E3S Web of Conferences (Jan 2023)

Primer concentration and Pre-denaturation Time Effect on cyt-K Bacillus cereus Detection using Real-Time PCR Method

  • Azzahra M.,
  • Nurjayadi M.,
  • Pramudiyasih N. A.,
  • Kusumawati R. N.,
  • Maulana I.,
  • Declan J. L.,
  • Putri G. I.,
  • Juliansyah D. A.,
  • Krisdawati I.,
  • Kurniadewi F.,
  • Kartika I. R.,
  • Sukmawati D.,
  • Nastassya L.,
  • Saamia V.,
  • Oktaviani D.A.S.,
  • Wiranatha M.,
  • Ali El-Enshasy H.,
  • Abomoelak B.

DOI
https://doi.org/10.1051/e3sconf/202340004011
Journal volume & issue
Vol. 400
p. 04011

Abstract

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Foodborne disease is a global threat that can affect all sections of society, both in developed or developing countries. Bacillus cereus is a Gram-positive bacteria that can cause food poisoning disease in humans. [2] Real-Time PCR detection method is one of the molecular marker methods that has been widely recognized as a fast, reliable, sensitive and specific detection tool for detecting pathogenic bacteria. In previous studies, the optimum condition and formulas applied for cyt-K 2 primer pairs have been obtained using Real-Time PCR. The purpose of this study is to find out the best conditions work of the primer pair cyt-K Bacillus cereus on detecting bacteria target using variations of pre-denaturation time and primer concentration with Real-Time PCR method. The annealing temperature used for PCR is at 60°C with sample concentration 50 ng/µL of B. cereus. Real-time PCR detection of variations in pre-denaturation time and primer concentration obtained the best conditions for primer pair cyt-K work at minute 4 with a primer concentration of 10 pmol and successfully amplifying the target by producing a Ct value of B. cereus at 13.04. Based on the results of the study, the primer pair cyt-K were reproducible in detecting the target gene and in the further step, this research can be continued to developed a prototype detection kit for foodborne pathogen bacteria using Real-Time PCR method.