» Articles » PMID: 20521115

The Supramolecular Architecture, Function, and Regulation of Thylakoid Membranes in Red Algae: an Overview

Overview
Journal Photosynth Res
Publisher Springer
Date 2010 Jun 4
PMID 20521115
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Red algae are a group of eukaryotic photosynthetic organisms. Phycobilisomes (PBSs), which are composed of various types of phycobiliproteins and linker polypeptides, are the main light-harvesting antennae in red algae, as in cyanobacteria. Two morphological types of PBSs, hemispherical- and hemidiscoidal-shaped, are found in different red algae species. PBSs harvest solar energy and efficiently transfer it to photosystem II (PS II) and finally to photosystem I (PS I). The PS I of red algae uses light-harvesting complex of PS I (LHC I) as a light-harvesting antennae, which is phylogenetically related to the LHC I found in higher plants. PBSs, PS II, and PS I are all distributed throughout the entire thylakoid membrane, a pattern that is different from the one found in higher plants. Photosynthesis processes, especially those of the light reactions, are carried out by the supramolecular complexes located in/on the thylakoid membranes. Here, the supramolecular architecture, function and regulation of thylakoid membranes in red algal are reviewed.

Citing Articles

Structure, biogenesis, and evolution of thylakoid membranes.

Ostermeier M, Garibay-Hernandez A, Holzer V, Schroda M, Nickelsen J Plant Cell. 2024; 36(10):4014-4035.

PMID: 38567528 PMC: 11448915. DOI: 10.1093/plcell/koae102.


Single-cell transcriptome sequencing revealing the difference in photosynthesis and carbohydrate metabolism between epidermal cells and non-epidermal cells of (Rhodophyta).

Chen H, Hu Y, Li P, Feng X, Jiang M, Sui Z Front Plant Sci. 2022; 13:968158.

PMID: 36466256 PMC: 9714639. DOI: 10.3389/fpls.2022.968158.


Increased CO Relevant to Future Ocean Acidification Alleviates the Sensitivity of a Red Macroalgae to Solar Ultraviolet Irradiance by Modulating the Synergy Between Photosystems II and I.

Zhang D, Xu J, Beer S, Beardall J, Zhou C, Gao K Front Plant Sci. 2021; 12:726538.

PMID: 34603355 PMC: 8481898. DOI: 10.3389/fpls.2021.726538.


Comparative Transcriptome Profiling of (Rhodophyta, Solieriaceae) in Response to Light of Different Wavelengths and Carbon Dioxide Enrichment.

Thien V, Rodrigues K, Voo C, Wong C, Lym Yong W Plants (Basel). 2021; 10(6).

PMID: 34204578 PMC: 8234600. DOI: 10.3390/plants10061236.


Photosynthesis of the Cyanidioschyzon merolae cells in blue, red, and white light.

Parys E, Krupnik T, Kulak I, Kania K, Romanowska E Photosynth Res. 2020; 147(1):61-73.

PMID: 33231791 PMC: 7728651. DOI: 10.1007/s11120-020-00796-x.


References
1.
Loll B, Kern J, Saenger W, Zouni A, Biesiadka J . Towards complete cofactor arrangement in the 3.0 A resolution structure of photosystem II. Nature. 2005; 438(7070):1040-4. DOI: 10.1038/nature04224. View

2.
Delphin E, Duval J, Etienne A, Kirilovsky D . State transitions or delta pH-dependent quenching of photosystem II fluorescence in red algae. Biochemistry. 1996; 35(29):9435-45. DOI: 10.1021/bi960528+. View

3.
Mustardy L, Cunningham Jr F, Gantt E . Photosynthetic membrane topography: quantitative in situ localization of photosystems I and II. Proc Natl Acad Sci U S A. 1992; 89(21):10021-5. PMC: 50269. DOI: 10.1073/pnas.89.21.10021. View

4.
DELPHIN , DUVAL , ETIENNE , Kirilovsky . DeltapH-dependent photosystem II fluorescence quenching induced by saturating, multiturnover pulses in red algae . Plant Physiol. 1998; 118(1):103-13. PMC: 34847. DOI: 10.1104/pp.118.1.103. View

5.
Wehrmeyer W, Morschel E, Vogel K . Core substructure in phycobilisomes of red algae. II. The central part of the tricylindrical core--APCM--a constituent of hemidiscoidal phycobilisomes of Rhodella violacea. Eur J Cell Biol. 1993; 60(1):203-9. View