Automatic polymerase chain reaction product detection system for food safety monitoring using zinc finger protein fused to luciferase

作者：Yoshida Wataru; Kezuka Aki; Murakami Yoshiyuki; Lee Jinhee; Abe Koichi; Motoki Hiroaki; Matsuo Takafumi; Shimura Nobuaki; Noda Mamoru; Igimi Shizunobu; Ikebukuro Kazunori^*

来源：Analytica Chimica Acta, 2013, 801: 78-83.

DOI：10.1016/j.aca.2013.08.019

• Zinc finger protein
• Luciferase
• Polymerase chain reaction
• Pathogen detection
• Automatic analyzer

An automatic polymerase chain reaction (PCR) product detection system for food safety monitoring using zinc finger (ZF) protein fused to luciferase was developed. ZF protein fused to luciferase specifically binds to target double stranded DNA sequence and has luciferase enzymatic activity. Therefore, PCR products that comprise ZF protein recognition sequence can be detected by measuring the luciferase activity of the fusion protein. We previously reported that PCR products from Legionella pneumophila and Escherichia coli (E. coli) 0157 genomic DNA were detected by Zif268, a natural ZF protein, fused to luciferase. In this study, Zif268-luciferase was applied to detect the presence of Salmonella and coliforms. Moreover, an artificial zinc finger protein (B2) fused to luciferase was constructed for a Norovirus detection system. In the luciferase activity detection assay, several bound/free separation process is required. Therefore, an analyzer that automatically performed the bound/free separation process was developed to detect PCR products using the ZF-luciferase fusion protein. By means of the automatic analyzer with ZF-luciferase fusion protein, target pathogenic genomes were specifically detected in the presence of other pathogenic genomes. Moreover, we succeeded in the detection of 10 copies of E. coli BL21 without extraction of genomic DNA by the automatic analyzer and E. coli was detected with a logarithmic dependency in the range of 1.0 x 10 to 1.0 x 10(6) copies.

• 出版日期2013-11-1