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Table 4 Mutant genotypes and corresponding site-specific primer sequences (F, forward; R, reverse) used for verification a

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

Mutant genotype

Primer

Primer sequence

Δpgi

Δpgi- F

5′- GATCACGCGTATCCCTTCTCCGGCATC- 3′

 

Δpgi- R

5′- GATCTCTAGATCCAGCGACACGAATAATC- 3′

ΔpurA

ΔpurA- F

5′- GATCTCTAGAATGGATCGGATGTGACG- 3′

 

ΔpurA- R

5′- GATCACGCGTCAATCGGTCAACCTGGT- 3′

ΔguaB2

ΔguaB2- F

5′- GATCACGCGTGAGTTTCTACCGGAGGA- 3′

 

ΔguaB2- R

5′- GATCTCTAGATCAGACTGGAAGTAACG- 3′

purF K348Q

purFK348Q- F

5′- GATCACGCGTGATTGCGGACTGGTTAC- 3′

 

purFK348Q- R

5′- GATCTCTAGACTCCTGCTGCTGCGTATG- 3′

 

K348Q- 1

5′- GGCCAAGGCATGGTCCAG AACGCCTACGTTGGC- 3′

 

K348Q- 2

5′- GCCAACGTAGGCGTTCTG GACCATGCCTTGGCC- 3′

  1. a For the single amino acid substitution in purFK348Q, sequences for fusion primers (K348Q-1, K348Q-2) containing the point mutation (underlined) are denoted.