Maximal cyclic electron flow rate is independent of PGRL1 in Chlamydomonas

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...

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Published in	Biochimica et biophysica acta. Bioenergetics Vol. 1860; no. 5; pp. 425 - 432
Main Authors	Nawrocki, W.J., Bailleul, B., Cardol, P., Rappaport, F., Wollman, F.-A., Joliot, P.
Format	Journal Article Web Resource
Language	English
Published	Netherlands Elsevier B.V 01.05.2019 Elsevier
Subjects	Anoxia Biochemistry, biophysics & molecular biology Biochimie, biophysique & biologie moléculaire Biologie végétale (sciences végétales, sylviculture, mycologie...) Chemical Sciences Chlamydomonas reinhardtii Cyclic electron flow Cytochrome b6f electrons Life Sciences mutants oxidoreductases oxygen Photosynthesis Photosystem I Phytobiology (plant sciences, forestry, mycology...) reducing agents Sciences du vivant spectroscopy Vegetal Biology Photosystem I Cytochrome b6f Cyclic electron flow Anoxia Photosynthesis photosystem I cytochrome b6f anoxia cyclic electron flow
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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. [Display omitted] •The maximal rate of cyclic electron flow is independent of PGRL1 in vivo.•Oxygen availability modifies the duration, but not the maximal rate of CEF.•The rate of CEF is determined by the redox state of both PSI donor and acceptor side.
AbstractList	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. 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.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. 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 reductase involved in the CEF mechanism. 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 b f. 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. 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. [Display omitted] •The maximal rate of cyclic electron flow is independent of PGRL1 in vivo.•Oxygen availability modifies the duration, but not the maximal rate of CEF.•The rate of CEF is determined by the redox state of both PSI donor and acceptor side.
Author	Nawrocki, W.J. Wollman, F.-A. Cardol, P. Rappaport, F. Joliot, P. Bailleul, B.
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Keywords	Photosystem I Cytochrome b6f Cyclic electron flow Anoxia Photosynthesis photosystem I cytochrome b6f anoxia cyclic electron flow
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Snippet	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...
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SubjectTerms	Anoxia Biochemistry, biophysics & molecular biology Biochimie, biophysique & biologie moléculaire Biologie végétale (sciences végétales, sylviculture, mycologie...) Chemical Sciences Chlamydomonas reinhardtii Cyclic electron flow Cytochrome b6f electrons Life Sciences mutants oxidoreductases oxygen Photosynthesis Photosystem I Phytobiology (plant sciences, forestry, mycology...) reducing agents Sciences du vivant spectroscopy Vegetal Biology
Title	Maximal cyclic electron flow rate is independent of PGRL1 in Chlamydomonas
URI	https://dx.doi.org/10.1016/j.bbabio.2019.01.004 https://www.ncbi.nlm.nih.gov/pubmed/30711358 https://www.proquest.com/docview/2179540206 https://www.proquest.com/docview/2221023937 https://hal.sorbonne-universite.fr/hal-02351657 http://orbi.ulg.ac.be/handle/2268/236838
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