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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:基于高强度超声处理的新提取方法研究丝状纤维素薄膜薄膜螺纹的RNA调节

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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 × 10 8 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分子调节。这些方法必须粘合细胞而不会降解遗传物质。对于蓝藻,这可能是由于蓝细菌细胞包膜的存在而特别具有挑战性。蓝细菌形状和大小(单细胞,殖民或丝状多细胞)的大量呼吸产生了各种细胞裂解方法。然而,仍然缺乏可靠的核酸萃取用于若干类型的蓝细菌的技术。在这里,我们在丝状蓝色细胞薄膜刺激神李基上设计和测试了15种提取方法。基于使用珠子,超声处理和热冲击的技术似乎太软而无法破坏浮动桥agardhii细胞包络,而基于使用洗涤剂的技术降解了细胞包络,但也是RNA。允许两种协议成功获得高质量的RNA。第一种方案包括用杵手动压碎冷冻细胞颗粒,第二种方案基于使用高强度超声波处理。当比较这两个时,高强度超超声协议比液氮杵协议相比,更快,更快,更快,更快地提取3.5倍的RNA。然后在五个Planktothrix菌株上测试高强度超声超声协议,该方案允许获得&8.5μg的RNA,用于近似3.5×10 8细胞。提取的RNA以260/280和260/230的比例和gt表征。对于2,表明样品缺乏污染物,以及RNA质量编号&对于7,意味着通过这种提取方法保留了RNA的完整性。总之,我们基于高强度超声波开发的方法证明了其在综合桥RNA的提取中的功效,并且可能有助于其他类型的样品。

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