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. 2003 Oct;69(10):5928–5934. doi: 10.1128/AEM.69.10.5928-5934.2003

TABLE 1.

Bacterial strains, plasmids, and PCR primers used in this study

Strain, plasmid, or primer Relevant characteristic(s) or sequence Source or reference
V. fischeri
    ES114 Wild-type light-organ isolate from E. scolopes 5
    ESR1 Spontaneous Rfr mutant of ES114 14
    JRM100 to JRM104 Five ES114 clones with mini-Tn7 insertion; Emr This study
    JRM200 ES114 clone with mini-Tn7 insertion; Cmr This study
E. coli
    BW23474 Δlac-169 robA1 creC510 hsdR514 uidAMluI)::pir116 endA(BT33) recA1 28
    CC118λpir Δ(ara-leu) araD ΔlacX74 galE galK phoA20 thi-I rpsE rpoB argE(Am) recA1; lysogenized with λpir 16
Plasmids
    pEVS94S R6K ori oriT Emr 41
    pEVS104 Derivative of pRK2013; conjugal tra and trb genes 41
    pEVS107 pEVS94S derivative, mini-Tn7; mob; Emr Knr This study
    pUXBF13 R6K ori; tns genes; Apr 4
    pCR2.1 PCR product cloning vector; ColE1 ori; Apr Knr Invitrogen Inc.
    pJRM3 pEVS107 with Cmr replacing Emr This study
    pEVS35 CmrXbaI fragment cloned into XbaI site of pBC 39
Primers
    JM1 5′ GTTACACGTTACTAAAGGG 3′ This study
    JM2 5′ ACCAGACCGTTCAGCTGG 3′ This study
    JM3 5′ GGAACATGTGTGGTATGG 3′ This study
    JM4 5′ GACAGTCATCTATTCAAC 3′ This study