Literature DB >> 2404979

Movement of newly imported light-harvesting chlorophyll-binding protein from unstacked to stacked thylakoid membranes is not affected by light treatment or absence of amino-terminal threonines.

B D Kohorn1, D Yakir.   

Abstract

In higher plants and algae, the transduction of captured light energy is highly regulated as excess excitation of photosystem II (PSII) reaction centers can be redirected to photosystem I (PSI) reaction centers. Models that attempt to explain this phenomenon involve light-harvesting chlorophyll-protein complexes (LHCII) that capture light energy and migrate between PSII and PSI. This report shows that in pea chloroplasts, the major protein component of LHCII, light-harvesting chlorophyll-binding protein (LHCP), can indeed migrate within the thylakoid membrane. We show, however, that although newly imported LHCP inserts into both stacked and unstacked thylakoid membranes, it then moves only from the unstacked, PSI-rich membranes to the stacked, PSII-rich membranes. The observed migration is not affected by light treatment that induces a redistribution of captured light energy (state I-state II transition) that previously was thought to induce LHCP to migrate in the opposite direction, from stacked to unstacked membranes. A mutation that removes the site of LHCP phosphorylation, the proposed trigger of state transitions, also has no effect on the integration and movement of LHCP, but does render LHCP more susceptible to proteolytic degradation. These results are not consistent with current models that deal with the short-term change in the distribution of light energy.

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Year:  1990        PMID: 2404979

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  7 in total

1.  Assembly of the chlorophyll-protein complexes.

Authors:  R Nechushtai; Y Cohen; P R Chitnis
Journal:  Photosynth Res       Date:  1995-05       Impact factor: 3.573

2.  State adaptations in the cyanobacterium Synechcoccus 6301 (PCC): Dependence on light intensity or spectral composition?

Authors:  D Rouag; P Dominy
Journal:  Photosynth Res       Date:  1994-04       Impact factor: 3.573

3.  Soluble Chloroplast Enzyme Cleaves preLHCP Made in Escherichia coli to a Mature Form Lacking a Basic N-Terminal Domain.

Authors:  M S Abad; J E Oblong; G K Lamppa
Journal:  Plant Physiol       Date:  1991-08       Impact factor: 8.340

4.  Proteomics of Chlamydomonas reinhardtii light-harvesting proteins.

Authors:  Einar J Stauber; Andreas Fink; Christine Markert; Olaf Kruse; Udo Johanningmeier; Michael Hippler
Journal:  Eukaryot Cell       Date:  2003-10

5.  Component specificity for the thylakoidal Sec and Delta pH-dependent protein transport pathways.

Authors:  H Mori; E J Summer; X Ma; K Cline
Journal:  J Cell Biol       Date:  1999-07-12       Impact factor: 10.539

6.  Proteomics Evidence of a Systemic Response to Desiccation in the Resurrection Plant Haberlea rhodopensis.

Authors:  Petko Mladenov; Diana Zasheva; Sébastien Planchon; Céline C Leclercq; Denis Falconet; Lucas Moyet; Sabine Brugière; Daniela Moyankova; Magdalena Tchorbadjieva; Myriam Ferro; Norbert Rolland; Jenny Renaut; Dimitar Djilianov; Xin Deng
Journal:  Int J Mol Sci       Date:  2022-07-31       Impact factor: 6.208

7.  Determinants for cleavage of the chlorophyll a/b binding protein precursor: a requirement for a basic residue that is not universal for chloroplast imported proteins.

Authors:  S E Clark; G K Lamppa
Journal:  J Cell Biol       Date:  1991-08       Impact factor: 10.539

  7 in total

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