TY - JOUR
T1 - Phylloquinone is the principal Mehler reaction site within photosystem I in high light
AU - Kozuleva, Marina
AU - Petrova, Anastasia
AU - Milrad, Yuval
AU - Semenov, Alexey
AU - Ivanov, Boris
AU - Redding, Kevin E.
AU - Yacoby, Iftach
N1 - Publisher Copyright:
© 2021 American Society of Plant Biologists. All rights reserved.
PY - 2021/8
Y1 - 2021/8
N2 - Photosynthesis is a vital process, responsible for fixing carbon dioxide, and producing most of the organic matter on the planet. However, photosynthesis has some inherent limitations in utilizing solar energy, and a part of the energy absorbed is lost in the reduction of O2 to produce the superoxide radical (O 2 ) via the Mehler reaction, which occurs principally within photosystem I (PSI). For decades, O2 reduction within PSI was assumed to take place solely in the distal iron-sulfur clusters rather than within the two asymmetrical cofactor branches. Here, we demonstrate that under high irradiance, O2 photoreduction by PSI primarily takes place at the phylloquinone of one of the branches (the A-branch). This conclusion derives from the light dependency of the O2 photoreduction rate constant in fully mature wild-type PSI from Chlamydomonas reinhardtii, complexes lacking iron-sulfur clusters, and a mutant PSI, in which phyllosemiquinone at the A-branch has a significantly longer lifetime. We suggest that the Mehler reaction at the phylloquinone site serves as a release valve under conditions where both the iron-sulfur clusters of PSI and the mobile ferredoxin pool are highly reduced.
AB - Photosynthesis is a vital process, responsible for fixing carbon dioxide, and producing most of the organic matter on the planet. However, photosynthesis has some inherent limitations in utilizing solar energy, and a part of the energy absorbed is lost in the reduction of O2 to produce the superoxide radical (O 2 ) via the Mehler reaction, which occurs principally within photosystem I (PSI). For decades, O2 reduction within PSI was assumed to take place solely in the distal iron-sulfur clusters rather than within the two asymmetrical cofactor branches. Here, we demonstrate that under high irradiance, O2 photoreduction by PSI primarily takes place at the phylloquinone of one of the branches (the A-branch). This conclusion derives from the light dependency of the O2 photoreduction rate constant in fully mature wild-type PSI from Chlamydomonas reinhardtii, complexes lacking iron-sulfur clusters, and a mutant PSI, in which phyllosemiquinone at the A-branch has a significantly longer lifetime. We suggest that the Mehler reaction at the phylloquinone site serves as a release valve under conditions where both the iron-sulfur clusters of PSI and the mobile ferredoxin pool are highly reduced.
UR - http://www.scopus.com/inward/record.url?scp=85111267808&partnerID=8YFLogxK
U2 - 10.1093/plphys/kiab221
DO - 10.1093/plphys/kiab221
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C2 - 34618103
AN - SCOPUS:85111267808
SN - 0032-0889
VL - 186
SP - 1848
EP - 1858
JO - Plant Physiology
JF - Plant Physiology
IS - 4
ER -