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. 2018 Apr 26;62(5):e02318-17. doi: 10.1128/AAC.02318-17

TABLE 1.

Genes and primers used for qPCR in this study

Gene Primer sequence (5′–3′)
Forward primer
Reverse primer
Product size (bp) Reference
Forward Reverse BPa GCb TMc BP GC TM
lasI TGTTCAAGGAGCGCAAAGG ATGGCGAAACGGCTGAGTT 19 52.6 62.4 19 52.6 63 244 58
lasR AGCGACCTTGGATTCTCGAAG CGAAGAACTCGTGCTGCTTTC 21 52.4 63 21 52.4 62.5 226 58
rhlI TGCTCTCTGAATCGCTGGAA GTTTGCGGATGGTCGAACTG 20 50 59.1 20 55 59.83 154 58
rhlR TTGCTGAGCGTGCTTTCC AGGATGATGGCGATTTCCC 19 52.6 62.6 19 52.6 62.1 228 58
rpsLd CCTCGTACATCGGTGGTGAAG CCCTGCTTACGGTCTTTGACAC 21 57.1 62.8 22 54.5 63.1 148 59
proDd GGGCGAAGAAGGAAATGGTC CAGGTGGCGTAGGTAGAGAA 20 55 63.1 20 55 58 178 60
a

BP, primer length (base pairs).

b

GC, G-C content of primer.

c

TM, melting temperature of primer.

d

Reference/endogenous control gene.