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. 2006 Jun;188(12):4362–4372. doi: 10.1128/JB.01922-05

TABLE 2.

Plasmids used in this worka

Plasmid Relevant features Reference
pBT205 Vector for integration into B. subtilis chromosome, promoterless lacZ gene, ColE1 ori Apr Cmr 14
pBT205O+E pBT205 with ω gene with its promoter, Pω, and part of the ɛ gene This work
pBT233 pSM19035 derivative, accession no. X64695 11
pBT346 pHP13 with δ, ω, ɛ, and ζ genes (pDB101 coordinates 4696 to 8271), HincII-HincII pBT233 fragment cloned into SmaI siteb 11
pBT346-5 pHP13 with ω gene (pDB101 coordinates 6312 to 6894) (sixth triplet mutated into a stop codon)b 14
pDO1000 pUC18 with δ and ω genes (pDB101 coordinates 5382 to 6740)b This work
pDO1030 pUC18 with δ and ω genes, with δ truncated after the 23rd codon This work
pDO1040 pUC18 with δ and ω genes, with δ truncated after the 40th codon This work
pDO1212 pUC18 with δ gene promoter (Pδ) This work
pDO1340 pUC18 with δ and ω genes, with δ's Walker motif A deleted This work
pDO3000 pUC18 with δ and ω genes, with δ promoter (Pδ) replaced with copS promoter (PcopS) This work
pDO3212 pUC18 with copS gene promoter (PcopS) This work
pDO7000 pUC18 with δ and ω genes, with δ promoter (Pδ) replaced with ω promoter (Pω) This work
pDO7212 pUC18 with ω gene promoter (Pω) This work
pHP13 Shuttle vector for E. coli/B. subtilis, with high copy number in E. coli and low copy number in B. subtilis, ColE1 ori/pTA1060 ori Err Cmr 25
pHP1000 pHP13 with δ and ω genes This work
pHP1340 pHP13 with δ and ω genes, with δ's Walker motif A deleted This work
pHV1436 Shuttle vector for E. coli/B. subtilis, with high copy number in E. coli and low copy number in B. subtilis, ColE1 ori/pTB19 ori Apr Cmr 30
pOSE10 pBT205 with inactivated ω gene with its promoter, Pω, and part of the ɛ gene This work
pOSZ5 pHP13 with inactivated ω gene with its promoter, Pω, and the ɛ and ζ genes This work
pRC1 pDB101 derivative carrying copS with its promoter and the repS and erm genes 14
pRP346-5 pHP13 with δ, ω, ɛ, and part of the ζ gene (pDB101 coordinates 4693 to 7251)b Laboratory collection
pUC18 E. coli general cloning vector, ColE1 ori Apr 51
pUCRC pUC18 with pRC1 fragment encompassing repS, α, and β genes (pDB101 coordinates 20 to 4103)b This work
pUCRS pUCRC derivative with HindIII site in repS gene converted into a StuI site This work
pUHC13 Shuttle vector for E. coli/B. subtilis, with high copy number in E. coli and low copy number in B. subtilis, ColE1 ori/pTB19 ori Apr Cmr This work
pUHC1000 pUHC13 with δ and ω genes This work
pUHC1340 pUHC13 with δ and ω genes, with δ's Walker motif A deleted This work
pUHC1212 pUHC13 with δ gene promoter (Pδ) This work
pUHC3212 pUHC13 with copS gene promoter (PcopS) This work
pUHC7212 pUHC13 with ω gene promoter (Pω) This work
pUSE2 Shuttle vector for E. coli/B. subtilis, with high copy number in E. coli and low copy number in B. subtilis, ColE1 ori/pSM19035 ori Apr Emr This work
pUSE1000 pUSE2 with δ and ω genes This work
pUSE1030 pUSE2 with δ and ω genes, with δ truncated after the 23rd codon This work
pUSE1040 pUSE2 with δ and ω genes, with δ truncated after the 40th codon This work
pUSE1340 pUSE2 with δ and ω genes, with δ's Walker motif A deleted This work
pUSE3000 pUSE2 with δ and ω genes, with δ promoter (Pδ) replaced with copS promoter (PcopS) This work
pUSE7000 pUSE2 with δ and ω genes, with δ promoter (Pδ) replaced with ω promoter (Pω) This work
a

Plasmid construction details are given in the text.

b

pDB101 is a pSM19035 derivative which contains the two long inverted repeats and possesses all functions associated with replication, copy control, stable maintenance, and antibiotic resistance (accession no. X66468).