首页> 美国卫生研究院文献>BMC Microbiology >DNA repair genes RAD52 and SRS2 a cell wall synthesis regulator gene SMI1 and the membrane sterol synthesis scaffold gene ERG28 are important in efficient Agrobacterium-mediated yeast transformation with chromosomal T-DNA
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DNA repair genes RAD52 and SRS2 a cell wall synthesis regulator gene SMI1 and the membrane sterol synthesis scaffold gene ERG28 are important in efficient Agrobacterium-mediated yeast transformation with chromosomal T-DNA

机译:DNA修复基因RAD52和SRS2细胞壁合成调节基因SMI1和膜固醇合成支架基因ERG28在农杆菌介导的染色体T-DNA高效转化酵母中很重要

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摘要

BackgroundPlant pathogenic Agrobacterium strains can transfer T-DNA regions of their Ti plasmids to a broad range of eukaryotic hosts, including fungi, in vitro. In the recent decade, the yeast Saccharomyces cerevisiae is used as a model host to reveal important host proteins for the Agrobacterium-mediated transformation (AMT). Further investigation is required to understand the fundamental mechanism of AMT, including interaction at the cell surface, to expand the host range, and to develop new tools. In this study, we screened a yeast mutant library for low AMT mutant strains by advantage of a chromosome type T-DNA, which transfer is efficient and independent on integration into host chromosome.
机译:背景植物致病性土壤杆菌菌株可以在体外将其Ti质粒的T-DNA区域转移到各种真核宿主中,包括真菌。在最近的十年中,酵母酿酒酵母被用作模型宿主,以揭示农杆菌介导的转化(AMT)的重要宿主蛋白。需要进一步研究以了解AMT的基本机制,包括细胞表面的相互作用,扩大宿主范围并开发新工具。在这项研究中,我们利用染色体类型T-DNA筛选了低AMT突变菌株的酵母突变体文库,该方法高效且独立于宿主染色体整合而转移。

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