Related Experiment Video
Updated: Jan 25, 2026

Oral Transmission of Listeria monocytogenes in Mice via Ingestion of Contaminated Food
Published on: May 6, 2013
The Use of Bacteriocin-Producing Pediococcus acidilactici to Control Postprocessing Listeria monocytogenes
Elaine D Berry1, Robert W Hutkins1, Roger W Mandigo1
1Department of Food Science and Technology, University of Nebraska-Lincoln, Lincoln, Nebraska 68583-0919 and Department of Animal Science, University of Nebraska-Lincoln, Nebraska 68583-0908.
Abstract:
The ability of a bacteriocin-producing Pediococcus acidilactici to control postprocessing Listeria monocytogenes contamination of frankfurters was examined. Bacteriocin-producing P. acidilactici JD1-23 or its plasmid-cured derivative JD-M and a five-strain composite of L. monocytogenes were inoculated onto fully processed frankfurters. Under normal storage conditions at 4°C under vacuum, L. monocytogenes without added pediococci grew from an initial level of 104 CFU/g to a final level of 106 CFU/g over 60 d, with a lag time of 20-30 d. Under the same conditions, high levels (107 CFU/g) of either pediococcal strain inhibited growth of L. monocytogenes up to 60 d, although no reduction of cells occurred. With low levels of pediococci (103-104 CFU/g), Listeria grew, although the lag time was increased, and a bacteriocin effect was observed on frankfurters inoculated with JD1-23. In additional experiments done at 4°C and 15°C under aerobic and anaerobic conditions, levels of 107-108 CFU/g of either pediococci were observed to control Listeria growth on frankfurters at 15°C under anaerobic conditions for up to 15 d. At 4°C under aerobic conditions, L. monocytogenes grew on frankfurters inoculated with JD-M, while JD1-23 inhibited growth of the organism up to 30 d. At 15°C under aerobic conditions, L. monocytogenes grew in the presence of either pediococci, although a bacteriocin effect was indicated. Package atmosphere was observed to affect L. monocytogenes growth on this product.
Related Concept Videos
Contaminants and Errors
Another key consideration is determining the appropriate number of samples required to...
Control System Problem
When forming a closed-loop system, issues can arise if the poles cross into the unstable region, leading to potential...
SN1 Reaction: Stereochemistry
In the first step of an SN1 reaction, the bond between the electrophilic carbon and the leaving group ionizes to generate the carbocation intermediate. The second step of the mechanism is the nucleophilic attack.
In the formed carbocation, the positively charged carbon is sp2 hybridized with a trigonal planar geometry. As all the three substituents lie on the same plane, a plane of symmetry for the...
SN1 Reaction: Kinetics
However, Sir Christopher Ingold and Edward D. Hughes, who studied the kinetics of various nucleophilic substitution reactions, noticed that a tertiary alkyl halide does undergo a nucleophilic substitution reaction in the presence of a weak nucleophile. While studying the substitution...
SN1 Reaction: Mechanism
Firstly, the haloalkane ionizes to generate a carbocation intermediate and a halide ion. This heterolytic cleavage is highly endothermic with large activation energy. The ionization of the substrate, facilitated by a...
Acidity of 1-Alkynes
The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.

