Rapid evolution of a bacterial iron acquisition system.

Mol Microbiol

Department of Biochemistry, Jacobs School of Medicine and Biomedical Sciences, The University at Buffalo, 955 Main Street, Room 4102, Buffalo, NY, 14203-1121, USA.

Published: April 2018

AI Article Synopsis

  • Bacteria under iron limitation use siderophores to acquire ferric iron from their environment for nutrition.
  • In Bradyrhizobium japonicum, mutations in outer membrane transporter genes allow cells to utilize a variety of natural and synthetic iron siderophores, indicating adaptability in siderophore uptake.
  • The process involves a cytoplasmic membrane transporter that facilitates the reduction of ferric iron to ferrous iron, enabling efficient cellular entry after dissociation from chelators.

Article Abstract

Under iron limitation, bacteria scavenge ferric (Fe ) iron bound to siderophores or other chelates from the environment to fulfill their nutritional requirement. In gram-negative bacteria, the siderophore uptake system prototype consists of an outer membrane transporter, a periplasmic binding protein and a cytoplasmic membrane transporter, each specific for a single ferric siderophore or siderophore family. Here, we show that spontaneous single gain-of-function missense mutations in outer membrane transporter genes of Bradyrhizobium japonicum were sufficient to confer on cells the ability to use synthetic or natural iron siderophores, suggesting that selectivity is limited primarily to the outer membrane and can be readily modified. Moreover, growth on natural or synthetic chelators required the cytoplasmic membrane ferrous (Fe ) iron transporter FeoB, suggesting that iron is both dissociated from the chelate and reduced to the ferrous form within the periplasm prior to cytoplasmic entry. The data suggest rapid adaptation to environmental iron by facile mutation of selective outer membrane transporter genes and by non-selective uptake components that do not require mutation to accommodate new iron sources.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867251PMC
http://dx.doi.org/10.1111/mmi.13918DOI Listing

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