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首页> 外文期刊>International Journal of Food Microbiology >Evaluation of DNA extraction methods for Bacillus anthracis spores spiked to food and feed matrices at biosafety level 3 conditions.
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Evaluation of DNA extraction methods for Bacillus anthracis spores spiked to food and feed matrices at biosafety level 3 conditions.

机译:在生物安全等级为3的条件下,掺入食品和饲料基质的炭疽杆菌孢子的DNA提取方法的评估。

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The DNA extraction efficiency from milk, whey, soy, corn gluten meal, wheat powders and heat-treated corn grain that were spiked with Bacillus anthracis and Bacillus thuringiensis spores was determined. Two steps were critical: lysis of the spores and binding of the free DNA to the DNA binding magnetic beads in the presence of the interfering powders. For the guanidine-thiocyanate based Nuclisens lysis buffer from Biomerieux we found that between 15 and 30% of the spores survived the lysis step. As most lysis buffers in DNA/RNA extraction kits are guanidine based it is likely that other lysis buffers will show a similar partial lysis of the Bacillus spores. Our results show that soybean flour and wheat flour inhibited the DNA extraction process strongest, leading to unreliable DNA extractions when using too much of the matrix. For corn gluten meal, heat-treated corn grain and milk powders, DNA extraction efficiencies in the presence of 100 mg and 10 mg of powder resulted in 70%-95% reduced DNA recoveries. The inhibition was, however, reliable and intermediate compared to the inhibition by soy and wheat. Whey powder had the lowest inhibitory effect on DNA-extraction efficiency and recoveries of 70-100% could be reached when using 10 mg of powder. The results show that reducing the amount of matrix leads to better DNA-extraction efficiencies, particularly for strongly inhibiting powders such as soy and wheat. Based on these results, a standard protocol to directly isolate DNA from micro-organisms present in complex matrixes such as food and feed powders was designed.
机译:确定了从掺有炭疽杆菌和苏云金芽孢杆菌孢子的牛奶,乳清,大豆,玉米面筋粉,小麦粉和热处理的玉米粒中提取DNA的效率。至关重要的两个步骤是:在存在干扰粉的情况下,裂解孢子和将游离DNA结合到与DNA结合的磁珠上。对于来自Biomerieux的基于胍硫氰酸盐的Nuclisens裂解缓冲液,我们发现15%至30%的孢子在裂解步骤中存活了下来。由于DNA / RNA提取试剂盒中的大多数裂解缓冲液均基于胍,因此其他裂解缓冲液可能也会显示出芽孢杆菌孢子的类似部分裂解。我们的结果表明,大豆粉和小麦粉对DNA提取过程的抑制作用最强,当使用过多的基质时会导致DNA提取不可靠。对于玉米蛋白粉,热处理的玉米谷物和奶粉,在100 mg和10 mg粉末存在下的DNA提取效率导致DNA回收率降低70%-95%。然而,与大豆和小麦的抑制作用相比,这种抑制作用是可靠且中间的。乳清粉对DNA提取效率的抑制作用最低,当使用10 mg乳清粉时,回收率可达到70-100%。结果表明,减少基质的量会导致更好的DNA提取效率,特别是对于强抑制性粉末(如大豆和小麦)而言。基于这些结果,设计了一种标准协议,可以直接从复杂基质(例如食物和饲料粉)中存在的微生物中分离DNA。

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