Photoinhibition-like damage to the photosynthetic apparatus in plant leaves induced by submergence treatment in the dark

Submergence is a common type of environmental stress for plants. It hampers survival and decreases crop yield, mainly by inhibiting plant photosynthesis. The inhibition of photosynthesis and photochemical efficiency by submergence is primarily due to leaf senescence and excess excitation energy, cau...

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Veröffentlicht in:PloS one 2014-02, Vol.9 (2), p.e89067
Hauptverfasser: Fan, Xingli, Zhang, Zishan, Gao, Huiyuan, Yang, Cheng, Liu, Meijun, Li, Yuting, Li, Pengmin
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Liu, Meijun
Li, Yuting
Li, Pengmin
description Submergence is a common type of environmental stress for plants. It hampers survival and decreases crop yield, mainly by inhibiting plant photosynthesis. The inhibition of photosynthesis and photochemical efficiency by submergence is primarily due to leaf senescence and excess excitation energy, caused by signals from hypoxic roots and inhibition of gas exchange, respectively. However, the influence of mere leaf-submergence on the photosynthetic apparatus is currently unknown. Therefore, we studied the photosynthetic apparatus in detached leaves from four plant species under dark-submergence treatment (DST), without influence from roots and light. Results showed that the donor and acceptor sides, the reaction center of photosystem II (PSII) and photosystem I (PSI) in leaves were significantly damaged after 36 h of DST. This is a photoinhibition-like phenomenon similar to the photoinhibition induced by high light, as further indicated by the degradation of PsaA and D1, the core proteins of PSI and PSII. In contrast to previous research, the chlorophyll content remained unchanged and the H2O2 concentration did not increase in the leaves, implying that the damage to the photosynthetic apparatus was not caused by senescence or over-accumulation of reactive oxygen species (ROS). DST-induced damage to the photosynthetic apparatus was aggravated by increasing treatment temperature. This type of damage also occurred in the anaerobic environment (N2) without water, and could be eliminated or restored by supplying air to the water during or after DST. Our results demonstrate that DST-induced damage was caused by the hypoxic environment. The mechanism by which DST induces the photoinhibition-like damage is discussed below.
doi_str_mv 10.1371/journal.pone.0089067
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It hampers survival and decreases crop yield, mainly by inhibiting plant photosynthesis. The inhibition of photosynthesis and photochemical efficiency by submergence is primarily due to leaf senescence and excess excitation energy, caused by signals from hypoxic roots and inhibition of gas exchange, respectively. However, the influence of mere leaf-submergence on the photosynthetic apparatus is currently unknown. Therefore, we studied the photosynthetic apparatus in detached leaves from four plant species under dark-submergence treatment (DST), without influence from roots and light. Results showed that the donor and acceptor sides, the reaction center of photosystem II (PSII) and photosystem I (PSI) in leaves were significantly damaged after 36 h of DST. This is a photoinhibition-like phenomenon similar to the photoinhibition induced by high light, as further indicated by the degradation of PsaA and D1, the core proteins of PSI and PSII. In contrast to previous research, the chlorophyll content remained unchanged and the H2O2 concentration did not increase in the leaves, implying that the damage to the photosynthetic apparatus was not caused by senescence or over-accumulation of reactive oxygen species (ROS). DST-induced damage to the photosynthetic apparatus was aggravated by increasing treatment temperature. This type of damage also occurred in the anaerobic environment (N2) without water, and could be eliminated or restored by supplying air to the water during or after DST. Our results demonstrate that DST-induced damage was caused by the hypoxic environment. 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It hampers survival and decreases crop yield, mainly by inhibiting plant photosynthesis. The inhibition of photosynthesis and photochemical efficiency by submergence is primarily due to leaf senescence and excess excitation energy, caused by signals from hypoxic roots and inhibition of gas exchange, respectively. However, the influence of mere leaf-submergence on the photosynthetic apparatus is currently unknown. Therefore, we studied the photosynthetic apparatus in detached leaves from four plant species under dark-submergence treatment (DST), without influence from roots and light. Results showed that the donor and acceptor sides, the reaction center of photosystem II (PSII) and photosystem I (PSI) in leaves were significantly damaged after 36 h of DST. This is a photoinhibition-like phenomenon similar to the photoinhibition induced by high light, as further indicated by the degradation of PsaA and D1, the core proteins of PSI and PSII. In contrast to previous research, the chlorophyll content remained unchanged and the H2O2 concentration did not increase in the leaves, implying that the damage to the photosynthetic apparatus was not caused by senescence or over-accumulation of reactive oxygen species (ROS). DST-induced damage to the photosynthetic apparatus was aggravated by increasing treatment temperature. This type of damage also occurred in the anaerobic environment (N2) without water, and could be eliminated or restored by supplying air to the water during or after DST. Our results demonstrate that DST-induced damage was caused by the hypoxic environment. 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adverse effects</topic><topic>Electron Transport</topic><topic>Environmental stress</topic><topic>Euonymus - physiology</topic><topic>Euonymus - radiation effects</topic><topic>Flowers &amp; plants</topic><topic>Gas exchange</topic><topic>Hemerocallis - physiology</topic><topic>Hemerocallis - radiation effects</topic><topic>Hydrogen peroxide</topic><topic>Hydrogen Peroxide - metabolism</topic><topic>Hypoxia</topic><topic>Inhibition</topic><topic>Laboratories</topic><topic>Leaves</topic><topic>Life sciences</topic><topic>Light</topic><topic>Oryza</topic><topic>Oxygen</topic><topic>Photochemicals</topic><topic>Photoinhibition</topic><topic>Photosynthesis</topic><topic>Photosynthesis - physiology</topic><topic>Photosynthesis - radiation effects</topic><topic>Photosynthetic apparatus</topic><topic>Photosystem I</topic><topic>Photosystem I Protein Complex - metabolism</topic><topic>Photosystem II</topic><topic>Photosystem II Protein Complex - metabolism</topic><topic>Physics</topic><topic>Physiology</topic><topic>Plant biochemistry</topic><topic>Plant biology</topic><topic>Plant Leaves - 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It hampers survival and decreases crop yield, mainly by inhibiting plant photosynthesis. The inhibition of photosynthesis and photochemical efficiency by submergence is primarily due to leaf senescence and excess excitation energy, caused by signals from hypoxic roots and inhibition of gas exchange, respectively. However, the influence of mere leaf-submergence on the photosynthetic apparatus is currently unknown. Therefore, we studied the photosynthetic apparatus in detached leaves from four plant species under dark-submergence treatment (DST), without influence from roots and light. Results showed that the donor and acceptor sides, the reaction center of photosystem II (PSII) and photosystem I (PSI) in leaves were significantly damaged after 36 h of DST. This is a photoinhibition-like phenomenon similar to the photoinhibition induced by high light, as further indicated by the degradation of PsaA and D1, the core proteins of PSI and PSII. In contrast to previous research, the chlorophyll content remained unchanged and the H2O2 concentration did not increase in the leaves, implying that the damage to the photosynthetic apparatus was not caused by senescence or over-accumulation of reactive oxygen species (ROS). DST-induced damage to the photosynthetic apparatus was aggravated by increasing treatment temperature. This type of damage also occurred in the anaerobic environment (N2) without water, and could be eliminated or restored by supplying air to the water during or after DST. Our results demonstrate that DST-induced damage was caused by the hypoxic environment. The mechanism by which DST induces the photoinhibition-like damage is discussed below.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24586508</pmid><doi>10.1371/journal.pone.0089067</doi><tpages>e89067</tpages><oa>free_for_read</oa></addata></record>
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subjects Biology
Chemistry
Chlorophyll
Chlorophyll content
Crop yield
Damage accumulation
Darkness - adverse effects
Electron Transport
Environmental stress
Euonymus - physiology
Euonymus - radiation effects
Flowers & plants
Gas exchange
Hemerocallis - physiology
Hemerocallis - radiation effects
Hydrogen peroxide
Hydrogen Peroxide - metabolism
Hypoxia
Inhibition
Laboratories
Leaves
Life sciences
Light
Oryza
Oxygen
Photochemicals
Photoinhibition
Photosynthesis
Photosynthesis - physiology
Photosynthesis - radiation effects
Photosynthetic apparatus
Photosystem I
Photosystem I Protein Complex - metabolism
Photosystem II
Photosystem II Protein Complex - metabolism
Physics
Physiology
Plant biochemistry
Plant biology
Plant Leaves - metabolism
Plant Leaves - physiology
Plant Leaves - radiation effects
Plant photosynthesis
Plant Roots - metabolism
Plant species
Plants
Proteins
Reactive oxygen species
Reactive Oxygen Species - metabolism
Roots
Salix - physiology
Salix - radiation effects
Senescence
Studies
Submergence
Temperature
Zea mays
Zea mays - physiology
Zea mays - radiation effects
title Photoinhibition-like damage to the photosynthetic apparatus in plant leaves induced by submergence treatment in the dark
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