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. 2019 Jan 9;85(2):e01873-18. doi: 10.1128/AEM.01873-18

TABLE 1.

Strains and plasmids used in this study

Strain or plasmid Relevant feature(s)a Reference or sourceb
Strains
    Rhodobacter sphaeroides
        2.4.1 WT strain NBRC
        Δccr mutant In-frame deletion mutant of RSP_0960 This study
        ΔphaC1 mutant In-frame deletion mutant of RSP_0382 This study
    Escherichia coli
        HST02 Cloning strain TaKaRa
        BL21(DE3) Protein production strain Novagen
        S17-1 Conjugation strain NBRC
Plasmids
    pUC18 Cloning vector, Apr TaKaRa
    pET22b (+) Expression vector in E. coli, Apr Novagen
    pETRcAceB Production of C-terminal His6-tagged RcAceB, Apr This study
    pK19mobsacB Mobilizable suicide vector for gene deletion, Kmr 42
    pKDRsccr pK19mobsacB backbone, deletion of RSP_0960, Kmr This study
    pKDRsphaC1 pK19mobsacB backbone, deletion of RSP_0382, Kmr This study
    pMG170 Shuttle vector stably maintained in R. sphaeroides, Kmr 43
    pMG180 lac promoter removed from pMG170, Kmr This study
    pMGccr pMG180 backbone, RSP_0960 with 241-bp upstream region, Kmr This study
    pMGphaC1 pMG180 backbone, RSP_0382 with 350-bp upstream region, Kmr This study
    pMGP pMG180 backbone, puc promoter from R. capsulatus, Kmr This study
    pMGPaceBA pMGP backbone, aceBA from R. capsulatus, Kmr This study
a

Apr, ampicillin resistance; Kmr, kanamycin resistance.

b

NBRC, National Institute of Technology and Evaluation (NITE) Biological Resource Center.