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Biosynthesis of the Escherichia coli Siderophore Enterobactin: Sequence of the entF Gene, Expression and Purification of EntF, and Analysis of Covalent Phosphopantetheine

  • Frank Rusnak
  • , Masahiro Sakaitani
  • , Dale Drueckhammer
  • , Janice Reichert
  • , Christopher T. Walsh
  • Harvard University

Research output: Contribution to journalArticlepeer-review

133 Scopus citations

Abstract

The sequence of the entF gene which codes for the serine activating enzyme in enterobactin biosynthesis is reported. The gene encodes a protein with a calculated molecular weight of 142006 and shares homologies with the small subunits of gramicidin S synthetase and tyrocidine synthetase. We have subcloned and overexpressed entF in a multicopy plasmid and attempted to demonstrate l-serine-dependent ATP-[32P]PPi exchange activity and its participation in enterobactin biosynthesis, but the overexpressed enzyme appears to be essentially inactive in crude extract. A partial purification of active EntF from wild-type Escherichia coli, however, has confirmed the expected activities of EntF. In a search for possible causes for the low level of activity of the overexpressed enzyme, we have discovered that EntF contains a covalently bound phosphopantetheine cofactor.

Original languageEnglish
Pages (from-to)2916-2927
Number of pages12
JournalBiochemistry
Volume30
Issue number11
DOIs
StatePublished - Mar 1 1991

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