Hudspeth M E, Shumard D S, Tatti K M, Grossman L I
Biochim Biophys Acta. 1980 Dec 11;610(2):221-8. doi: 10.1016/0005-2787(80)90003-9.
A procedure is presented for the rapid isolation of mitochondrial DNA (mtDNA) in high yield from Saccharomyces cerevisiae. Yeast cells, which may be grown to late stationary phase, are broken by a combination of enzymatic and mechanical means; mtDNA is then isolated from a crude mitochondrial lysate by a single cycle of bisbenzimide-CsCl buoyant density centrifugation. mtDNA so isolated is at least 99.5% pure, and has a mean duplex molecular weight of 24.5 . 10(6). In addition to mtDNA and bulk nuclear DNA, several other yeast nucleic acid species, identified as ribosomal DNA and a mixture of duplex RNAs, form discrete bands in these gradients.
本文介绍了一种从酿酒酵母中快速高产分离线粒体DNA(mtDNA)的方法。可培养至稳定期末期的酵母细胞通过酶解和机械方法相结合进行破碎;然后通过单轮双苯甲酰亚胺-CsCl浮力密度离心从粗制线粒体裂解物中分离mtDNA。如此分离得到的mtDNA纯度至少为99.5%,平均双链分子量为24.5×10⁶。除了mtDNA和大量核DNA外,其他几种酵母核酸种类,被鉴定为核糖体DNA和双链RNA混合物,在这些梯度中形成离散条带。