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Table 4 Bacterial strains and plasmids used in this work

From: Developing a genetic engineering method for Acetobacterium wieringae to expand one-carbon valorization pathways

Strain or plasmid

Relevant characteristics

Source

Strains

 Acetobacterium wieringae strain JM

Wild type

Lab stock

 Acetobacterium wieringae DSM 1911 T

Wild type

DSMZ collection

 Acetobacterium woodii DSM 1030 T

Wild type

DSMZ collection

 Clostridium acetobutylicum DSM 792 T

Wild type

DSMZ collection

 Escherichia coli DH5α

fhuA2∆(argF-lacZ)U169 phoglnV44 Φ80 ∆(lacZ)M15 gyrA96 recA1 relA1 endA1 thi-1 hsdR17

NZYTech

 Escherichia coli TOP10

F- mcrA Δ(mrr-hsdRMS-mcrBC) Φ80lacZΔM15 ΔlacX74 recA1 araD139 Δ(ara-leu)7697 galgalrpsL (StrR) endA1 nupG

Invitrogen

 Escherichia coli CA434

E. coli HB101 containing plasmid R702

thi-1 hsdS20 (r-B, m-B) supE44 recAB ara-14 leuB5proA2 lacY1galK rpsL20 (strR) xyl-5 mtl-1

[28]

Plasmids

 R702

Tra+, Mob+ conjugative plasmid

[28]

 pMTL82151

Gram+: pBP1, catP; Gram: ColE1, catP; application: MCS

[28]

 pMTL83151

Gram+: pCB102; catP; Gram: ColE1, catP; application: MCS

[28]

 pMTL84151

Gram+: pCD6; catP; Gram: ColE1, catP; application: MCS

[28]

 pMTL85151

Gram+: pIM13, catP; Gram: ColE1, catP; application: MCS

[28]

 pMTL83_APO

pMTL83151, PthlA, thlA, ctfAB, adc from C. acetobutylicum

This study