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. 2009 Jul 31;191(19):6012–6019. doi: 10.1128/JB.00604-09

TABLE 2.

Bacillus subtilis plasmids and oligonucleotides

Plasmid Oligonucleotidea Sequenceb Vector
pDPV220 DLP179 CGGAATTCCACCATATTAAAAATATCAGC pMUTIN4
DLP180 CGGGATCCTCCCGCAGTATAAAGCGAGGC pMUTIN4
pDPV221 DLP175 CGGAATTCAATCCTAAGTTTCATGAAAGC pMUTIN4
DLP176 CGGGATCCGAAATCAGCACAGCCATGTCC pMUTIN4
pDPV222 DLP177 CGGAATTCAAAGGGGATTATGAGACAAGC pMUTIN4
DLP178 CGGGATCCACTCAATAGAAAGATGATGCG pMUTIN4
pDPV283 DLP311 GCTCTAGAAGTCTGAAAAAGAGTTGC pBKJ236
DLP312 CTTCAATTCGCGGGGATCCCACAAATCGATTCATGATG pBKJ236
DLP313 GAATCGATTTGTGGGATCCCCGCGAATTGAAGGATG pBKJ236
DLP314 GAACTGCAGGTGATGATATGATACTCC pBKJ236
pDPV337 DLP307 GCTCTAGAAGTGCTGATTTGTGATCG pBKJ236
DLP308 CCATTTTGTTCGGATCCTATTGAATCGTCCATCC pBKJ236
DLP309 GGACGATTCAATAGGATCCGAACAAAATGGCGGGTAA pBKJ236
DLP310 GAACTGCAGGAAGCCGTCATTTGGTCG pBKJ236
pDPV338 DLP315 GCTCTAGACTTCCTTCAATTGAATGC pBKJ236
DLP316 CTGCATGTCTGCCGGATCCCAGTTTGCTTGACATGTTTC pBKJ236
DLP317 GTCAAGCAAACTGGGATCCGGCAGACATGCAGGCTG pBKJ236
DLP318 GAACTGCAGATCTGTGATTTTAAATGG pBKJ236
pDPV411 DLP468 GCGCTTAATTAAATGGTGATGAAGAAACATGTC pSWEET-bgaB
DLP469 GCGCGGATCCTCATCAGCCTGCATGTCTGCC pSWEET-bgaB
pDPV412 DLP466 GCGCTTAATTAAGGGAAGGAGCTTTTGGATGG pSWEET-bgaB
DLP467 GCGCGGATCCCGACGACTGTAATTTTACCC pSWEET-bgaB
a

The two or four oligonucleotides listed for each plasmid were used to perform PCR as described in Materials and Methods to produce fragments that were cloned into the indicated vector.

b

Underlined sequences indicate restriction sites used to clone PCR products to the indicated vector. Bold sequences indicate the BamHI sites inserted within in-frame deletion sites.