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Development of a new extraction method based on high-intensity ultra-sonication to study RNA regulation of the filamentous cyanobacteria Planktothrix

机译:基于高强度超声波的新型提取方法的研究,以研究丝状蓝细菌浮游藻的RNA调控

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摘要

Efficient RNA extraction methods are needed to study transcript regulation. Such methods must lyse the cell without degrading the genetic material. For cyanobacteria this can be particularly challenging because of the presence of the cyanobacteria cell envelope. The great breath of cyanobacterial shape and size (unicellular, colonial, or filamentous multicellular) created a variety of cell lysis methods. However, there is still a lack of reliable techniques for nucleic acid extraction for several types of cyanobacteria.Here we designed and tested 15 extraction methods using physical, thermic or chemical stress on the filamentous cyanobacteria Planktothrix agardhii. Techniques based on the use of beads, sonication, and heat shock appeared to be too soft to break the Planktothrix agardhii cell envelope, whereas techniques based on the use of detergents degraded the cell envelope but also the RNA. Two protocols allowed to successfully obtain good-quality RNA. The first protocol consisted to manually crush the frozen cell pellet with a pestle and the second was based on the use of high-intensity ultra-sonication. When comparing these two, the high-intensity ultra-sonication protocol was less laborious, faster and allowed to extract 3.5 times more RNA compared to the liquid nitrogen pestle protocol. The high-intensity ultra-sonication protocol was then tested on five Planktothrix strains, this protocol allowed to obtain >8.5 μg of RNA for approximatively 3.5 × 108 cells. The extracted RNA were characterized by 260/280 and 260/230 ratio > to 2, indicating that the samples were devoid of contaminant, and RNA Quality Number > to 7, meaning that the integrity of RNA was preserved with this extraction method. In conclusion, the method we developed based on high-intensity ultra-sonication proved its efficacy in the extraction of Planktothrix RNA and could be helpful for other types of samples.
机译:需要有效的RNA提取方法来研究转录物调控。这些方法必须裂解细胞而不降解遗传物质。对于蓝细菌,由于蓝细菌细胞包膜的存在,这可能特别具有挑战性。蓝细菌形状和大小(单细胞,结肠或丝状多细胞)的巨大呼吸创造了多种细胞裂解方法。然而,仍然缺乏可靠的技术来提取几种类型的蓝细菌的核酸。在此,我们设计并测试了15种利用物理,热或化学应力对丝状蓝细菌浮游细菌琼脂(Planktothrix agardhii)进行提取的方法。基于使用磁珠,超声处理和热休克的技术似乎太软而无法破坏浮游植物琼脂糖细胞包膜,而基于清洁剂的技术则降解细胞包膜和RNA。有两种方案可以成功获得高质量的RNA。第一个方案是用杵手动压碎冷冻的细胞沉淀,第二个方案是基于高强度超声的使用。比较这两种方法时,高强度超声处理方案省时,省力,速度快,并且提取的RNA比液氮杵方案高3.5倍。然后在五种Planktothrix菌株上测试了高强度超声处理方案,该方案可为大约3.5×10 8 细胞获得> 8.5μgRNA。提取的RNA的特征是260/280和260/230的比率>等于2,表明样品中没有污染物,RNA质量数大于等于7,这意味着该提取方法可保持RNA的完整性。总之,我们基于高强度超声处理开发的方法证明了其在提取Planktothrix RNA中的功效,并可能对其他类型的样品有所帮助。

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