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PLANT PHYSIOLOGY , Vol 105, Issue 2 619-627, Copyright © 1994 by American Society of Plant Biologists
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ENVIRONMENTAL AND STRESS PHYSIOLOGY |
Acclimation, Hydrogen Peroxide, and Abscisic Acid Protect Mitochondria against Irreversible Chilling Injury in Maize Seedlings
T. K. Prasad, M. D. Anderson and C. R. Stewart
Department of Botany, Iowa State University, Ames, Iowa 50011
Our previous results indicated that 3-d-old dark-grown chilling-sensitive
maize (Zea mays L.) seedlings did not survive 7 d of 4[deg]C chilling
stress, but 69% of them survived similar stress when the seedlings were
either preexposed to 14[deg]C for 3 d or pretreated with 0.1 mM H2O2 for 4
h at 27[deg]C (T.K. Prasad, M.D. Anderson, B.A. Martin, C.R. Stewart [1994]
Plant Cell 6: 65-74) or 1 mM abscisic acid (ABA) for 24 h at 27[deg]C (M.D.
Anderson, T.K. Prasad, B.A. Martin, C.R. Stewart [1994] Plant Physiol 105:
331-339). We discovered that chilling imposed oxidative stress on the
seedlings. Since H2O2 accumulated during the periods of both acclimation
and nonacclimation, we concluded that H2O2 had dual effects at low
temperature: (a) During acclimation, its early transient accumulation
signals the induction of antioxidant enzymes such as catalase 3 and
peroxidase to scavenge H2O2; and (b) at 4[deg]C in nonacclimated seedlings,
it accumulates to damaging levels in the tissues because of low levels of
these and perhaps other antioxidant enzymes. Three-day-old seedlings
pretreated with H2O2 (a mild oxidative stress) or ABA showed induced
chilling tolerance. In the present study, we investigated whether
mitochondria are a target for chilling-induced oxidative stress and, if so,
what differences do acclimation, H2O2, or ABA make to protect mitochondria
from irreversible chilling injury. The results indicated that chilling, in
general, impairs respiratory activity, the cytochrome pathway of electron
transport, and ATPase activity regardless of the treatment. In pretreated
seedlings, the activities of catalase 3 and peroxidase in the mitochondria
increased severalfold compared with control and nonacclimated seedlings.
The increases in these antioxidant enzymes imply that mitochondria are
under oxidative stress and such increases could initiate a protective
mechanism in the mitochondria. Mitochondrial respiration is partially
cyanide resistant during chilling stress and also after the 1st d of
recovery. Upon further recovery over 3 d, in contrast to nonacclimated
seedlings, the mitochondria of acclimation-, H2O2-, and ABA-treated
seedlings showed the following recovery features. (a) The mitochondrial
respiration changed from a cyanide-resistant to a cyanide-sensitive
cytochrome pathway, (b) cytochrome oxidase activity recovered to control
levels, (c) the ability of mitochondria to generate ATP was regained, and
(d) the antioxidant enzyme activities remained at or above control levels.
Based on these results, we conclude that chilling impairs mitochondrial
function and that chilling-induced oxidative stress seems to be a factor,
at least in part, for causing possible irreversible damage to the
mitochondrial membrance components. Acclimation, H2O2, and ABA provide a
protective mechanism by inducing antioxidant enzymes to protect
mitochondria from irreversible oxidative damage that is absent in
nonacclimated seedlings. Therefore, we conclude that the ability of the
seedlings to recover from chilling injury is, at least in part, due to the
ability of the mitochondria to resume normal function.
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