Three isolates of Brevibacterium (B.) linens from the brine of a red s
mear cheese manufacturer produced Listeria inhibiting principles which
could be demonstrated by deferred stab inoculation, spot on the lawn
technique, well assay, associate growth and in cellfree fluid culture.
The antimicrobial agent was dialyzable through tubing MWCO 1 kDa, sta
ble at pH 4,0-9,0 and after heating (80 degrees C, 30 min) at acid pH,
but not at alkaline pH, remained active after treatment with protease
s, catalase and lipase, was soluble in water and ethanol and insoluble
in acetone. Its mode of action was dependent on the strain of L. mono
cytogenes and the activity was more efficient at pH 7,6 than at pH 5,7
. The spectrum of activity comprised 96 % of strains of L. monocytogen
es (n = 48) and all strains of L. innocua (n = 20), L. seeligeri (n =
3), L. ivanovii (n = 2) and L. welshimeri (n = 2). L. monocytogenes co
uld not be detected after associate growth with B. linens on agar for
at least five days at 16 degrees C, if the inocula of L. monocytogenes
was was very low and that of B. linens very high. L. monocytogenes wa
s, however, detectable inoculated in enrichments of agar culture of B.
linens. Hence microbiological control of growth of Listeria by antago
nistic active strains of B. linens cannot replace hygiene concepts for
controlling L. monocytogenes.