Le. Hersman et al., Siderophore production and iron reduction by Pseudomonas mendocina in response to iron deprivation, GEOMICROB J, 17(4), 2000, pp. 261-273
In aerobic environments microorganisms are faced with a discrepancy of simi
lar to 10 orders of magnitude between the available Fe (similar to 10(-17)
M) and their metabolic requirement for it (similar to 10(-7) M). In contras
t to facultative anaerobic environments, where dissimilatory iron-reducing
bacteria (DIRB) are often abundant, few studies have detailed microbial int
eractions with Fe(III) (hydr) oxides in aerobic environments. To better und
erstand acquisition of Fe from Fe(III) (hydr)oxides, we investigated the pr
oduction of siderophore and Fe(III) reduction by a strict aerobe in the pre
sence of synthetic hematite as a source of Fe. Pseudomonas mendocina grew b
est when Fe was supplied as FeEDTA (similar to1.8 x 10(8) colony-forming un
its [CFU] ml(-1)), grew abundantly when Fe was supplied as hematite (simila
r to1.2 x 10(8) CFU ml(-1)), and grew poorly when Fe was withheld from the
medium (similar to5.5 x 10(7) CFU ml(-1)). As expected, negligible sideroph
ore was produced per cell when Fe was supplied as FeEDTA and more sideropho
re was produced in the hematite flasks than in the controls. Thus, growth o
f P. mendocina and the production of siderophore in the presence of hematit
e present compelling evidence that siderophore was produced as a mechanism
to acquire Fe from hematite. For the Fe reduction experiments, Fe reduction
by components of the supernatant fluid was induced weakly when Fe was supp
lied as hematite or as FeEDTA, but much more when the cells were cultured u
nder extreme Fe deprivation. In fact, 16 times as much Fe reduction occurre
d in the controls as in the presence of either of the FeEDTA or hematite am
endments. Our results, which contravene the long-held assumptions that Fe a
cquisition was facilitated solely by siderophores, provides a new perspecti
ve regarding microbial interactions with Fe-bearing minerals.