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Table 1 Sequences of primers used in quantitative real time PCR (qPCR) transcriptional analysis, with sizes of amplified fragments and annealing temperatures

From: Transcriptional analysis of genes related to biofilm formation, stress-response, and virulence in Listeria monocytogenes strains grown at different temperatures

Gene

Nucleotide sequence

Amplicon size (bp)

Annealing temperature (°C)

agrA

5′ CGGGTACTTGCCTGTATGAA 3′

149

58.65

5′ TGAATAGTTGGCGCTGTCTC 3′

59.03

degU

5′ GGCGCGTATATTCATCCAC 3′

150

58.96

5′ TACCTCGCACTCTCTATGCG 3′

59.20

luxS

5′ CATTTGATGGCAGAACTTGC 3′

127

59.28

5′ TGATTTCGAGTGCATCATCA 3′

58.73

prfA

5′ GGAAGCTTGGCTCTATTTGC 3′

145

59.07

5′ ACAGCTGAGCTATGTGCGAT 3′

58.65

hly

5′ AGCTCATTTCACATCGTCCA 3′

124

59.24

5′ TGGTAAGTTCCGGTCATCAA 3′

58.97

actA

5′ AGAAATCATCCGGGAAACAG 3′

147

58.98

5′ CCTCTCCCGTTCAACTCTTC 3′

58.87

flaA

5′ GTAAGCATCCAAGCGTCTGA 3′

148

59.03

5′ AAGAATCAGCATCAGCAACG 3′

59.03

sigB

5′ TGGTGTCACGGAAGAAGAAG 3′

135

58.85

5′ TCCGTACCACCAACAACATC 3′

59.27

ltrC

5′ TACGGCGTCGATGAGATACT 3′

144

58.35

5′ GAATGTGTGAACGGCGATAC 3′

59.01

sufS

5′ GAATTTGGCGGAGAAATGAT 3′

137

58.98

5′ TCTGCCAAGTAATCAATCGC 3′

58.87

sufU

5′ TTCAGAAATGGTGCAAGGTC 3′

135

58.70

5′ ATCGCTCTCTCCATTGCTTT 3′

59.03