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. 2010 Dec 23;77(4):1214–1220. doi: 10.1128/AEM.02316-10

TABLE 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Characteristics Reference or source
Strains
    M. goodii 12523 Wild type 20
    M. smegmatis mc2155 Wild type, ATCC 700084 ATCC
    M. smegmatis mc2155 ΔmimA M. smegmatis strain mc2155 with mimA deletion This study
    Gordonia sp. strain TY-5 Wild type 7
    Gordonia sp. strain TY-5 prmB::Kanr Gordonia sp. strain TY-5 with prmB disruption 7
    E. coli DH5α Host used for cloning Takara Bio
Plasmids
    pET21a Vector used for cloning Novagen
    pETmimABCDgo pET21a containing mimABCDgo of M. goodii 12523 This study
    pETmimABCDsm pET21a containing mimABCDsm of M. smegmatis mc2155 This study
    pK18mobsacB Vector used for deletion mutagenesis, aph sacB NBRP (NIG, Japan)
    pKΔmimA pK18mobsacB containing a deleted mimA gene of M. smegmatis mc2155 This study
    pRHK1 Rhodococcus (Mycobacterium)-E. coli shuttle vector, Kanr 6
    pUCkap1 pUC18 containing the kap1 promoter region from R. erythropolis 13
    pRHKkap1 pRHK1 containing the kap1 promoter region This study
    pRHKkap1mimAgo pRHKkap1 containing the mimAgo gene under the control of the kap1 promoter This study
    pRHKkap1mimAsm pRHKkap1 containing the mimAsm gene under the control of the kap1 promoter This study