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Table 1 Strains and plasmids used in this study

From: Metabolic pathway engineering for production of 1,2-propanediol and 1-propanol by Corynebacterium glutamicum

Strain or plasmid

Relevant characteristics

Source or reference

C. glutamicum strains

WT

Wild type (ATCC13032)

[76]

Δcg1497

In-frame deletion of cg1497 in C. glutamicum WT

This work

ΔhdpA

In-frame deletion of hdpA (cg2474) in C. glutamicum WT

This work

Δcg1497ΔhdpA

In-frame deletion of hdpA (cg2474) in C. glutamicum Δcg1497

This work

ΔhdpAΔldh

In-frame deletion of ldh (cg3219) in C. glutamicum ΔhdpA

This work

Plasmids

pK19mobsacB

Kana, mobilizable E. coli vector for the construction of insertion and deletion mutants of C. glutamicum (oriV, sacB, lacZ)

[75]

pEKEx3

Speca; C. glutamicum/E. coli shuttle vector (Ptac, lacI b; pBL1, OriVC.g., OriVE.c.)

[45]

pVWEx1

Kana; C. glutamicum/E. coli shuttle vector for regulated gene expression (Ptac, lacIb, pHM1519, oriVC.g., oriVE.c.)

[77]

pK19mobsacB-Δcg1497

Kana, pK19mobsacB with the deletion construct for cg1497

This work

pK19mobsacB-ΔhdpA

Kana, pK19mobsacB with the deletion construct for hdpA (cg2474)

This work

pK19mobsacB-Δldh

Kana, pK19mobsacB with the deletion construct for ldh (cg3219)

[28]

pEKEx3-mgsA-gldA

Derived from pEKEx3 for IPTG-inducible overexpression of mgsA and gldA from E. coli with artificial ribosome binding site in front of each gene

This work

pEKEx3-mgsA-yqhD-gldA

Derived from pEKEx3 for IPTG-inducible overexpression of mgsA, yqhD, and gldA from E. coli with artificial ribosome binding site in front of each gene

This work

pEKEx3-mgsA-yqhD-fucO-gldA

Derived from pEKEx3 for IPTG-inducible overexpression of mgsA, yqhD, fucO, and gldA from E. coli with artificial ribosome binding site in front of each gene

This work

pVWEx1-ppdABC

Derived from pEKEx3 for IPTG-inducible overexpression of ppdABC from K. oxytoca DSM4798 with artificial ribosome binding site in front of the gene cluster

This work

  1. aResistance gene
  2. bQuantity