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Table 3 Genetically modified organisms constructed in the present study: Mutant strains of C. glutamicum based on the wild type strain (ATCC 13032) were constructed by site-directed mutagenesis

From: Metabolic engineering of the purine biosynthetic pathway in Corynebacterium glutamicum results in increased intracellular pool sizes of IMP and hypoxanthine

Strain

Genotype

Reference

C. glutamicum ATCC 13032

wild type

American Type Culture Collection

C. glutamicum Δpgi

deletion of the pgi gene (NCgl0817)

This work

C. glutamicum ΔpurA

deletion of the purA gene (NCgl2669)

This work

C. glutamicum ΔguaB2

deletion of the guaB2 gene (NCgl0578)

This work

C. glutamicum purF K348Q

Nucleotide exchange K348Q in the purF gene (NCgl2495)

This work

C. glutamicum ΔpurA ΔguaB2

double deletion of purA and guaB2 genes

This work

C. glutamicum ΔpurA ΔguaB2 purF 348 Δpgi

deletion of purA, guaB2 and pgi genes and allelic amino acid substitution K348Q in the purF gene

This work

E. coli DH5α

F−endA1, hsdR17(rk−mk+) supE44, thi-1λ− recAI gyrA96 relA1 Φ80ΔlacAm15

[48]

E. coli NM522pTC

supE thi-1 Δ(lac-proAB) Δ(mcrB-hsdSM)5 (r K−m K+) [F′ proAB lacI qZΔM15]

Stratagene

  1. E. coli strains were employed for plasmid construction.