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Engineering the Chloroplast Genome of Oleaginous Marine Microalga Nannochloropsis oceanica

机译:改造油生海洋微藻的叶绿体基因组 Nannochloropsis oceanica

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Plastid engineering offers an important tool to fill the gap between the technical and the enormous potential of microalgal photosynthetic cell factory. However, to date, few reports on plastid engineering in industrial microalgae have been documented. This is largely due to the small cell sizes and complex cell-wall structures which make these species intractable to current plastid transformation methods (i.e., biolistic transformation and polyethylene glycol-mediated transformation). Here, employing the industrial oleaginous microalga Nannochloropsis oceanica as a model, an electroporation-mediated chloroplast transformation approach was established. Fluorescent microscopy and laser confocal scanning microscopy confirmed the expression of the green fluorescence protein, driven by the endogenous plastid promoter and terminator. Zeocin-resistance selection led to an acquisition of homoplasmic strains of which a stable and site-specific recombination within the chloroplast genome was revealed by sequencing and DNA gel blotting. This demonstration of electroporation-mediated chloroplast transformation opens many doors for plastid genome editing in industrial microalgae, particularly species of which the chloroplasts are recalcitrant to chemical and microparticle bombardment transformation.
机译:塑料质工程为填补微藻光合细胞工厂的技术潜力和巨大潜力之间的空白提供了重要工具。然而,迄今为止,关于工业微藻类中的质体工程的报道很少。这主要是由于小细胞大小和复杂的细胞壁结构,使这些物种难以被当前的质体转化方法(即,生物弹转化和聚乙二醇介导的转化)所吸引。在此,以工业产油微藻Nannochloropsis oceanica为模型,建立了电穿孔介导的叶绿体转化方法。荧光显微镜和激光共聚焦扫描显微镜证实了绿色荧光蛋白的表达,该蛋白由内源性质体启动子和终止子驱动。 Zeocin抗性选择导致获得同质菌株,通过测序和DNA凝胶印迹揭示了其同质菌株在叶绿体基因组内的稳定和位点特异性重组。电穿孔介导的叶绿体转化的这一展示为工业微藻,特别是其中叶绿体对化学和微粒轰击转化不起作用的物种的质体基因组编辑打开了许多大门。

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