DNA Extraction- and Amplification-Free Nucleic Acid Biosensor for the Detection of Foodborne Pathogens Based on CRISPR/Cas12a and Argonaute Protein-Mediated Cascade Signal Amplification-Reference-Cited by-同舟云学术

DNA Extraction- and Amplification-Free Nucleic Acid Biosensor for the Detection of Foodborne Pathogens Based on CRISPR/Cas12a and Argonaute Protein-Mediated Cascade Signal Amplification

Published:2023-11-10 Issue:46 Volume:71 Page:18037-18045
ISSN:0021-8561
Container-title:Journal of Agricultural and Food Chemistry
language:en
Short-container-title:J. Agric. Food Chem.

Author:

Chen Rui¹,Zhao Junpeng¹,Han Minjie¹,Dong Yongzhen²,Jiang Feng³,Chen Yiping²^ORCID

Affiliation:

1. College of Food Science and Technology, Huazhong Agricultural University, Wuhan, Hubei 430070, China

2. State Key Laboratory of Marine Food Processing and Safety Control, Dalian Polytechnic University, Dalian, Liaoning 116034, China

3. Key Laboratory of Detection Technology of Focus Chemical Hazards in Animal-derived Food for State Market Regulation, Wuhan 430075, China

Funder

National Natural Science Foundation of China

Key R&D Program of Hubei Province

Key Laboratory of Detection Technology of Focus Chemical Hazards in Animal-derived Food for State Market Regulation

Publisher

American Chemical Society (ACS)

Subject

General Agricultural and Biological Sciences,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jafc.3c06530

Reference35 articles.

1. Rapid and visual detection of enterovirus using recombinase polymerase amplification combined with lateral flow strips

2. Biosensors for rapid detection of Salmonella in food: A review

3. Research Note: Repetitive element–based polymerase chain reaction genotyping improves efficiency of Salmonella surveillance in a model broiler production system

4. Fat removal with hydrolyzed corn starch for real-time qPCR detection of Salmonella enterica in ground beef in 4.5 hours without enrichment

5. Sensitive and rapid visual detection of Salmonella Typhimurium in milk based on recombinase polymerase amplification with lateral flow dipsticks

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