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Magnetic Ionic Liquids as Solvents for RNA Extraction and Preservation

机译:磁离子液体作为RNA提取和保存的溶剂

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Ribonucleic acid (RNA) is particularly sensitive to enzymatic degradation by endonucleases prior to sample analysis. In-field preservation has been a challenge for RNA sample preparation. Very recently, hydrophobic magnetic ionic liquids (MIL) have shown significant promise in the area of RNA extraction. In this study, MILs were synthesized and employed as solvents for the extraction and preservation of RNA in aqueous solution. RNA samples obtained from yeast cells were extracted and preserved by the trihexyl(tetradecyl) phosphonium tris(hexafluoroacetylaceto)cobaltate(II) ([P_(66614)~(+)][Co(hfacac)_(3)~(–)]) and trihexyl(tetradecyl) phosphonium tris(phenyltrifluoroacetylaceto)cobaltate(II) ([P_(66614)~(+)][Co(Phtfacac)_(3)~(–)]) MIL with a dispersion of the supporting media, polypropylene glycol, at room temperature for up to a 7 and 15 day period, respectively. High-quality RNA treated with ribonuclease A (RNase A) was recovered from the tetra(1-octylimidazole)cobaltate(II) di(l-glutamate) ([Co(OIM)_(4)~(2+)][Glu~(–)]_(2)) and tetra(1-octylimidazole)cobaltate(II) di(l-aspartate) ([Co(OIM)_(4)~(2+)][Asp~(–)]_(2)) MILs after a 24 h period at room temperature. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) and agarose gel electrophoresis were used to determine the effect of RNA preservation. Furthermore, the preservation mechanism was investigated by exploring the partitioning of RNase A into the MIL using high-performance liquid chromatography.
机译:在样品分析之前,核糖核酸(RNA)对内切核酸酶的酶促降解特别敏感。现场保存是RNA样品制备的挑战。最近,疏水性磁离子液体(MIL)在RNA提取区域中显示出显着的希望。在该研究中,合成米尔并用作水溶液中RNA的提取和保存的溶剂。从酵母细胞中获得的RNA样品被三己烯(四烷基)鏻三(六氟乙酰丙酮)钴酸钴(II)([P_(66614)〜(+)] [CO(HFACAC)_(3)〜( - )]。 )和三己基(四烷基)鏻三(苯三氟乙酰丙酮)钴酸盐(II)([P_(66614)〜(+)] [CO(pHTFACAC)_(3)〜( - )])米尔,具有支撑介质的分散,聚丙二醇,在室温下,分别为高达7和15天的时间。用核糖核酸酶(RNasea)处理的高质量RNA(RNasea)从四(1-辛基咪唑)钴酸盐(II)二(L-谷氨酸)([CO(OIM)_(4)〜(2 +)] [glu 〜( - )] _(2))和四(1-辛基咪唑)钴酸盐(II)二(L-天冬氨酸)([CO(OIM)_(4)〜(2 +)] [ASP〜( - )] _(2))室温下24小时后米尔。定量逆转录聚合酶链反应(QRT-PCR)和琼脂糖凝胶电泳用于确定RNA保存的作用。此外,通过使用高效液相色谱法探讨RNaseA进入MIL的分配来研究保存机制。

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