Figure 1.

(A) List of fluorescence transcriptional reporters used by Diacovich et al. They were made by cloning the promoter region of selected genes upstream of the fluorescent reporter gene gfpmut3A. The reporters are functional for FACS and microscopy read-outs. (B) Schematic representation of the catabolic part of the central carbon metabolism in S. enterica and elements that were studied by Diacovich et al. The enzymes that correspond to the studied transcriptional fusions are indicated in red and other relevant metabolic enzymes are highlighted in green (eda: 2-keto-3-deoxygluconate-6-phosphate aldolase and fadI: acetyl-CoA acyltransferase). The scheme was generated using the BioCyc Database Collection.¹¹