Comparative evaluation of Salicornia bigelovii oil planted under different treatments

El-Araby, R.; Rezk, A. I.; El-Enin, S. A. Abo; Nofal, O. A.; El-Nasharty, A. B.

doi:10.1186/s42269-020-00388-8

Research
Open Access
Published: 12 August 2020

Comparative evaluation of Salicornia bigelovii oil planted under different treatments

R. El-Araby¹,
A. I. Rezk²,
S. A. Abo El-Enin¹,
O. A. Nofal³ &
A. B. El-Nasharty²

Bulletin of the National Research Centre volume 44, Article number: 133 (2020) Cite this article

1086 Accesses
2 Citations
Metrics details

Abstract

Background

Assessment of the oil % in a representative sample of Salicornia bigelovii seeds with different extraction methods using some of the organic solvents to reach the best economic one and determination of the effect of S. bigelovii cultivation under different conditions of irrigation and fertilization on the percentage, composition, and nutrition value of oil were done. From the International Training Centre-Mariut, Alexandria, we obtained representative samples of Salicornia bigelovii seeds which are collected from the sea coast and 17 samples of S. bigelovii seeds which are subjected to different treatments of irrigation and fertilization. The oil % in a blank sample (B) was determined using different solvents (hexane, hexane-isopropanol, and ethanol) with variant methods (shaker, conventional, and ultrasonic). Oil % in 17 samples was evaluated by the ultrasonic probe technique using ethanol. The oil composition was determined in all samples by GC analysis. The phenolic and flavonoid contents in the residue were determined with the Folin-Ciocalteu reagent and colorimetric method, respectively.

Results

The ethanol has higher extraction efficiency and the ultrasonic probe recovered higher oil % in the blank sample. Seventeen samples of S. bigelovii cultivated under different combined treatments of fertilization and irrigation recorded oil % less than the blank sample. The fatty acids profile cleared that the oil of cultivated samples (17 samples) had power for biodiesel production with high ignition properties and good stability due to the high cetane number and a high percentage of palmitic acid. The nutrition value of the blank sample is higher than that of the other 17 samples. The polyunsaturated fatty acids in the blank sample represent > 63% of the total fatty acids.

Conclusion

The different combined treatments of fertilization and irrigation of S. bigelovii changed the fatty acid profiles of all samples, palmitic, stearic, oleic, and linoleic acids were recognized as the most abundant saturated fatty acids. The total phenolic and flavonoid contents differed in the sample to another one but less than their contents in the blank sample.

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

Full size table

Work steps are as follows:

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.
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.
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.
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.
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.
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):

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

(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

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).
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.

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

Full size table

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

Full size table

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

Full size table

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.