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. 2015 Nov 25;10(11):e0143898. doi: 10.1371/journal.pone.0143898

Table 1. Bacterial strains and plasmids used in this study.

Strains and plasmids Characteristics Reference
Strains
E. coli DH5a Cloning strain
V. atypica OK5 Wild type [9]
V. parvula PK1910 Wild type This work
V. parvula OK1 Wild type This work
V. atypica OK2 Wild type This work
V. rogosae OK3 Wild type This work
V. dispar OK4 Wild type This work
V. atypica OK6 Wild type This work
V. atypica OK7-1 Wild type This work
V. dispar OK7-2 Wild type This work
V. dispar OK8 Wild type This work
V. dispar OK9 Wild type This work
V. dispar OK10 Wild type This work
V. rogosae OK11 Wild type This work
S. gordonii DL1 Wild type [10]
Δhsa DL1 hsa deletion mutant This work
ΔsrtA DL1 srtA deletion mutant [11]
ΔsspA/B DL1 sspA/B deletion mutant This work
S. gordonii-hsa::luc DL1 hsa promoter luciferase reporter This work
Δhsa-hsa::luc hsa promoter luciferase reporter in hsa mutant This work
Plasmids
pFW5-hsa p-luc Suicide vector pFW5::luc of S. gordonii with hsa promoter region; Specr This work
pAS8741 Plasmid containing the complete hsa gene [12]
pAS8748 Deletion of SR1 and NR2 regions in Hsa [12]
pAS8744 Deletion of SR1 region in Hsa [12]
pAS8746 Deletion of NR2 region in Hsa [12]
pAS8749 Deletion of part of SR2 region in Hsa [12]
pAS8375 Deletion of part of SR2 region in Hsa [12]
pAS8165 Deletion of SR2 region in Hsa [12]
pAS8164 Deletion of SR1 and SR2 regions in Hsa [12]