Background

One of the problems facing the world is how to provide food needs in the frame of limiting soils for cultivation and not enough water sources with increasing population problem. Egypt, like other developing countries of the arid and semi-arid regions, faces four major problems, namely high rate of population increases, limited natural sources of good quality water, the existence of salt-affected land, and shortage of food and feed (Koyro et al., 2011). In the agriculture regions, the change in the climate of a decrease in rainfall and an increase in temperature means a water crisis (Fan et al., 2014). Therefore, it requires a change in the established agricultural operations management and taking the non-traditional direction to maintain productivity and increase sustainability (García-Caparrós et al., 2018).

The recent technique for solving many of the agricultural problems is finding 97% of the global water in the seas and oceans while the territorial land is about 43% arid or semi-arid. Presence parts of these areas near the sea are a serious solution for agricultural irrigation, so some wild plants which are tolerant of salinity, namely Halophytes, can be grown. Salicornia (S.) is one of the halophytes plants which contain a high percentage of oil.

Synthetic fertilizers play a significant role in soil and groundwater pollution, causing the crop to be more prone to diseases. Therefore, organic farming becomes an important demand because of healthy food and a clean environment. The essential components of organic farming are biofertilizers. Biofertilizers are the substances that contain living microorganisms and are used in the fields of agriculture to keep the soil rich in all kinds of micro- and macro-nutrients. They are improving soil fertility via nitrogen fixation, phosphate, and potassium solubilization or mineralization, production of antibiotics, and biodegradation of organic matter in the soil (Sheraz Mahdi et al., 2010; Kaushal Kumar et al., 2013; Bhardwaj et al., 2014).

The greenhouse experiment studied the effect of irrigation with diluted seawater (12.5%, 25.0%, 37.0%, and 50.0%) on the halophytic plants (e.g., Sporobolus, Leplochloa, and Salicornia europa), and found that increasing seawater concentration increased the succulence, Na/K ratio, and the content of proline, sodium, pigment, carbohydrates, and protein in the plants at the different cuttings (Yuan et al., 2019; Tawfik et al., 2013).

Tawfik (Tawfik, 2007) pointed out that the nutritional status of the halophytes forages plants concentrated on the quantity of protein, phosphorus, and plant content of produced energy. However, Fang et al. (Yuan et al., 2019) indicated that potassium is an important nutrient and plays an essential role in water relations, osmotic adjustment, stomatal movement, and finally resistance to drought. Nitrogen metabolism is the most important factor that influences plant growth and performance, some studies showed the reduction of nitrate uptake and a decrease in nitrate reductase activity under water stress (Ismail & Hiroshi, 2012).

The algae are used as a biofertilizer for many plants to overcome the difficult conditions such as high alkaline degree, salinity, and content of calcium. El-Sayed et al. (El-Sayed et al., 2015) showed that the application of algae foliar at a rate of 300 g/fed achieved the highest values of the fresh and dry weight of the plant. Abd El-Baky et al. (Abd El-Baky et al., 2016) cleared that the algae foliar extracts can improve non-enzymatic and enzymatic antioxidant defense systems in potatoes cultivated under drought stress conditions.

Oil is considered the largest energy source which is playing a central role in human nutrition and to maintain food security (Shahi et al., 2014). The saltwater crops are considered of oil production sources, such as Salicornia spp. which are leafless, succulent, and small-seeded and used as conventional oil crops (Abideen et al., 2015). The physical and chemical analysis of oils showed that their fatty acid composition is similar to other common edible vegetable oils. Salicornia fruticose lipid analysis revealed the presence of 11 fatty acids such as palmitic acid (32.4%) and linoleic acid (14.16%) (Radwan et al., 2007). Salicornia bigelovii is very rich in linoleic acid (about 70%) with a fatty acid profile that is similar to sunflower oil (Gouda & Elsebaie, 2016). The seed contains about 26–33% oil (similar to safflower oil), 35% protein, and salt content of about 3% (Garcia, 2010).

The most common types of plant oils are waxes, triglycerides, and phospholipids. The molecular structure of triglycerides consists of three fatty acid molecules bonded to one glycerol molecule. Triglycerides are used as an energy source stored mostly in seeds and to a lesser extent within the plant itself. The phospholipid consists of two fatty acids bonded to glycerol with a phosphate functional group (Falasca et al., 2014).

The oil was extracted from the seeds through solvent extraction methods (Narasimha Rao et al., 2015). Elsebaie et al. (Elsebaie et al., 2013) evaluated the methods of oil extraction from glasswort seeds and reported that chloroform and methanol mixture (2:1 v:v) gave the maximum amount extracted from seeds (28.59%). Adewale et al. (Folayan et al., 2019) used the supercritical fluid extraction process (SFE) as a viable alternative to liquid extraction.

The Salicornia oil will be a candidate for biofuel production for containing a small amount of C18:3 (Ruana et al., 2008). The high percentage of polyunsaturated fatty acids (> 40%) is referring to the nutraceutical and pharmaceutical components in such oil (Kang et al., 2011; Hammami et al., 2018).

The research is focused on the effect of Salicornia bigelovii cultivation under different conditions of irrigation and fertilization on both the percentages and fatty acids composition of the oil. The capability of this oil is to produce biofuel and finally for nutritional, cosmeceutical, and pharmaceutical applications. The characterizations of samples will compare with blank samples that were collected from the desert coastal area of the saline aquatic environment.

Methods

From the International Training Centre-Mariut, Alexandria, we obtained of the following:

  • The blank samples of S. bigelovii seeds which are collected from the desert coastal area of the saline aquatic environment

  • Test samples of S. bigelovii seeds (17 samples) which are subjected to different cultivation conditions of irrigation and fertilization, as shown in Table 1.

  • All chemicals were used from the analytical grade

Table 1 Samples key under different combined treatments of fertilization and irrigation

Work steps are as follows:

  1. 1.

    From the desert of the North West Coast areas, the following were collected:

    1. (a)

      A representative sample of S. bigelovii seeds for testing as a blank one

    2. (b)

      Representative samples of soil, ground well water, and seawater

  2. 2.

    Comparative tests were conducted to identify the most successful cultivation method of S. bigelovii by using either seeds or semi-cuts or hard-cuts or transplants were tested by using some growth regulators (indole butyric acid and gibberellic acid for activate seeds germination and rooting the cuts).

  3. 3.

    Greenhouse experiments using Salicornia transplants were conducted. Saline well water or/and diluted seawater as a source of irrigation (4 treatments) combined with four fertilization treatments including algae (Amphora) extract (as a source of biofertilizer), NPK, and micronutrients during an integrated and balanced fertilizer program were conducted (Table 1).

  4. 4.

    Whole plants were collected and the seeds were brought out to evaluate oil percentage at different conditions of cultivation and to identify the viability of oil for human consumption and to be used as a biofuel.

  5. 5.

    The blank samples of S. bigelovii seeds were subjected to the following tests:

    1. (a)

      Determination the humidity percentage

    2. (b)

      A certain weight W0 of S. bigelovii seeds was dried at 85 °C until constant weight W1. The percentage of humidity will be calculated after cooling.

    3. (c)

      Oil extraction

    4. (d)

      The total oil from the dried seeds after grinding was extracted using different solvents of hexane, hexane to isopropanol mixture (3:2 v/v), and ethanol through different techniques, at ratio 1:6 wt./v of dry biomass to solvent, as follows:

    5. (e)

      Shaker (Elsebaie et al., 2013)

      Mixing of 10 g of ground seeds with solvent in a conical flask was done. The mixture was subject to agitation, at ambient temperature for 24 h using a shaker (Model3060, ORBITAL SHAKER), at 150 rpm. In the end, the reaction mixture was filtrated and the solvent will be evaporated by using a rotary vacuum evaporator.

    6. (f)

      Conventional method (Basily et al., 2018a)

    7. (g)

      Ground seeds (10 g) with organic solvent were placed in a flask. The suspensions were continuously stirred using a magnetic stirrer at constant temperature (65 5C) for 2 h with reflux. After extraction time and filtration, the oil will be separated from the solvent using a rotary evaporator.

    8. (h)

      Ultrasonic probe technique (Basily et al., 2018a)

    9. (i)

      The same steps as in conventional method except that the suspension will be subjected to ultrasonic generator probe Model Sollics Vibra Cell V500 at room temperature, for 15 min. After extraction and filtration, the oil will be separated from the solvent using a rotary vacuum evaporator.

    10. (j)

      The oil samples after all the extraction processes are transferred to sealed glass vials and stored at 5 °C for further analysis.

    11. (k)

      The samples of S. bigelovii seeds which are subject to different treatments of irrigation and fertilization as shown in Table 1 will be dried and ground to prepare for the oil extraction process by ultrasonic generator probe Model Sollics Vibra Cell V500 at room temperature, for 15 min using a solvent system of ethanol. After extraction and filtration, the oil will be separated from the solvent using a rotary vacuum evaporator.

  6. 6.

    Gas chromatography analysis of extracted oil

    1. (a)

      For all extraction processes, the fatty acids profiles for oil samples were determined using chromatography (GC) provided with a split automatic injector and silica capillary column DB-5 (length, 60 m; ID, 0.32 mm). Helium is used as a carrier gas at a flow rate of 1 mL/min. The column was held at 150 °C for 1 min and ramped to 240 °C, at a rate of 30 °C/min, and held at 240 °C, for 30 min. Standards are used to give rise to well-individualized peaks that allow the identification of the fatty acid composition.

    2. (b)

      Cetane number of the produced oil can be calculated from the fatty acid profiles according to the following equation (Clements 1996; Hawash and AboElenin, 2015):

$$ \mathrm{CM}=\Sigma\;\mathrm{XME}\;\left(\mathrm{wt}.\%\right).\mathrm{CNME} $$
  1. (c)

    where CN is the cetane number of biodiesel, XME is the weight percentage of each methyl ester, and CNME is a cetane number of individual methyl ester

  1. 7.

    Extraction of phenolic compounds

    1. (a)

      Four grams of de-oiled biomass was suspended in 20 ml of 80% ethanol, homogenized for 3 min at 4 °C to disrupt cells. The homogenate was centrifuged at 2000 rpm for 15 min at 4 °C.

    2. (b)

      The resulting supernatant was centrifuged again at 2000 rpm for 10 min. the residue was repeatedly extracted with the same solvent until they were colorless. Then, the supernatant was filtered through Millipore filters. The filtrate was evaporated to dryness to give a crude ethanolic extract (enriched in phenolic compounds) and immediately analyzed (Sarojini et al., 2013; Basily et al., 2018b).

    3. (c)

      Total phenols extracts were determined in triplicate by the Folin-Ciocalteu reagent using gallic acid as a standard (Singleton & Rossi, 1965; Anandjiwala, 2007).

  2. 8.

    Extraction of flavonoids compounds (Baviskar & Khandelwal, 2015)

    1. (a)

      One gram of de-oiled biomass was crushed in motor, added 5 ml of distilled water, centrifuged at 1000 rpm for 15 min, and incubated at 4 °C for 20 min. Then, it was transferred to the water bath adjusted at 100 °C for 20 min. The supernatant was filtrated through filter paper No. 1 the filtrate was adjusted to 25 ml with 95% methanol solution and incubated at room temperature for 48 h for the determination of flavonoid content. Total flavonoid was measured by a colorimetric assay according to Kim et al. (Dae-Ok et al., 2003) with some modifications (Khaleghnezhad et al., 2019). Flavonoid content (FC) was expressed as mg Rutin equivalents per gram of dried biomass (mg RE g−1) (Massoumeh et al., 2014).All samples were analyzed three times.

Results

Humidity percentage

The percentage of water in the dried seeds at 85 °C until a constant weight had recorded an average of 8% dry weight.

Oil content of blank sample

The yield percentage of oil extracted from dry biomass of blank samples of S. bigelovii seeds by different methods (shaker, conventional, and ultrasonic probe) using different organic solvents are reported in Fig. 1.

Fig. 1
figure 1

Effect of different solvent with variant extraction methods on the oil percentage of blank sample

The oil percentage obtained by using the ultrasonic probe is more than that by the conventional method which recorded a percentage of oil more than that of the shaker process. The ethanol in all extraction techniques produced a maximum yield of oil. Hexane-isopropanol recovered an oil percentage higher than hexane.

Fatty acid profile of blank sample

Gas chromatography analysis of the fatty acids composition of blank samples oils, which are extracted by three methods (shaker, conventional, and ultrasonic probe) using ethanol solvent represented in Table 2.

Table 2 Fatty acids profile of blank samples oil extracted by different methods using ethanol

The GC analysis showed eleven fatty acids distinctly. Six were saturated and five unsaturated. The palmitic (C16:0) was the dominant saturated fatty acids (18.6–19.5%), while linoleic-ω6 acid (18:2) was the major unsaturated fatty acid (34.3–35.3%), oleic acid (18:1) as mono-unsaturated fatty acid recorded 16–17.5% of total fatty acids. The unsaturated FA (USFA) was almost twice saturated FA (SFA).

Effect of different cultivation treatments on

Oil yield

The cultivation of S. bigelovii plant under variant mixed treatments of irrigation and fertilizing was affected on its oil content as clearing in Table 3.

Table 3 Total oil % of S. bigelovii seeds cultivated under different combined treatments

The recovered oil, by ethanol with an ultrasonic probe, from the blank sample (B) which was a representative sample from the desert of the North West Coast, was 36.3%. However, the highest percentage of oil was 35% obtained from sample No. 16, which was subjected to 75% well water for irrigation and fertilized with a combination of NPK + micro + algae. The control sample No. 17 was grown under the same environmental conditions of cultivation as the other samples (1–16), excluding irrigation and fertilization. It produced an acceptable amount of oil (25%), but less than the oil % in the blank sample (B).

Fatty acid composition

The oil compositions of different cultivation treatments samples (1–17) were determined by GC analysis, as shown in Table 4.

Table 4 The fatty acid profile and cetane No. of oil in samples cultivated under different treatments

The different combined treatments of fertilization and irrigation of S. bigelovii have changed the fatty acid profiles of all samples, where the saturated FA (SFA) was more than the unsaturated FA (USFA), except two samples No. 10 and 16 where the USFA percentage is higher than SFA, by 2–6%.

The most abundant saturated fatty acids were palmitic acid (C16:0) and stearic acid (C18:0). Oleic acid (C18:1) and linoleic acid (C18:2) were the most unsaturated fatty acid present.

Nutrition activity

Fatty acids

Generally, the ratio of polyunsaturated fatty acid (PUFA) to saturated fatty acid (SFA) is used to evaluate the nutritional value of oil (Choi et al., 2014; López-Yerena et al., 2018). The effects of MUFA and PUFA+MUFA/SFA on the plasma and liver lipid concentrations in rats were examined by Chang and Huang (López-Yerena et al., 2018). They concluded that MUFA/SFA must be < 1, PUFA/SFA < 2, and PUFA/MUFA > 2 and PUFA+MUFA/SFA must not exceed than 2, for lowering the effects of triacylglycerol and cholesterol on the plasma and liver lipid concentrations.

The ratio of polyunsaturated fatty acid to saturated fatty acid for the blank sample was in agreement with Chang and Huang, where

MUFA/SFA = 0.5, PUFA / SFA = 1.3, PUFA/MUFA = 2.5, and PUFA+MUFA/SFA = 1.8.

The GC analysis of oil samples (Table 3), recorded that, all of them are not rich in PUFA.

The ratios of PUFA/SFA for nutrition value were not revealed for most samples.

Total phenolic and flavonoid content

The total polyphenolic content of investigated samples 1–17 according to the Folin method differed from one to another between 2.13 and 3.66 mg Gallic/1 g dry weights of de-oiled biomass, as shown in Fig. 2. The colorimetric determination of total flavonoid content in the samples recorded a variation from 1.28 to 2.44 mg/1 g dry weight in flavonoid content. The samples with higher oil % recorded low phenolic and flavonoid content, whereas the phenolic and flavonoid content in the blank sample was higher value, 4.5 and 2.9 mg/1 g, respectively.

Fig. 2
figure 2

The polyphenolic and flavonoids content in samples, 1–17 and blank (B)

Discussion

Oil content of blank sample

The results show that ethanol has higher extraction efficiency than the other used solvents. This is for the fact that the efficiency of oil extraction is mostly dependent on the solvent polarity (Basily et al., 2018a).

The polar solvents can open the wall of cells and thus allow more extraction of the cell contents (Tir et al., 2012), so it is the most promising solvent for oil extraction. The ethanol and isopropanol as polar solvents of short-chain alcohols are used in several studies as alternative solvents for extraction because they are safer (Rodrigues et al., 2010; Russin et al., 2010).

The ultrasonic probe systems recorded maximum oil % with all solvents used for extraction process. The performance of ultrasonic technique is based on an electromagnetic transducer (i.e., converting mechanical energy or electrical one to big frequency sound) as an ultrasound power, commonly operating at a frequency of 20 kHz, and the ultrasonic probe energy is introducing directly into the extraction vessel not transfer through the liquid medium to the cells (Basily et al., 2018a).

Fatty acid profile of blank sample

There are slight differences in the fatty acid composition of the oil extracted either by different methods or with various organic solvents. This means that the extraction method and the solvent are affecting in the oil yield percentage, not in the oil composition. The result is in agreement with previous studies (Basily et al., 2018a).

Effect of different cultivation treatments on

Oil yield

The environmental conditions of cultivation are primary factors in the oil yield percentage. Previous researches (Yuan et al., 2019; Tawfik et al., 2013; Tawfik, 2007) studied the effect of different cultivation treatments on the productivity of the halophyte plants. From the percentages of oil in our study, it can be concluded that the well water and NPK + micro + algae have a significant effect to increase the percentage of oil recovery from the seeds. Samples 4, 8, 12, and 16 were cultivated under the same treatments of fertilization of micronutrients, NPK, and biofertilizer of algal extract and different irrigation system at well water percentage of 100, 0, 50, and 75%. The lowest oil % was recorded from sample 8 due to the absence of well water in its irrigation system, and increases with the increasing percentage of well water to reach a higher value at sample 16 with inserting 25% seawater. This is in agreement with other studies (Bhardwaj et al., 2014; Tawfik et al., 2013), where the moderate salinity and biofertilizer improve the productivity of halophyte and its contents of protein and carbohydrate. The other combined treatments of fertilization and irrigation of S. bigelovii recorded lower oil percentages.

Fatty acid composition

In previous research (Knothe, 2012), palmitic, stearic, oleic, and linoleic acids were recognized as the most common fatty acids that were suitable for biodiesel production. In particular, oils with oleic acid (C18-1) content have been reported to have a feasible balance of fuel properties (Gopinath et al., 2015). That agrees with our results as clear in a Table 4, the calculated cetane number of FA components higher than 50 for all samples. Overall, the oil of cultivated samples is reasonable for biodiesel production with good quality (Gopinath et al., 2015). The stability of the oil is better than the other commercial oils because of the small amount of linolenic acid C18:3 (5.2–5.5%) (Gopinath et al., 2015).

Comparing with the blank sample (B) found that it contains FAs with a carbon chain of more than 18 as C20, C20-1 C22-2, and C24. The percentage of palmitic A. and stearic A. is very low, 19.5% and 2.5%, respectively. Its cetane No. is too small (29.6). As a result, the oil of this sample (B) is not promising enough for biofuel production.

Nutrition activity

Fatty acids

The unsaturated fatty acids of the blank sample were recorded > 63% of the total FAs. Such FAs composition has an important role in cosmetology and medical applications (Minzangi et al., 2011; Torri et al., 2019). The free FAs can be generated in the skin as a result of triglycerides decomposition by bacteria. The destruction of the epidermal protective layer and loss of skin water leads the epidermis to produce more lipids in the lamellar granules of the stratum granulose. The regeneration of the lipids decreases with aging, so the oil-containing FAs of omega-6 series increase the lipid’s reproduction in the lamellar granules (Zare et al., 2019). The blank sample oil was rich in polyunsaturated fatty acids, especially, oleic acid (17.5%) and linoleic acid (36.5%), which have a medical effect. Naturally, the linoleic C18:2 is a component of sebum, and decreasing its content assists to block skin pores leading to the formation of eczemas and comedos. So the linoleic can be used for solving the problems of skin care and skin richness (Zielińska & Nowak, 2014).

Total phenolic and flavonoid content

The total phenolic concentrations of investigated samples based on the Folin method were varied from sample to another one (Fig. 2). This agrees with previous studies that demonstrated that culture parameters and the type of plant are affected in the concentration and composition of phenolic compounds of biomass (Safafar et al., 2015). Phenolic compounds are considered to be biologically active components with various health beneficial properties (Zhao et al., 2014).

The colorimetric determination of flavonoid content clarifies a variation in flavonoid content which may be due to the difference in physicochemical parameters of cultivation. Flavonoids are secondary metabolites and have the capacity to act as strong antioxidants capable to scavenge free radicals which are harmful to the human body and food products (Shashank & Abhay, 2013).

With the increasing demand for natural products in pharmaceuticals, nutraceuticals, and cosmetic industries, flavonoids and phenolic are gaining vital importance with their multiple activities as antioxidants by inhibition of reactive oxygen species (ROS) generation and direct or indirect scavenging of free radicals. Recently, natural antioxidants discovered in plants have attracted some interest as anti-microbial, anti-cancer, and anti-diabetic. They have the capacity to improve food quality and stability (Esmaeili et al., 2015).

Conclusion

The different combined treatments of fertilization and irrigation of S. bigelovii changed the fatty acid profiles of all samples than the blank one, where the saturated FA became more than the unsaturated FA. Except for two samples 10 and 16, there is no significant difference between the SFA and USFA percentages. Such oil is being more reasonable for biodiesel production. The most abundant saturated fatty acids were palmitic acid (C16:0) and stearic acid (C18:0). Oleic acid (C18:1) and linoleic acid (C18:2) were the most abundant unsaturated fatty acid. In palmitic, stearic, oleic, and linoleic acids were recognized as the most common fatty acids for biodiesel. In particular, oils with oleic acid content have been reported to have a feasible balance of fuel properties that agrees with our results. The higher cetane number than 50 for all samples is referring to this oil has power for biodiesel production with good ignition properties. The nutrition activity of the blank sample was higher than the recultivated samples. The omega series acids ω-9 (oleic), ω-6 (linoleic), and ω-3 (α-linolenic) have wide applications in cosmetic industries as thickening agents, water-binding agents, and antioxidants in facial and skin care products. Phenolic compounds have an important role in human health as radical scavengers. Flavonoids are secondary metabolites with multiple activities as anti-microbial, anti-cancer, and anti-diabetic.