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. 2008 Jan 18;190(6):2031–2038. doi: 10.1128/JB.01625-07

TABLE 1.

Strains and plasmids used

Strain or plasmid Genotype and description Source and/or reference
B. subtilis strains
    168 Wild type, trp Laboratory stock
    PS832 Wild type, trp+ revertant of strain 168 Laboratory stock
    PS356a ΔsspA ΔsspB αβ 10
    PERM450a ΔsspA ΔsspB ΔexoA::tet Δnfo::neo αβ Neor Tetr 20
    PERM452a ΔexoA::tet Tetr 20
    PERM453a Δnfo::neo Neor 20
    PERM454a ΔexoA::tet Δnfo::neo Neor Tetr 20
    YB300 recA Cmr R. Yasbin (36)
    PERM662a recA Cmr (YB300 → PS832)b
    PERM663a recA ΔexoA::tet Cmr Tetr (pPERM374 → PS599)c
    PERM665a recA ΔexoA::tet Δnfo::neo Cmr Tetr Neor (pPERM337 → PERM663)c
    PS599a uvrA42 trp+ P. Setlow
    PERM515a uvrA ΔexoA::tet Tetr (pPERM374 → PS599)c
    PERM517a uvrA ΔexoA::tet Δnfo::neo Tetr Neor (pPERM337 → PERM515)c
Plasmids
    pPERM337 1.3-kb SmaI-SmaI fragment containing a Neor cassette inserted into the NaeI site of nfo in pPERM282; Ampr Neor 20
    pPERM374 469-bp XbaI-BamHI fragment (3′ region of exoA) and 537-bp EcoRI-HindIII fragment (5′ region of exoA) flanking the tetracycline gene of pDG1515; Ampr Tetrd 20
a

The background for this strain is PS832.

b

Chromosomal DNA from the strain to the left of the arrow was used to transform the strain to the right of the arrow.

c

DNA of the plasmid to the left of the arrow was used to transform the strain to the right of the arrow.

d

See reference 6.