Amin-ul Mannan M, Sharma Sushma, Ganesan K
Institute of Microbial Technology (Council of Scientific and Industrial Research), Sector 39-A, Chandigarh 160036, India.
Anal Biochem. 2009 Jun 1;389(1):77-9. doi: 10.1016/j.ab.2009.03.014. Epub 2009 Mar 18.
Conventional methods of RNA isolation are not suitable for yeast cells from stationary phase and fermentation broth. Methods specially reported for such cells are cumbersome and do not lend themselves for use with large number of samples. Here we report a facile method of RNA isolation from such recalcitrant yeast cells. The entire procedure is performed in microcentrifuge tubes and, thus, is ideal for faster processing of multiple samples. The method consistently gives high quality and quantity of RNA, which was found to be suitable for downstream applications such as quantitative real-time polymerase chain reaction. Besides Saccharomyces cerevisiae, the method was found to work equally well with other yeast species; thus, it is likely to have wider applicability.
传统的RNA提取方法不适用于来自稳定期的酵母细胞和发酵液。专门报道的针对此类细胞的方法繁琐,不适用于大量样本。在此,我们报道一种从这种难处理的酵母细胞中提取RNA的简便方法。整个过程在微量离心管中进行,因此非常适合快速处理多个样本。该方法始终能获得高质量和高产量的RNA,发现其适用于下游应用,如定量实时聚合酶链反应。除了酿酒酵母,该方法对其他酵母物种同样有效;因此,它可能具有更广泛的适用性。