清脆的
环介导等温扩增
食物腐败
计算生物学
DNA
生物
聚合酶链反应
细菌
基因组
食品科学
化学
遗传学
基因
作者
Qingzhou Meng,Hongmei Yang,Guiquan Zhang,Wenjun Sun,Peixiang Ma,Xinyi Liu,Lu Dang,Guanglei Li,Xingxu Huang,Xinjie Wang,Jianghuai Liu,Qibin Leng
标识
DOI:10.1016/j.ifset.2021.102854
摘要
Beer spoilage bacteria present severe challenges for the beer fermentation industry. Here, we establish a rapid, specific and highly portable CRISPR/Cas12a-based key beer spoilage bacterial scanning method, dubbed CRISPR-Beer Scan. With the variable 16S rDNA segments of these major spoilage microbe species serving as targets, highly efficient and specific crRNAs were determined. By coupling with recombinase polymerase isothermal amplification, CRISPR-Beer Scan could detect as low as 10 copies of DNA targets. Indeed, trace amounts of target genome DNAs can be accurately identified within a mixture of genome DNAs conditioned in beer. Moreover, the extracted genome DNA samples can be conveniently distinguished through the visual fluorescent signals excited by blue light in 45 min with CRISPR-Beer Scan Method. Taken together, the CRISPR-Beer Scan represents a widely applicable microbe-monitoring platform for not only breweries, but also other industries.
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