Table 2. EQI decreases malonyl-CoA levels in S. aureus.
Fold-change (EQI vs. DMSO) | p-value | ||
---|---|---|---|
Malonyl-CoA | 0.20 | <0.01 | |
AMP | 0.27 | 0.01 | |
NAD+ | 0.48 | 0.16 | |
ADP | 0.71 | 0.01 | |
ATP | 0.79 | 0.14 | |
GDP | 0.87 | 0.50 | |
NADP+ | 0.91 | 0.62 | |
Adenine | 0.94 | 0.70 | |
Pyruvate | 0.96 | 0.94 | |
Acetyl-CoA | 1.21 | 0.26 | |
Glycerol-3P | 1.31 | 0.20 | |
NADH | 1.37 | 0.70 | |
Glutamate | 1.38 | <0.01 | |
BSSB | 1.42 | 0.21 | |
CoASH | 1.49 | 0.38 | |
Proline | 1.56 | <0.01 | |
Alanine | 1.60 | <0.01 | |
Succinate | 1.67 | <0.01 | |
BSH | 1.70 | <0.01 | |
Glutamine | 1.79 | <0.01 | |
Fumarate | 1.95 | <0.01 | |
GTP | 2.11 | 0.01 | |
NADPH | 3.24 | 0.07 | |
Adenosine | 4.21 | <0.01 | |
Malate | 5.52 | 0.03 | |
Lactate | 7.13 | 0.07 |
S. aureus cultures were treated with EQI (4.36 μM) for 2 h in quintuplicate. Metabolites were quantified by LC-MS. Metabolites were normalized to bacterial concentrations and fold-changes were determined in comparison to DMSO. Significance of fold-change was determined using a two-tailed, unpaired t tests; DMSO vs EQI. Analytes with a p < 0.05 are indicated in red.