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. 2013 Jan;20(1):56–65. doi: 10.1128/CVI.00550-12

Table 1.

Strains and plasmids used in this study

Strain or plasmid Relevant characteristics Source or reference
Strains
    E. coli
        Top10 High-competency cloning strain Life Technologies
        INV110 dam dcm mutant strain used to produce unmethylated plasmid DNA Life Technologies
    B. anthracis
        Ames pXO1+/pXO2+ 30
        Ames ΔbclA pXO1+/pXO2+ ΔbclA::kan 39
        Sterne 34F2 pXO1+/pXO2 NMRCa
    B. cereus
        569-UM20 Plasmidless, nonencapsulated, anthranilic acid-negative strain derived from B. cereus 569 40
        dcG9241 pBCXO1/pBC210/pBClin29+ 18
        dcG9241 ΔbclA pBCXO1/pBC210/pBClin29+ ΔbclA::kan This work
Plasmids
    pGEM-T TA-based E. coli cloning vector; Ampr Promega
    pUTE583 Dual E. coli and Bacillus vector; Cmr in E. coli, Emr in Bacillus 41
    pUTE618 Source of Ωkan cassette for gene replacement; Cmr Spr 41
    pBclA-U 1-kb region upstream from bclA in pGEM-T; Ampr This work
    pBclA-D 1-kb region downstream from bclA in pGEM-T; Ampr This work
    pBclA-UD 1-kb regions upstream and downstream of bclA in pGEM-T; Ampr This work
    pBclA-UΩD Ωkan cassette between 1-kb regions upstream and downstream of bclA in pGEM-T; Ampr This work
    p583BclA-UΩD Ωkan cassette between 1-kb region upstream and downstream of bclA in pUTE583; Cmr in E. coli, Emr in Bacillus This work
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NMRC, Naval Medical Research Center.