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Designer diatom episomes delivered by bacterial conjugation

机译:通过细菌结合递送设计师硅藻附加体

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摘要

Eukaryotic microalgae hold great promise for the bioproduction of fuels and higher value chemicals. However, compared with model genetic organisms such as Escherichia coli and Saccharomyces cerevisiae, characterization of the complex biology and biochemistry of algae and strain improvement has been hampered by the inefficient genetic tools. To date, many algal species are transformable only via particle bombardment, and the introduced DNA is integrated randomly into the nuclear genome. Here we describe the first nuclear episomal vector for diatoms and a plasmid delivery method via conjugation from Escherichia coli to the diatoms Phaeodactylum tricornutum and Thalassiosira pseudonana. We identify a yeast-derived sequence that enables stable episome replication in these diatoms even in the absence of antibiotic selection and show that episomes are maintained as closed circles at copy number equivalent to native chromosomes. This highly efficient genetic system facilitates high-throughput functional characterization of algal genes and accelerates molecular phytoplankton research.
机译:真核微藻有望用于生物生产燃料和更高价值的化学物质。但是,与模型遗传生物(如大肠杆菌和酿酒酵母)相比,藻类的复杂生物学和生化特性以及菌株改良的表征受到效率低下的遗传工具的阻碍。迄今为止,许多藻类物种只能通过粒子轰击才能转化,并且所引入的DNA随机整合到核基因组中。在这里,我们描述了第一个用于硅藻的核游离载体,以及通过从大肠杆菌到硅藻Phaeodactylum tricornutum和Thalassiosira pseudonana缀合的质粒递送方法。我们确定了酵母来源的序列,即使在没有选择抗生素的情况下,也能在这些硅藻中进行稳定的附加体复制,并显示附加体以闭合环的形式维持在与天然染色体相等的拷贝数上。这种高效的遗传系统有助于藻类基因的高通量功能表征,并加速了分子浮游植物的研究。

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