Skip to main content
. 2021 Jan 27;6(1):e01321-20. doi: 10.1128/mSphere.01321-20

TABLE 1.

Plasmids used in this study

Plasmid Description Resistance phenotypea Reference
pRMH977 IS26 in pUC19 Ap 6
pRMH1011 IS1006 in pUC19b,c Ap This study
pRMH1012 IS1008 in pUC19c,d Ap This study
pRMH1013 IS1006/1008 in pUC19c,e Ap This study
pRMH1015 IS26 with internal catA1 gene in pUC19c,f Ap Cm C. J. Harmer and R. M. Hall, submitted for publication
pRMH762 IS26 in pUC19 Ap 6
pRMH962 IS26-FS-L in pUC19 Ap 6
R388 IncW plasmid Su Tp 22
R388::IS26 IS26 in R388 Su Tp 6
R388::IS26-2 IS26 in R388g Su Tp This study
R388::IS26-FS-R R388::IS26 frameshift mutant Su Tp 6
R388::IS1006 IS1006 in R388b,g Su Tp This study
R388::IS1008 IS1008 in R388d,g Su Tp This study
R388::IS1006/1008 IS1006/1008 in R388e,g Su Tp This study
a

Ap, ampicillin; Su, sulfamethoxazole; Tp, trimethoprim.

b

Bases 39531 to 40583 from pD36-4 (GenBank accession no. CP012956).

c

Insert cloned into the pUC19 BamHI site by Gibson assembly.

d

Bases 88655 to 90375 from pA297-3 (GenBank accession no. KU744946).

e

Bases 42241 to 43233 from pJ9-3 (GenBank accession no. CP041590).

f

Synthetic construct, equivalent to pRMH977, with bases 133211 to 133909 of pRMH760 (GenBank accession no. KF976462) containing the catA1 gene and its natural promoter inserted between bases 775 and 776 of IS26.

g

Insert cloned between the two R388 HindIII sites by Gibson assembly.