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. 2018 Mar 19;84(7):e02762-17. doi: 10.1128/AEM.02762-17

TABLE 2.

Oligonucleotides used in this study

Oligonucleotide name Sequence (5′–3′)a Function
ndvBp-F-2b cttctcctttactcatatgtatatctccttcAGAGATGAAACCAGGTTCCGG PndvB-gfp fusion
ndvBp-R-2b caaaaacgcgtaacaaaagtgtctataatcaACCCGGCAGGCCGGGTTG PndvB-gfp fusion
AH-GFP-Tag-Fb tcatccgccaaaacagccaagcttgcatgcctgcagactagtGGAGTCCAAGCTCAGCTAATTAAGC GFP stability tag
AH-GFP-Tag-Rb acagctgctgggattacacatggcatggatgaactatacaaaAGGCCTGCAGCAAACGACGAA GFP stability tag
rpoSdel1 ATCCATGGATCCTAGTCTGATCGGCCGTTTTG rpoS deletion
rpoSdel2 ATCATCGTGGTCAAACTCCG rpoS deletion
rpoSdel3 CGGAGTTTGACCACGATGATGACAAGCAGCGTGAGGTGGT rpoS deletion
rpoSdel4 ATCCATCTGCAGTGCCAGAAAACCCAGCGAAG rpoS deletion
rpoScompF AATAATGGTACCCTGCGAGCGGTAGTCTGATC rpoS complementation
rpoScompR CATCATAAGCTTATCTACTTAGGCTCACACGC rpoS complementation
ndvBp-lacZ for ATCCATCTGCAGGGACTAGACTTGCAACAGAC PndvB-lacZ fusion
ndvBp-mut-lacZ forc ATCCATCTGCAGGGAAGAGACTTGCAACAGAC Mutant PndvB-lacZ fusion
ndvBp-lacZ rev ATCCATAAGCTTAGAGATGAAACCAGGTTCCG PndvB-lacZ fusion
Tn7R CACAGCATAACTGGACTGATTTC Tn7 insertion verification
glmS-down GCACATCGGCGACGTGCTCTC Tn7 insertion verification
ndvB-F ACAAGGGCTTCTTCCACATC ndvB qPCR
ndvB-R TCTTCGGTGATGCACCATTC ndvB qPCR
rpoD-F TCCATCGCCAAGAAGTACAC rpoD qPCR
rpoD-R TTGTAGCCACGACGGTATTC rpoD qPCR
rpoS-F CGAACCTTCACCCGAAGAAA rpoS qPCR
rpoS-R AAGAGAGACGTCTACCGAAGT rpoS qPCR
gfp-gsp1 AGCACGTGTCTTGTAGTTCC 5′ RACE
gfp-gsp2 ATCTGGGTATCTCGCAAAGC 5′ RACE
gfp-gsp3 CTACAGGATCCGAAAGTAGTGACAAGTGTTGG 5′ RACE
3′ RACE adapter primer GGCCACGCGTCGACTAGTAC(T)17 5′ RACE
AUAP GGCCACGCGTCGACTAGTAC 5′ RACE
M13R TCACACAGGAAACAGCTATGAC Sequencing
a

Restriction sites are indicated in bold.

b

Primer used for yeast-recombination cloning. Uppercase in the sequence indicates sequences targeted for PCR amplification. Lowercase in the sequence indicates sequences homologous to the vector used for recombination.

c

Primer contains two changes (underlined) to the predicted ndvB promoter element.