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An ancient light-harvesting protein is critical for the regulation of algal photosynthesis
- Source :
- Nature. 462:518-521
- Publication Year :
- 2009
- Publisher :
- Springer Science and Business Media LLC, 2009.
-
Abstract
- Light is necessary for photosynthesis, but its absorption by pigment molecules such as chlorophyll can cause severe oxidative damage and result in cell death. The excess absorption of light energy by photosynthetic pigments has led to the evolution of protective mechanisms that operate on the timescale of seconds to minutes and involve feedback-regulated de-excitation of chlorophyll molecules in photosystem II (qE). Despite the significant contribution of eukaryotic algae to global primary production, little is known about their qE mechanism, in contrast to that in flowering plants. Here we show that a qE-deficient mutant of the unicellular green alga Chlamydomonas reinhardtii, npq4, lacks two of the three genes encoding LHCSR (formerly called LI818). This protein is an ancient member of the light-harvesting complex superfamily, and orthologues are found throughout photosynthetic eukaryote taxa, except in red algae and vascular plants. The qE capacity of Chlamydomonas is dependent on environmental conditions and is inducible by growth under high light conditions. We show that the fitness of the npq4 mutant in a shifting light environment is reduced compared to wild-type cells, demonstrating that LHCSR is required for survival in a dynamic light environment. Thus, these data indicate that plants and algae use different proteins to dissipate harmful excess light energy and protect the photosynthetic apparatus from damage.
- Subjects :
- Chlorophyll
Time Factors
Photosystem II
Cell Survival
Acclimatization
Light-Harvesting Protein Complexes
Chlamydomonas reinhardtii
Chlorophyta
Photosynthetic pigment
Photosynthesis
Fluorescence
chemistry.chemical_compound
Algae
Botany
RNA, Messenger
Multidisciplinary
biology
Algal Proteins
Genetic Complementation Test
Chlamydomonas
biology.organism_classification
chemistry
Mutation
Subjects
Details
- ISSN :
- 14764687 and 00280836
- Volume :
- 462
- Database :
- OpenAIRE
- Journal :
- Nature
- Accession number :
- edsair.doi.dedup.....a0dc259b15395efdb3a722c8d1394a52