Affiliation:
1. Department of Microbiology, University of Mississippi School of Medicine, Jackson, Mississippi 39216
Abstract
The fate of the hydroxamic acid-iron transport cofactors during iron uptake from the
59
Fe
3+
chelates of the
3
H-labeled hydroxamates schizokinen and aerobactin was studied by assay of simultaneous incorporation of both
59
Fe
3+
and
3
H. In the schizokinen-producing organism
Bacillus megaterium
ATCC 19213 transport of
59
Fe
3+
from the
3
H-schizokinen-
59
Fe
3+
chelate at 37 C was accompanied by rapid uptake and release (within 2 min) of
3
H-schizokinen, although
3
H-schizokinen discharge was temperature-dependent and did not occur at 0 C. In the schizokinen-requiring strain
B. megaterium
SK11 similar release of
3
H-schizokinen occurred only at elevated concentrations of the double-labeled chelate; at lower chelate concentrations,
3
H-schizokinen remained cell-associated. Temperature-dependent uptake of deferri (iron-free)
3
H-schizokinen to levels equivalent to those incorporated from the chelate form was noted in strain SK11, but strain ATCC 19213 showed only temperature-independent binding of low concentrations of deferri
3
H-schizokinen. These results indicate an initial temperature-independent binding of the ferric hydroxamate which is followed rapidly by temperature-dependent transport of the chelate into the cell and an enzyme catalyzed separation of iron from the chelate. The resulting deferri hydroxamate is discharged from the cell only when a characteristic intracellular concentration of the hydroxamate is exceeded, which happens in the schizokinen-requiring strain only at elevated concentrations of the chelate. This strain also appears to draw the deferri hydroxamate into the cell by a temperature-dependent mechanism. The aerobactin-producing organism
Aerobacter aerogenes
62-1 also demonstrated rapid initial uptake and temperature-dependent discharge of
3
H-aerobactin during iron transport from
3
H-aerobactin-
59
Fe
3+
, suggesting a similar ferric hydroxamate transport system in this organism.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
44 articles.
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