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. 2010 Apr 23;76(12):3978–3988. doi: 10.1128/AEM.00493-10

TABLE 2.

Oligonucleotides used in this study

Name Sequencea Purpose
LuxpXen5F 5′ ATAAAAGAATTCGACTCCTGTGAAATGATC Amplification of the lux operon and kanamycin gene from pXen5
LuxpXen5R 5′ AAAAAACTCGACCGGATGTACTTCAGAAAAGA
pKGT1F 5′ AAAAAAGCGGCCGCATCACGCCGCTAGAGCTT Inverse PCR amplification of pKGT452Cβ to clone lux operon from pXen5
pKGT1R 5′ AAAAAACTCGAGTCAGAGAAGGTGAGGGCCTC
KanF 5′ GAAGCGTTTGATAGTTAAGT For confirmation of EZ::TN<lux-kan> integration into chromosome
KanR 5′ GGTACTAAAACAATTCATCC
LuxpXen5F2 5′ ATAAAAGCGGCCGCGAAACAGCTATGACCATGAT Amplification of the lux operon from pXen5
LuxpXen5R2 5′ AAAAAACTCGAGTTATTATTTCCCTCCTCGAC
pKGT2F 5′ AAAAAACTCGAGATCACGCCGCTAGAGCTTGG Inverse PCR amplification of pKGT452Cβ to clone lux operon from pXen13
pKGT2R 5′ AAAAAGCGGCCGCTCAGACAAGGTGAGGGCCTC
CmxF 5′ AGAGTACTGCCGACGCCGA Confirmation of Tn1409-lux integration into chromosome
CmxR 5′ ACTGTCGATCCTGCTCTCCG
LuxCF 5′ GTTGATGAATATCCACCTCT Confirmation of Tn1409-lux integration into chromosome
LuxCR 5′ GGACATACATTCGTGACTTA
Xu3F 5′ GGATTTGTCGGGGTGTTTCG Mapping of insertion site of Tn1409-lux in C. michiganensis subsp. michiganensis genome
Xu3R 5′ CGGCCCCACAGAAGCAATTA
a

Restriction sites added to the 5′ end of each primer are underlined.