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. 2009 Oct 16;75(24):7838–7849. doi: 10.1128/AEM.01603-09

TABLE 2.

Primers used in this study

Name Sequence (5′-3′)a Use
PPK1 F ATAAAAGGTACCATTTAGCCATAAAACTCCCG Amplification of 81-176 ppk1 region
PPK1 R AAAAAACTGCAGGCGATAGGTTTGAACCTTTA
PPK1 INV F ATAAAAGGATCCTACAGATCAAAGTCGTGCAA Amplification of pDG1 except ppk1
PPK1 INV R AAAAAAGGATCCGAACATTGGTCTAAAACACG
PPK1 COMP F AAATAACTGCAGGTCCTAAACCACTTTGCGCT Amplification of ppk1 gene for complementation
PPK1 COMP R AAATAAGGTACCCCTCGCTTCCACCAGTTTTA
CsrA F TTATCGGAGAAGGTATAG Real-time quantitative PCR amplification of cDNA from ppk2, csrA, spoT, phosR, cmeC, pstS, pstC, and CJJ81176_0750 from 81-176 strain
CsrA R TTTCTAAGTATCATAAGGG
SpoT F GTAACCACTCGCACAATATC
SpoT R GATGTCGCAGTTTATTCTCC
PhosR F GCAAACATAATCATCACAACCAC
PhosR R GAGAGCAAGGATACAAAGAAGC
CmeC F GCTGCTGCTCAATTAGGTATAG
CmeC R GCTTCATAATCATACTCACTTGC
PstS F CCTTATACAAACTGGAATCAAATC
PstS R GACACATCACTCATTACAAGC
PstC F CGCTTATGCTTTAGGTATGAC
PstC R GCTGCCATCACCACTATC
CJJ81176_0750 F GGTCTTGTTGCCTTATTG
CJJ81176_0750 R GTATCGCTATGTTCTATGC
PPK2 F ATCTAATACTCCAACTTGTC
PPK2 R TTCTTCTTCTCCACTACG
a

Underlining indicates restriction sites added to the 5′ end of each primer.