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Siponen, M. I.

Publications and source records attributed to Siponen, M. I..

3 recordsLinked to original sources

The Posidonia oceanica Large PSI-LHCII supercomplex reveals the molecular basis of PSI spectral diversification in higher plants

Higher plant Photosystem I (PSI) can capture low-energy photons and convert them into chemical energy through special far-red absorbing chlorophylls, the red-forms. Across higher-plant evolution, red-form spectral range has shifted to match differences in far-red availability across various habitats, despite broad conservation of the antenna system and canonical red-form architecture. Here, we report the 1.9 A cryo-EM structure of a large and blue shifted PSI light-harvesting complex I and II supercomplex (L-PSI-LHCI-LHCII) from the Mediterranean seagrass Posidonia oceanica, a marine angiosperm adapted to blue-enriched underwater light depleted in far-red wavelengths. Although the PSI core remains conserved, the antenna system was selectively remodeled through incorporation of an additional Lhca1-Lhca4 heterodimer at a previously undescribed binding site, together with pigment remodeling in the LHCI and the LHCII that enhanced blue-cyan light harvesting. Comparative structural analyses identified recurrent amino-acid sites within the far-red domains that influence red-forms geometry and whose residue composition diverges strongly among blue-shifted and red-shifted plant species. These findings establish a common structural basis underlying the spectral diversification of PSI toward contrasting light environments, accounting for both seagrass adaptation to the seawater light regime and the broad range of far-red absorption in higher plants.

plant biology↗

Cryo-EM structure of the Rhodobaca bogoriensis RC-LH1-PufX dimeric complex at 2.9 angstrom

The reaction centre-light harvesting 1 (RC-LH1) complex is essential for converting light into proton motive force in photosynthetic bacteria. RC-LH1 is a monomer in most purple bacteria, but in Rhodobacter species, it is a dimer. Its assembly depends on an accessory polypeptide (PufX) and, ultimately, on photosynthetic growth. To date, knowledge on the RC-LH1-PufX structure, where the dimer has two incomplete C-shaped antenna rings surrounding an RC, is mainly limited to the model organism Rhodobacter sphaeroides. Here we present a cryo-electron microscopy structure at 2.9 [A] from Rhodobaca bogorensis strain LBB1. RCs are surrounded by 30 antennas and incorporate protein Y and PufX. RCs are stably connected by PufX, which self-interacts, electrostatically attracts cytochrome c2 (cyt c2) and forms extensive networks with co-factors. This structure underlines coordinated energy transfer in a combinatorial manner, providing a basis to describe bacterial photosynthesis within a dimeric photosynthetic apparatus.

biophysics↗

The Rhodobacter sphaeroides methionine sulfoxide reductase MsrP can reduce R- and S- diastereomers of methionine sulfoxide from a broad-spectrum of protein substrates.

Methionine (Met) is prone to oxidation and can be converted to Met sulfoxide (MetO), which exists as R- and S-diastereomers. MetO can be reduced back to Met by the ubiquitous methionine sulfoxide reductase (Msr) enzymes. Canonical MsrA and MsrB were shown as absolutely stereospecific for the reduction of S- and R-diastereomer, respectively. Recently, the molybdenum-containing protein MsrP, conserved in all gram-negative bacteria, was shown to be able to reduce MetO of periplasmic proteins without apparent stereospecificity in Escherichia coli. Here, we describe the substrate specificity of the Rhodobacter sphaeroides MsrP. Proteomics analysis coupled to enzymology approaches indicate that it reduces a broad spectrum of periplasmic oxidized proteins. Moreover, using model proteins, we demonstrated that RsMsrP preferentially reduces unfolded oxidized proteins and we confirmed that this enzyme, like its E. coli homolog, can reduce both R- and S-diastereomers of MetO with similar efficiency.

biochemistry↗