Isolation of the PufX protein from Rhodobacter capsulatus and Rhodobacter sphaeroides: Evidence for its interaction with the α- polypeptide of the core light-harvesting complex

Paul A. Recchia, Christine M. Davis, Timothy G. Lilburn, J. Thomas Beatty, Pamela S. Parkes-Loach, C. Neil Hunter, Paul A. Loach*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

50 Scopus citations

Abstract

Using mutant strains of Rhodobacter capsulatus and Rhodobacter sphaeroides in which the pufX gene had been deleted, it was possible to identify by HPLC membrane protein components present in pufX+ cells but absent in pufX- cells. In parallel preparations, membrane proteins soluble in chloroform/methanol containing ammonium acetate were first extracted from lyophilized membrane fractions of the pufX+ cells and separated from pigments and larger protein material by gel-filtration chromatography. Protein-containing fractions were examined by HPLC, and several peaks were collected from pufX+ material that were not present in pufX- material. From N-terminal amino acid sequencing, the PufX protein of Rb. capsulatus was identified, and from positive interaction with a PufX protein antibody, the Rb. sphaeroides PufX protein was identified. Although overall yields were very small, sufficient quantities of these proteins were isolated to evaluate their effect on the reconstitution of the core light-havesting antenna (LH1) and its subunit complex. From the behavior of the PUfX protein and the α- polypeptide of LH1 on HPLC, qualitative evidence was obtained that the two proteins have a high affinity for each other. In reconstitution assays with bacteriochlorophyll (Bchl) and the LH1 α- and β-polypeptides of Rb. capsulatus, the PufX protein of Rb. capsulatus was inhibitory to LH1 formation at low concentration. A similar inhibition was exhibited by Rb. sphaeroides PufX protein for reconstitution of LH1 with Bchl and the LH1 α- and β-polypeptides of Rb. sphaeroides. In both cases, the ratios of concentrations of the PufX protein to the α-polypeptide causing 50% inhibition were approximately 0.5. Formation of the heterologous (αβ) subunit-type complex formed with Bchl and the α- and β-polypeptides of LH1 of Rb. capsulatus was also inhibited by low concentrations of the Rb. capsulatus PufX protein (approximately 50% inhibition at PufX:α-polypeptide ratios = 0.5). However, neither PufX protein inhibited formation of a homologous (ββ) subunit-type complex, which indicates that the PUfX proteins do not interact with the β-polypeptides.

Original languageEnglish (US)
Pages (from-to)11055-11063
Number of pages9
JournalBiochemistry
Volume37
Issue number31
DOIs
StatePublished - Aug 4 1998

ASJC Scopus subject areas

  • Biochemistry

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