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. 2020 Apr 15;20:93. doi: 10.1186/s12866-020-01763-1

Table 3.

Plasmids and bacterial strains constructed in the study

Plasmid Source of description Reference/origin
E. coli DH5α FendA1 glnV44 thi-1 recA1 relA1 gyrA96 deoR nupG ϕ80dlacZΔM15 Δ(lacZYA-argF)U169, hsdR17(rK-mK+), λ- Invitrogen
E. coli BL21 (DE3) FompT gal dcm lon hsdSB(rBmB) λ(DE3 [lacI lacUV5-T7 gene 1 ind1 sam7 nin5] Invitrogen
M. smegmatis mc2155 Lab stock
pGEX 4 T-1 lacTq, 4.9 kb, Ampr, GST gene fusion vector GE Healthcare
pRSET-B lacTq, 2.8 kb, AmpR, 6xHis (N-term) gene fusion vector Invitrogen
p0004- Sac B Suicide recombination delivery vector carrying hygR-SacB for gene disruption, hygR
PhAE159 Conditionally replicating shuttle phasmid vector William R Jacobs Jr (unpublished)
pMV261 E. coli mycobacterial shuttle vector, KanR, hsp60 promoter Strover et al. (1991)
Constructs in this study
 pGBRJ1 pRSET-B vector carrying the coding region of Rv0148 gene from M. tuberculosis, AmpR This study
 pGBRJ2 pGEX 4 T-1 vector carrying the coding region of Rv0148 gene from M. tuberculosis, AmpR This study
 pGBRJ3 pRSET-B vector carrying the coding region of Htdy gene from M. tuberculosis, AmpR This study
 Δ0148 The deletion of Rv0148 gene from M. tuberculosis This study
 CΔ0148 pMV261 vector carrying the coding region of Rv0148 gene from M. tuberculosis, KanR expressed in M. tuberculosis (complementation) This study