TY - DATA T1 - MOESM3 of Deletion of the 2-acyl-glycerophosphoethanolamine cycle improve glucose metabolism in Escherichia coli strains employed for overproduction of aromatic compounds PY - 2015/12/01 AU - CĂŠsar Aguilar AU - NoemĂ­ Flores AU - Fernando Riveros-McKay AU - Diana Sahonero-Canavesi AU - Susy Carmona AU - Otto Geiger AU - Adelfo Escalante AU - Francisco BolĂ­var UR - https://springernature.figshare.com/articles/journal_contribution/MOESM3_of_Deletion_of_the_2-acyl-glycerophosphoethanolamine_cycle_improve_glucose_metabolism_in_Escherichia_coli_strains_employed_for_overproduction_of_aromatic_compounds/4351277 DO - 10.6084/m9.figshare.c.3607286_D3.v1 L4 - https://ndownloader.figshare.com/files/7077326 KW - Metabolic engineering KW - Metabolic plasticity KW - PTS system KW - Escherichia coli KW - Adaptive laboratory evolution KW - 2-Acyl-glycerophosphoethanolamine cycle KW - Glycerol metabolism KW - Glucose metabolism N2 - Additional file 3: Figure S1. RT-qPCR values of central metabolism and regulatory genes. Relative mRNA concentrations of central metabolism and regulatory genes of PB12 and PB13 strains, grown in glucose as the sole carbon source were determined by RT-qPCR. The PB12 values have been previously reported [2, 6, 7] and are presented here for discussion and comparison purposes. Data in this Figure are reported as relative expression levels of the parental strain JM101. The mRNA level of each gene in the parental strain was used as control to normalize the data, assigning it the value of one (see Materials and Methods). ER -