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. 2008 Jan 22;7:1. doi: 10.1186/1475-2859-7-1

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]