Features of the Effect of Quercetin on Different Genotypes of Wheat under Hypoxia

1. Introduction

Plants, due to their immobile nature, are very dependent on environmental conditions and suffer from its adverse effects. To counteract negative factors, plants have developed a powerful defense system. Various enzymes and numerous secondary metabolites are involved in the protective functions [1]. Wheat is one of the most important agricultural crops. The survival of half of the population of our planet depends on the yield of this crop and the quality of grain. In mid-latitudes with a temperate climate, which is most favorable for the normal growth of wheat, there is an increase in wetland crop lands associated with heavy seasonal rainfall.

O₂ is an essential element for plant survival. O₂ deficiency, which is formed as a result of heavy rainfall, interferes with respiration and other biochemical processes [2]. In addition, several other conditions can also lead to hypoxia, for example, salt stress can disrupt symplastic connections between cells,

During heavy rainfall, there is a deficiency of O₂, which is necessary for the normal development of the plant. Most terrestrial plants can temporarily survive O₂ deficiency by either accelerating shoot growth or by slowing growth and becoming dormant. Reduced O₂ content in flooded plants causes growth inhibition and cell damage. With prolonged exposure to hypoxia, these effects are enhanced [7]. The stage of plant development when it is immersed in water is of great importance for the effect of damage. This is especially observed during seed germination, early development, also flooding has a negative effect during flowering [8,9]. Plant recovery after O₂ deficiency is also one of the most important factors determining plant tolerance to hypoxia [10]. One of the visual indicators of plant response to hypoxia is the destruction of chlorophyll, the so-called chlorosis, which occurs when there is a lack of O₂ [11]. As a result of hypoxia, chlorophyll degradation occurs, the degree of which depends on the duration of hypoxia. However, chlorosis in plants can continue even after normal conditions are restored [12,13].

Stress factors lead to damage causing increased ROS production [14,15]. A significant increase in ROS is called oxidative stress. ROS generation is carried out mainly by mitochondria during oxidative phosphorylation reactions in the electron transport chain [16,17]. Changes in mitochondria lead to the release of intermembrane proteins, disruption of the electron transport chain, changes in the transmembrane potential difference, and the formation of excess ROS [18]. An increase in lipid oxidation in mitochondrial membranes disrupts their integrity and leads to swelling and lysis of mitochondria. This disrupts the energy supply of cells and reduces their adaptive ability to stress factors. During hypoxia, phosphatidic acid is released, which activates type D phospholipase, which triggers the regulation of the production of ROS and calcium [19]. Wheat plants tolerate hypoxia stress by regulating lipid remodeling, causing multiple changes in endogenous lipid levels [20].

The level of formation of highly toxic ROS in plant cells is controlled by antioxidants [21]. Plants have protective mechanisms against oxidative stress, leading to a decrease in the production of ROS and their destruction [22]. The antioxidant system of plants consists of enzymatic (superoxide dismutase, ascorbate peroxidase, guaiacol peroxidase, catalase, etc.) and non-enzymatic antioxidants (flavonoids, carotenoids, ascorbate, glutathione, tocopherols, etc.) [23,24].

Low molecular weight antioxidants belong to the secondary antioxidant system, as they are activated under severe oxidative stress, when the enzymatic antioxidant system can no longer cope with excess ROS. The main role of low molecular weight antioxidants is to detect and chelate free radicals. Flavonoids are one of the main classes of secondary plant metabolites and belong to the group of low molecular weight antioxidants [25]. More than 9000 flavonoid derivatives have been identified in various plants, which are further divided into different subfamilies depending on the modification of their basic structure [26,27]. Flavonoids contain several subgroups, including anthocyanidins, flavones, flavanols, flavanones, etc.

Quercetin (3,3',4', 5,7-pentahydroxyflavone) is one of the most abundant flavonoids in plants. Quercetin (Qu), classified as a phenolic compound, has strong antioxidant effects as it helps maintain oxidative balance [28]. This flavonoid is found in the outer membrane layer of the chloroplast membrane [29]. Due to this localization, Qu is involved in the regulation of the intensity of light exposure to plants [30]. Qu plays an important role in the process of protecting plants from the effects of stress, such as ultraviolet radiation or osmotic stress, which has been confirmed in numerous studies [32,33,34].

To increase the efficiency of agricultural production, a variety of plant protection products are widely used. However, these products often have adverse effects on the environment and human health. Therefore, more and more attention is being paid to the use of safe agents. The exogenous use of various bioregulators is very promising due to their cost-effectiveness compared to traditional breeding or transgenic approaches for increasing plant tolerance. Currently, more and more data are emerging on the use of Qu as a protective element against various stress factors [35]. However, despite the large number of publications on the effect of exogenous application of phenolic substances, including Qu, on physiological processes occurring in plants [36], information about it in wheat seedlings is insufficient [37]. The purpose of the study was to evaluate the effectiveness of using exogenous Qu on wheat seedlings of two genotypes exposed to hypoxia. The results obtained will allow future studies to evaluate the usefulness of this flavonoid as a preventive agent that protects plants from biotic and abiotic stresses.

2. Results

2.1. Growth Condition

Deficiency O₂ has the greatest negative effect on seed germination and in the early stages of plant development [8,9]. The effect of hypoxia was studied on 6-day-old wheat seedlings grown in roll culture. To study the reduction of excess ROS formed during hypoxia, treatment of seedlings of two varieties of Orenburgskaya 22 (Triticum aestivum) and Zolotaya (Triticum durum) with Qu was used before and after hypoxia for antioxidant systems, according to the scheme below (Figure 1).

In Table 1 shows the morphometric parameters of plant changes in response to O₂ deficiency in 6-day-old seedlings of two wheat varieties before and after treatment with 0.03% Qu.

The total length of seedlings of the Zolotaya variety practically does not change under hypoxia. O₂ deficiency leads to a decrease in shoot height by 1.21 times, but at the same time the root lengthens by 1.17 times. Hypoxia causes dramatic morphological changes in the Orenburgskaya 22 variety. The total length of seedlings during hypoxia decreases by 1.96 times: at the same time, the length of the roots decreased, in contrast to the Zolotaya variety, by 1.15 times. The height of shoots in the Orenburgskaya 22 variety also decreased by 1.23 times, as in the Zolotaya variety. Qu does not affect the morphometric parameters of the Zolotaya variety grown under normal conditions, and also does not affect the morphometric parameters under conditions of O2 deficiency. However, Qu promotes the development of the Orenburgskaya 22 variety, and leads to a slight elongation of the roots by 1.05 times. Although pre-treatment with Qu variety Orenburgskaya 22 before hypoxia (path A) is accompanied by morphometric changes: a decrease in the total length of the seedling by 1.08 times and a decrease in shoot height by 1.13 times is observed, while the length of the roots remains practically unchanged. However, treatment with Qu after hypoxia reveals inhibition of growth of both roots and shoots in the Orenburgskaya 22 variety. Probably, this fact indicates that for the Orenburgskaya 22 variety, reoxygenation is the most limiting stage after hypoxia. Unlike the Orenburgskaya 22 variety, the Zolotaya wheat variety is tolerant of O₂ deficiency, its total seedling length remains virtually unchanged and treatment with Qu does not affect morphometric parameters.

2.2. Сytological Analysis

The structure of root cells of two wheat genotypes grown under different conditions leading to the formation of vacuoles in the cytoplasm was studied. As a result, cell types with vacuoles were identified that differed in size, shape and localization in the cytoplasm. No changes in the cytoplasm were detected in the cells of control plants of both wheat varieties (Figure 2, Table 2).

Under hypoxic conditions, with a decrease in the availability of O2, small and narrow, elongated vacuoles near the nuclear membrane were detected in the root cells of the Zolotaya variety. However, most cells contained giant vacuoles near the nucleus, causing the nucleus to move toward the cytoplasmic membrane. In most cells of the Orenburgskaya 22 variety, elongated vacuoles near the nucleus were detected. In some cells, irregularly shaped vacuoles were randomly located throughout the cytoplasm. Invaginations of the plasma membrane were detected on the cell surface.

When seedlings of the Orenburg variety were treated with Qu, 22 irregularly shaped vacuoles were detected only in dividing root cells. In some cells of the Zolotaya variety, large vacuoles around the nucleus are found in the cytoplasm. Most cells had one giant vacuole around the nucleus.

Pre-treatment with Qu before exposure to hypoxia on seedlings of the Orenburgskaya 22 variety is accompanied by the formation of giant vacuoles, which can lead to kernel deformation. However, there are cells with a granular structure. In the Zolotaya variety, interphase (G2) and prophase cells are characterized by granularity of the cytoplasm at the G2 and prophase stages.

Treatment with Qu after hypoxia in cells of the Orenburgskaya 22 variety is accompanied by the formation of a fine-grained structure of the cytoplasm. In most cells, vacuoles of irregular shape are concentrated around the nucleus. In the Zolotaya variety, under the same conditions, cells with numerous small vacuoles are found, forming necklaces around the nuclei.

2.3. Chlorophyll Content

Plant stress negatively affects photosynthetic electron transfer in PSI and PSII and chlorophyll biosynthesis [15,38]. Therefore, the photosynthetic apparatus is a sensor of various environmental stresses, which may be responsible for the imbalance of cellular energy due to modification of the redox status [39]. From the data in Table 3 it is clear that hypoxia leads to a decrease in the content of Chl a and Chl b in the leaves of the wheat variety Orenburgskaya 22 (3.3 times and 3.7 times, respectively). However, in the leaves of the Zolotaya variety, the effect of hypoxia is of a different nature; even a slight increase in the content of Chl a and b is observed. It should be noted that the content of Chl a and Chl b in the Zolotaya variety in the control is lower than in the Orenburgskaya 22 variety (1.7 times and 1.9 times, respectively). The Chl a/Chl b ratio in the Zolotaya variety is higher than in the Orenburgskaya 22 variety due to the lower Chl b content. Under O₂ deficiency, the Chl a/Chl b ratio increased relative to the control in both the Orenburgskaya 22 wheat and the Zolotaya variety, although not as significantly.

The addition of Qu leads to an increase in the content of Chl a and Chl b in the leaves of the wheat variety Orenburgskaya 22 and has virtually no effect on their content in the Zolotaya variety. The addition of Qu before hypoxia (path A) prevents a decrease in the content of Chl a and Chl b in the leaves of the Orenburgskaya 22 variety), thereby not disrupting the process of photosynthesis, and even higher content of Chl a and Chl b is observed than in the control. The addition of Qu after hypoxia (Figure 1, path B) leads to an increase in the content of Chl a and Chl b, but does not lead to their complete recovery. Thus, in the leaves of the Orenburgskaya 22 variety, the process of destruction of chlorophylls (chlorosis) occurs during hypoxia. Qu prevents the process of chlorosis, however, reoxygenation in the leaves is so significant that Qu does not completely prevent the degradation of chlorophylls after hypoxia.

It is interesting to note that treatment with Qu before and after hypoxia leads to a decrease in the content of Chl a and Chl b in the leaves of the wheat variety Zolotaya compared to control. It can be assumed that in the Zolotaya variety there is a different set of non-enzymatic antioxidants, in contrast to the Orenburgskaya 22 variety, which actively protects green pigments from destruction during hypoxia. The addition of Qu competes with other low molecular weight metabolites and, as a result, an increase in the process of chlorosis is observed.

2.4. Content ROS

Abiotic and biotic stress factors induce a reaction in plants, during which ROS production in cells increases and a series of cascade reactions are triggered to neutralize excess ROS. ROS targets in cells can be various biochemical and physiological reactions, as well as cellular structures, depending on the degree of damage to which cell metabolism is rearranged and plants acclimatize to stress conditions or one or another variant of programmed cell death (PCD) is triggered [40,41,42].

Excessive production of ROS during oxidative stress is part of many stressful situations, including hypoxia. In the transition from normal to hypoxia, there is an increase in the formation of ROS, plant mitochondria undergo swelling, releasing Ca2⁺ and cytochrome c. Transmission electron microscopy under hypoxic conditions in wheat roots visualized the presence of H₂O₂ in the apoplast and in association with the plasma membrane [43]. If in the control wheat mitochondria were characterized by an electron-dense matrix, intact membranes and distinct cristae, then under the influence of hypoxia mitochondria are characterized by an increase in volume, a decrease in matrix density and disintegration of cristae associated with deep swelling [44]. Under conditions of hypoxic stress, evidence of ROS formation under conditions of low oxygen content was found [45]. The decrease in the ATP content observed during hypoxia increases the likelihood of ROS formation due to the inhibition of the mitochondrial electron transport chain [46].

Our studies have shown that cultivated wheat plants under the action of hypoxia (24 h), when staining the roots of varieties Orenburgskaya 22 and Zolotaya with the ROS marker Carboxy-H2DFF, contain different amounts of ROS production, determined by the intensity of fluorescence. In the roots of Orenburgskaya 22 wheat grown under control conditions, the fluorescence intensity is 1.22 times lower than in the roots of the Zolotaya variety (Figure 3 and Figure 4). Root zones were noted from the most intense fluorescence to its absence. The data obtained show that during hypoxia, the most intense ROS staining is observed in the areas of the cap and fission. At the same time, compared with the control, the increase in the level of ROS is most observed in the cells of the epidermis and cortex, and to a lesser extent in the cells of the central cylinder (Figure 3).

O₂ deficiency induces the formation of ROS in both wheat genotypes. But if in the Zolotaya variety the amount of ROS increased only 1.06 times, then in the Orenburgskaya 22 variety this increase was 2.69 times. As a result of exposure to hypoxia, the ROS content in the roots of the Orenburgskaya 22 variety exceeded that in the Zolotaya variety by more than 2 times.

Qu significantly reduces the amount of ROS by 1.51 times in the roots of the Orenburgskaya 22 variety and has virtually no effect on the Zolotaya variety. Treatment with Qu, both before and after hypoxia, practically did not change the level of ROS in the roots of the Zolotaya variety. However, pre-treatment with Qu before exposure to hypoxia reduced the production of ROS in the Orenburgskaya 22 variety by 2.45 times and approached almost the level of ROS in the control roots. Although treatment with Qu decreased after hypoxia, it was not as effective as compared to pre-treatment.

2.5. Content H₂O₂

The H₂O₂ content in the control shoots of both wheat varieties is close in value (Figure 5). In the roots of the Zolotaya variety, the H₂O₂ content is slightly higher (1.1 times) than in the roots of the Orenburgskaya 22 variety. Moreover, the H₂O₂ content in the roots of both wheat varieties exceeds the H₂O₂ value in the shoots: in the Orenburgskaya 22 variety by 6.26 times, in the Zolotaya variety - by 7.24 times. The effect of hypoxia leads to an increase in the H₂O₂ content in both roots and shoots. However, the accumulation of H₂O₂ in different organs of different wheat genotypes has a different tendency. If in the roots of the variety Orenburgskaya 22 H₂O₂ increases only by 1.49 times, then in the shoots - by 1.64, and in the Zolotaya variety in the roots - by 1.15 times, and in the shoots - by 1.08. Qu reduces the H₂O₂ content only in the roots and shoots of the Orenburgskaya 22 variety; and in the Zolotaya variety, added Qu even leads to an increase in H₂O₂ content. Treatment with Qu before exposure to O2 deficiency on the Orenburgskaya 22 variety resulted in a 1.28-fold decrease in H₂O₂ content in roots compared to exposure to hypoxia, and in seedlings by 1.23-fold. Treatment with Qu after exposure to hypoxia in seedlings of the Orenburgskaya 22 variety even led to an increase in the accumulation of H₂O₂ compared to hypoxia by 1.13 times. Treatment of the Zolotaya variety with Qu did not lead to significant changes in the H₂O₂ content in the roots. It should be noted that treatment of this wheat variety with Qu was accompanied by an increase in the H₂O₂ content in the shoots by 1.52 times. O₂ deficiency in the shoots of the Zolotaya variety was not accompanied by the accumulation of H₂O₂, however, treatment with Qu before and after hypoxia led to an increase in H₂O₂.

2.6. Antioxidant System

Various abiotic stresses lead to an overproduction of ROS in plants, which are highly reactive and toxic and cause damage to proteins, lipids, carbohydrates and DNA, which ultimately leads to oxidative stress [47]. The antioxidant system protects plants from damage caused by oxidative stress [41]. The antioxidant system (AOS) includes a complex of enzymes involved in detoxification and the conversion of superoxide ions into peroxide and then into water, and a complex of low molecular weight components. Therefore, the antioxidant activity (AOA) value depends on the extraction method. We used two test systems, which are based on different methods of extraction of the material under study: water and alcohol. (R)-4-[1-Hydroxy-2-(methylamino)ethyl]-benzene-1,2-diol (HMAEB) and 2,2-diphenyl-1-picrylhydrazyl (DPPH) were used as substrates (Table 4).

The AOA value in the wheat variety Orenburgskaya 22 in the roots is 1.09 times higher than in Zolotaya, and in the shoots of the Zolotaya 22 variety it is 1.03 times higher than in Orenburgskaya 22 (Table 3). A decrease in O₂ levels leads to a decrease in AOA levels in both roots and shoots of both wheat genotypes. However, the decrease in AOA in the Orenburgskaya 22 variety is more significant than in the Zolotaya variety (in roots by 1.50 and 1.14, respectively, and in shoots by 1.55 and 1.1, respectively).

Qu increases AOA in the roots of the Orenburgskaya 22 variety by 1.18 times, and in the shoots only by 1.03 times. It is interesting to note that in the shoots of the Zolotaya variety, Qu reduces AOA by 1.03 times. Pre-treatment of the Orenburgskaya 22 variety with Qu does not protect the roots from hypoxia and AOA remains at the same level as under hypoxia. A slight increase in AOA is observed only in the shoots of this variety. And treatment of the Orenburgskaya 22 variety with Qu after O2 deficiency leads to an even greater drop in AOA. Similar to the Zolotaya variety, treatment with Qu after hypoxia reduces the total level of AOA in both roots and shoots. However, pre-treatment of the Zolotaya variety with Qu leads to an increase in AOA in shoots by 1.13 times.

The ARA value is significantly higher than the AOA, but its changes have the same trend as the AOA. The ARA value in the shoots of the Zolotaya variety is also higher than in the Orenburgskaya 22 variety, and lower in the roots. It should be noted that the differences in the content of the two wheat varieties in ARA values are less significant than AOA. This is probably due to the fact that the amount of low molecular weight antioxidants in the Zolotaya variety is higher than in the Orenburgskaya 22 variety, since the determination of ARA uses alcoholic extraction of plant materials, which promotes the extraction of low molecular weight antioxidants, such as polyphenols and flavonoids.

2.6.1. Content Glutathione

Glutathione (GSH) is one of the low molecular weight components of AOS involved in H₂O₂ detoxification [24]. Glutathione is a tripeptide (L-glutamyl-L-cysteinylglycine. The protective effect of GSH is accompanied by its oxidation sulfhydryl group and conversion to glutathione disulfide (GSSG). A high GSH/GSSG ratio and the activity of enzymes associated with GSH metabolism are among the markers of plant resistance to stressors [48].

The GSH content in the roots of the Zolotaya variety (2.43 mM) is 1.87 times higher than in the Orenburgskaya 22 variety (1.32 mM) (Fig. 6), and in the shoots it is 1.42 times higher (Figure 6). A decrease in O₂ level leads to a sharp increase in GSH concentration, especially in the shoots of the Zolotaya variety by 7.68 times. At the same time, in the Orenburgskaya variety, the increase in GSH content increases only by 1.21 times. Although the GSH content in the roots of the Orenburgskaya 22 variety increases more significantly than in the shoots (1.76 times), and in the Zolotaya variety in the roots less significantly (2.58 times) compared to the shoots, the total GSH content in the roots of the Zolotaya variety is nevertheless higher in 2.75 times.

Qu has a positive effect on the Orenburgskaya 22 variety, especially on the roots: the GSH content increases by 1.77 times. At the same time, in the roots of the Zolotaya variety, Qu inhibits the synthesis of GSH: its content decreases by 1.58 times. Qu has little effect on the GSH content in the shoots of both wheat varieties. Treatment with Qu both before and after hypoxia, variety Orenburgskaya 22, increases the GSH content, especially in the roots (before by 1.98 times, after by 1.44 times). If treatment of the roots of the Zolotaya variety with Qu is not as effective as for the Orenburgskaya 22 variety, then this treatment has a negative effect on the shoots: the GSH content decreases (before 1.36 times, after -1.6 times).

2.6.2. Expression of Genes

The antioxidant system protects plants from damage caused by oxidative stress. ROS also influence the expression of a number of genes and therefore control many processes such as growth, cell cycle, PCD, abiotic stress responses, pathogen defense, systemic signaling, and development. In this review, we describe the biochemistry of ROS and their sites of production, as well as the antioxidant defense mechanisms that scavenge ROS. Superoxide ion (O^2-.) is the most toxic molecule that accumulates in plants as a result of exposure to abiotic stress. Superoxide dismutases (SOD) convert O^2-. into H₂O₂ [24]. Increased SOD activity represents one of the most important protective mechanisms that reduces oxidative damage caused by stress. However, increased H₂O₂ content is reactive and toxic and must be removed. The conversion of H₂O₂ involves a number of enzymes that convert H₂O₂ into H₂O. CAT, PX and GPX, are among the most active enzymes involved in the neutralization of H₂O₂ [49].

Depending on the metal interacting with the active site, enzymes can be divided into three types: FeSOD, MnSOD, Cu/ZnSOD [23]. Different isoforms of SOD with similar functions have different metal cofactors, amino acid sequences, crystal structures and subcellular localizations and exhibit different sensitivity to H₂O₂ in vitro [50,51]. Cu/ZnSOD, which are mainly located in chloroplasts, cytoplasm and/or extracellular space, are present in some bacteria and all eukaryotic species [52], while MnSODs are mainly found in plant mitochondria [53,54]. FeSOD are common in prokaryotes, protozoa, usually localized in chloroplasts and plant cytoplasm [55].

The expression of the mitochondrial MnSOD gene in the Orenburgskaya 22 variety is higher than in the Zolotaya variety; in the roots by 2.42 times, in the shoots it decreased by 1.03 times. (Figure 7). It should be noted that in the roots of the Orenburgskaya 22 variety, MnSOD activity is 2.12 times higher than in the shoots. In the Zolotaya variety, there is a slight excess of MnSOD activity in the shoots than in the roots (1.1 times). O₂ deficiency causes a significant increase in MnSOD activity in both roots and shoots of both wheat varieties. It should be noted that hypoxia stimulates MnSOD activity in the Zolotaya variety (2.92 times in roots, 2. 2 times in shoots) more significantly than in the Orenburgskaya 22 variety (1.74 times in roots, 1.95 times in shoots).

Treatment with Qu leads to a significant increase in the level of MnSOD expression in the roots of the Orenburgskaya 22 variety by 2.88 times and in the shoots by 2.22 times. However, changes in expression levels are less significant, especially in roots; only 1.08 times. Pre-treatment with Qu before decreasing the O₂ content is accompanied by an increase in MnSOD activity in both the roots and shoots of the Orenburgskaya 22 variety (2.01 and 2.49 times, respectively). And treatment with Qu after exposure to hypoxia is not as effective as pre-treatment. In contrast to the variety Orenburgskaya 22. In the variety Zolotaya, pretreatment is much less significant; moreover, it even leads to a decrease in the level of MnSOD expression, especially in the roots (2.48 times).

In control samples of wheat Orenburgskaya 22, the level of expression of chloroplast Cu/ZnSOD is higher than in the Zolotaya variety, especially in the roots (2.23 times). It should be noted that the Cu/ZnSOD activity in the shoots of the Orenburgskaya 22 variety is slightly lower than in the roots (1.09 times), and in the Zolotaya variety the opposite picture is observed: in the shoots the Cu/ZnSOD activity is 1.35 times higher than in the roots. A decrease in O₂ content is accompanied by an increase in the expression of Cu/ZnSOD, this is especially noticeable for the Zolotaya variety: in the roots it increases by 5.02 times, and in the shoots by 2.64 times.

Qu stimulates the activity of Cu/ZnSOD especially in the roots of the Orenburgskaya 22 variety by 2.96 times. At the same time, in the shoots of the Zolotaya variety, a slight drop in Cu/ZnSOD activity is observed. Treatment with Qu before or after hypoxia induces different expression responses of Cu/ZnSOD in roots and shoots of different wheat genotypes. If in the Orenburgskaya 22 variety, treatment with Qu leads to activation of Cu/ZnSOD, especially in the shoots (pathway a, 1.92 times), then in the Zolotaya variety, under the same conditions, Cu/ZnSOD activity is inhibited in the shoots.

One of the main enzymes involved in the conversion of H₂O₂ to H₂O and O₂ is catalase (CAT) [56,57]. Based on the data obtained, it follows that CAT is more active in shoots than in roots in both wheat genotypes: in Orenburgskaya 22 by 4.55 times, in Zolotoy by 1.45 times. It is interesting to note that CAT is most active in the roots of the Zolotaya variety and in the shoots of the Orenburgskaya 22 variety. Hypoxia leads to an increase in activity in the Zolotaya variety in both roots and shoots (1.59 times, 1.47 times, respectively). If O₂ deficiency is not accompanied by changes in the expression of CAT in the shoots of the Orenburgskaya 22 variety, a significant drop in CAT activity by 1.43 times is observed in the roots. Qu causes activation of CAT expression in the roots of Orenburgskaya 22 (1.96 times), and in the Zolotaya variety inhibition of CAT activity is observed. In the shoots of both wheat varieties, Qu did not have a significant effect on CAT levels. Pretreatment with Qu leads to a sharp increase in the level of CAT expression in the roots of both wheat varieties. especially in the roots of the Orenburgskaya 22 variety (4.09 times). In shoots of the Zolotaya variety, there is also an increase in CAT activity before and after treatment with Qu, and in shoots of the Orenburgskaya 22 variety, under the same conditions, CAT activity decreases.

Peroxidase (PX) is also involved in the neutralization of H₂O₂ [58]. The highest PX activity was observed in the roots of Orenburgskaya 22 compared to the roots of the Zolotaya variety (5.93 times). In shoots there is no longer such a big difference in PX activity between varieties (1.85 times). But if in the roots and shoots of the Orenburgskaya 22 variety the levels of PX expression are close, then in the shoots of the Zolotaya variety the level of PX activity is 3.07 times higher. than in the roots. Hypoxia causes a sharp increase in activity in the roots of the Zolotaya variety by 5.53 times. PX activity in the roots of the Zolotaya variety also increases significantly with the addition of Qu (4.08 times). The level of activity during pre-treatment with Qu before reducing the O₂ level in the roots of the Zalotaya variety also contributes to the activation of PX. In shoots of the Zolotaya variety, a decrease in PX activity is observed, especially in the case of treatment with Qu after hypoxia by 3.16 times. If O₂ deficiency leads to a slight increase in PX activity in the Orenburgskaya 22 variety, then Qu in all variants causes a significant decrease in PX activity in both roots and shoots.

Another enzyme involved in the neutralization of H₂O₂ is glutathion peroxidase (GPX) [59,60]. GPX activity in control samples of wheat variety Orenburgskaya 22 in both roots and shoots is higher than in the Zolotaya variety (1.24 times and 2.20 times, respectively). Noted, that GPX activity is higher in the shoots of Orenburgskaya 22. than in the roots by 1.06 times, and in the Zolotaya variety it is higher in the roots, than in escapes at 1.66. O₂ deficiency leads to a decrease in GPX activity in all variants. Qu also inhibits GPX activity. Only in the case of treatment with Qu before and after exposure to hypoxia in the shoots of the Zolotaya variety is an increase in GPX activity observed.

Glutathion-S- transferase (GST) responsible for detoxification has approximately the same level of activity in all control samples [61,62]. Changes in growing conditions for the Orenburgskaya 22 variety practically did not lead to significant changes. A decrease in O₂ content significantly stimulated an increase in activity GST in the Zolotaya variety: in the roots by 2.78 times, in the shoots by 1.93 times. It is interesting to note that the addition of Qu decreased the level of GST expression in the shoots of the Orenburgskaya 22 variety and increased it in the shoots of the Zolotaya variety.

3. Disscussion

Oxygen (O₂) is an important element for normal plant development [63]. O₂ deficiency resulting from heavy precipitation impairs respiration and other biochemical processes [63]. In addition, a number of other conditions can lead to hypoxia, for example, salt stress can disrupt symplastic connections between cells, resulting in a decrease in cell permeability to O₂ [64]

Plants are very plastic and quickly adapt to changing unfavorable environmental conditions. Depending on the mechanisms and speed of adaptation, plants can be divided into varieties tolerant and sensitive to abiotic stress. Hypoxia is one of the most important abiotic stresses. In addition, plants often experience physiological hypoxia in tissues and organs due to limited O₂ diffusion or rapid O₂ consumption [65].

Hypoxia-tolerant plants tolerate long-term reductions in O₂ availability by accelerating shoot growth and thereby increasing O₂ or, conversely, by slowing growth while conserving nutrient resources [6]. To survive O₂ deficiency, plants use various strategies through biochemical, anatomical and morphological changes. For example, the distribution of O₂ from the aerial parts to the roots is facilitated by the formation of aerenchyma [66,67]. Similarly, the formation of adventitious roots can also improve O2 levels in plants under waterlogged conditions [68]. Meanwhile, balanced ROS production and increased antioxidant activity can improve tolerance to hypoxia and anoxia in plants [69].

Abiotic stresses lead to a decrease in the content of chlorophyll (Chl) and carotenoids, leaf necrosis and a decrease in metabolic functions in the cell, including photosynthesis [70]. Osmotic stress associated with ion imbalance as well as hypoxia can lead to oxidative damage [15]. Analysis of chlorophyll a and b content is an excellent tool for quantifying damage to the photosynthetic apparatus caused by abiotic stress [71].

Stress negatively affects photosynthetic electron transfer in PSI and PSII and Chl biosynthesis in plants [72]. Therefore, the photosynthetic apparatus is a sensor of various environmental stresses, which may be responsible for the imbalance of cellular energy due to modification of the redox status.

All significant changes occurring in the roots and shoots of two wheat genotypes grown under different conditions are presented in diagrams (Figure 8, Figure 9, Figure 10 and Figure 11). Under normal development conditions, the content of Chl a and Chl b in the Orenburgskaya 22 variety is significantly higher. than that of the Zolotaya variety by 1.67 and 1.92 times, respectively. It can be assumed that the slowdown in the process of photosynthesis in the Zolotaya variety is due to slower access of O₂ and its absorption compared to the Orenburgskaya 22 variety. From the data in the figure it can be seen that O₂ deficiency leads to a decrease in the content of Chl a and Chl b in the leaves of the wheat variety Orenburgskaya 22, a in the Zolotaya variety it even increases. Hypoxia and the associated O₂ deficiency turned out to be not critical for the biosynthesis of Chl in the Zolotaya variety, since the Zolotaya variety is adapted to O₂ deficiency.

When exposed to various unfavorable stresses, including hypoxia, the level of ROS in plants increases [41]. The accumulation of the fluorescent ROS marker Carboxy-H2DFFDA in the cells and tissues of the roots of wheat seedlings under the influence of oxidative stress induced by hypoxia indicates a disruption of ROS homeostasis. In the variety Orenburgskaya 22, under hypoxia, a significant increase in ROS is observed compared to the variety Zolotaya. In particular, in the Orenburgskaya 22 variety there is a more significant accumulation of H₂O₂ both in the roots and in the shoots compared to the Zolotaya variety. Increased ROS production triggers antioxidant defense in wheat. In the process of evolution, plants have developed a powerful antioxidant system to protect against external influences. A decrease in the availability of O₂ during hypoxia leads to a decrease in the overall activity of AOA, with the most significant drop in activity noted in the roots of the Orenburgskaya 22 variety, and the least significant drop occurs in the shoots of the Zolotaya variety.

AOS includes both an enzymatic complex and low molecular weight antioxidants. The enzyme complex mainly includes SOD, which is divided into different isoforms depending on the metal cofactor [53]. Depending on the cofactor, the localization of SOD is determined [54,55]. The most important isoform of the enzyme is MnSOD, since it is localized in mitochondria, the main sources of ROS.

The greatest activity of mitochondrial MnSOD is manifested in the roots of the Orenburgskaya 22 variety. O2 deficiency leads to an increase in the level of MnSOD expression, this is especially noticeable in the roots of the Zolotaya variety. However, the overall level of MnSOD activity remains higher in the Orenburgskaya 22 variety. Under normal growth conditions in the roots and shoots of the Orenburgskaya 22 variety, the level of activity of another SOD, chloroplast Cu/ZnSOD, exceeds that of the Zolotaya variety. However, under hypoxic conditions, this form of SOD is most activated in the Zolotaya variety, especially in the roots. Consequently, in the Orenburgskaya 22 variety, mitochondrial MnSOD is most responsible for the conversion of superoxide ion into peroxide under O2 deficiency, and in the Zolotaya variety, it is chloroplast Cu/ZnSOD.

Further detoxification associated with the conversion of H₂O₂ into H₂O and free O₂ occurs with the help of a number of enzymes, the most important of which is catalase [56,57]. It should be noted that catalase activity depends on the level of H₂O₂. However, the greatest accumulation of H₂O₂ occurs in the roots of the Orenburgskaya 22 variety, but at the same time the activity of CAT decreases. Although the H₂O₂ content in the roots of the Zolotaya variety increases slightly under hypoxia, the expression of the CAT gene has the greatest activity. Another enzyme involved in the detoxification of Н₂О₂ -_РХ also does not show an increase in activity in the Orenburgskaya 22 variety under hypoxia, in contrast to the Zolotaya variety, in which, especially in the roots, the activity of РХ increases sharply.

Under stressful circumstances, when ROS accumulate in plants and enzymatic AOS is unable to neutralize excess ROS, low molecular weight antioxidants are activated in plants. One of the most important antioxidants is GSH [24]. The main place of its localization is chloroplasts. GSH is often used as a marker of plant resistance to stressors [48]. In the roots, the GSH content of the Zolotaya variety is almost 2 times higher than that of the Orenburgskaya 22 variety. As a result of a decrease in O₂ levels, an increase in GSH content is observed in all wheat genotypes, both in shoots and roots. But if the increase in GSH in the Orenburgskaya 22 variety is not so significant, then in the roots of the Zolotaya variety the GSH increase occurs more than 7 times. Such a high GSH content in the Zolotaya variety may be due to the fact that the functioning of chloroplasts plays a special role in the Zolotaya variety under O₂ deficiency. This assumption is also confirmed by the special activity of chloroplast Cu/ZnSOD under hypoxic conditions. One of the evidence of the special role of GSH in the Zolotaya variety under hypoxia is the activation of GST-glutathione-S-transferase, an enzyme involved in detoxification together with GSH [61,62].

Using cytological analysis, different types of changes in the structure of the cytoplasm in root cells of two wheat genotypes were identified. In most Zolotaya wheat cells, under hypoxia, giant vacuoles formed around the nucleus. In cells of the Orenburgskaya 22 variety, cells with irregularly shaped vacuoles, randomly located throughout the cytoplasm, were observed. Different changes in the structure of the cytoplasm indicate different methods of protection against O₂ deficiency. The formation of giant vacuoles probably contributes to better adaptation to hypoxia in the Zolotaya variety compared to the Orenburgskaya 22 variety.

The greatest changes occur in the root cells of the Zolotaya variety during pretreatment with Qu (path A). These changes are associated with the formation of a fine-grained structure of the cytoplasm. Individual cells with a similar structure are also found in the variety Orenburgskaya 22. There are significantly more such cells in Orenburgskaya 22 when seedlings are treated with Qu after hypoxia.

In stressful factors, phytoprotectors are used that protect plants and mitigate the effects of stress [73]. These metabolites include phenolic compounds, one of which is Qu. Qu is a flavonoid that plays an important role in maintaining a balanced concentration of ROS in cells and in enhancing physiological functions, providing tolerance to biotic and abiotic stresses. Qu reduces the level of H₂O₂, absorbs ROS, inhibiting their aggregation. The antioxidant effect of Qu was confirmed in studies by [74], in which various plant species were subjected to paraquat stress, where Qu was shown to be an effective protective agent against the harmful effects of ROS on plants. Therefore, this flavonoid has a beneficial effect on plant resistance to oxidative stress due to the inactivation of reactive oxygen and the interaction of ROS with the electron transport of chloroplasts and mitochondria [36].

The addition of exogenous Qu to the Orenburgskaya 22 variety had a beneficial effect on both morphometric parameters and Chls content (Figure 9). Moreover, a decrease in ROS and H₂O₂ levels was noted. Total AOA increased, and MnSOD and Cu/ZnSOD activities also increased, especially in roots. But at the same time, inhibition of the activity of enzymes involved in the neutralization of H₂O₂ was observed. One can guess that exogenous Qu activates SOD enzymes itself actively participates in the neutralization of H₂O₂, inhibiting enzyme activity, participating in this process.

Unlike the Orenburgskaya 22 variety, treatment with Qu on the Zolotaya variety does not have a noticeable effect on morphometric parameters and Chls content. Moreover, a decrease in AOA and an increase in H₂O₂ content were noted. In addition, the content of the important AOS component for the Zolotoy variety, GSH, decreased slightly in the roots, while the activity of the MnSOD and Cu/ZnSOD genes remained virtually unchanged. or even decreased. It should be noted that in the roots of the Zolotaya variety, treatment with Qu significantly increased the activity of PX. It can be assumed that in the Zolotaya variety there is competition between endogenous GSH and exogenous Qu. As a result of this, low-molecular antioxidants were excluded from the process of H₂O₂ neutralization, which led to a slight increase in the H₂O₂ content.

Pre-treatment with Qu before the negative impact of hypoxia on the Orenburgskaya 22 variety has a positive effect (Figure 10). Although, in comparison with the sample of wheat treated with Qu, there is a decrease in morphometric parameters with further hypoxia, but in comparison with the sample after exposure to hypoxia (without pre-treatment with Qu), the shoot height and root length of the Orenburgskaya 22 variety are higher. The chlorophyll content in shoots of Orenburgskaya 22 does not decrease with O₂ deficiency, which also indicates the protective mechanism of Qu. It should be noted that pre-treatment with Qu helps to reduce ROS compared to hypoxia, however, compared to the control, H₂O₂ accumulates in the shoots of the Orenburgskaya 22 variety. Total AOA decreases, especially in the roots, and pretreatment with Qu does not improve the situation. Under these conditions, in the roots of the Orenburgskaya 22 variety, the activities of MnSOD and Cu/ZnSOD, as well as enzymes involved in the neutralization of H₂O₂, except for CAT, are significantly reduced. However, it should be noted that the GSH content simultaneously increases. It is interesting to note that a different picture is observed in the shoots: the activity of MnSOD and Cu/ZnSOD and the activity of PX and GPX increase. Thus, it can be assumed that pre-treatment with Qu on the Orenburgskaya 22 variety has a positive protective effect mainly on the development of shoots and changes the defense mechanism in the roots, placing the main emphasis on GSH.

Pre-treatment with Qu before hypoxia in the Zolotaya variety has its own characteristics. This treatment does not lead to the accumulation of ROS, the H₂O₂ content also does not increase in the roots, only in the shoots, while the chlorophyll content decreases. Under these conditions, in the Zolotaya variety, as well as in the Orenburgskaya 22 variety, the activity of MnSOD and Cu/ZnSOD, as well as enzymes involved in the neutralization of H₂O₂, with the exception of CAT, is significantly reduced. At the same time, the GSH content increases significantly. Thus, we can conclude that Qu does not have a positive effect on the Zolotaya variety, and hypoxia even helps to restore the normal development of the Zolotaya variety.

The process of plant reoxygenation - recovery from hypoxia - is also a stress state in plants [10]. During this period, plants experience oxidative stress, associated with excess O₂, resulting in cellular damage. Depending on the duration of the reoxygenation process, when the water level slowly decreases, in the case of poor adaptation of the plant to the reoxygenation process, especially at an early stage of development, cellular damage can be significant and can lead to death. To facilitate the recovery of wheat after hypoxia, we used Qu treatment (Figure 11).

Treatment with Qu after hypoxia promotes root elongation and an increase in shoot height in the Orenburgskaya 22 variety, as well as an increase in Chls content, although there is no complete restoration to the control level. Especially, after stress treatment with Qu effectively affects the shoots of the Orenburgskaya 22 variety. Against the background of inactivation of redox processes in the roots, these processes are significantly activated in the shoots. Perhaps the Orenburgskaya 22 variety requires a longer period to fully recover from hypoxia. But even based on these indicators, we can talk about the positive effect of treating the Orenburgskaya 22 variety, which is sensitive to O₂ deficiency, with Qu.

Treatment of the Zolotaya variety with Qu during reoxygenation gives a different effect. If the morphometric parameters remain practically unchanged, then the Chls content decreases both in comparison with control shoots and with shoots under hypoxia. Moreover, almost all participants in redox processes are inactivated in both shoots and roots. Consequently, this experiment also confirms the conclusion that the Zolotaya variety is a wheat variety with a low level of redox balance, O₂ deficiency is the norm for its development and an increase in the activity of oxidative processes leads to significant damage.

Abiotic and biotic stresses cause degradation of intracellular components through the process of autophagy [75]. Increased ROS generation under stress conditions promotes the induction of autophagy, which attenuates oxidative stress [76], thus representing a regulatory cycle. It was previously established that autophagy is induced in wheat cells of the Orenburgskaya 22 and Zolotaya varieties under stress [77]. depending on the degree of damage to cellular structures, at which a restructuring of cellular metabolism occurs and plants acclimatize to stressful conditions, or one or another variant of PCD is triggered [76,77,78,79,80]. Two pathways of plant PCD are known: “apoptosis-like”, the markers of which are DNA breaks, release of cytochrome c from mitochondria and transfer of phosphatidylserine to the outer layer of the membrane, and “vacuolar death”, characterized by the formation of large vacuoles and autophagosomes [81].

O₂ deficiency causes an increase in nuclei with DNA breaks in seedling root cells (our article). In the variety Orenburgskaya 22, breaks were found in 11% of root cells, and in the variety Zolotaya - in 8%. Under hypoxic conditions, the root cells of Orenburgskaya 22 were noticeably larger than those of the Zolotaya variety; cells in the G2 period and prophase predominated. Many binucleated cells were observed, which indicates a violation of cytokinesis; the cytoplasm of these cells was vacuolated. The appearance of DNA breaks in the nuclei of root cells indicates the role of hypoxia as an inducer of cell death along an apoptosis-like pathway. When exposed to hypoxia, phosphatidylserine was detected on the plasma membrane of both wheat varieties, and the cell nuclei are stained with propidium iodide, which indicates their necrotic death.

Immunodetection of cytochrome c revealed the release of cytochrome c from mitochondria into the cytoplasm of cells in both wheat varieties, but in the Orenburgskaya variety there were significantly more 22 death cells than in the Zolotaya variety. These indicators indicate the mitochondrial pathway of apoptosis under hypoxia in two wheat genotypes. During hypoxia, giant vacuoles are formed in the Zolotaya variety, which are one of the protective mechanisms against O₂ deficiency.

Qu activates protective mechanisms when O2 availability decreases only in the case of the Orenburgskaya 22 variety. Pre-treatment with Qu helps to increase the tolerance of the Orenburgskaya 22 variety. However, under the same conditions, maximum changes in cell structure are observed in the Zolotaya variety.

Thus, the use of Qu to strengthen the protective mechanisms of plants against the effects of abiotic stress is possible only after a preliminary comprehensive study of its effect on the plant.

4. Materials and Methods

4.1. Plants

Two wheat varieties Orenburgskaya 22 (Triticum aestivum) and Zolotaya (Triticum durum) were developed by the Orenburg Research Institute of Agriculture of the Steppe Ecological Detachment (Federal Scientific Center of the Russian Academy of Sciences, Orenburg, Russia). The effect of hypoxia and treatment with 0.03% Qu on the antioxidant system of two wheat varieties was studied. In an experiment on wheat seedlings, a Qu solution was used. Plants were grown in rolls [82] according to the scheme (Figure 1). The addition of Qu before (pathway A) or after stress (pathway B) wheat allowed us to determine the protective properties of Qu for the antioxidant system.

4.2. Chlorophyll Content Analysis

Chlorophyll was extracted using 80% acetone extraction [83]. Chlorophyll levels were determined by absorbance values at 665 nm and 649 nm, which were measured on an IMPLEN nanophotometer. The content of chlorophyll a and b was determined using the formulas:

chl a = [(11.63 x A665) – (2.39 x A649)] x Vml/ 1000 x Wmg

chl b = [(20.11 x A649) – (5.18 x A665)] x Vml/ 1000 x Wmg

where Vml is the total volume of the extract, W mg is the plant sample

Data were expressed as mean ± standard deviation (SD; n = 30), and significant differences were defined as p < 0.05.значимые различия были oпределенo р < 0,05.

4.3. Fluorescence Microscopy

To visualize and determine the level of ROS in the cells of root tips (4–5 mm) of 6 day old wheat seedlings, 25–50 nM carboxy-H2DFFDA (Thermo Fisher Scientific, USA) was used for 30 min, then washed three times. The samples were analyzed under an Olympus BX51 fluorescence microscope (Japan), x 10 objective, wavelength 490 nm. Images were obtained using Color View digital camera and Cell software (Germany). ImageJ software was used to measure fluorescence intensity.

4.4. Light Microscopy

6-day-old seedlings, sections (5 mm) of the root tip were fixed in a 4% solution of paraformaldehyde (Sigma Aldrich, USA) in PHEM buffer, pH = 6.9 (60 mM PIPES (Sigma Aldrich, USA), 25 mM HEPES (Sigma Aldrich, USA), 10 mM EGTA (Sigma Aldrich, USA) and 2 mM MgCl2 (Sigma Aldrich, USA) for 1.5 h at room temperature. The fixative was washed with PHEM buffer. The samples were incubated 7 minutes in 0.4 M mannitol containing 4% cellulase (Sigma Aldrich, USA) and 5 mM EGTA, then washed with PBS buffer, after incubation in the enzyme, the roots were transferred to coverslips and separated into individual cells. The prepared preparations were dried in the refrigerator at +4 ° C for 24 hours. and placed in Mowiol U-44 (Hoechst, Germany) with the addition of DAPI (1 μl/1 ml) (4,6-diamidino-2-phenylindole) (Sigma Aldrich, USA). The samples were analyzed under an Olympus BX51 fluorescence microscope (Japan), x 100 objective. Images were obtained using Color View digital camera and Cell software (Germany). ImageJ software was used to measure fluorescence intensity.

4.5. Biochemical Analysis

Antioxidant activity (AOA) was determined by blocking the oxidation process of a 0.1% aqueous solution of (R)-4-[1-hydroxy-2-(methylamino)ethyl]benzene-1,2-diol (HMAEB). Absorbance was measured at λ= 347 nm [84] Antiradical activity (ARA) was determined by the method

decrease in color of a 5x10-5M alcohol solution of 2,2-diphenyl-1-picrylhydrazyl (DPPH). Absorbance was measured at λ= 517 nm [85] The concentration of peroxide in aqueous solutions of plants was determined by the decrease in color of a 0.02 M KMnO4 solution. Absorbance was measured at λ=480 nm [86]. The content of glutathione (GSH} in mM was determined by the Elman method by the appearance of color after adding a 0.01 M alcohol solution. Absorbance was measured at λ = 412 nm [87]

4.6. Total RNA Isolation and Gene Expression Analysis

The analysis was carried out using a standard kit for RNA isolation “Extran RNA Synthol” (Russia). RNA was isolated from the roots and shoots of wheat grown under different conditions. cDNAs were synthesized by reverse transcription using standard methods (Syntol, Moscow, Russia). The cDNA concentration was determined spectrophotometrically using an IMPLEN nanophotometer. RT-PCR using SYBR Green I (Syntol) was carried out in a CFX 96 real-time thermal cycler (BioRad, USA). Information on the structure of Cu/ZnSOD, MnSOD, Per, GPX, CAT and GST genes in wheat was obtained from NCBI. Primers for the genes were synthesized by Syntol (Table S1). Each RT-PCR reaction was performed in triplicate.

4.7. Statistical Methods

Statistica 6.0 and STATAN programs were used for statistical calculations using Student's t test (DPS software). Different letters indicate significant differences at p < 0.05. Values are presented as means ± standard deviations of triplicate biological copies, significant differences at p < 0.05.

5. Conclusions

Wheat is the most common agricultural plant species. During cultivation, wheat is exposed to both biotic and abiotic stress factors, which damage plants and contribute to inhibition of their growth and reduction of grain yield [5]. Under natural conditions, plants are often exposed to various stresses that affect their growth and development. One of the visible symptoms of abiotic stress is impaired seedling development. The greatest morphometric changes are caused by the effect of hypoxia on the Orenburgskaya 22 variety (Triticum aestivum). Using cytological analysis, various types of cytoplasmic changes in root cells under hypoxic conditions were identified. The formation of giant vacuoles during hypoxia in the Zolotaya variety (Triticum durum) is one of the protective mechanisms. Various stress factors lead to an increase in ROS and increased damage to various plant tissues. Increased ROS production under abiotic stress triggers antioxidant defense in wheat. In the Orenburgskaya 22 variety, the most active components of the antioxidant system are MnSOD and Cu/ZnSOD, and in the Zolotaya variety - GSH. The antioxidant quercetin reduces the formation of ROS. Pre-treatment of wheat seedlings with 0.3% quercetin has a protective effect against O₂ deficiency on seedlings of the Orenburgskaya 22 variety, but has a negative effect on seedlings of the Zolotaya variety. Treatment of seedlings of the Orenburgskaya 22 variety with quercetin after exposure to hypoxia helps restore their development. Quercetin is effective and helps protect against oxidative stress for seedlings of the Orenburgskaya 22 variety. Thus, under hypoxia, quercetin has a different effect on two wheat genotypes.