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. 2009 Jul 6;191(17):5489–5498. doi: 10.1128/JB.00590-09

TABLE 2.

Plasmids used in this study

Plasmid Description Source/reference
pGEM-T PCR cloning vector Promega
pGEMA9V pGEM-T spo0A(A257V) gene This study
pGEMSpo0A pGEM-T with spo0A sequence from RBS to E263 This study
pET16b Protein expression vector Novagen
pET16b0A pET16b with an 848-bp NcoI-BamHI insert bearing the spo0A gene 8
pET16bA9V pET16b with an 848-bp NcoI-BamHI insert bearing the spo0A(A257V) gene This study
pUCIIGtrpA pUC19 with spoIIG promoter and proximal transcript fused to trpA terminator 36
pJM5134 Cloning vector with abrB promoter 30
pUCIIGAtrpASS1 pUCIIGtrpA with a single mutation in site 2 0A boxes This study
pUCIIGAtrpASS2 pUCIIGtrpA with two mutations in site 2 0A boxes This study
pUCIIGAtrpASS3 pUCIIGtrpA with three mutations in site 2 0A boxes This study
pUCIIGAtrpASS4 pUCIIGtrpA with four mutations in site 2 0A boxes This study
pUCIIGAtrpASS5 pUCIIGtrpA with five mutations in site 2 0A boxes This study
pDH32 amyE integrative vector for lacZ fusions 42
pDH32SSIIG1 pDH32 containing an EcoRI-BamHI fragment from pUCIIGtrpASS1 This study
pDH32SSIIG2 pDH32 containing an EcoRI-BamHI fragment from pUCIIGtrpASS2 This study
pDH32SSIIG3 pDH32 containing an EcoRI-BamHI fragment from pUCIIGtrpASS3 This study
pDH32SSIIG4 pDH32 containing an EcoRI-BamHI fragment from pUCIIGtrpASS4 This study
pDH32SSIIG5 pDH32 containing an EcoRI-BamHI fragment from pUCIIGtrpASS5 This study