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. 2002 Oct;184(20):5661–5671. doi: 10.1128/JB.184.20.5661-5671.2002

TABLE 2.

Plasmids used in this study

Plasmid Characteristics Reference
pUB110 Kmr 9
pKTH10 pUB110 derivative; encodes the α-amylase (AmyQ) of B. amyloliquefaciens; Kmr 17
pKTH10L pKTH10 derivative; Kmr 11
pMutin4 pBR322-based integration vector for B. subtilis; contains a multiple-cloning site downstream of the Pspac promoter and a promoterless lacZ gene preceded by the RBSa of the spoVG gene; Apr/Emr 26
pDL Vector for the integration of transcriptional promoter-bgaB gene fusions in the amyE locus of B. subtilis; Apr Cmr 30
pDN220 pDL containing the complete cssR-cssS control region on a PCR-amplified fragment; Apr Cmr This study
pDN221 pMutin4 containing the complete cssR-cssS control region on a PCR-amplified fragment; Apr Emr This study
pDN222 pMutin4 containing the complete cssR-cssS control region, with the A → G mutation at position −60 relative to the start codon of cssR; Apr Emr This study
pDN223 pDL containing the htrB control region with the T → C change at position −218 relative to the start codon of htrB; Apr Cmr This study
pX Vector for the integration of genes in the amyE locus; the integrated gene will be transcribed from the xylA promotor; carries the xylR gene; Apr Cmr 12
pXcssS pX derivative; carries cssS downstream of the xylA promoter; Apr Cmr This study
a

RBS, ribosome-binding site