文献类型： 外文期刊
作者： Soleimani-Delfan, Abbas 1 ; Bouzari, Majid 1 ; Wang, Ran 2 ;
作者机构： 1.Univ Isfahan, Fac Biol Sci & Technol, Dept Cell & Mol Biol & Microbiol, HezarJereeb St, Esfahan 8174673441, Iran
2.Jiangsu Acad Agr Sci, Inst Food Safety & Nutr, Nanjing, Jiangsu, Peoples R China
关键词： Bacteriophage precipitation; DNA extraction; Rapid method; Next-generation sequencing
期刊名称：JOURNAL OF VIROLOGICAL METHODS （ 影响因子：2.014； 五年影响因子：2.001 ）
ISSN： 0166-0934
年卷期： 2021 年 293 卷
页码：
收录情况： SCI
摘要： The bacteriophage (phage) DNA extraction methods for genomics analysis is a critical and time-consuming process. Hence, a rapid and cost-effective method for DNA extraction of phages is favorable for phage biologists. In the present study, a cost-effective, simple and rapid procedure for phage genome extraction in less than 10 min is introduced. Highly concentrated phage lysates were prepared using acetone precipitation followed by extraction using various methods such as commercial kits, TES lysis buffer, potassium iodide, and sodium iodide. The quality of the extracted DNA was analyzed by agarose gel electrophoresis and UV absorbance of DNA at 260 and 280 nm. Finally, the extracted DNA was subjected to restriction digestion and next-generation sequencing to approve the efficiency of the method. Based on the time, cost, and quality of obtained DNA, the acetone precipitation of phages and extraction by potassium iodide or sodium iodide method was determined to be the best method for phage DNA extraction tested in this study. Moreover, the extracted genomic DNA using this method is suitable for phage genomic analysis such as restriction enzyme studies, preparation of DNA library, and also next-generation sequencing.
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