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Table 2 Strains and plasmids used in this study

From: Engineering NAD+ availability for Escherichia coli whole-cell biocatalysis: a case study for dihydroxyacetone production

Strains or plasmids

Genotype or characteristic

Resources or references

E. coli Strains

  

DH5α

F-, φ80d/lacZ∆M15, ∆(lacZYA-argF)U169, deoR, recA1, endA1, hsdR17(rk-, mk+), phoA, supE44, λ-, thi-1, gyrA96, relA1

TaKaRa

DH10B

F-,mcr A, ∆(mrr-hsd RMS-mcr BC), φ80lac Z∆M15, ∆lac X74, rec A1, end A1, ara D139, ∆ (ara, leu)7697, gal U, gal K, λ-, rps L, nup G/pMON14272/pMON7124

Invitrogen

DH1

F-, glnV44(AS), λ-, rfbC1, gyrA96(NalR), recA1, endA1, thi-1, hsdR17

CGSC

(No. 6040)

MG1655

F-, λ-, rph-1

CGSC

(No. 6300)

BW25113

rrnB3, ∆lacZ4787, hsdR514, ∆(araBAD)567, ∆(rhaBAD)568 rph-1

CGSC

(No. 7636)

Bl21(DE3)

F–, dcm, ompT, hsdS(rB–, mB–), gal, λ(DE3)

Novagen

YJE005

DH5α/pTrc99A-gldA-nox

This study

YJE006

DH5α/pTrc99A-gldA-nox + ntt4

This study

Plasmids

  

pMD18-T

lacZ, pBR322 ori, bla, cloning vector

TaKaRa

pTrc99A

lacI, pBR322 ori, bla, expression vector

Amersham Pharmacia

pET15K-ntt4

ntt4 inserted within Nde I and Bam H I sites, kan

[11]

pBCTC-ntt4

ntt4 inserted within Sac I and Bam H I sites, kan

This study

pBCTD-ntt4

ntt4 inserted within Sac I and Bam H I sites, kan

This study

pTrc99A-gldA-nox

gldA and nox transcription under Trc promoter

This study

pTrc99A-gldA-nox + ntt4

gldA and nox transcription under Trc promoter, ntt4 under gntT105p promoter.

This study