Isolation and characterization of nisin-producing Lactococcus lactis subsp. lactis from bean-sprouts |
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Authors: | Y. Cai,L.-K. Ng,& J.M. Farber |
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Affiliation: | Department of Microbiology and Immunology, University of Ottawa, Ottawa, Ontario,Canada,;National Laboratory for Enteric Pathogens, Bureau of Microbiology, Laboratory Centreof Disease Control, Ottawa, Ontario, Canada,;Microbiology Research Division, Bureau of Microbial Hazard, Food Directorate, HealthCanada, Ottawa, Ontario, Canada |
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Abstract: | ![]() Bacterial isolates from bean-sprouts were screened for anti- Listeria monocytogenes bacteriocins using a well diffusion method. Thirty-four of 72 isolates inhibited the growth of L.monocytogenes Scott A. One, HPB 1688, which had the biggest inhibition zone against L.monocytogenes Scott A, was selected for subsequent analysis. Both ribotyping and DNAsequencing of 16S ribosomal RNA gene demonstrated that the isolate was Lactococcus lactis subsp. lactis . Polymerase chain reaction and nucleotide sequencing revealed that thegenomic DNA of the bean-sprout isolates contained a nisin Z structural gene. In MRS broth,bean-sprout isolate HPB 1688 survived at 3–4·5°C for at least 20 d, grew at 4°Cand produced anti-listerial compoundsat 5°C. When co-cultured with L. monocytogenes in MRS broth, the isolate inhibited thegrowth of L. monocytogenes at 4°C after 14d and at 10°C after 2 d. When co-inoculatedwith 102cells g−1 of L.monocytogenes on fresh-cut ready-to-eat Caesar salad, L. lactis subsp. lactis (108cells g−1) was able to reduce the number of L. monocytogenes by 1–1·4 logs after storage for 10 d at 7° and 10°C. A bacteriocin-producing Enterococcusfaecium was also able to reduce the numbers of L. monocytogenes onCaesar salad, butdid not act synergistically when co-inoculated with L. lactis subsp. lactis . |
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