DNA提取
色谱法
溶解
检出限
洗脱
多路复用
固相萃取
裂解缓冲液
聚合酶链反应
萃取(化学)
化学
生物
生物化学
生物信息学
基因
作者
Xuanhua Du,Man Lu,Hangzhen Lan,Zhendong Cai,Daodong Pan,Yichun Wu
标识
DOI:10.1016/j.jfca.2024.105977
摘要
A rapid, portable, simple, low-cost, and high-throughput DNA isolation method was developed for the quantitative identification of meat adulteration based on mesoporous UiO-66 coated solid phase microextraction (SPME) devices. The high-throughput DNA extraction system consists of 96 UiO-66 SPME devices and a polyformaldehyde plate, which can extract DNA from 96 livestock and poultry meat samples simultaneously. At the same time, several parameters of the high throughput DNA isolation method were optimized, including lysis buffer volume, elution buffer volume, lysis time and elution time, etc. Compared with the single DNA isolation device, the 96-SPME high-throughput extraction system maintains the original good universality, reproducibility, chemical stability, and reusability. On this basis, it obtained higher DNA concentration (80±34 ng μL-1), satisfactory DNA purity (A260/A280=2.4) and shorter extraction time (less than 7.2 seconds per sample), which are much more convenient and efficient than the conventional kit method and the single SPME DNA isolation method. In addition, the conventional multiplex polymerase chain reaction and real-time polymerase chain reaction techniques were used for the qualitative and quantitative detection of meat adulteration. The DNA obtained from this extraction method is highly reproducible and sensitive for the identification of duck ingredients in beef, with a detection range of 1-100% and a minimum detection limit of 1% (w/w).
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