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Biochim Biophys Acta Bioenerg ; 1860(5): 433-438, 2019 05 01.
Article in English | MEDLINE | ID: mdl-30827891

ABSTRACT

Apart from the canonical light-driven linear electron flow (LEF) from water to CO2, numerous regulatory and alternative electron transfer pathways exist in chloroplasts. One of them is the cyclic electron flow around Photosystem I (CEF), contributing to photoprotection of both Photosystem I and II (PSI, PSII) and supplying extra ATP to fix atmospheric carbon. Nonetheless, CEF remains an enigma in the field of functional photosynthesis as we lack understanding of its pathway. Here, we address the discrepancies between functional and genetic/biochemical data in the literature and formulate novel hypotheses about the pathway and regulation of CEF based on recent structural and kinetic information.


Subject(s)
Adenosine Triphosphate/metabolism , Chloroplasts/enzymology , Photosynthesis/physiology , Photosystem I Protein Complex/metabolism , Photosystem II Protein Complex/metabolism , Electron Transport/physiology , Kinetics
2.
Biochim Biophys Acta Bioenerg ; 1860(5): 425-432, 2019 05 01.
Article in English | MEDLINE | ID: mdl-30711358

ABSTRACT

Cyclic electron flow (CEF) is defined as a return of the reductants from the acceptor side of Photosystem I (PSI) to the pool of its donors via the cytochrome b6f. It is described to be complementary to the linear electron flow and essential for photosynthesis. However, despite many efforts aimed to characterize CEF, its pathway and its regulation modes remain equivocal, and its physiological significance is still not clear. Here we use novel spectroscopic to measure the rate of CEF at the onset of light in the green alga Chlamydomonas reinhardtii. The initial redox state of the photosynthetic chain or the oxygen concentration do not modify the initial maximal rate of CEF (60 electrons per second per PSI) but rather strongly influence its duration. Neither the maximal rate nor the duration of CEF are different in the pgrl1 mutant compared to the wild type, disqualifying PGRL1 as the ferredoxin-plastoquinone oxidoreductase involved in the CEF mechanism.


Subject(s)
Chlamydomonas reinhardtii/metabolism , Membrane Proteins/metabolism , Chlamydomonas reinhardtii/genetics , Electron Transport/physiology , Membrane Proteins/genetics , Oxidation-Reduction
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