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. 2018 Mar 13;8(19):10284–10293. doi: 10.1039/c7ra11823f

Minimum inhibitory concentrations of COE1-3C, COE1-3Py and daptomycin.

Strain Description Growth conditions MIC
COE1-3C COE1-3Py Daptomycin
E. faecalis OG1RF Wild type BHI 2 μM 1 μM 1.23 μM
EFC3Ca COE1-3C resistant BHI 8 μM 1 μM 9.87 μM
EFC3Pyb COE1-3Py resistant BHI 8 μM 16 μM 9.87 μM
DAP 21c Daptomycin resistant BHI 2 μM 1 μM 78.96 μM
DAP 22d Daptomycin resistant BHI 2 μM 1 μM 78.96 μM
E. faecalis OG1RF Wild type BHI + palmitic acid C16:0 (10 μg mL−1) 2 μM 1 μM ND
E. faecalis OG1RF Wild type BHI + cis-vaccenic acid C18:1 ω7c (10 μg mL−1) 8 μM 2 μM ND
E. faecalis OG1RF Wild type BHI + cis-9,10-methyleneoctadecanoic acid C19:0 cyclo ω8c (12.5 μg mL−1) 8 μM 4 μM ND
a

COE1-3C resistant strains with in frame deletion in liaF at position 179 and a substitution in the intergenic region between treB (PTS family trehalose porter, IIBC component) and gloA6 (lactoylglutathione lyase).

b

COE1-3Py resistant strains with a non-synonymous substitution at position 97 in the liaR gene.

c

DAP21 strains have mutations in cardiolipin synthase 1 (cls1; RF10364), a gene encoding a putative chaperone protein regulated by the liaFSR operon (RF11464) and hypothetical membrane protein (RF11507).21

d

DAP22 strains have mutations in gene encoding a putative chaperone protein regulated by the liaFSR operon (RF11464) and hypothetical membrane protein (RF11507) along with mutations in cardiolipin synthase 2 (cls2; RF11324) and a putative metal-dependent HD-domain-containing hydrolase (RF11901).21 ND – not determined.