Skip to main content
. 2018 Sep 17;84(19):e01150-18. doi: 10.1128/AEM.01150-18

TABLE 2.

Primers used in this study

Primer Sequence (5′–3′) Purpose
27F AGAGTTTGATCCTGGCTCAG To amplify the 16S ribosomal RNA gene
1492R TACGGCTACCTTGTTACGACTT
IH-F TAAGAAGGAGATATACATATGTCAGATCAGTTGTGGTCAAAGAGTG Construction of plasmid pET-ipaH
IH-R GTGGTGGTGGTGGTGCTCGAGACCAGCGTTGATGAACGGC
KA-F TATGACCATGATTACGAATTCTTGGGGGAAGGCGCCATA Construction of plasmid pEX-ipaH
KA-R CAGGTCGACTCTAGAGGATCCTCAGTAGCCAGCCGCGGC
KT-F TCCGACCCAGCGGGAGACC Detect integrated sequence in strain YJN-5M
KT-R GCCGTGCGAGTCAGATGGA
CP-F GATAAGCTTGATATCGAATTCCGCGATGAGAAAGCAGAAATG Construction of plasmid pBBR1-ipaH
CP-R CGCTCTAGAACTAGTGGATCCCTAACCAGCGTTGATGAACGG
ipaH-A ATGTCAGATCAGTTGTGGTCAAAGAGTGCTA Amplify ipaH gene
ipaH-B CTAACCAGCGTTGATGAACGGCGAGA
K82A-F CCCGATCACCCTCGCGGTGAATATTGACCTCGTCGGT Amplify mutant gene ipaH-K82A with Lys82 replaced Ala82
K82A-R CAATATTCACCGCGAGGGTGATCGGGACGC
S157A-F GCTGGCGGAGCGTCAGGCGGCGAG Amplify mutant gene ipaH-S157A with Ser157 replaced to Ala157
S157A-R GCCTGACGCTCCGCCAGCCGTGC
S181A-F GATCTCGTTGGTGCGCTGCGGAATCCTGCG Amplify mutant gene ipaH-S181A with Ser181 replaced to Ala181
S181A-R GATTCCGCAGCGCACCAACGAGATCATTCCCGAC