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Development of a New Recombineering System for Agrobacterium Species

机译:农杆菌菌种新组合系统的开发

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The discovery of new and efficient genetic engineering technologies for Agrobacterium will broaden the capacity for fundamental research on this genus and its utilization as a transgenic vehicle. In this study, we aim to develop an efficient recombineering system for Agrobacterium species. We examined isolates of Agrobacterium and the closely related genus Rhizobium to identify pairs of ET-like recombinases that would aid in the recombineering of Agrobacterium species. Four pairs of ET-like recombinases, named RecETh1h2h3h4(AGROB6), RecETh1h2P3(RHI597), RecET(RHI145), and RecETh(RHI483), were identified in Agrobacterium tumefaciens strain B6, Rhizobium leguminosarum bv. trifolii WSM597, Rhizobium sp. strain LC145, and Rhizobium sp. strain Root483D2, respectively. Eight more candidate recombineering systems were generated by combining the new ET-like recombinases with Red gamma or Plu gamma. The Plu gamma ETRHI145 system, the RecETh1h2h3h4(AGROB6 )system, and the Plu gamma EThRHI483 system were determined to be the most efficient recombineering systems for the type strains A. tumefaciens C58, A. tumefaciens EHA105, and Rhizobium rhizogenes NBRC 13257, respectively. The utility of these systems was demonstrated by knocking out the istB-istA fusion gene in C58, the celI gene in EHA105, and the 3'-to-5' exonuclease gene and endoglucanase gene in NBRC 13257. Our work provides an effective genetic manipulation strategy for Agrobacterium species. IMPORTANCE Agrobacterium is a powerful transgenic vehicle for the genetic manipulation of numerous plant and fungal species and even animal cells. In addition to improving the utility of Agrobacterium as a transgenic vehicle, genetic engineering tools are important for revealing crucial components that are functionally involved in transfer DNA (T-DNA) translocation events. This work developed an efficient and versatile recombineering system for Agrobacterium. The successful genome modification of Agrobacterium strains revealed that this new recombineering system could be used for the genetic engineering of Agrobacterium.
机译:农杆菌新的高效基因工程技术的发现将扩大该属的基础研究及其作为转基因载体的利用能力。在这项研究中,我们旨在开发一种有效的农杆菌物种重组系统。我们检查了农杆菌和密切相关的根瘤菌属的分离物,以确定有助于农杆菌物种重组的ET样重组酶对。在根癌农杆菌菌株B6、豆科植物Bv中鉴定出4对ET样重组酶,分别命名为RecETh1h2h3h4(AGROB6)、RecETh1h2P3(RHI597)、RecET(RHI145)和RecETh(RHI483)。分别是三叶菌WSM597、根瘤菌菌株LC145和根瘤菌菌株Root483D2。通过将新的ET样重组酶与Red gamma或Plu gamma相结合,又产生了8个候选重组系统。Plu gamma ETRHI145体系、RecETh1h2h3h4(AGROB6 )体系和Plu gamma EThRHI483体系分别是根癌曲霉C58型、根癌菌EHA105型和根瘤菌型NBRC 13257菌株最有效的重组体系。通过敲除 C58 中的 istB-istA 融合基因、EHA105 中的 celI 基因以及 NBRC 13257 中的 3'-to-5' 核酸外切酶基因和内切葡聚糖酶基因来证明这些系统的效用。我们的工作为农杆菌物种提供了一种有效的遗传操作策略。重要性 农杆菌是一种强大的转基因载体,用于对多种植物和真菌物种甚至动物细胞进行基因操作。除了提高农杆菌作为转基因载体的效用外,基因工程工具对于揭示在功能上参与转移 DNA (T-DNA) 易位事件的关键成分也很重要。这项工作开发了一种高效且多功能的农杆菌重组系统。农杆菌菌株的成功基因组改造表明,这种新的重组系统可用于农杆菌的基因工程。

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