The GRAS (for Generally Regarded As Safe) bacterium, Lactococcus lactis, is
a good candidate to produce heterologous proteins of vaccinal, medical or
technological interest. The secretion of such proteins would allow a direct
contact between the protein and its target and therefore would be a better
mode of production than intracellular production. To develop heterologous
protein export systems in L. lactis, we used the staphylococcal nuclease. W
e combined these secretion tools to the Nisin-Inducible Controlled Expressi
on system. We first developed two new expression vectors allowing the induc
ible production of Nuc intra- and extracellularly. We then used them to pro
duce in L. lactis two heterologous proteins of therapeutical interest: (i)
the ovine omega interferon which possesses antiviral properties and which w
ill be useful to enhance immune response in the case of the use of L. lacti
s as antigen delivery vehicle and (ii) a fusion protein between the Blg41-6
0 epitope and the mature part of Nuc.