Skip to main content
. 2020 Aug 25;202(18):e00282-20. doi: 10.1128/JB.00282-20

FIG 1.

FIG 1

Overview of the SNAP, phoZ, and gusA reporter constructs. Each reporter was cloned into the C. difficile shuttle plasmid pMTL84151 and placed under transcriptional fusion with a 402-bp region (−399 to +3), including 399 bp directly upstream of hpdBCA, to the hpdB start codon (ATG).