Five phosphonate operon gene products as components of a multi-subunit complex of the carbon-phosphorus lyase pathway

Bjarne Jochimsen, Signe Lolle, Fern R. McSorley, Marih Nabi, Jens Stougaard, David L. Zechel, Bjarne Hove-Jensen

    Research output: Contribution to journalJournal articleResearchpeer-review

    Abstract

    Organophosphonate utilization by Escherichia coli requires the 14 cistrons of the phnCDEFGHIJKLMNOP operon, of which the carbon-phosphorus lyase has been postulated to consist of the seven polypeptides specified by phnG to phnM. A 5,660-bp DNA fragment encompassing phnGHIJKLM is cloned, followed by expression in E. coli and purification of Phn-polypeptides. PhnG, PhnH, PhnI, PhnJ, and PhnK copurify as a protein complex by ion-exchange, size-exclusion, and affinity chromatography. The five polypeptides also comigrate in native-PAGE. Cross-linking of the purified protein complex reveals a close proximity of PhnG, PhnI, PhnJ, and PhnK, as these subunits disappear concomitant with the formation of large cross-linked protein complexes. Two molecular forms are identified, a major form of molecular mass of approximately 260 kDa, a minor form of approximately 640 kDa. The stoichiometry of the protein complex is suggested to be PhnG4H2I2J2K. Deletion of individual phn genes reveals that a strain harboring plasmid-borne phnGHIJ produces a protein complex consisting of PhnG, PhnH, PhnI, and PhnJ, whereas a strain harboring plasmid-borne phnGIJK produces a protein complex consisting of PhnG and PhnI. We conclude that phnGHIJK specify a soluble multisubunit protein complex essential for organophosphonate utilization.
    Original languageEnglish
    JournalProceedings of the National Academy of Sciences of the United States of America
    Volume108
    Issue number28
    Pages (from-to)11393-11398
    ISSN0027-8424
    DOIs
    Publication statusPublished - 2011

    Cite this