In this thesis, we show the effect of the global regulators CRP, IHF and Fis in the flagella-biofilm transcriptional regulatory network and show that, despite its important role to regulate the system, those GRs are not entirely necessary, since remotion of any GRs studied leads, despite affected, to motility and biofilm formation. Altogether, this data strongly suggest that the flagella-biofilm network present an intrinsic capacity to support nodes remotion, and supporting the robustness of the flagella-biofilm transcriptional regulatory network. One of the synthetic biology aims is to standardize and understand the signal integration and the behavior of biological parts for its eventual circuit integration and properly function. Due this, as a first part of my PhD, I worked to generate synthetic cis-elements that will be recognized by three transcriptions factors as well as understand the regulatory mechanisms which drives this sequence in bacteria (Attached article). For this, we based our study on the well-known transcription activation and repression mechanisms of gene expression in bacteria (Browning and Busby, 2016). Specifically, we used the principle of CCR induction in bacteria, in which a specific cis-element recognized by CRP global regulator is sufficient to modulate cognate genes, as for wild type lac promoter. Therefore, in order to evaluate the hypothesis of "compress information", we wondering whether it could be possible to generate a synthetic sequence that would be recognized by three different global regulators. First, we unveil the consensus sequences that are recognized by CRP, IHF and Fis and we used an evolutionary algorithm to generate a synthetic cis-element that does not exist in bacteria and, that in principle, would be recognized by the three different transcription factors. Next, those sequences were cloned upstream of a GFPlva reporter system to determine the functionality of the sequences. For this, bacteria transformed with the reporter systems were surveyed in vivo to determine its dynamic of gene expression. The results shown that (i) the synthetic sequence, that does not exist in bacteria, is completely functional. (ii) The synthetic promoter regions generated were, in fact, modulated by three GRs, showing that it is possible to compress information. This concept was published in ACS Syntheticc Biology by the end of 2015 and the article is attached in this thesis.