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Probing protein structural requirements for formation of the core light-harvesting complex of photosynthetic bacteria using hybrid reconstitution methodology
Authors:Paul A. Loach  Pamela S. Parkes-Loach  Christine M. Davis  Barbara A. Heller
Affiliation:(1) Department of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Hogan 2-100, 60208-3500 Evanston, IL, USA
Abstract:The agr- and beta-polypeptides of LH1 isolated from four different photosynthetic bacteria (Rhodospirillum rubrum, Rhodobacter sphaeroides, Rhodobacter capsulatus and Rhodopseudomonas viridis) were used for homologous and hybrid reconstitution experiments with bacteriochlorophyll a. Formation of B820-type subunit complexes and LH1-type complexes were evaluated. The beta-polypeptides of R. rubrum, Rb. sphaeroides and Rb. capsulatus behaved similarly and formed B820-type subunit complexes in the absence of an agr-polypeptide. The agr- and beta-polypeptides were both required to form a LH1-type complex with each of these three homologous systems. In hybrid experiments where the beta-polypeptides were tested for reconstitution with agr-polypeptides other than their homologous partners, half of the twelve possible combinations resulted in formation of both B820- and LH1-type complexes. Three of the combinations that did not result in formation of a LH1-type complex involved the beta-polypeptide of R. rubrum. It is suggested that these latter results can be explained by charge repulsion between the Lys at position-17 (assigning the conserved His located nearest to the C-terminus as position 0) in the beta-polypeptide of R. rubrum and each of the heterologous agr-polypeptides tested, all of which have an Arg at this location. Conclusions that can be derived from these experimental results include: (1) the experimental data support the idea that a central core region of approximately 40 amino acids exists in each of the polypeptides, which contains sufficient information to allow formation of both the B820- and LH1-type complexes and (2) a specific portion of the N-terminal hydrophilic region of each polypeptide was found in which ion pairs between oppositely charged groups on the agr- and beta-polypeptides seem to stabilize complex formation.Abbreviations BChl a bacteriochlorophyll a - BChl BChl a is implied - BChl aP BChl a containing phytol as the esterifying alcohol - BChl agg BChl a containing geranylgeraniol as the esterifying alcohol - LH1 the core light-harvesting complex - B873 the core light-harvesting complex of the G-9 mutant (carotenoidless) of R. rubrum or of the wild-type light-harvesting complex after benzene extraction (both with absorption maxima at 873 nm) - B820 the subunit form of B873 consisting of native agr- and beta-polypeptides with the same stoichiometry of agr1beta1·2BChl as LH1 - B820-type complex a complex exhibiting absorption and CD spectra indistinguishable from B820 but composed of either the beta-polypeptide only, or of a heterologous mixture of agr- and beta-polypeptides - RC reaction center - PRC photoreceptor complex consisting of the RC and LH1 - CD circular dichroism - OG n-octyl beta-d-glucopyranoside - HFA hexafluoroacetone trihydrate
Keywords:bacteriochlorophyll  pigment-protein complex
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