Isolation, amplification and characterization of foodborne pathogen disease bacteria gene for rapid kit test development
Author(s) -
Muktiningsih Nurjayadi,
Iman Santoso,
Irma Ratna Kartika,
Fera Kurniadewi,
V. Saamia,
W. Sofihan,
D. Nurkhasanah
Publication year - 2017
Publication title -
aip conference proceedings
Language(s) - English
Resource type - Conference proceedings
SCImago Journal Rank - 0.177
H-Index - 75
eISSN - 1551-7616
pISSN - 0094-243X
DOI - 10.1063/1.4991181
Subject(s) - primer (cosmetics) , polymerase chain reaction , isolation (microbiology) , food safety , salmonella , bacteria , food poisoning , pathogen , pathogenic bacteria , foodborne pathogen , biology , gene , in silico , computational biology , microbiology and biotechnology , genetics , food science , chemistry , organic chemistry , listeria monocytogenes
There is a lot of public concern over food safety. Food-safety cases recently, including many food poisoning cases in both the developed and developing countries, considered to be the national security threats which involved police investigation. Quick and accurate detection methods are needed to handle the food poisoning cases with a big number of sufferers at the same time. Therefore, the research is aimed to develop a specific, sensitive, and rapid result molecular detection tool for foodborne pathogen bacteria. We, thus, propose genomic level approach with Polymerase Chain Reaction. The research has successfully produced a specific primer to perform amplification to fim-C S. typhi, E. coli, and pef Salmonella typhimurium genes. The electrophoresis result shows that amplification products are 95 base pairs, 121 base pairs, and 139 base pairs; and all three genes are in accordance with the size of the in silico to third genes bacteria. In conclusion, the research has been successfully designed a specifi...
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