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. 2014 Jul;196(13):2472–2480. doi: 10.1128/JB.01512-14

TABLE 4.

Metabolite profiles of E. faecalis strains cultured under each conditiona

Strain Carbon source O2 Concn of consumed carbon source (mM) Metabolite concn (mM)
Carbon balance (%)b
AAL Acetate Acetoin Ethanol Formate d-Lactate l-Lactate
W11 Glucose + 50 <0.1 35.1 19.1 <0.1 0.2 0.1 18.5 92
50 <0.1 <0.1 0.3 6.2 11.7 0.1 78.8 88
Δpfl mutant Glucose + 50 <0.1 37.1 15.6 <0.1 0.2 0.1 36.9 105
50 <0.1 0.9 0.2 <0.1 0.2 0.1 90.1 92
W11 Glycerol + 100 <0.1 55.0 12.9 <0.1 0.1 0.2 7.7 89
100 <0.1 <0.1 0.3 61.3 62.1 0.2 33.8 96
Δpfl mutant Glycerol + 100 <0.1 75.2 13.0 1.1 <0.1 0.1 6.6 109
36 <0.1 2.6 0.2 5.4 0.2 0.2 34.3 119
W11 DHA + 100 <0.1 79.8 4.3 <0.1 1.4 1.6 0.3 90
100 <0.1 24.3 0.5 10.7 26.7 1.6 45.6 83
Δpfl mutant DHA + 100 <0.1 78.5 1.9 <0.1 <0.1 1.3 3.6 87
100 <0.1 17.8 0.2 11.6 0.1 1.2 58.8 90
a

E. faecalis strains were cultured in M-MRS broth containing 50 mM glucose, 100 mM glycerol, or 100 mM DHA for 36 h under aerobic (+) and anaerobic (−) conditions. M-MRS broth contains 36 mM acetate, 0.5 mM ethanol, 0.1 mM formate, 0.3 mM d-lactate, and 11.1 mM l-lactate; metabolite concentrations are presented exclusive of these initial amounts. The results are the means of results from three experiments. The standard errors were all <10%. AAL, acetaldehyde.

b

The concentrations of CO2 (mM) generated by the Pdh and AlsS reactions were calculated as follows. CO2 (Pdh) = (AAL [mM] + acetate [mM] + ethanol [mM]) − formate (mM). CO2 (AlsS) = acetoin (mM).