What You Need to Know
The method relies on extracting microbial DNA, amplifying the 16S rRNA gene via PCR, and sequencing the amplicons to profile community composition. Quantitative PCR targets specific spoilage organisms such as Listeria monocytogenes, providing rapid detection limits. Integration of growth kinetics with community dynamics enables early spoilage risk assessment.
The Science
Primary Reaction
PCR amplification of 16S rRNA gene fragments