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Table 5 Primers used in this study

From: Chromosomal evolution of Escherichia coli for the efficient production of lycopene

Primers

Sequence and purposea

BLP1

5′- ATCGCCTGTATGAACCTG -3′, Diagnostic PCR in attPP21 integration

BLP4

5′- TAGAACTACCACCTGACC -3′, Diagnostic PCR in attPP21 integration

AHP2

5′- ACACTTAACGGCTGACATGG -3′, Diagnostic PCR in attPP21 integration

AHP3

5′- AACGAGTATCGAGATGGCAC -3′, Diagnostic PCR in attPP21 integration

CGA

5′- TCAAGAATCTGGTGACCGAGGAG -3′, Diagnostic PCR in attPP21 integration

CGB

5′- ACGCCGCTTCAATGACGCTG -3′, Diagnostic PCR in attPP21 integration

VCA1

GTCGTCAGGCTACTGCGTATG. Diagnostic PCR in recA deletion

VCA2

CACGATCCAACAGGCGAG. Diagnostic PCR in recA deletion

NDF

5′- TGGTAATAATGGCTTCGTCTG -3′, qPCR for the minD gene

NDR

5′- GCGATAAAGATGCCCTCAC -3′, qPCR for the minD gene

QCF

5′- CCAGGAGGGATATTTGC -3′, qPCR for the crtI gene

QCR

5′- CAGGGAGTGGAACGAGAAG -3′, qPCR for the crtI gene

wrbAR

5′- CGGTCGACGCGTATCCTCCTGTTGAAGATTAG CCGTT -3′

yedeOF

5′- GCGTCGACAGGAGAGATAAAATGTCGCTCGT TTGTTCT -3′

ydeOR

5′- GGTCTCTGCAGTCAAATAGCTAAAGCATTCATCGT -3′

atpEF

5′- GAGAGCTCAGGAGGACTGTCATGGAAAACCTGAAT -3′

atpER

5′- CGGGGTACCTAAATAAAAGCAACGCTTACTACGC -3′

dxsF

5′-CTGGGATCCAGGAGATCCGCTATGGATCTTTTATCAATACAGGAC-3′

dxsR

5′- CCGGGTACCGCTGTCATGATCCAATTCCTTTATGT -3′

idiF

5′-GAGGTACCAGGAGTTGTTCGATGTCCAACAATG-3′

idiR

5′-GGCTCTAGATTATTTAAGCTGGGTAAATGCAG-3′

appYF

5′-GCCTGCAGAGGAGGTGCAAGATGGATTATGT-3′

appYR

5′-CCGCATGCTTATCAGTCAATTGTTTTG-3′

pckF

5′-GGAATTCTCAATGCGCGTTAACAATGGTT-3′

pckR

5′-CTCCCATGGTTACAGTTTCGGACCAGCC-3′

ppsF

5′-GAGGTACCAGGAGTTGTTCGATGTCCAACAATG-3′

ppsR

5′-CGTCCCGGGTTATTTCTTCAGTTCAGCCAGG-3′

rpoSF

5′-GCCTCTAGAAGGAGCCACCTTATGAGTCAGAATAC-3′

rpoSR

5′-GGTCGACTTACTCGCGGAACAGCGCTT-3′

ycgWF

5′-CGGCATGCAGGAGATAACAAATGAAGTGGATAGT-3′

ycgWR

5′-GCCAAGCTTTAGCATATCGAGCATATTT-3′

yjiDF

5′-GGTCGACAGGAGGCGCAAAATGATGCGACAAT-3′

YJIDR

5′-GGCTGCAGTTAGCTGACATTCTCCAGCG-3′

APFP

5′- CTCCGTATAGAGTTCCATCGT -3′, Diagnostic PCR in the replacement of appY promoter

APRP

5′- GCCACATTTCTGGGCTACGAC -3′, Diagnostic PCR in the replacement of appY promoter

IKFP

5′- TGTTTATCAAGAGTGTCTGAGCGT -3′, Diagnostic PCR in the deletion of the iclR gene

IKRP

5′- CGTTTTCACCGCAAATACCG -3′, Diagnostic PCR in the deletion of the iclR gene

  1. a Restriction enzyme sites are underlined.