Based on several experiences of microbial release using genetically modifie
d Rhizobium leguminosarum, we have highlighted a number of aspects related
to the suitability of introduced markers such as resistance to mercury and
P-galactosidase activity, the latter serving the function of high-expressio
n level reporter gene obtained by the introduction of a synthetic promoter
conferring strong inducible expression in Gram-negative bacteria. In vitro
expression and in vivo performances of the chosen examples have been follow
ed in model strains comparing gene dosage and expression levels. The techni
cal possibility of unambiguously monitoring the marked GMM has been evaluat
ed in medium- and long-term experiments carried out both in microcosms and
soil, also including the presence of the plant symbiotic host. Marker stabi
lity, regardless the nature of the gene, was shown to be dependent on the l
ocation of the genetic modification and on its degree of gene expression re
gulation. Reporter strength was found to be an advantage allowing the disti
nction of marker-bearing bacteria while negatively affecting their genetic
stability. Plasmid-borne regulated reporters were found to be stable up to
the stages of rhizosphere colonization, but were more critically selected a
gainst upon symbiotic host invasion.