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Amino acid deletions in the cytosolic domains of the chlorophyll alpha-binding protein CP47 slow Q(A)(-) oxidation and/or prevent the assembly of Photosystem II
Umeå University, Faculty of Science and Technology, Chemistry.
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2002 (English)In: PLANT MOLECULAR BIOLOGY, ISSN 0167-4412, Vol. 50, no 3, 563-72 p.Article in journal (Refereed) Published
Abstract [en]

The Photosystem II (PSII) core antenna chlorophyll alpha-binding protein, CP47, contains six membrane-spanning a-helices separated by five hydrophilic loops: A-E. To identify important hydrophilic cytosolic regions, oligonucleotide-directed mutagenesis was employed to introduce short segment deletions into loops B and D, and the C-terminal domain. Four strains carrying deletions of between three and five residues were created in loop B. Two strains, with deletions adjacent to helices II and III, did not assemble PSII; however, the mutants Delta(F123-D125) and Delta(R127-S131) remained photoautotrophic with near wild-type levels of assembled reaction centers. In contrast, all deletions introduced into loop D, connecting helices IV and V, failed to assemble significant levels of PSII and were obligate photoheterotrophic mutants. However, deletions in the C-terminal domain did not prevent the assembly of PSII reaction centers although the mutant Delta(S471-T473), with a deletion adjacent to helix VI, exhibited retarded Q(A)(-) oxidation kinetics and the PSII-specific herbicide, atrazine, bound less tightly in the Delta(S471-T473) and Delta(F475-D477) strains. Deletions in the C-terminal domain also created mutants with large protein aggregates that were recognized by an antibody raised against the PSII reaction center D1 protein. Low-temperature fluorescence emission spectra of photoautotrophic strains carrying deletions in either the C-terminal domain or loop B did not provide evidence for impaired energy transfer from the phycobilisomes to the PSII reaction center. The data therefore suggest an important structural role for loop D in the assembly of PSII and a potential interaction between the C-terminal domain of CP47 and the PSII reaction center that, when perturbed, results in photoinduced protein aggregates involving the D1 protein.

Place, publisher, year, edition, pages
2002. Vol. 50, no 3, 563-72 p.
Keyword [en]
CP47, D1, oligonucleotide-directed mutagenesis, Photosystem II, synechocystis
URN: urn:nbn:se:umu:diva-8786OAI: diva2:148457
Available from: 2008-02-12 Created: 2008-02-12 Last updated: 2011-01-13Bibliographically approved

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