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Rapid and Effective DNA Extraction Method with Bead Grinding for a Large Amount of Fungal DNA

机译:珠粒研磨快速有效地提取大量真菌DNA的DNA方法

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摘要

To identify a rapid method for extracting a large amount of DNA from fungi associated with food hygiene, extraction methods were compared using fungal pellets formed rapidly in liquid media. Combinations of physical and chemical methods or commercial kits were evaluated with 3 species of yeast, 10 species of ascomycetous molds, and 4 species of zygomycetous molds. Bead grinding was the physical method, followed by chemical methods involving sodium dodecyl sulfate (SDS), cetyl trimethyl ammonium bromide (CTAB), and benzyl chloride and two commercial kits. Quantity was calculated by UV absorbance at 260 nm, quality was determined by the ratio of UV absorbance at 260 and 280 nm, and gene amplifications and electrophoresis profiles of whole genomes were analyzed. Bead grinding with the SDS method was the most effective for DNA extraction for yeasts and ascomycetous molds, and bead grinding with the CTAB method was most effective with zygomycetous molds. For both groups of molds, bead grinding with the CTAB method was the best approach for DNA extraction. Because this combination also is relatively effective for yeasts, it can be used to extract a large amount of DNA from a wide range of fungi. The DNA extraction methods are useful for developing gene indexes to identify fungi with molecular techniques, such as DNA fingerprinting.
机译:为了确定从与食品卫生有关的真菌中提取大量DNA的快速方法,使用在液体培养基中快速形成的真菌沉淀物对提取方法进行了比较。评估了物理和化学方法或商业试剂盒的组合,其中包括3种酵母,10种子囊霉菌和4种合子霉菌。珠磨是物理方法,然后是化学方法,包括十二烷基硫酸钠(SDS),十六烷基三甲基溴化铵(CTAB)和苄基氯以及两种商业试剂盒。通过260nm处的UV吸光度计算数量,通过260nm和280nm处的UV吸光度之比确定质量,并分析整个基因组的基因扩增和电泳图谱。用SDS方法进行的珠磨对于酵母和子囊霉菌的DNA提取最有效,而使用CTAB方法的磨珠在合子菌霉菌中最为有效。对于两组模具,使用CTAB方法进行珠磨是提取DNA的最佳方法。由于这种组合对酵母菌也相对有效,因此可用于从多种真菌中提取大量DNA。 DNA提取方法可用于开发利用分子技术(例如DNA指纹图谱)鉴定真菌的基因索引。

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  • 来源
    《Journal of food protection》 |2010年第6期|P.1077-1084|共8页
  • 作者单位

    Division of Microbiology, National Institute of Health Sciences, Kamiyoga 1-18-1, Setagaya-ku, Tokyo 158-8501, Japan;

    rnVeterinary Medical Science, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo 113-8657, Japan;

    rnFood Research Laboratories, Mitsui Norin Co., Ltd., Miyabara 223-1, Fujieda-shi, Shizuoka 426-0133, Japan;

    rnVeterinary Medical Science, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo 113-8657, Japan;

    rnDivision of Microbiology, National Institute of Health Sciences, Kamiyoga 1-18-1, Setagaya-ku, Tokyo 158-8501, Japan;

    rnDivision of Microbiology, National Institute of Health Sciences, Kamiyoga 1-18-1, Setagaya-ku, Tokyo 158-8501, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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