AI Article Synopsis

  • Researchers aimed to identify genes in Helicobacter pylori that enable it to utilize haem as an iron source by transforming an Escherichia coli mutant with a cosmid library from H. pylori.
  • Four unique cosmids were found that could help the E. coli mutant grow on iron-deficient media with various haem compounds, but no growth differences were observed among them.
  • One cosmid showed it could complement another E. coli mutant and also produced proteins that were immunoreactive to H. pylori, with one of these proteins being similar in size to a known iron-repressible protein from H. pylori.

Article Abstract

To identify genes responsible for the utilization of haem as an iron source in Helicobacter pylori, a siderophore synthesis mutant of Escherichia coli was transformed with an ordered cosmid library of H. pylori NCTC 11638. Four independent cosmids were found that were able to complement this mutant on iron-restrictive solid media containing different haem compounds as the sole source of iron. Hybridization experiments revealed that the four cosmids contained unrelated DNA fragments. No major differences were observed in the growth of the four transformants on iron-restrictive solid media to which different haem compounds had been added. None of the cosmids could confer the ability to use haem as an iron source to an E. coli aroB tonB mutant, which means that transport of iron and/or haem across the outer membrane requires a functional TonB protein. Further characterization of the cosmids revealed that one of them was also able to complement E. coli aroB hemA, indicating that the haem molecule is taken up as a whole by this haem-biosynthesis mutant. Expression of this haem-uptake system could not be repressed by excess iron. Another cosmid expressed two polypeptides in E. coli which were specifically immunoreactive with a polyclonal antiserum raised against whole cells of H. pylori. The production of these proteins appeared to be iron repressible. One of these proteins has the same molecular mass as a previously described 77 kDa haem-binding iron-repressible outer-membrane protein (IROMP) of H. pylori.

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http://dx.doi.org/10.1099/13500872-145-3-681DOI Listing

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