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Background  The cyclic diguanylate (c-di-GMP) is currently considered an ubiquitous second messenger in bacteria that influences a wide range of cellular processes. One of the methodological approaches to unravel c-di-GMP regulatory networks involves raising the c-di-GMP intracellular levels, e.g. by expressing a diguanylate cyclase (DGC), to provoke phenotypic changes.    Results  We have constructed mini-Tn 7  delivery vectors for the integration and stable expression of the  pleD * gene encoding a highly active DGC, which can be used to artificially increase the intracellular levels of c-di-GMP in Gram negative bacteria. The functionality of these new vectors has been validated in several plant-interacting α- and γ-proteobacteria. Similarly to vector plasmid-borne  pleD *, the genome-borne mini-Tn 7 pleD* constructs provide significant increases in intracellular c-di-GMP, provoking expected phenotypic changes such as enhanced polysaccharide production, biofilm formation and reduced motility. However, the mini-Tn 7 pleD* constructs resulted far more stable in the absence of antibiotics than the plasmid-based  pleD * constructs. Furthermore, we have also implemented an inducible system to modulate  pleD * expression and intracellular c-di-GMP rises “on demand”.    Conclusions  mini-Tn 7 pleD* constructs are very stable and are maintained during bacterial free-living growth as well as during interaction with eukaryotic hosts, in the absence of selective pressure. This high stability ensures experimental homogeneity in time and space with regard to enhancing c-di-GMP intracellular levels in bacteria of interest.    Electronic supplementary material  The online version of this article (doi:10.1186/s12866-015-0521-6) contains supplementary material, which is available to authorized users.

Mini-Tn7 vectors for stable expression of diguanylate cyclase PleD* in Gram-negative bacteria