeon.
机译:我们最近通过利用pyrF缺陷型突变体KU25作为宿主菌株,并以pyrF基因作为选择标记,为高嗜温古生柯达热球菌开发了一种基因破坏系统。为了在体内对基因进行更高级的功能分析以实现多种遗传操作,有必要建立多个宿主标记系统或开发一种可以重复利用一个标记基因的系统。在这项研究中,我们首先通过同源重组特异性和几乎完全删除内源性pyrF,构建了一个新的宿主菌株KU216(ΔpyrF)。在这种精致的宿主中,无需考虑由随机诱变引起的未知突变,并且与以前的宿主KU25不同,几乎没有(如果有的话)在标记基因和染色体等位基因之间发生意外重组的可能性。此外,开发了新的trpE缺失宿主KW128(ΔpyrFΔtrpE:: pyrF)和trpE基因的宿主标记组合。该系统使得可以通过更简单的选择程序分离转化体以及推导转化效率,从而克服了第一个系统的实际缺点。还使用该系统研究了转化条件的影响。最终,我们还建立了一个系统,在该系统中,通过弹出重组将其切除,可以重复利用可逆选择的pyrF标记。内源序列和外源序列都可以应用,作为标记pyrF侧翼的串联重复用于弹出重组。用弹出策略构建的双缺失突变体KUW1(ΔpyrFΔtrpE)被证明是双标记pyrF和trpE的有用宿主。同样,也可以构建三重缺失突变体KUWH1(Δ pyrF Δ trpE Δ hisD )。现在,在此开发的转化系统为这种超嗜热古细菌提供了广泛的遗传研究手段。

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