CRISPR/Cas-based Nucleic Acid Detection and Its Application in Rapid Detection for Food Safety

被引:0
|
作者
Zhai B. [2 ]
Cheng N. [3 ]
Wang H. [2 ]
Xu Y. [1 ]
机构
[1] Faculty of Environment and Life, Beijing University of Technology, Beijing
[2] Henan Railway Food Safety Management Engineering Technology Research Center, Zhengzhou
[3] College of Food Science & Nutritional Engineering, China Agriculture University, Beijing
关键词
clustered regularly interspaced short palindromic repeats (CRISPR); food safety; nucleic acid biosensor; rapid detection;
D O I
10.16429/j.1009-7848.2023.02.037
中图分类号
学科分类号
摘要
In recent years, rapid detection technology has become one of the most important topics in the scope of food safety. CRISPR/Cas system consists of clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated protein (Cas). Due to its superior targetability, CRISPR/Cas system has been widely used in the nucleic acid detection. CRISPR/Cas nucleic acid biosensor has become the research hotspot of rapid detection, because of its high sensitivity, strong specificity and good timeliness, driving the development of rapid detection for food safety. This review summarized the development of CRISPR/Cas system, introducing CRISPR/Cas systems combined with different nucleic acid amplification technologies, and their applications in target detection. Furthermore, the use of CRISPR/Cas nucleic acid biosensors in rapid detection for food safety was discussed, and future research directions was proposed. Overall, this review provides references and ideas for developing novel rapid detection methods utilizing CRISPR/Cas nucleic acid biosensors. © 2023 Chinese Institute of Food Science and Technology. All rights reserved.
引用
收藏
页码:383 / 397
页数:14
相关论文
共 61 条
  • [51] NIU C Q, WANG C Y, LI F, Et al., Aptamer assisted CRISPR -Cas12a strategy for small molecule diagnostics, Biosensors and Bioelectronics, 183, (2021)
  • [52] SHA Y, HUANG R, HUANG M Q, Et al., Cascade CRISPR/Cas enables amplification -free microrna sensing with fm-sensitivity and single-base-specificity, Chemical Communications, 57, 2, (2021)
  • [53] PENG L, ZHOU J, YIN L J, Et al., Integration of logic gates to CRISPR/Cas12a system for rapid and sensitive detection of pathogenic bacterial genes, Analytica Chimica Acta, 1125, (2020)
  • [54] LI F, YE Q H, CHEN M T, Et al., An ultrasensitive CRISPR/Cas12a based electrochemical biosensor for Listeria monocytogenes detection, Biosensors and Bioelectronics, 179, (2021)
  • [55] SHEN J J, ZHOU X M, SHAN Y Y, Et al., Sensitive detection of a bacterial pathogen using allosteric probe-initiated catalysis and CRISPR-Cas13a amplification reaction, Nature Communications, 11, 1, (2020)
  • [56] ABNOUS K, DANESH N M, RAMEZANI M, Et al., A novel colorimetric aptasensor for ultrasensitive detection of aflatoxin M<sub>1</sub> based on the combination of CRISPR -Cas12a, rolling circle amplification and catalytic activity of gold nanoparticles, Analytica Chimica Acta, 1165, (2021)
  • [57] WANG P, LIU Y M, YU Y, Et al., Hydrazone ligation assisted dnazyme walking nanomachine coupled with CRISPR-Cas12a for lipopolysaccharide analysis, Analytica Chimica Acta, 1174, (2021)
  • [58] XIONG Y, ZHANG J J, YANG Z L, Et al., Functional DNA regulated CRISPR -Cas12a sensors for point-of-care diagnostics of non-nucleic-acid targets, Journal of the American Chemical Society, 142, 1, (2019)
  • [59] WU H, QIAN C, WU C, Et al., End -point dual specific detection of nucleic acids using CRISPR/ Cas12a based portable biosensor, Biosensors and Bioelectronics, 157, (2020)
  • [60] LIU H, WANG J B, ZENG H J, Et al., Rpa - Cas12a-fs: A frontline nucleic acid rapid detection system for food safety based on CRISPR -Cas12a combined with recombinase polymerase amplification, Food Chemistry, 334, (2021)