TABLE 1.
Category | Value (mol × 1017 cells−1) for: |
||||||
---|---|---|---|---|---|---|---|
Intracellular R.S.C.a | Hydrogen excreted | Acetate excreted | Lactate excreted | Alanine excreted | CO2 excretedc | Excess equivalents excretedd | |
WT cells (measured) | 31 ± 14 | 2.9 ± 0.3 | 6.5 ± 0.4 | 60 ± 7 | 1.8 ± 0.8 | 6.5 | |
nifJ cells (measured) | 26 ± 5 | 2.3 ± 0.2 | 3.0 ± 0.4 | 51 ± 7 | 3.0 ± 1.0 | 3 | |
Carbon equivalents per moleculeb | −6 | 0 | 2 | 3 | 3 | 1 | |
NADH equivalents per moleculeb | −2 | 1 | −1 | 1 | 1 | 0 | |
WT carbon equivalents | −186 | 0 | 13 | 180 | 5.4 | 6.5 | 18.9 |
nifJ carbon equivalents | −156 | 0 | 6 | 153 | 9 | 3 | 15 |
WT NADH equivalents | −62 | 2.9 | −6.5 | 60 | 1.8 | 0 | −3.8 |
nifJ NADH equivalents | −52 | 2.3 | −3 | 51 | 3 | 0 | 1.3 |
R.S.C., reduced sugars catabolized.
Values represent theoretical equivalents of carbon (row 3) and reductant (row 4 [as NADH]) per catabolized glucose equivalent during fermentation.
CO2 values were not directly measured and are set equal to the acetate concentration, since CO2 forms stoichiometrically and concomitantly with acetyl-CoA via the PFOR or PDC reaction (Fig. 1). Additionally, the reductant formed in this reaction is accounted for in the acetate column only to avoid double counting.
Excreted equivalents that were excreted in excess of the carbohydrate catabolized. Based on the systematic error determined for each detection method, the propagated systematic error for this column is ±15 for carbon equivalents (rows 5 and 6) and ±5 for NADH equivalents (rows 7 and 8) based on the systematic error for each detection method.