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Appl. Environ. Microbiol., Apr 1996, 1252-1256, Vol 62, No. 4
A Coffey, FM Rombouts and T Abee
The ability to produce phosphatidylcholine phospholipase C (lecithinase) is
associated with virulence in pathogenic species of Listeria. Levels of
production vary greatly among members of the genus, and this virulence
factor is not readily detectable in many members of the pathogenic species
on conventional agar media containing egg yolk, a common substrate for the
enzyme. In this study, the influence of a variety of environmental
parameters, including temperature, pH, and salt concentration, on the
production of lecithinase by a number of strains was evaluated. Lecithinase
production by Listeria monocytogenes LO28 in brain heart infusion medium
was optimal at 1.75 to 2.0% NaCl; pH 7.0 to 7.3, and 37 to 40 degrees C,
and the presence of oxygen had no effect. In a chemically defined medium,
the optimal NaCl concentration and temperature were lower at 0.75 to 1.0%
NaCl and 33.5 degrees C. As detection of virulence factors is useful to
assist in the identification and differentiation of Listeria species, this
report shows that lecithinase activity can conveniently be detected within
36 h on a relatively inexpensive medium. Under the conditions described, L.
monocytogenes could be distinguished from other members of the genus as a
result of distinct lecithin degradation which was not evident in L.
innocua, L. seeligeri, L. ivanovii, L. welshimeri, or L. murrayi/grayi.
Copyright © 1996, American Society for Microbiology
Influence of environmental parameters on phosphatidylcholine phospholipase C production in Listeria monocytogenes: a convenient method to differentiate L. monocytogenes from other Listeria species
Department of Food Science, Wageningen Agricultural University, Netherlands.
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