Skip to main content
. 2016 Nov 21;82(24):7052–7062. doi: 10.1128/AEM.01771-16

TABLE 2.

Primers used in this study

Primer DNA sequence (5′ to 3′)a Description
pnr-F GGAATTCCATATGATCAAAACAAACGATTTTATGG Forward primer to amplify pnr with a NdeI site
pnr-R CCGCTCGAGTTTCCATTCTGCAATTGTATCAATC Reverse primer to amplify pnr with a XhoI site
RT-16SF CCAGCATTCAGTTGGGCACTCTAAG Forward primer of quantitative real-time PCR to amplify a 173-bp fragment of 16S rRNA sequence
RT-16SR ACTGAGAACAGATTTGTGGGATTGG Reverse primer of quantitative real-time PCR to amplify a 173-bp fragment of 16S rRNA sequence
RT-PF GCCGCCGTTCTATTCGCAACTATG Forward primer of quantitative real-time PCR to amplify a 113-bp fragment of pnr sequence
RT-PR CCATGGCTGCGCGTTAACAGAAGAT Reverse primer of quantitative real-time PCR to amplify a 113-bp fragment of pnr sequence
a

Underlined sequences refer to the restriction sites.