Activation of cyclic electron flow by hydrogen peroxide in vivo

Strand, Deserah D.; Livingston, Aaron K.; Satoh-Cruz, Mio; Froehlich, John E.; Maurino, Veronica G.; Kramer, David M.

doi:10.1073/pnas.1418223112

Title: Activation of cyclic electron flow by hydrogen peroxide in vivo

Journal Article · Mon Apr 13 00:00:00 EDT 2015 · Proceedings of the National Academy of Sciences of the United States of America

DOI:https://doi.org/10.1073/pnas.1418223112· OSTI ID:1235192

Strand, Deserah D. ^[1]; Livingston, Aaron K. ^[2]; Satoh-Cruz, Mio ^[3]; Froehlich, John E. ^[4]; Maurino, Veronica G. ^[5]; Kramer, David M. ^[6]

Plant Research Laboratory and, Departments of bPlant Biology and
School of Molecular Biosciences and, Institute for Biological Chemistry, Washington State University, Pullman, WA 99164, and
Plant Research Laboratory and
Plant Research Laboratory and, Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48824,
Institute of Developmental and Molecular Biology of Plants, Plant Molecular Physiology and Biotechnology Group, Heinrich-Heine-Universität, Cluster of Excellence on Plant Sciences (CEPLAS), 40225 Düsseldorf, Germany
Plant Research Laboratory and, Departments of bPlant Biology and, Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48824,

Cyclic electron flow (CEF) around photosystem I is thought to balance the ATP/NADPH energy budget of photosynthesis, requiring that its rate be finely regulated. The mechanisms of this regulation are not well understood. We observed that mutants that exhibited constitutively high rates of CEF also showed elevated production of H₂O₂. We thus tested the hypothesis that CEF can be activated by H₂O₂ in vivo. CEF was strongly increased by H₂O₂ both by infiltration or in situ production by chloroplast-localized glycolate oxidase, implying that H₂O₂ can activate CEF either directly by redox modulation of key enzymes, or indirectly by affecting other photosynthetic processes. CEF appeared with a half time of about 20 min after exposure to H₂O₂, suggesting activation of previously expressed CEF-related machinery. H₂O₂-dependent CEF was not sensitive to antimycin A or loss of PGR5, indicating that increased CEF probably does not involve the PGR5-PGRL1 associated pathway. In contrast, the rise in CEF was not observed in a mutant deficient in the chloroplast NADPH:PQ reductase (NDH), supporting the involvement of this complex in CEF activated by H₂O₂. In conclusion, we propose that H₂O₂ is a missing link between environmental stress, metabolism, and redox regulation of CEF in higher plants.

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Research Organization:: Washington State Univ., Pullman, WA (United States); Michigan State Univ., East Lansing, MI (United States). MSU-DOE Plant Research Laboratory; Heinrich Heine Univ., Dusseldorf (Germany)

Sponsoring Organization:: USDOE Office of Science (SC), Basic Energy Sciences (BES); German Research Foundation (DFG)

Grant/Contract Number:: FG02-11ER16220; SC0007101; FG02-04ER15559; FG02-91ER20021; MA2379/11-1

OSTI ID:: 1235192

Alternate ID(s):: OSTI ID: 1348375

Journal Information:: Proceedings of the National Academy of Sciences of the United States of America, Journal Name: Proceedings of the National Academy of Sciences of the United States of America Vol. 112 Journal Issue: 17; ISSN 0027-8424

Publisher:: Proceedings of the National Academy of SciencesCopyright Statement

Country of Publication:: United States

Language:: English

Citation Metrics:

Cited by: 100 works

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reactive oxygen species
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Title: Activation of cyclic electron flow by hydrogen peroxide in vivo

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