The influence of Fe(II) on the dissimilatory bacterialreduction of an Fe(III) aqueous complex (Fe(III)-citrate
aq)was investigated using
Shewanella putrefaciens strainCN32. The sorption of Fe(II) on CN32 followed a Langmuirisotherm. Least-squares fitting gave a maximum sorptioncapacity of
Qmax = 4.19 × 10
-3 mol/10
12 cells (1.19 mmol/m
2 of cell surface area) and an affinity coefficient of log
K = 3.29. The growth yield of CN32 with respect toFe(III)
aq reduction showed a linear trend with an averagevalue of 5.24 (±0.12) × 10
9 cells/mmol of Fe(III). Thereduction of Fe(III)
aq by CN32 was described by Monodkinetics with respect to the electron acceptor concentration,Fe(III)
aq, with a half-saturation constant (
Ks) of 29 (±3)mM and maximum growth rate (
max) of 0.32 (±0.02) h
-1.However, the pretreatment of CN32 with Fe(II)
aq significantlyinhibited the reduction of Fe(III)
aq, resulting in a lagphase of about 3-30 h depending on initial cell concentrations.Lower initial cell concentration led to longer lag phaseduration, and higher cell concentration led to a shorter one.Transmission electron microscopy and energy dispersivespectroscopy revealed that many cells carried surfaceprecipitates of Fe mineral phases (valence unspecified)during the lag phase. These precipitates disappeared afterthe cells recovered from the lag phase. The cell inhibitionand recovery mechanisms from Fe(II)-induced mineralprecipitation were not identified by this study, but severalalternatives were discussed. A modified Monod modelincorporating a lag phase, Fe(II) adsorption, and aqueouscomplexation reactions was able to describe theexperimental results of microbial Fe(III)
aq reduction andcell growth when cells were pretreated with Fe(II)
aq.