Abstract

The light-harvesting proteins in plastids of different lineages including algae and land plants represent a superfamily of chlorophyll-binding proteins that seem to be phylogenetically related, although some of the light-harvesting complex (LHC) proteins bind different carotenoids. LHCs can be divided into chlorophyll a/b-binding proteins found in green algae, euglenoids, and higher plants and into chlorophyll a/c-binding proteins of various algal taxa. LHC proteins from diatoms are named fucoxanthin-chlorophyll a/c-binding proteins (FCP). In contrast to chlorophyll a/b-binding proteins, there is no information so far about the way FCPs integrate into thylakoid membranes. The diatom FCP preproteins have a bipartite presequence that is necessary to enable transport into the four membrane-bound diatom plastids, but similar to chlorophyll a/b-binding proteins there is apparently no presequence present for targeting to the thylakoid membrane. By establishing an in vitro import assay for diatom thylakoids, we demonstrated that thylakoid integration of diatom FCP depends on the presence of stromal factors and GTP. This indicates that a pathway involving signal recognition particles (SRP) is involved in membrane integration just as shown for LHCs in higher plants. We also demonstrate integration of diatom FCP into thylakoids of higher plants and vice versa SRP-dependent targeting of LHCs from pea and Arabidopsis into diatom thylakoids. The similar SRP-dependent modes of thylakoid integration of land plant LHCs and FCPs support recent analyses indicating a common origin of chlorophyll a/b- and a/c-binding proteins.

Highlights

  • Photosynthetic organisms possess protein complexes that harvest light energy and transfer it to the reaction centers

  • By establishing an in vitro import assay for diatom thylakoids, we demonstrated that thylakoid integration of diatom fucoxanthin-chlorophyll a/c-binding proteins (FCP) depends on the presence of stromal factors and GTP

  • The integration process of the light-harvesting complex (LHC) from land plants into thylakoid membranes involves binding to a chloroplast signal recognition particle (SRP), which consists of at least two proteins named cpSRP54 and cpSRP43, and to a further protein, FtsY [11,12,13]. cpSRP54 and cpSRP43 are related to homologous proteins that are major factors of the cotranslational protein import pathway into the endoplasmic reticulum of eukaryotes [14]

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Summary

FCP Integration into Diatom Thylakoid Membranes

These so-called complex plastids depends on a bipartite presequence and occurs in at least two steps [19]. Several different Fcp genes have already been found in diatoms, and it is likely that there are even more present [20, 21]. There are no reports about functional aspects of FCPs with respect to integration into thylakoid membranes and cooperation with the diatom photosystems. We present the first data on thylakoid membrane integration of a member of the FCP family using a respective protein from the diatom Odontella sinensis. We have established an in vitro thylakoid import assay from purified diatom plastids enabling the study of FCP integration. Our results suggest that FCPs are integrated mainly by an SRP-dependent integration mechanism as found for LHCs. Complementary integration experiments were performed using LHC and FCP proteins as well as thylakoid membranes from land plant and diatom plastids

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