A. Ehrenreich et F. Widdel, ANAEROBIC OXIDATION OF FERROUS IRON BY PURPLE BACTERIA, A NEW-TYPE OFPHOTOTROPHIC METABOLISM, Applied and environmental microbiology, 60(12), 1994, pp. 4517-4526
Anoxic iron-rich sediment samples that had been stored in the light sh
owed development of brown, rusty patches. Subcultures in defined miner
al media with ferrous iron (10 mmol/liter, mostly precipitated as FeCO
3) yielded enrichments of anoxygenic phototrophic bacteria which used
ferrous iron as the sole electron donor for photosynthesis. Two differ
ent types of purple bacteria, represented by strains L7 and SW2, were
isolated which oxidized colorless ferrous iron under anoxic conditions
in the light to brown ferric iron. Strain L7 had rod-shaped, nonmotil
e cells (1.3 by 2 to 3 mu m) which frequently formed gas vesicles. In
addition to ferrous iron, strain L7 used H-2+CO2, acetate, pyruvate, a
nd glucose as substrates for phototrophic growth. Strain SW2 had small
rod-shaped, nonmotile cells (0.5 by 1 to 1.5 mu m). Besides ferrous i
ron, strain SW2 utilized H-2+CO2, monocarboxylic acids, glucose, and f
ructose; Neither strain utilized free sulfide; however, both strains g
rew on black ferrous sulfide (FeS) which was converted to ferric iron
and sulfate. Strains L7 and SW2 grown photoheterotrophically without f
errous iron were purple to brownish red and yellowish brown, respectiv
ely; absorption spectra revealed peaks characteristic of bacteriochlor
ophyll a. The closest phototrophic relatives of strains L7 and SW2 so
far examined on the basis of 16S rRNA sequences were species of the ge
nera Chromatium (gamma subclass of proteobacteria) and Rhodobacter (al
pha subclass), respectively. In mineral medium, the new isolates forme
d 7.6 g of cell dry mass per mol of Fe(II) oxidized, which is in good
agreement with a photoautotrophic utilization of ferrous iron as elect
ron donor for CO2 fixation. Dependence of ferrous iron oxidation on li
ght and CO2 was also demonstrated in dense cell suspensions. In media
containing both ferrous iron and an organic substrate (e.g., acetate,
glucose), strain L7 utilized ferrous iron and the organic compound sim
ultaneously; in contrast, strain SW2 started to oxidize ferrous iron o
nly after consumption of the organic electron donor. Ferrous iron oxid
ation by anoxygenic phototrophs is understandable in terms of energeti
cs. In contrast to the Fe3+/Fe2+ pair (E(0) = +0.77 V) existing in aci
dic solutions, the relevant redox pair at pH 7 in bicarbonate-containi
ng environments, Fe(OH)(3)+HCO3-/FeCO3, has an E(0) of +0.2 V. Ferrous
iron at pH 7 can therefore donate electrons to the photosystem of ano
xygenic phototrophs, which in purple bacteria has a midpoint potential
around +0.45 V. The existence of ferrous iron-oxidizing anoxygenic ph
ototrophs may offer an explanation for the deposition of early banded-
iron formations in an assumed anoxic biosphere in Archean times.