We inserted such a kanamycin marker downstream of araC with the following primers: 5′_araC_yabI_insert AATCAGACAATTGACGGCTTGACGGAGTAGCATAGGGTTTTGTGTAGGCTGGAGCTGCTTC; 3′_araC_yabI_insert GCATAATGTGCCTGTCAAATGGACGAAGCAGGGATTCTGCCATATGAATA

TCCTCCTTAGTTCCTAT. The insertion was done in DY330 following the protocol described by [42], verified by PCR and moved to MG1655 by P1 transduction, Ferrostatin-1 price thus generating TB55. TB55 was subsequently used to generate a PCR product that spanned the kanamycin cassette adjacent to araC, araC, the full intergenic region between araC and araB, and 42 basepairs at the 5′ and 3′ -prime ends that were homologous to the upstream and 5′-coding region of ygjD, dnaT ,fldA or ffh. The sequence of the primers was ygjD_insert5′ AGTTTTACATCAACCCGCATTGGTCCTACACTGCGCGGTAATAATGTGCCTGTCAAATGGACG ygjD_insert3′ GCCGGTTTCATCGCAGGAAGTTTCAATACCCAGTACACGCATCGTTTCACTCCATCCAAAAAA dnaT_insert5′ TCCGTGTGTTACTATAAAAGTTATCTCCCTTCTCGTTCATCGAATGTGCC TGTCAAATGGACG dnaTC_insert3′ GTCAATACCAACGACGTCCGGGGTCAAAACTCTGGAAGACATCGTTTCAC

TCCATCCAAAAAA ffh_insert5′ GACGCCTTCATGTTATACTGCGGCAAAATACTGATGATGTGTAATGTGCC TGTCAAATGGACG ffh_insert3′ GCGCAGCGTGCGCGACAAACGATCGGTTAAATTATCAAACATCGTTTCAC TCCATCCAAAAAA fldA_insert5′ TGCCTTTATCCGTGGGCAATTTTCCACCCCCATTTCAATAAGAATGTGCC TGTCAAATGGACG fldA_insert3′ ATTACCGGTGTCGCTGCCGAAAAAGATGCCAGTGATAGCCATCGTTTCAC TCCATCCAAAAAA DY330 cells were grown in LB medium supplemented with 0.2% Blasticidin S datasheet L-arabinose and made electro- and recombination competent [42], and electroporated with the above described PCR product. After electroporation,

cells Tozasertib concentration were transferred to LB medium containing 0.1% L-arabinose and incubated at 32° for 1.5 hours prior to plating on LB plates agar containing L-arabinose (0.1%) and kanamycin (50 μg/ml, Sigma). Clones were checked on LB agar plates supplemented with 0.4% glucose to confirm that they were unable to grow in the presence of glucose. The promoter fusions and the adjacent araC gene were verified by sequencing with the following primers: araC_FW GCTACTCCGTCAAGCCGTCA; triclocarban ygjD_RW GGCAATTGGTCTGGGGAGCA. dnaTC_RW AGAGTTGATCGTCCAGAGCG ffh_RW ATTTTGACGAACTCCTGCCC fldA_RW CGAGAGTCGGGAAGAAGTCA The constructs were then moved by P1 transduction into MG1655. To construct TB80 the kanamycin cassette was removed with pCP20. The knockout ΔrelA::kan was derived from the KEIO library clone JW2755 [2] and P1-transduced into TB82. ΔspoT::kan was introduced using AB1058) as donor strain for P1 transduction. To measure activity of the promoters Para, Prsd and Papt, MG1655 and TB80 were transformed [37] with plasmids that contain transcriptional promoter-gfp fusions [29]. Microscopy LB agar pads were prepared by filling a cavity of a sterile microscope cavity slide with a drop of freshly melted LB agar, and covering it with a cover slip to attain a flat surface. The cavity slide was transferred to a fridge for a short time to allow the agar to solidify.