Table 5.
Escherichia coli strains and plasmids used in this work.
| Strain or plasmid | Relevant genotype | Reference |
| JM101 | supE, thi Δ(lac-proAB), F' traD36 proA+ proB+ lacIq lacZΔM15 | [31] |
| PB12 | This strain was derived from PB11PTS-Glc-, a ptsHIcrr deletion derivative of strain JM101. PB12 has the same genotype of PB11 and at least three additional mutations (arcB, rpoS and a mutation responsible for the upregulation of genes involved in the ppGpp metabolism) that appeared during the selection of this fast growing mutant on glucose. | [7,9,21] |
| PB12aroB- | PB12aroB::cat | This work |
| pRW300 | aroGfbr is under the control of the IPTG inducible promoter lacUV5; carrying tetracycline resistance. Replication origin of pBR322. | [16] [10] |
| pCLtktA | tktA is under its constitutive promoter carrying spectinomycin resistance. Replication origin of pACYC184. | [16] |