TABLE 1.
Summary of growth yields for S. oneidensis strain MR-1 utilizing a variety of electron acceptors after 70 h in culturea
| Culture treatment | Concn of total cell carbon (μg liter−1) | Concn of e-reduced (mM)b | Growth (107 cells ml−1) | Growth per cell (10−14 g of C cell−1) | Yield (g of C mol of e−−1) |
|---|---|---|---|---|---|
| FeOOH | 1,600 ± 209 | 10.2 | 12.6 ± 0.3 | 1.3 | 0.169 |
| FeOOH + AQDS | 1,744 ± 244 | 24.0 | 14.7 ± 0.3 | 1.2 | 0.073 |
| Smectitec | 2.8 | 9.0 ± 0.4 | |||
| Smectite + AQDSc | 4.0 | 12.0 ± 0.3 | |||
| Fe(III) citrate | 10,885 ± 1,293 | 48.6 | 16.5 ± 0.7 | 6.6 | 0.198 |
| O2 | 25,490 ± 3,062 | 20.0 | 14.8 ± 0.2 | 17.2 | 1.29 |
Each value is the mean ± 1 standard deviation or the average from the same triplicate cultures per treatment presented in Fig. 2.
Average concentration of electron acceptor reduced measured in triplicate cultures. Oxygen utilization was calculated from the stoichiometry presented in Table 2, assuming complete utilization of the lactate added.
It was not possible to resolve cell carbon or yield in smectite cultures due to the presence of background carbon impurities.