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A comparison of methods used to extract bacterial DNA from raw milk and raw milk cheese.

机译:从原料奶和原料奶奶酪中提取细菌DNA的方法比较。

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Aims: In this study, we compare seven different methods which have been designed or modified to extract total DNA from raw milk and raw milk cheese with a view to its subsequent use for the PCR of bacterial DNA. Materials and Results. Seven extraction methods were employed to extract total DNA from these foods, and their relative success with respect to the yield and purity of the DNA isolated, and its quality as a template for downstream PCR, was compared. Although all of the methods were successful with respect to the extraction of DNA naturally present in cheese, they varied in their relative ability to extract DNA from milk. However, when milk was spiked with a representative Gram-positive (Listeria monocytogenes EGDe) or Gram-negative (Salmonella enterica serovar Typhimurium LT2) bacterium, it was established that all methods successfully extracted DNA which was suitable for subsequent detection by PCR. Conclusions. Of the seven approaches, the PowerFoodTM Microbial DNA Isolation kit (MoBio Laboratories Inc.) was found to most consistently extract highly concentrated and pure DNA with a view to its subsequent use for PCR-based amplification and also facilitated accurate detection by real-time quantitative PCR. Significance and Impact of the Study: Accurately assessing the bacterial composition of milk and cheese is of great importance to the dairy industry. Increasingly, DNA-based technologies are being employed to provide an accurate assessment of this microbiota. However, these approaches are dependent on our ability to extract DNA of sufficient yield and purity. This study compares a number of different options and highlights the relative success of these approaches. We also highlight the success of one method to extract DNA from different microbial populations as well as DNA which is suitable for real-time PCR of microbes of interest, a challenge often encountered by the food industry. copyright 2012 The Authors. Journal of Applied Microbiology copyright 2012 The Society for Applied Microbiology.
机译:目的:在这项研究中,我们比较了设计或修改的七种不同方法,这些方法已被设计或改进以从生乳和生乳干酪中提取总DNA,以期将其随后用于细菌DNA的PCR。材料和结果。使用了七种提取方法从这些食物中提取总DNA,并比较了它们相对于分离出的DNA的产量和纯度以及作为下游PCR模板的质量的相对成功。尽管所有方法均能成功提取奶酪中天然存在的DNA,但它们从牛奶中提取DNA的相对能力却有所不同。但是,在牛奶中加入代表性的革兰氏阳性菌(单核细胞增生李斯特菌EGDe)或革兰氏阴性菌(肠沙门氏菌血清鼠伤寒沙门氏菌LT2)细菌时,可以确定所有方法成功提取了适合后续PCR检测的DNA。结论。在这七种方法中,发现PowerFood TM 微生物DNA分离试剂盒(MoBio Laboratories Inc.)能够最稳定地提取高浓度和纯净的DNA,以用于随后的基于PCR的扩增以及实时定量PCR有助于准确检测。研究的意义和影响:准确评估牛奶和奶酪的细菌组成对乳业至关重要。越来越多地使用基于DNA的技术来提供对该微生物群的准确评估。但是,这些方法取决于我们提取足够产量和纯度的DNA的能力。这项研究比较了许多不同的选择,并强调了这些方法的相对成功。我们还强调了一种从不同微生物种群中提取DNA的方法的成功以及适用于目标微生物实时PCR的DNA的成功,这是食品行业经常遇到的挑战。版权2012作者。应用微生物学期刊版权所有2012应用微生物学会。

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