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. 2005 Jan;71(1):261–269. doi: 10.1128/AEM.71.1.261-269.2005

TABLE 1.

Oligonucleotide primers used for RT-PCR and construction of various mutant strains

Primer Sequence (5′-3′)a Use
CAF1 CGTATTGCCCTAAGCTCGGTTGAA RT-PCR
CAR1 GCGATGCGCTCGATGGCTTT RT-PCR
CAF2 GCGCCCAAGCTGCTGTATGC RT-PCR
CAR2 CGATCTCGGCCAGCAAAAGGTAG RT-PCR
clpF1 GAGCTCGATCTCCGCCACATCCGTCA Upstream flank for construction of mutant strains DC211 and DCA2422; SstI
clpR1 GAATTCGAGCCGGAGACGACATAATAGAGG Upstream flank for construction of mutant strains DC211 and DCA2422; EcoRI
clpF2 GAATTCCGGCCGCGTGCTCAAGAAG Downstream flank for construction of mutant strain DC211; EcoRI
clpR2 CTCGAGGCCCAGCGTCTTGACGAACTTG Downstream flank for construction of mutant strain DC211; SstI
clpF3 GAATTCGCCATACCCGCTACTCGCTGAC Upstream flank for construction of mutant strain DC2422; EcoRI
clpR3 CTCGAGCGCGGCGATCGGACATAAG Downstream flank for construction of mutant strain DC2422; SstI
PIF1 GACGGGCGAGGGCCGCGA Amplification of clp for construction of P1, complementation strain of mutant 5E4
PIR1 GGCGCGTCCCATCGGGGC Amplification of clp for construction of P1, complementation strain of mutant 5E4
a

The underlined sequences are added restriction enzyme sites for the enzymes indicated in the column on the right.