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首页> 外文期刊>BMC Microbiology >Comparison of the efficiency of different cell lysis methods and different commercial methods for RNA extraction from Candida albicans stored in RNAlater
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Comparison of the efficiency of different cell lysis methods and different commercial methods for RNA extraction from Candida albicans stored in RNAlater

机译:不同细胞裂解方法效率的比较及不同商业方法的RNA innalater annalater的念珠菌提取

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BackgroundObtaining sufficient RNA yield and quality for comprehensive transcriptomic studies is cumbersome for clinical samples in which RNA from the pathogen is present in low numbers relative to the nucleic acids from the host, especially for pathogens, such as yeasts, with a solid cell wall. Therefore, yeast cell lysis including cell wall disruption constitutes an essential first step to maximize RNA yield. Moreover, during the last years, different methods for RNA extraction from yeasts have been developed, ranging from classic hot phenol methods to commercially available specific kits. They offer different RNA yield and quality, also depending on the original storage medium, such as RNAlater.ResultsWe observed that, for C. albicans cells stored in Tryptic Soy Broth with 15% glycerol, 10?min of bead beating in a horizontal position in RiboPure Lysis Buffer provided complete cell lysis. Cell lysis efficiency was decreased to 73.5% when cells were stored in RNAlater. In addition, the RiboPure Yeast Kit (Ambion) offered the highest RNA yield in comparison with the automated platform NucliSENS easyMAG total nucleic extraction (bioMérieux) and the RNeasy Mini Kit (Qiagen) according to NanoDrop and Fragment Analyzer. Moreover, we showed that, in spite of the decrease of cell lysis efficiency after RNAlater storage, as compared to storage in TSB?+?15% glycerol, RNAlater increased RNA yield during RNA extraction with both RiboPure Yeast Kit and easyMAG, as confirmed by Fragment Analyzer analysis and by RT-qPCR of the RNA from the Internal Transcribed Spacer 2.ConclusionsIn our hands, the most efficient cell lysis and highest RNA yield from C. albicans cells stored in RNAlater was obtained by horizontal bead beating in RiboPure Lysis Buffer followed by RNA extraction with the RiboPure Yeast Kit.
机译:背景技术对于综合转录组研究的足够的RNA产率和质量对于临床样本有麻烦,其中来自病原体的RNA相对于来自宿主的核酸存在于低位,特别是对于具有固体细胞壁的病原体,例如酵母。因此,包括细胞壁破坏的酵母细胞裂解构成最大化RNA产率的主要第一步。此外,在过去几年中,已经开发出不同的RNA提取方法,从经典的热酚方法到市售的特定试剂盒。它们提供不同的RNA产量和质量,也取决于原始的存储介质,如RNALATER.Resultwe观察到,对于含有15%甘油的胰蛋白酶,对于胰蛋白酶粒细胞,10?min在水平位置处跳动。核平裂解缓冲液提供完全的细胞裂解。当细胞储存在大萜酯中时,细胞裂解效率降至73.5%。此外,根据纳米二氢纤维和片段分析仪,核素酵母试剂盒(AMACION)提供了最高的RNA产量,与自动化平台核素核酸easymag总核萃取(BioFérieux)和rneasy迷你套件(qiagen)进行了比较。此外,我们表明,尽管在RNALATER储存后细胞裂解效率降低,与TSB?+ + +β1.15%甘油中的储存相比,RNATATER在RNA提取期间用核武器酵母试剂盒和Easymag增加了RNA产量,如片段分析仪分析和通过内部转录的间隔物的RNA的RT-QPCR。通过核化裂解缓冲液中的水平珠跳动获得储存在RNALATER中的C. albicans细胞的最有效的细胞裂解和最高的RNA产量。通过RNA提取核桃酵母试剂盒。

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