Møller Ian Max, Rasmusson Allan G
Department of Molecular Biology and Genetics, Aarhus University, Slagelse, Denmark.
Department of Biology, Lund University, Lund, Sweden.
Methods Mol Biol. 2022;2363:39-50. doi: 10.1007/978-1-0716-1653-6_4.
The isolation of mitochondria from potato tubers (Solanum tuberosum L.) is described, but the methodology can easily be adapted to other storage tissues. After homogenization of the tissue, filtration and differential centrifugation, the key step is a Percoll density gradient centrifugation. The Percoll gradient contains two parts: a bottom part containing Percoll in 0.3 M sucrose, and a slightly less dense top part containing Percoll in 0.3 M mannitol. After centrifugation, a density gradient is formed that is almost linear in the central part, and this is where the band containing the purified intact mitochondria is formed. This method makes it possible to process large amounts of plant material (2-6 kg) and saves at least 1.5 h on the preparation time compared to methods where two consecutive purification methods are used. Nonetheless, it yields large amounts of mitochondria (50-125 mg protein) of very high purity, intactness and functionality.
本文描述了从马铃薯块茎(Solanum tuberosum L.)中分离线粒体的方法,但该方法可轻松适用于其他贮藏组织。组织匀浆、过滤和差速离心后,关键步骤是进行Percoll密度梯度离心。Percoll梯度包含两部分:底部部分含有0.3 M蔗糖中的Percoll,顶部部分密度稍低,含有0.3 M甘露醇中的Percoll。离心后,形成一个在中心部分几乎呈线性的密度梯度,含有纯化完整线粒体的条带就在此处形成。与使用两种连续纯化方法的方法相比,该方法能够处理大量植物材料(2 - 6 kg),并且在制备时间上至少节省1.5小时。尽管如此,它能产生大量纯度、完整性和功能性都非常高的线粒体(50 - 125 mg蛋白质)。