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Table 3 Escherichia coli strains and plasmids used in this work

From: Metabolic engineering for improving anthranilate synthesis from glucose in Escherichia coli

Strain/Plasmid

Characteristics

Reference

Strains

  

PB11

JM101 [supE, thi, Δ(lac-proAB), F'] ΔptsHI, crr::kmR, glucose-

[10]

W3110 trpD9923

W3110 [F-λ- INV (rrn D-rrn E) 1] tryptophan auxotroph, randomly mutagenized by treatment with ultraviolet radiation.

[5]

W3110 trpD9923 PTS-

As W3110 trpD9923 but ΔptsHI, crr::kmR, glucose-

This work

Plasmids

  

pJLBaroGfbr

aroGfbr expressed from the lacUV5 promoter, lacIq and tet genes, tetracycline resistance, pACYC184 replication origin.

[14]

pv5Glk5GalP

glk and galP genes expressed from the trc5 promoter, spectinomycin resistance. pCL1920 replication origin.

[13]

pJLBaroGfbrtkt A

pJLBaroGfbr derivative, containing the tktA gene with its native promoter.

This work