The development of chilling and freezing injury symptoms in plants is known to frequently coincide with peroxidation of free fatty acids [1]. Peroxide and malondialdehyde levels are often increased by freezing and thawing stress suggesting peroxidation of lipids [2] that result in structural and functional membrane and membrane protein changes [3]. It has been shown that mitochondria are one of the major sources of superoxide, which is a powerful oxidant radical, in chilling-sensitive plant tissues at low temperatures [4]. Even in non-stress conditions, 1–2 % of oxygen reduced in mitochondria by iron-sulfur centers in complex I and partially by reduced ubiquinone and cytochrome b in complex III is constitutively converted to superoxide [5, 6]. Mitochondria are also a major site for the accumulation of low molecular weight Fe²⁺ complexes, which induce lipid peroxidation in membranes [7, 8].

It has also been shown that cold stress causes an increase in antioxidant levels in many plant species. Furthermore, it has been found that different isoenzymes of glutathione reductase are expressed during cold acclimation of red spruce (Picea rubens) needles. One of them has been proposed to be a cold-acclimation protein [9]. Recently it was suggested that in mitochondria there was another physiological mechanism involved into antioxidant defense system of cell. V.P. Skulachev supposed that uncoupling of oxidation and phosphorylation in mitochondria during oxidative stress could decrease ROS generation by mitochondrial respiratory chain [10]. This point of view was supported by recent studies of plant UCP-like uncoupling proteins such as PUMP and others. For example, it was found that the inhibition of PUMP activity in isolated potato tuber mitochondria significantly increased mitochondrial H₂O₂ generation. It was also found that such substrates of UCP-like uncoupling proteins as linoleic acid and other free fatty acids reduced mitochondrial H₂O₂ generation [11, 12]. However, it is necessary to note that reactions of isolated organelles and whole plant cell on the same treatment can differ. At the same time, it is known that PUMP and other UCP-like proteins are not the only uncoupling system in plant mitochondria. All the plants have such a mechanism in mitochondria as alternative cyanide-resistant oxidase (AOX) whose activation during cold stress causes uncoupling of respiration and oxidative phosphorylation [13]. Recently it has been found that in cereals, such as winter wheat and winter rye, cold stress protein CSP 310 is present [14] and also causes uncoupling of respiration and oxidative phosphorylation in mitochondria during cold stress [15]. It was found that an addition of CSP 310 to isolated winter wheat mitochondria induced ascorbat-dependent and NADH-dependent lipid peroxidation systems unlike other known uncoupling proteins [16]. On the other hand, it has been shown that inhibition of CSP 310 by specific antiserum increases lipid peroxidation in isolated mitochondria [17]. Therefore, it is interesting to determine what CSP 310 activity, prooxidant or antioxidant is the most pronounced in whole winter wheat shoots during cold stress.

Meanwhile, the presence of a "family" of proteins immunochemically related to CSP 310 in cereals has been established. Earlier it has been shown that CSP 310-like native proteins are present in cytoplasm [18] and mitochondria [19] of cereals with different cold tolerance, and that CSP 310 could associate with and dissociate from mitochondria [20]. At the same time, CSP 310 was found in mitochondrial proteins of all species investigated, but this protein was found in winter rye and in lower amounts in winter wheat cytoplasmic proteins only. By using affine chromatography on a column with immobilized on BrCN-activated Sepharose anti-CSP 310 antiserum preparations of CSP 310-like cytoplasmic proteins from winter rye, winter wheat, maize and Elymus were obtained. These preparations consisted of 470 KD, 310 kD, 230 kD, about 140 kD, 66 kD and 56 kD proteins from winter rye, 310 kD, 230 kD, about 140 kD, 66 kD and 56 kD from winter wheat, 230 kD, about 140 kD, 66 kD and 56 kD from maize and 380 – 330 kD, 230 kD, about 140 kD, 66 kD and 54 kD proteins from Elymus. All these proteins consist of two types of subunits [18]. At the same time, this difference in spectra of native cereal proteins allows us to suppose a difference between their influence on mitochondrial energetic activity and lipid peroxidation.

The aim of this work is to examine the influence of proteins related to CSP 310 from some cereal species on energetic activity and lipid peroxidation in winter wheat mitochondria in vitro we also aim to examine the influence of activation of plant uncoupling systems on lipid peroxidation in winter wheat seedlings shoots during cold stress.

The study of the influence of CSP 310-like cytoplasmic proteins from winter rye, winter wheat, maize and Elymus on lipid peroxidation shows that immunochemically related to CSP 310 proteins from winter wheat, maize and Elymus did not have such prooxidant effect as CSP 310-like proteins from winter rye (Fig. 1). At the same time if proteins from winter wheat and maize did not have significantly influence on lipid peroxidation, proteins from Elymus do have an antioxidant activity in all systems studied (Fig. 1). In particular, proteins from CSP 310 "family" from Elymus inhibit NADH-dependent lipid peroxidation more than two times as compared to the variant without addition of any proteins.

All the proteins of CSP 310 "family" were previously shown to consist of two types of subunits [18]. The difference between these proteins is only in different composition of two types of subunits in native proteins. In accordance with this fact, the difference between their influence on energetic activity and lipid peroxidation can deal with the difference between their native structures. Therefore, we suppose that non-active low molecular weight combinations of CSP 310 subunits can be a "depot" that allows to rapidly increase CSP 310 concentration during cold stress. Because the reaction of isolated mitochondria and of the whole plant on CSP 310 treatment can differ, we studied an influence of CSP 310 infiltration of winter wheat seedlings shoots on lipid peroxidation and oxygen consumption.

The results obtained showed that cold stress treatment caused about 20 % increasing of dienic conjugates formation in winter wheat shoots tissues (Fig. 2). These data are well correlated with data obtained by many investigators on the influence of cold stress on lipid peroxidation in plant tissues [1, 2]. At the same, time we observed a slightly increase of oxygen consumption of winter wheat shoots during cold stress (Fig. 3).

An infiltration of winter wheat shoots by all plant uncoupling mitochondrial systems activators investigated (pyruvate, that activate AOX [13], linoleic acid, which is a substrate and activator of PUMP [12] and CSP 310) reduced the rate of lipid peroxidation during cold stress (Fig. 2). It is interesting to note, that all of them caused about 30 % decrease of dienic conjugates formation, and these values were slightly lower but were not statistically different from the value of dienic conjugate contents in non-stressed winter wheat shoots (Fig. 2). The study of an influence of these activators on oxygen consumption in winter wheat shoots during cold stress showed that all of them caused an increase of oxygen consumption values (Fig. 3). It is necessary to note, that, if the infiltration of winter wheat shoots by pyruvate and CSP 310 caused about 20–25 % increasing of oxygen consumption, their infiltration by linoleic acid caused about 100 % increasing of oxygen consumption. These data allow us to suppose that infiltration of winter wheat shoots by linoleic acid can strongly activate UCP-like plant uncoupling proteins and other members of the mitochondrial carrier protein family. On the other hand, this effect can deal not only with PUMP activation but also with the direct uncoupling effect of free fatty acids that are powerful uncouplers by themselves. Similarly, the influence of pyruvate infiltration on lipid peroxidation may be caused by its own antioxidant effect, but at the same time its effect on oxygen consumption during cold stress allows us to suppose that it can deal with its influence on mitochondrial energetic activity too.

So, based on the data obtained we can conclude that during cold stress all the studied winter wheat uncoupling systems can be involved in plant defense against oxidative stress. Low-molecular weight CSP 310-like proteins obtained from cereals investigated decreased lipid peroxidation in mitochondria but did not influence the energetic activity of plant mitochondria. Only CSP 310 increased lipid peroxidation in mitochondria damaged by inducing ascorbat-dependent and NADH-dependent lipid peroxidation systems.

Three day old etiolated shoots of winter wheat (Triticum aestivum L., cv. Irkutskaya Ozimaya) grown on moist paper at 26°C, were used in this work.

Crude and purified mitochondria were isolated from winter wheat shoots by the method described previously using discontinuous Percoll gradient consisting of 18%, 23%, 40% Percoll [15, 21]. Purity and integrity of mitochondria were determined by measurement of cytochrome c oxidase activity (EC 1.9.3.1) [22]. The mitochondrial proteins were measured by the Lowry method [23].

The isolated mitochondria were resuspended in the following medium: 20 mM MOPS-KOH buffer (pH 7.4), 300 mM sucrose, 10 mM KC1, 5 mM EDTA, 1 mM MgCl₂, 4 mM ATP, 4 mM ADP, 10 mM malate and 10 mM glutamate. In these experiments 0.5 mg of immunochemically related to CSP 310 proteins were added to mitochondrial suspension per 1 mg of mitochondrial protein. Energetic activity of mitochondria was analyzed immediately after isolation and after 30 min of incubation at 0°C. The aliquots of mitochondrial suspension were taken and the mitochondrial energetic activity was recorded polarographically at 27°C. The reaction medium contained 125 mM KCl, 18 mM KH₂PO₄, 1 mM MgCl₂ and 5 mM EDTA, pH 7.4. 10 mM malate in the presence of 10 mM glutamate was used as an oxidation substrate. Polarogrammes were used to calculate the rates of phosphorylative respiration (state 3), non-phosphorylative respiration (state 4), respiratory control by Chance-Williams and the ADP:O ratio [24].

Proteins, immunochemically related to winter rye stress protein CSP 310 from winter rye, winter wheat, Elymus and maize were isolated as described previously using affine chromatography on a column with BrCN-activated Sepharose with immobilized anti-CSP 310 antiserum [18].

The rate of lipid peroxidation was determined by measurement of the primary products of lipid peroxidation – conjugated diene formation. Mitochondria were incubated in the incubation media contained 175 mM KCl and 25 mM Tris-HCl (pH 7.4). For induction of the ascorbate – dependent lipid peroxidation system 1 mM ascorbate, 1 mM ADP and 20 mkM Fe²⁺ were added to the incubation media. For induction of the NADH – dependent lipid peroxidation system 1 mM NADH, 1 mM ADP and 20 mkM Fe²⁺ were added to the incubation media. For measurement of the dienic conjugate contents mitochondrial lipids were extracted by hexane – isopropanol (1:1 v/v) mixture (9 ml per 1 ml of the sample) by shaking. After shaking 1 ml H₂O was added to the mixture to stratify hexane and isopropanol phases. Measurement of dienic conjugate contents was made in the hexane phase at 233 nm on spectrophotometer "SF-46" ("LOMO", USSR). The dienic conjugate contents in the sample were calculated according to 233 nm molar extinction coefficient to polyunsaturated fatty acids conjugated dienes 2,2 × 10⁵ × M^-1 sm^-1[25].

Winter wheat shoots samples (3 g) were infiltrated by 1) Water, 2) Pyruvate (40 mM), 3) Linoleic acid (40 mM) and 4) CSP 310 (1 mg/mL) for 1 h and were packed in paper containers for stress treatment. Cold stress of winter wheat shoots was performed in thermostat at -4°C for 1 h. The control variant was not placed in stress conditions.

The oxygen uptake of winter wheat shoots was analyzed polarographically at 27°C using a platinum electrode of a closed type in a 1.4 mL volume cell. The reaction mixture contained 175 mM KCl and 25 mM Tris-HCl (pH 7.4).

All the experiments were made in six preparations. The data obtained were analyzed statistically, i.e. arithmetic means and standard errors were determined.