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. 2016 Mar 31;198(8):1250–1259. doi: 10.1128/JB.00937-15

TABLE 1.

Strains and plasmids used in the study

Strain or plasmid Description Source or reference
M. extorquensa
    AM1 Rifr derivative (wild type) 43
    CM194.1 ΔmxaF 44
    ES890 xoxF1::Km 22
    ES970 ΔxoxF2 22
    ES1022 ΔxoxF2 xoxF1::Km 22
    ES1017 ΔmxaF xoxF1::Km This study
    ES2288 ΔmxaF ΔxoxF2 This study
    ES1100 ΔmxaF ΔxoxF2 xoxF1::Km 22
E. coli
    TOP10 Competent cells for cloning (Smr) Invitrogen
    S17-1 Helper strain for conjugation (Tpr Smr) 30
Plasmids
    pAYC61 Allelic exchange suicide vector (Tcr Apr) 33
    pAP5 Promoterless venus fusion vector constructed from pCM62 (Tcr) 22
    pCM157 cre expression vector (Tcr) 34
    pCM184 Allelic exchange suicide vector (Kmr Tcr Apr) 34
    pES134-135 pCM184 with xoxF2 upstream and downstream flanks (Kmr Tcr Apr) 22
    pES502 pAP5 containing the mxa promoter region (Tcr) 22
    pES503 pAP5 containing the xox1 promoter region (Tcr) 22
    pHV-F2 pAP5 containing the xoxF2 promoter region (Tcr) This study
    pLC6168 pAYC61 with xoxF1 upstream and downstream flanks (Kmr Tcr Apr) 20
    pRK2013 Conjugative helper plasmid (Kmr) 31
a

All M. extorquens AM1 strains used in the study are isogenic.