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Table 1 Promoters analysed in this study. The promoters (column 1 and 4) were amplified by PCR using the template DNA (column 2) and the primers (column 3) listed in the table.

From: Viral promoters can initiate expression of toxin genes introduced into Escherichia coli

Promoter fragment

Template DNAa

Primer sequenceb

Size of promoter-fragment

P PH: Polyhedrin promoter from baculovirus

pBacPAK8 [29]

PH-1: GCCCGGGCCATCTCGCAAATAAATAAG

PH-2: GTCTAGACAGGGATCCGTATTTATAGG

78 bp

P CMV: Enhancer and immediate early promoter from CMV

pRL-CMV [30]

CMV-1: GCCCGGGGATCTTCAATATTGGCCATTAGCC

CMV-2: GTCTAGACACTGACTGCGTTAGCAATTTAAC

802 bp

P SV40: Early promoter from SV40

pGL3 [31]

SV40-1: GCCCGGGCTAGCCCGGGCTCGAGATCTG

SV40-2: GTCTAGATTTGCAAAAGCCTAGGCCTCC

223 bp

P TK Thymidine kinase promoter from HSV1

pRL-TK [32]

TK-1: GCCCGGGATCTAAATGAGTCTTCGGACCTCGC

TK-2: TCTAGACGAGACTGTTGTGTCAGAAGAATCAAGC

788 bp

P LTR HIV-1 subtype D 5'LTR promoter

isolate 92UG021

LTR-1: GGCCCGGGATTAGATATCCACTGACCTTTGGATGGTGC

LTR-2: GGTCTAGATTAAGCAGTGGGTTCCCTAGCTAGCC

412 bp

P NPTIII: nptIII promoter

pBin19 [33, 34]

NPTIII-S: GCGCCCGGGCATAATTGTGGTTTCAAAATCGGC

NPTIII-AS: GGGTCTAGATTATTATTTCCTTCCTCTTTTC

193 bp

P BLA: TEM-1 promoter

pKK232-8 [26, 35]

Amp-S: GCGCCCGGGCGTCAGGTGGCACTTTTCG

Amp-AS: GGGTCTAGAACTCTTCCTTTTTCAATATTATTG

134 bp

  1. apBacPAK8 was from Clontech (Palo Alto, CA, USA), pRL-CMV, pGL3 and pRL-TK were from Promega (Madison, WI, USA). The 5'LTR promoter sequence was kindly provided by S. Somogyi.
  2. bRestriction sites added to the primers for cloning purposes are italicised.