Unlike the great majority of the aerobactin-producing enteric bacteria documented in the literature, Enterobacter cloacae EK33, isolated from a case of human neonatal meningitis, did not show any homology at the DNA level with the prototype aerobactin system encoded by the ColV-K30 plasmid. However, both the nuclear magnetic resonance spectrum and fast-atom bombardment mass spectrometry of the siderophore purified from EK33 confirmed its identity with aerobactin. Bioassay screening of a gene library of total DNA of EK33 led to the isolation of several aerobactin-positive clones. Under conditions of iron limitation, these clones expressed in Eschericia coli a protein of 72 kilodaltons that reacted with antiserum raised against the pColV-K30 74-kilodalton aerobactin receptor, while the original E. cloacae strain synthesized an 85-kilodalton protein which also cross-reacted with the antiserum. Restriction endonuclease analysis of the cloned DNA confirmed the structural differences between the two aerobactin genetic systems.
CITATION STYLE
Crosa, L. M., Wolf, M. K., Actis, L. A., Sanders-Loehr, J., & Crosa, J. H. (1988). New aerobactin-mediated iron uptake system in a septicemia-causing strain of Enterobacter cloacae. Journal of Bacteriology, 170(12), 5539–5544. https://doi.org/10.1128/jb.170.12.5539-5544.1988
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