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. Author manuscript; available in PMC: 2020 Apr 1.
Published in final edited form as: Mol Microbiol. 2019 Feb 17;111(4):1039–1056. doi: 10.1111/mmi.14207

Table 1:

Strains and Plasmids used in this study.

Strains or plasmids Genotype/description Source/Reference

E.coli

DH5α E. coli DH5α for cloning Novagen
BL21 E. coli for protein expression Novagen
ALC8856 E. coli BL21 with pET14a-6x-His-YpdA This study
ALC8857 E. coli BL21 with pET14a-6x-His-YpdA-G10A This study

S. aureus

RN4220 Restriction minus NCTC8325-4 (Kreiswirth et al., 1983)
ALC7446 SH1000 corrected for BSH production (Posada et al., 2014)
ALC8254 ΔypdA::kan, ALC7446 with ypdA replaced by kanamycin cassette This study
ALC8638 ΔypdA::Δkan::ypdA, ALC8254 chromosomally complemented with ypdA This study
ALC8858 ALC7446 containing pALC8858 (promoter of ypdA driving venus) This study
ALC8859 ALC7446 containing pALC7925 (empty vector) This study
ALC8860 ALC7446 containing pALC7926 This study

Plasmids

pET14b E. coli expression vector Novagen
pMAD E. coli/S. aureus shuttle plasmid with the ori pE194ts; bgaB Ampr Ermr (Arnaud et al., 2004)
pSK236 Shuttle vector containing pUC19 cloned into the HindIII site of pC194 (Gaskill and Khan, 1988)
pALC7925 pALC2073 derivative with improved −10 binding site as described by Corrigan and Foster This study, (Bateman et al., 2001; Corrigan and Foster, 2009)
pALC7926 pALC7925 with ypdA for overexpression (pALC7925::ypdA) This study
pALC8858 pSK236 with promoter of ypdA driving venus This study