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. 2007 May 18;189(14):4975–4983. doi: 10.1128/JB.00207-07

TABLE 2.

Oligonucleotide primers used in this study

Primer 5′-to-3′ sequence (restriction site) Description Construct
PBP2-NTerm1 CTTTAAGAAGGAGATATACATATGCCGCAG (NdeI) Amplification of n-PB of P. aeruginosa PBP 2 pACBL17
PBP2-NTerm2 CCCGAAGCTTGCTCAGGACGATGTC (HindIII) Amplification of n-PB of P. aeruginosa PBP 2 pACBL17
EcPBP2-5 CCCGAAAACGCAGCATATGAAACTACAGAACTC (NdeI) Amplification of E. coli pbpA pACBL18
EcPBP2-2 CCGTCAAAGCTTATGGTCCTCCGCTG (HindIII) Amplification of E. coli pbpA pACBL18
EcPBP2-SA-SDM1 TCCTCCCGCGGCTACAGTTAAAC SDM of Ser→330Ala on E. coli pbpA pACBL19
EcPBP2-SA-SDM2 GTTTAACTGTAGCCGCGGGAGGA SDM of Ser→330Ala on E. coli pbpA pACBL19
EcPBP2-1 GAAAACGCAGCATATGAAACTACAGAACTC (NdeI) Amplification of n-PB of E. coli PBP 2 pACBL24
EcPBP2nPB-1 GAGTTTGAGAAGCTTCGTCAGGTAAATATC (HindIII) Amplification of n-PB of E. coli PBP 2 pACBL24
PaPBP3-1 GGTGGCCATATGAAACTGAATTATTTCCAGG (NdeI) Amplification of P. aeruginosa ftsI (pbpB) pACSR1
PaPBP3-2 GGCCCTCGAGGCCACGCCCTCC (XhoI) Amplification of P. aeruginosa ftsI (pbpB) pACSR1