R. Mazoy et Ml. Lemos, FERRIC-REDUCTASE ACTIVITIES IN WHOLE CELLS AND CELL-FRACTIONS OF VIBRIO (LISTONELLA) ANGUILLARUM, Microbiology, 142, 1996, pp. 3187-3193
The ability of Vibrio (Listonella) anguillarum strains from serotype g
roups O1 and O2 to reduce Fe3+ in the form of different chelates was i
nvestigated. All strains, grown in Mg minimal medium supplemented with
0.2 % Casamino acids, reduced Fe3+ complexed by citrate, nitrilotriac
etic acid and EDTA. In whole cells, the degree of reduction was depend
ent on the Fe3+ ligand and on the strain. with the greatest values cor
responding to ferric dicitrate and serotype group O1 strains, respecti
vely. The ferric-reductase activity increased, over the basal levels,
when the cells were grown with iron added as ferric dicitrate, haemin
oi haemoglobin. All strains also reduced ferricyanide, a compound that
is not transported into the bacterial cells. Ferricyanide reduction w
as also increased when the cells were grown in the presence of an iron
source. All of the cell fractions (periplasm, membranes and cytoplasm
) showed Fe3+-reducing activity, with the highest values observed in t
he presence of Mg2+, NADH and FAD in the assay buffer. Cytoplasmic fer
ric-reductase could be visualized using native polyacrylamide or starc
h gel electrophoresis. whereas the periplasmic and membrane reductase(
s) could only be detected on starch gels. The results indicate the pre
sence of different ferric-reductase activities in V. anguillarum, whic
h could be involved in the different iron-acquisition systems present
in this micro-organism, i.e. siderophore-mediated systems and sideroph
ore-independent mechanisms.