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OCL
Volume 32, 2025
Minor oils from atypical plant sources / Huiles mineures de sources végétales atypiques
Article Number 32
Number of page(s) 11
DOI https://doi.org/10.1051/ocl/2025027
Published online 07 October 2025

© A. A. Gotor et al., Published by EDP Sciences, 2025

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Highlights

  • Linseed oil is highly valued for its nutritional properties.

  • The growing location had a significant impact on the total tocopherol content.

  • Phytosterol content showed significant variation across locations and genotypes.

  • Abiotic stress controlled total tocopherol and phytosterol levels.

1 Introduction

Linseed, Linum usitatissimum L., oil is well known because of its high content of the essential oil alpha-linolenic acid (ω3) and the health benefits its intake may provide (Basch et al., 2007; Shim et al., 2014). Asia is the world's largest continent producing linseed oil with 0.32 Mt produced in 2020, followed by Europe with 0.27 Mt (FAOSTAT, 2023). In Europe, Belgium has the largest linseed oil production with 0.12 Mt in 2020. In France, linseed oil area of production reached 26 898 ha t in 2023 (Agreste, 2024). The crop is primarily cultivated in the North of France for fiber production, while oil production is extended from the north to the center of the country. The flax varieties used for fiber production have been bred specifically for their fiber quality; although their seeds are partially recovered, they are not used for oil extraction. On the contrary, linseed varieties are selected for their oil quality, but their fiber is not used as it does not meet the required quality standards. The L. usitatissimum oil contains a high content of bioactive minor components with interest for health or non-food uses. It contains high levels of phospholipids (Herchi et al., 2011), polyphenols (El-Beltagi et al., 2011), flavonols (El-Beltagi et al., 2011), tocopherols (Khattab and Zeitoun, 2013; Marquard et al., 1977; Oomah et al., 1997), and phytosterols (Herchi et al., 2009; Teneva et al., 2014).

Tocopherols represent a family of compounds, known as Vitamin E, with well-documented antioxidant properties. They play a crucial role in protecting against oxidative stress, with proven benefits in reducing the risk of cardiovascular diseases and exhibiting potential anti-cancer effects (Järvinen and Erkkilä, 2016; Shahidi and De Camargo, 2016). Total tocopherol content of L. usitatissimum oil ranged from 395 to 500 mg/kg based on varietal and location effects (Khattab and Zeitoun, 2013; Marquard et al., 1977). Moreover, Oomah et al. (Oomah et al., 1997) found that the average values for α, γ, δ, and total tocopherols in eight linseed cultivars were 1.5, 215.0, 5.6, and 221.9 mg/kg oil, respectively. In linseed, γ-tocopherols represent up to 97% of the total tocopherol content (Oomah et al., 1997), which corresponds to 90.4 mg/kg of seed, based on the average of seven cultivars. Studies on tocopherol content in linseed oils show significant variation, with values ranging from 153.5 mg/kg of oil (Choo et al., 2007) to 538 mg/kg of oil (Matthäus and Özcan, 2017), including plastochromanol-8 as part of the total tocopherol content. To our knowledge, no other study has been done to evaluate the variability in tocopherol content and composition across different genotypes and growing years in linseed.

The sterols are an important part of the unsaponifiable fraction in many plant oils. Several studies have proved that an intake of 2 g of sterols per day can lower plasma total and low-density lipoprotein (LDL) cholesterol levels (Musa-Veloso et al., 2011; Ras et al., 2013), which may help in reducing the coronary heart disease risk. Phytosterol contents and compositions are affected by species, genotypes, and growing conditions, especially during grain filling (Alignan et al., 2009; Amar et al., 2009; Ayerdi Gotor et al., 2015; Hamama et al., 2003). In linseed, the six major sterols present in the oil were β-sitosterol, cycloartenol, campesterol, 24-methylencycloartanol, Δ5-avenasterol, and stigmasterol that represent 96% of the total sterol content (Schwartz et al., 2008). However, little is known about the variability of these sterols within different genotypes or across growing years. This study compared several genotypes of L. usitatissimum over three years, grown in one southern (Lavaur) and two northern (Airaines and Poix-de-Picardie) locations in France.

The aim of this study was to evaluate both the content and composition of tocopherols and phytosterols, as well as to explore the effects of genotype, growing year, and location on their variation. Understanding these factors is essential for optimizing linseed oil quality for both food and non-food applications. This work is complementary to our previous analysis made on the impact of environmental factors and genotype on linseed composition and subsequent oil expression (Savoire et al., 2015).

2 Materials and methods

2.1 Chemicals

All reagents and standards used were of analytical grade from Sigma-Aldrich, St. Quentin Fallavier, France.

2.2 Samples collection

Samples were collected in two different locations in the North of France: Airaines (49° 57′ 57″ N, 1° 56′ 35″ E) and Poix-de-Picardie (49° 46′ 36″ N, 1° 59′ 07″ E) situated in the main linseed production area. The third location was in Lavaur (43° 41′ 59″ N, 1° 49′ 11″ E) in the South of France (Fig. 1). Experimental field trials were conducted using randomized plots with two replicates, following conventional agronomic practices. Sowing was carried out in the North between September 15th and September 25th, and in the South from October 1st till the 20th, depending on annual weather conditions. Fertilization included 80 kg of Nitrogen (N), 40 kg of phosphorus (P2O5), and 30 kg of potassium (K2O) per hectare, with a sowing density of 400 grains/m2. Experimentations in the North were conducted in deep silty clay soils, while those in the South were on clay-limestone soils with lower water retention capacity. All sites applied at least one herbicide to reduce the weeds presence. Up to ten winter linseed genotypes were studied during three growing seasons from 2013 to 2015. These numbered lines, in the final stage of the breeding process, were candidates for official seed catalogue registration within the next two to three years. Although no selection was made based on minor nutrient composition, these genotypes were selected for their high yield potential and overall disease resistance. This research was included in a larger project willing to determine the variability on fatty acids composition (Savoire et al., 2015). Grains were harvested at maturity, then stored in the dark at room temperature before oil extraction within two months after harvest.

thumbnail Fig. 1

Localization of trials, and main linseed production areas in France (in Green).

2.3 Oil extraction

Seed oil extraction was performed using our previously developed method with some modifications (Savoire et al., 2015). A hundred of seeds were oven dried at 110 °C for 24 h. Ten seeds were then transferred to a 1.5 mL screw tube and ball-milled three times for 1 min in 0.5 mL of isooctane using the FastPrep®-24 instrument (MP Biomedicals, Illkirch-Graffenstaden, France). Samples were centrifuged at 10 000 g for 5 min at room temperature. The supernatant containing solvent extraction and oil matter were recovered. Three supernatants of each sample were pooled into a vial and then evaporated under nitrogen to recover oil. The analyses below were carried out on freshly extracted oils. Oil extraction was made in triplicate.

2.4 Tocopherol analysis

Tocopherol analyses were performed according to our previous protocols, with a few minor modifications (Ayerdi Gotor et al., 2006; Rhazi et al., 2022). About 40 mg of oil sample were dissolved into 1 mL of isooctane. The high-performance liquid chromatography (HPLC) apparatus consisted of a surveyor system coupled to fluorometer detector (Thermo Fisher Scientific Corporation, Courtaboeuf, France). Tocopherols were separated using an Acclaim™ C30 analytical column, 150 × 4.6 mm, particle size 5 μm (Thermo Fisher Scientific Corporation, Courtaboeuf, France) connected in series with a pre-column with the same characteristics. The mobile phase was composed of methanol, acetonitrile, and tert-Butyl methyl ether HPLC-grade. The gradient profile was as described previously (Rhazi et al., 2022). The eluant was monitored with a fluorescence detector, and chromatograms were recorded at emission wavelength of 344 nm after excitation at excitation wavelength of 298 nm. The column was maintained at 30 °C during the run and the autosampler temperature was set at 10 °C to preserve tocopherols. The flow rate was 1.0 mL/min throughout the run. The injection volume was 30 μL. The identification was based on retention time, and the quantification of tocopherols was carried out using external calibration with standards. The peak areas of the individual tocopherols were plotted against the corresponding concentrations to construct the calibration graphs. Results were expressed as mg of tocopherols per kg oil.

2.5 Phytosterol analysis

Sterols extraction and gas chromatography-mass spectrometry (GC-MS) analysis were conducted as described previously (Ayerdi Gotor et al., 2007; Rhazi et al., 2022). Sterol quantification was carried out according to official procedure (ISO12228-1, 2014). About 40 mg of freshly obtained oil, and 200 μL of internal standard, were submitted to saponification reaction by adding 1 mL of ethanolic KOH (0.5 M) followed by incubation at 100 °C for 15 min. The solution of internal standard was prepared immediately before use by solubilizing 1 mg of betulin in 1 mL of acetone. Saponification was stopped by adding 1 mL of ethanol. The resulting solution was introduced into a glass column containing approximately 2 g of aluminum oxide powder soaked with ethanol. The unsaponifiable molecules were recovered into a new balloon by washing the column with 5 mL of ethanol and 30 mL of diethyl ether. Samples were concentrated using a rotavapor system and recovered with 2 mL of pyridine. Unsaponifiable matter (900 μL) was derivatized with 100 µL of N-methyl-N (trimethylsilyl)-heptafluorobutyramide (5:95 v/v) for 15 min at 105 °C in an oil bath. The trimethylsilyl derivatives of the phytosterols were determined by GC-MS using the Thermo Scientific GC-MS benchtop system that combines a Trace 1310 GC with an ISQ 7000 Single Quadrupole mass spectrometer (Thermo Fisher Scientific Corporation, Courtaboeuf, France). Separations were achieved employing Phenomenex fused silica capillary ZB-5 inferno column (30 m × 0.25 mm × 0.25 µm, Paris, France). The injector temperature was set at 320 °C and the oven was programmed as follows: initial temperature 240 °C, hold time 0 min, rate 4 °C/min, to 320 °C, and held for 10 min until it decreased to initial conditions. The mass spectrometer was used in electron impact mode (electron energy 70 eV). The transfer tube and source temperature were set at 250 °C and 200 °C, respectively. Helium carrier gas flow was set at 0.7 mL/min. Splitless injections were performed with 1 µL sample volume. The split valve was opened 3 min after injection. Identification of trimethylsilyl derivatives was based on their MS spectrum and retention time of standards and with the relative times to betulin given in the norm (ISO12228-1, 2014). The amount of phytosterol molecules was determined, based on the corresponding calibration curves. Analysis was realized in triplicates.

2.6 Weather

Weather parameters, namely: mean maximum temperature (TM, °C), mean minimum temperature (Tm, °C), and monthly rainfall during the critical growth period of linseed varieties (between March 1st to July 31st over the three years of the study), were recovered from the MétéoCiel database (https://www.meteociel.fr). Data for the Nord climatic conditions (N) were collected from a weather station located between Airianes and Poix-de-Picardie, while data for the South climatic conditions (S) were obtained from the Lavaur weather station.

2.7 Statistical analysis

After testing the homogeneity of variances and normality of obtained data using Levene and Shapiro-Wilk tests, respectively, analysis of variance (ANOVA) was used to evaluate the effects of variety and year and their interaction on tocopherols and phytosterols content and composition. The least significant difference (LSD) at the 0.05 significance level was used to distinguish differences among the mean values. All statistical analyses were performed using SPPS version 22.1.

3 Results

3.1 Environment and genotype effects

The meteorological dataset shows that 2015 was the hottest and driest year in both northern and southern France, although it was not exceptionally dry during the linseed growing period (Fig. 2). The southern regions were always hotter than the northern regions, with 2013 being the coldest year. In contrast, 2014 was the rainiest year. These significant variations in the weather during the growing period of linseed were probably responsible for the modifications in the content and composition of minor components, independent of genotype.

thumbnail Fig. 2

Meteorological data from trail sites in northern France (Airianes and Poix-de-Picardie; A, labelled N) and southern France (Lavaur; B, labelled S) during the 2013–2015 linseed growing seasons. Solid lines represent maximum temperatures (TM), and dotted lines denote minimum temperatures (Tm). Vertical bars indicate cumulative rainfall. Blue corresponds to northern France (2013–2015), and orange to southern France.

3.2 Oil content

The oil content was consistent across cultivars but lower at the southern site (Lavaur). Grain samples from 2015 presented a reduced oil content of 46%, compared to 48 and 49% in samples from 2013 and 2014, respectively (data not shown).

3.3 Tocopherols

The linseed oils had a mean total tocopherol content of 403.7 ± 37.0 mg/kg of oil (Tab. 1), with γ-tocopherol being the dominant isoform at 397.4 ± 39.2 mg/kg of oil. The mean total phytosterol content was 396.7± 89.4 mg/100 g of oil. Variety 07 had the highest tocopherol content with a total of 432.4 mg/kg, while variety 05 had the lowest at 351.4 mg/kg (Tab. 1). The two northern sites (Airanes and Poix-de-Picardie) presented significantly higher tocopherol content compared to the southern site (Lavaur). In 2015, the concentration of tocopherols in linseed oil was significantly lower than in 2013 and 2014.

The 2014 data were analyzed using ANOVA with a random model to highlight the contribution of each variance component: genotype (G), year of harvest (Y), and location (L) (Tab. 2) because it presented the larger number of the same cultivars cultivated in the three locations. The analysis showed that genotype and genotype × location were the main factors influencing total tocopherol, explaining 49 and 44% of the total variance, respectively. This variability presents an opportunity to increase the content on these two families of minor components through breeding, potentially leading to varieties with improved nutritional profiles and better oil quality preservation over a longer period.

The growing location had a significant impact on the total tocopherol content but not on the individual tocopherols, including γ- and δ-tocopherol (Tab. 2). Genotypes cultivated in Lavaur and Airaines showed a significantly lower content of total tocopherols (399.2 mg/kg of oil) compared to those grown in Poix-de-Picardie (412.7 mg/kg of oil) in 2014. The year 2014 had a significantly higher content of δ-tocopherol (p < 0.01) and total tocopherols (p < 0.001) compared to 2013 and 2015 (Tab. 2).

There were also significant differences between genotypes at the same location in 2014, with total tocopherol content ranging from 331.7 to 473.7 mg/kg of oil and γ-tocopherol content varying from 329.6 to 466.5 mg/kg of oil.

Table 1

Mean values of tocopherol content and isoform composition for 10 linseed genotypes, with location- and year-specific averages.

Table 2

Sum of squares from a combined analysis of variance for γ-tocopherol, δ-tocopherol and total tocopherol content in linseed for 10 varieties cultivated during the 2014 growing season across three locations (Airaines, Poix-de-Picardie, and Lavaur).

3.4 Phytosterols

Linseed oil contained six major phytosterols: campesterol, stigmasterol, β-sitosterol, Δ5-avenasterol, cycloratenol and Δ7-stigmasterol. Among these, β-sitosterol was the most important, comprising 36 ± 3% of the total phytosterol content, which corresponds to 146 ± 41 mg/100 g of oil, followed by cycloartenol at 22 ± 3%. A chromatogram of the phytosterol profile is presented in Figure 3.

Table 3 presents the content and composition of sterols in different linseed genotypes. Variety 06 had the highest total phytosterol content, with 501.34 mg/100 g of oil, while Variety 02 presented the lowest content, with 315.36 mg/100 g of oil. Significant differences in total phytosterol content were observed across years; 2015 had the lowest concentration, with a mean of 231.78 mg/100 g of oil, while 2013 presented the highest content, with 443.94 mg/100 g of oil. The highest phytosterol content was observed at the Poix-de-Picardie and Lavaur locations.

Analysis of variance showed significant differences in the content of the seven phytosterols, as well as in total phytosterols, total tocopherols, and α-tocopherol content across genotypes, locations, and years. Significant differences were also observed for the genotype × year interaction, except for β-sitosterol, avenasterol, and cycloartenol content, as well as for the genotype × location interaction with respect to Δ7-stigmasterol content.

Phytosterol content showed significant variation across sites and genotypes (Tab. 4). In the southern regions, there was a significant reduction in each individual phytosterol, as well as in total phytosterols. The total phytosterol content was largely influenced by location (44%). The Poix-de-Picardie location always presented the highest levels.

In 2014, the total phytosterol content was significantly higher (p < 0.01) compared to 2013 and 2015, with β-sitosterol also showing a significant increase (p < 0.001) (Tab. 4). This trend was observed for all phytosterols except Δ7-Stigmasterol.

There were also significative differences between genotypes at the same location in 2014, with total phytosterol content ranging from 192.3 to 519.6 mg/100 g of oil, β-sitosterol from 67.0 to 95.7 mg/kg of oil, and cycloartenol from 36.9 to 154.4 mg/kg of oil.

thumbnail Fig. 3

The upper figure (A) represents the GC chromatogram of silylated linseed oil sterols : 1: brassicasterol; 2: 24-methylene campesterol; 3: campesterol; 4: stigmasterol; 5: β-sitosterol; 6: Δ5-avenasterol; 7: cycloartenol; 8: Δ7-stigmasterol; 9: Δ7-avenasterol; and 10: betulin (internal standard); the B part mass spectrum of the cycloartenol at the retention time (RT) 12.58.
Table 3

Mean values of phytosterol content and isoform composition of 10 linseed genotypes, with location- and year-specific averages.

Table 4

Sum of squares of combined analysis of variance for individual phytosterols and total phytosterol content in linseed for 10 varieties cultivated during the 2014 growing season across three locations (Airaines, Poix-de-Picardie, and Lavaur).

4 Discussion

Previously, we have studied the effect of environmental factors and cultivar on linseed composition and subsequent oil expression (Savoire et al., 2015). Linseed oil content ranged between 30 and 50% of dry weight and contained 40 to 66% C18:3. The cultivar factor had a significant influence on oil and C18:3 content, while the growing location only affected lipid content. In addition, annual effects were noted on oil and C18:3 content. The observed increases in oil content can be explained by the increased degree day after flowering and sunshine duration while the significant decreases in C18:3 content were probably related to lower rainfall and a slightly lower temperature during seed filling.

This current study elucidates the intricate interplay of genetic, environmental, and G×E interactions that govern tocopherol and phytosterol variability in linseed oil. By assessing these compounds under realistic field conditions, our findings not only extend previous insights into oilseed variability but also provide a valuable framework for breeding and agronomic strategies aimed at sustaining oil quality amidst climate change.

Our study identifies γ-tocopherol as the predominant isoform in linseed oil (396.7 ± 39 mg/kg oil), as previous findings in other Linum varieties where γ-tocopherol typically constitutes 96–98% of total tocopherols (Gandova et al., 2023; Nykter et al., 2006; Oomah et al., 1997). These results also align with those reported by Marquard et al. (1977) and more recently by Dąbrowski et al. (2025), who observed tocopherol contents in linseed oil ranging from 395 to 500 mg/kg. The substantial reductions in tocopherol (365 mg/kg oil) and phytosterol (232 mg/100 g oil) content observed during the 2015 growing season underscore the sensitivity of these minor compounds to abiotic stress. The 2015 season experienced the more stressful weather conditions during pre-flowering, flowering and grain filling stages in both North and South locations, characterized by high temperatures and low precipitation. These factors significantly reduced total tocopherol levels compared to 2014 and 2013. In the South location, where temperatures were significantly higher than in the North locations, tocopherol content was further reduced. Previous studies have demonstrated that tocopherol levels fluctuate under heat stress, reflecting their dual role as antioxidants and stress indicators (Ali et al., 2022; Ayerdi Gotor et al., 2015). While elevated temperatures can enhance the activity of tocopherol biosynthetic enzymes such as homogentisate phytyltransferase (VTE2) and p-hydroxyphenylpyruvate dioxygenase (HPPD) (Marquard, 1990; Obranović et al., 2015), they can simultaneously impair chloroplast function, leading to excessive reactive oxygen species (ROS) accumulation, lipid peroxidation, and subsequent tocopherol depletion (Štolfa Čamagajevac et al., 2018). This phenomenon is well-documented in other oilseed crops, such as rapeseed, Brassica napus L., where heat stress during flowering exacerbates oxidative damage and reduces tocopherol content (Gawrysiak-Witulska et al., 2011), as well as in sunflower (Ayerdi Gotor et al., 2015).

Drought stress further alters plant metabolism by downregulating the mevalonate pathway, a crucial biosynthetic route for phytosterol production, as nicotinamide adenine dinucleotide phosphate (NADPH) is redirected toward essential stress responses such as glutathione synthesis (Zhang et al., 2023). This metabolic shift, evident in drought-induced lipid remodeling in soybean, Glycine max L. Merr. (Shahriari et al., 2022), highlights the importance of phytosterols as indicators of plant stress adaptation. While the suppression of the mevalonate pathway is a common stress response, some plants exhibit an upregulation of phytosterol biosynthesis under specific conditions, revealing a complex regulatory network that warrants further investigation (Zhang et al., 2020).

Beyond abiotic factors, the rhizosphere microbiome plays a pivotal role in modulating lipid metabolism through biotic interactions. Root exudates, including lipids, recruit beneficial microbes that enhance plant resilience by influencing lipid biosynthesis (Korenblum et al., 2022). Microbial metabolites can trigger systemic metabolic changes, leading to increased protective lipid production (Zhuang et al., 2024). Additionally, diverse microbial communities contribute to nutrient solubilization and hormone biosynthesis, further regulating lipid metabolism and overall plant health (Bharti et al., 2021). Despite these insights, the potential of microbial interactions in modulating linseed oil quality remains largely unexplored and represents a promising avenue for future research.

Phytosterol contents observed in this study are consistent with values reported in the literature, ranging from 315 to 508 mg/100mg of oil (Dąbrowski et al. (2025); Matthäus and Özcan, 2017). Shifts in phytosterol composition, particularly the balance between β-sitosterol and cycloartenol, reflect adaptive strategies for membrane stability and stress signaling. Sterols function as plant hormones and play an important role in protecting plants against environmental stress, as well as regulating growth and development. β-Sitosterol enhances membrane rigidity under abiotic stress (Rossi and Huang, 2022), while cycloartenol modulates stress-responsive pathways (Aboobucker and Suza, 2019; Du et al., 2022). Similar trends in quinoa (Schlag et al., 2022; Stoleru et al., 2022) and linseed (Choo et al., 2007; Herchi et al., 2009) underscore the ecological plasticity of oilseed crops, enabling them to fine-tune their lipid profiles for resilience across diverse climatic conditions. This plasticity highlights the potential for breeding strategies aimed at enhancing resilience to climate fluctuations (Donohue, 2016), although challenges persist in mitigating the adverse effects of G×E interactions, such as reduced oil yield under extreme environmental conditions.

The observed variation in phytosterol content across different locations, with notably high levels in Poix-de-Picardie (477 mg/100 g oil), underscores the potential of agroecological zoning to optimize crop value. In temperate regions, linseed presents a significant opportunity for the functional food market, particularly in cholesterol-lowering products (Čeh et al., 2020). However, the heightened susceptibility of linseed grown in southern locations to heat stress necessitates the development of heat-tolerant cultivars. Advances in gene editing, such as clustered regularly interspaced short palindromic repeats (CRISPR)-mediated modifications of thermotolerance genes, hold promise for maintaining oil quality under increasing temperatures (Clemis et al., 2023) and aligning with EU Farm-to-Fork and Green Deal objectives (Stavropoulos et al., 2023). For example, Saha et al. (Saha et al., 2019) identified 34 putative heat shock factor (HSF) genes in the L. usitatissimum genome and designed guide ribonucleic acid (RNA) sequences for precise gene editing with minimal off-target effects. Editing these HSF genes could lead to heat-tolerant linseed cultivars capable of maintaining oil quality under elevated temperatures. Similarly, overexpression of the drought-responsive element binding protein 2A (DREB2A) gene has been shown to confer drought tolerance in a transgenic line of linseed cv. Blanka (Tawfik et al., 2016). While selective breeding, leveraging traits with high heritability such as flowering time (Toor et al., 2024), offers immediate solutions, gene-editing technologies provide long-term resilience against climate uncertainties. These findings emphasize the importance of genetic diversity in linseed breeding programs aimed at improving oil quality and stability (Kaur et al., 2024; Shankar et al., 2024). While δ-tocopherol offers clear advantages in temperate climates, the potential benefits of γ-tocopherol in arid regions warrant further exploration, particularly in the context of shifting agricultural zones due to climate change.

Comparative studies across oilseed species underscore the need for crop-specific metabolic models to refine breeding strategies. The role of tocopherols, particularly γ-tocopherol and α-tocopherol, in enhancing the oxidative stability and stress resilience of G. max and other oilseed crops is well-documented. Genetic modifications and breeding strategies can optimize tocopherol profiles, improving nutritional value and shelf life across species. In G. max, γ-tocopherol is the predominant form, contributing to oxidative stability under environmental stress (Tavva et al., 2007). Genetic studies have identified quantitative trait loci (QTLs) linked to tocopherol synthesis, particularly those affecting the conversion of γ-tocopherol to α-tocopherol, which improves oil quality (Park et al., 2023). Similarly, in B. napus, genetic modifications targeting the γ-tocopherol methyltransferase (VTE4) gene have successfully increased α-tocopherol content, enhancing the oil's nutritional profile (Wang et al., 2025). In safflower, Carthamus tinctorius L., breeding efforts focus on optimizing tocopherol profiles, with metabolic flux analysis identifying key enzymatic control points in tocopherol biosynthesis to enhance oxidative resistance (Golkar, 2014). Sunflower (Helianthus annuus) seeds predominantly contain α-tocopherol, constituting more than 90% of total tocopherols (Velasco et al., 2014). Genetic modifications targeting HPPD, a key enzyme in the tocopherol biosynthesis pathway, have been shown to enhance α-tocopherol production, further emphasizing the importance of tocopherol biosynthesis in determining oil quality (Srinivasan et al., 2022).

While strategies to enhance tocopherol content show promise for improving oil quality and stability across different crops, it is essential to consider potential trade-offs in crop yield and other agronomic traits that may result from genetic modifications and breeding approaches. Genetic diversity in linseed (Kaur et al., 2024) provides a strong foundation for trait optimization. The variety 'Railinus' has been identified as a high-performing genotype, exhibiting significant levels of tocopherols and phytosterols, which are crucial for oil quality and stability (Matthäus and Özcan, 2017). In this study, Variety 06 was identified as a high-performing genotype (tocopherol: 431.94 mg/kg oil; phytosterol: 501.34 mg/100 g oil), demonstrating the potential of integrating multi-omics data with advanced breeding strategies. Transcriptomic analyses targeting key enzymes, such as tocopherol cyclase (VTE1) in tocopherol cyclization and Cytochrome P450 family 710 subfamily A (CYP710A) in sterol modification, could reveal regulatory hubs amenable to marker-assisted selection. Overexpression of VTE1 has been shown to significantly increase total tocopherol content in Arabidopsis leaves, underscoring its critical role in tocopherol biosynthesis (Kanwischer et al., 2005). Similarly, the CYP710A family encodes sterol C-22 desaturases involved in the biosynthesis of stigmasterol from β-sitosterol, as shown in studies on Arabidopsis and tomato (Morikawa et al., 2006). Moreover, predictive models have proven effective in assessing oilseed crop performance. The CAMEL model, developed for false flax, Camelina sativa L., successfully predicted seed yield, oil production, and key fatty acid accumulation under varying climatic conditions in Northern Italy (Cappelli et al., 2019). Adapting similar simulation frameworks for linseed could enhance breeding strategies by optimizing oil quality across diverse environmental conditions.

Despite the advances presented here, the three-year dataset in this study may not fully capture long-term climatic trends and extended multi-year trials are necessary to validate stress-response patterns. Additionally, the influence of the soil microbiome on lipid metabolism, a crucial factor in linseed rhizosphere interactions, remains unexplored. Future research should also incorporate economic analyses of breeding high-tocopherol linseed for both nutritional and industrial applications.

5 Conclusions

This study shows that tocopherol and phytosterol contents in linseed are governed by a complex interplay of genetic and environmental factors. Notably, high temperatures reduce the content of these bioactive compounds. This could be due to the protective role of tocopherols and phytosterols as antioxidants against hot stress, leading to a decrease of their content in the plant. The variability encountered within varieties allows the possibility to increase the content of these two families of components by breeding. By selecting varieties with superior tocopherol and phytosterol profiles, it may be possible to develop linseed cultivars that not only offer improved nutritional and cosmetic benefits but also maintain oil quality over longer storage periods. Future research should focus on integrating advanced breeding techniques to further exploit this variability for improved crop performance under changing climatic conditions.

Funding

Conseil Régional de Picardie (FUI project Granolin).

Conflicts of interest

The authors declare no conflict of interest

Author contribution statement

Conceptualization, Alicia Ayerdi Gotor, Brigitte Thomaset and Larbi Rhazi; Data curation, Alicia Ayerdi Gotor, Florentin Donot and Rachid Sabbahi; Methodology, Florentin Donot and Larbi Rhazi; Supervision, Thierry Aussenac and Larbi Rhazi; Validation, Alicia Ayerdi Gotor, Florentin Donot, Brigitte Thomaset and Thierry Aussenac; Writing − original draft, Alicia Ayerdi Gotor, Florentin Donot, Rachid Sabbahi and Larbi Rhazi; Writing − review & editing, Alicia Ayerdi Gotor, Brigitte Thomaset, Thierry Aussenac, Rachid Sabbahi and Larbi Rhazi.

All authors have read and agreed to the published version of the manuscript.

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Citation de l’article : Gotor AA, Donot F, Thomaset B, Aussenac T, Sabbahi R, Rhazi L. 2025. Genotypic and environmental variability of tocopherols and phytosterols in linseed (Linum usitatissimum L.) oil, OCL 32: 32. https://doi.org/10.1051/ocl/2025027

All Tables

Table 1

Mean values of tocopherol content and isoform composition for 10 linseed genotypes, with location- and year-specific averages.

In the text
Table 2

Sum of squares from a combined analysis of variance for γ-tocopherol, δ-tocopherol and total tocopherol content in linseed for 10 varieties cultivated during the 2014 growing season across three locations (Airaines, Poix-de-Picardie, and Lavaur).

In the text
Table 3

Mean values of phytosterol content and isoform composition of 10 linseed genotypes, with location- and year-specific averages.

In the text
Table 4

Sum of squares of combined analysis of variance for individual phytosterols and total phytosterol content in linseed for 10 varieties cultivated during the 2014 growing season across three locations (Airaines, Poix-de-Picardie, and Lavaur).

In the text

All Figures

thumbnail Fig. 1

Localization of trials, and main linseed production areas in France (in Green).
In the text
thumbnail Fig. 2

Meteorological data from trail sites in northern France (Airianes and Poix-de-Picardie; A, labelled N) and southern France (Lavaur; B, labelled S) during the 2013–2015 linseed growing seasons. Solid lines represent maximum temperatures (TM), and dotted lines denote minimum temperatures (Tm). Vertical bars indicate cumulative rainfall. Blue corresponds to northern France (2013–2015), and orange to southern France.
In the text
thumbnail Fig. 3

The upper figure (A) represents the GC chromatogram of silylated linseed oil sterols : 1: brassicasterol; 2: 24-methylene campesterol; 3: campesterol; 4: stigmasterol; 5: β-sitosterol; 6: Δ5-avenasterol; 7: cycloartenol; 8: Δ7-stigmasterol; 9: Δ7-avenasterol; and 10: betulin (internal standard); the B part mass spectrum of the cycloartenol at the retention time (RT) 12.58.
In the text

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