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Plant Signaling & Behavior 8:4, e23681; April 2013; 2013 Landes Bioscience
Introduction
Reactive oxygen species (ROS) is considered as unavoidable
chemical entity of aerobic life.1,2 They are considered as by
*Correspondence to: Sanjib Kumar Panda; Email: drskpanda@gmail.com
Submitted: 01/17/13; Accepted: 01/18/13
http://dx.doi.org/10.4161/psb.23681
Citation: Choudhury S, Panda P, Sahoo L, Panda SK. Reactive oxygen species
signaling in plants under abiotic stress. Plant Signal Behav 2013; 8: e23681
www.landesbioscience.com
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provide defense against the ROS.6 Antioxidants play the critical role of ROS removal and its activation is directly correlated
with defense against abiotic stress and plant development.6 The
survival in the stressed environment requires stable redox state,
which practically needs efficient antioxidant pathways to remove
the ROS in different cellular compartments.2,7,8 In order to have
an efficient antioxidant activity, cellular and physiological processes needs to be effective. ROS are produced in cells constantly
and any imbalance between ROS and antioxidants implicates to
oxidative stress.9 ROS generation is also genetically programmed.8
For examples, ROS like H2O2 and O2- acts as second messengers,
but its accumulation at high levels causes oxidative stress leading
to cell death.
The major antioxidants that play crucial role in ROS detoxification includes ascorbic acid (AA), -tocopherol, glutathione, catalase (CAT), peroxidases (POX), superoxide dismutase
(SOD), glutathione reductase (GR) etc. Synchronized action
of these antioxidants result in detoxification of ROS and limit
oxidative stress in plants (Fig. 2). Ascorbic acid is distributed
in almost all the plants. It is synthesized in the mitochondria
and transported to other parts of the plants.8,10,11 AA is used as
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Figure 1. Generation of reactive oxygen species (ROS) by various abiotic stress factors in plants.
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Figure 2. Antioxidant system in plants involved in detoxification of reactive oxygen species through various pathways.
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selectively. When the ROS concentration is increased, it conveys the change in gene expression. It was further stated that
such changes at gene level occurs via oxidation of components
of the signaling pathways resulting in the activation of transcription factors or possibly those transcription factors that are
redox sensitive.31 Studies on mitogen activated protein kinase
(MAPK) in Arabidopsis have revealed that H2O2 can activate
MAPK (AtMPK3 and At MPK6 ) and sturdily induces nucleotide diphosphate kinase 2 (AtNDPK2).31,33 Plants appear to be
tolerant to H2O2 due to controlled antioxidant system that helps
in the complete elimination of it and maintains the steady redox
state.34,35 In several reports, the role of glutathione and ascorbate
in redox signaling in plants have been emphasized.19,21,34,35 This
aspect has been critically discussed in one of the previous sections of this paper.
Chloroplast redox state has been well explored to understand
redox-regulated gene expression in plants.35,36 Any change in the
redox state of the chloroplast affects expression of chloroplast
proteins. In the chloroplast, plastoquinone (PQ), ascorbate, glutathione and ROS along with ferredoxin or thioredoxin system
are the key signaling components.36 The photosystem II (PSII) is
associated with production of 1O2 and both photosytem I (PSI)
and PSII with O2-.37-38 Studies on flu mutants of Arabidopsis have
shown that 1O2 signaling associated with programmed cell death
(PCD) possesses certain explicit characteristic in terms of gene
induction as compared with other ROS.30,40 Lee et al.41 identified
proteins associated with 1O2 signaling, the EXECUTOR 1 and 2
proteins, which repress the 1O2 induced cell death. Peroxisomes
are the major sites of H2O2 production thorough different biochemical reactions. During photosynthesis in C3 plants, peroxisomes generate high amount of H2O2 that is light dependent and
as such the antioxidant efficiency is extensively high in those
organelles.35 These include enzymes like CAT, APX and those
associated with ascorbate/glutathione system.35,42 These enzymes
are required for scavenging H2O2. The decline in the activity of
CAT during photorespiration leads to accumulation of oxidized
glutathione.35 It was also emphasized that the accumulation of
ascorbate and glutathione can balance CAT deficit briefly and the
glycollate oxidase reaction may be involved in passing the signal
from the chloroplast to peroxisomes.35,43 Such events have been
reported in plants under drought and high temperature stress.35
The cellular redox homeostasis has a direct correlation with
mitochondrial redox state. Since, the ROS scavenging capacity
of mitochondria is less as compared with chloroplast and peroxisomes, the stability of its own redox state decides the fate of total
cellular redox status.35
In comparison to mitochondria, the ROS production in chloroplast and peroxisomes is high. Despite of this fact, the amount
of oxidized protein in mitochondria is high.35,38 One of the explanations for presence of high concentration of oxidized protein
is possibly due to its susceptibility to ROS. Some of these oxidized proteins are part of mitochondrial electron transport complex I and III.38 The complexes are involved in ROS production,
which resulted in protein oxidation; moreover, certain proteins
are matrix proteins where oxidation takes place after ROS are
released from the inner mitochondrial membrane.38 Available
Conclusion
Aerobic life has made the presence of ROS inevitable. During
the course of evolution, plants have equipped themselves
to hunt the deleterious effects of ROS and subsequently use
them in different biological processes. High concentration of
ROS in cells as a result of abiotic stress limits plant growth
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