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Rapid Extraction of Genomic DNA from Medically Important Yeasts and Filamentous Fungi by High-Speed Cell Disruption

机译:通过高速细胞分裂从医学上重要的酵母和丝状真菌中快速提取基因组DNA

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摘要

Current methods of DNA extraction from different fungal pathogens are often time-consuming and require the use of toxic chemicals. DNA isolation from some fungal organisms is difficult due to cell walls or capsules that are not readily susceptible to lysis. We therefore investigated a new and rapid DNA isolation method using high-speed cell disruption (HSCD) incorporating chaotropic reagents and lysing matrices in comparison to standard phenol-chloroform (PC) extraction protocols for isolation of DNA from three medically important yeasts (Candida albicans, Cryptococcus neoformans, and Trichosporon beigelii) and two filamentous fungi (Aspergillus fumigatus and Fusarium solani). Additional extractions by HSCD were performed on Saccharomyces cerevisiae, Pseudallescheria boydii, and Rhizopus arrhizus. Two different inocula (108 and 107 CFU) were compared for optimization of obtained yields. The entire extraction procedure was performed on as many as 12 samples within 1 h compared to 6 h for PC extraction. In comparison to the PC procedure, HSCD DNA extraction demonstrated significantly greater yields for 108 CFU of C. albicans, T. beigelii, A. fumigatus, and F. solani (P ≤ 0.005), 107 CFU of C. neoformans (P ≤ 0.05), and 107 CFU of A. fumigatus (P ≤ 0.01). Yields were within the same range for 108 CFU of C. neoformans and 107 CFU of C. albicans for both HSCD extraction and PC extraction. For 107 CFU of T. beigelii, PC extraction resulted in a greater yield than did HSCD (P ≤ 0.05). Yields obtained from 108 and 107 CFU were significantly greater for filamentous fungi than for yeasts by the HSCD extraction procedure (P < 0.0001). By the PC extraction procedure, differences were not significant. For all eight organisms, the rapid extraction procedure resulted in good yield, integrity, and quality of DNA as demonstrated by restriction fragment length polymorphism, PCR, and random amplified polymorphic DNA. We conclude that mechanical disruption of fungal cells by HSCD is a safe, rapid, and efficient procedure for extracting genomic DNA from medically important yeasts and especially from filamentous fungi.
机译:从不同的真菌病原体中提取DNA的当前方法通常很耗时,并且需要使用有毒的化学物质。由于细胞壁或胶囊不易裂解,因此很难从某些真菌生物体中分离DNA。因此,我们与标准酚-氯仿(PC)提取方案相比,采用了离液剂和裂解基质的高速细胞破坏(HSCD)技术来分离新的快速DNA分离方法,该方法可从三种重要的医学酵母中分离出DNA(白色念珠菌,新型隐球菌和米氏Trichosporon)和两种丝状真菌(烟曲霉和茄形镰刀菌)。通过HSCD对啤酒酵母,波氏假单胞菌和阿扎根霉进行了其他提取。比较了两种不同的接种物(10 8 和10 7 CFU)以优化获得的产量。整个提取过程在1小时内对多达12个样品进行,而PC提取则为6小时。与PC程序相比,HSCD DNA提取显示白色念珠菌,米色锥虫,烟曲霉和茄形镰刀菌10 8 CFU的产量明显更高(P≤0.005),10 <新型梭菌的sup> 7 CFU(P≤0.05)和烟曲霉的10 7 CFU( P ≤0.01)。 10 8 CFU C的产率在相同范围内。 C的10 7 CFU。白色念珠菌可用于HSCD提取和PC提取。对于 T的10 7 CFU。 Beizelli ,PC提取的产量高于HSCD( P ≤0.05)。通过HSCD提取程序,丝状真菌从10 8 和10 7 CFU获得的产量显着高于酵母( P <0.0001)。通过PC提取程序,差异不显着。通过限制性片段长度多态性,PCR和随机扩增的多态性DNA证明,对于所有八个生物而言,快速提取程序均能获得良好的DNA产量,完整性和质量。我们得出结论,HSCD对真菌细胞的机械破坏是一种从医学上重要的酵母菌,尤其是丝状真菌中提取基因组DNA的安全,快速,有效的程序。

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