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Genetic transformation of duckweed Lemna gibba and Lemna minor

机译:浮萍Lemna gibba和Lemna minor的遗传转化

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摘要

We developed efficient genetic transformation protocols for two species of duckweed, Lemna gibba (G3) and Lemna minor (8627 and 8744), using Agrobacterium-medialed gene transfer. Partially differentiated nodules were co-cultivated with Agrobacteriumtumefaciens harboring a binary vector containing #bate#-glucuronidase and nptll expression cassettes. Transformed cells were selected and allowed to grow inlo nodules in the presence of kanamycin. Transgenic duckweed fronds were regenerated from selectednodules. We demonstrated that transgenic duckweed could be regenerated within 3 mo. after Agrobacterium-mediated transformation of nodules. Furthermore, we developed a method for transforming L. minor 8627 in 6 wk. These transformation protocols will facilitate genetic engineering of duckweed, ideal plants for bioremediation and large-scale industrial production of biomass and recombinant proteins.
机译:我们使用农杆菌介导的基因转移技术为两种浮萍(Lemna gibba(G3)和Lemna minor(8627和8744))开发了有效的遗传转化方案。将部分分化的结节与农杆菌共培养,该农杆菌携带含有#bate#-葡萄糖醛酸苷酶和nptII表达盒的二元载体。选择转化的细胞,并在卡那霉素存在下使其生长成结节。从选定的结节再生了转基因浮萍叶。我们证明转基因浮萍可以在3个月内再生。农杆菌介导的结节转化后。此外,我们开发了一种在6周内转化小L. 8627的方法。这些转化方案将促进浮萍的基因工程,浮萍是生物修复和大规模生产生物质和重组蛋白的理想植物。

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