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Article

Effects of Different Irrigation Regimes and Nitrogen Fertilization on the Physicochemical and Bioactive Characteristics of onion (Allium cepa L.)

by
Susana Marlene Barrales-Heredia
1,
Onécimo Grimaldo-Juárez
1,*,
Ángel Manuel Suárez-Hernández
2,
Ricardo Iván González-Vega
3,
Jairo Díaz-Ramírez
4,
Alejandro Manelik García-López
1,
Roberto Soto-Ortiz
1,
Daniel González-Mendoza
1,
Rey David Iturralde-García
5,
Ramón Francisco Dórame-Miranda
5 and
Carmen Lizette Del-Toro-Sánchez
5,*
1
Institute of Agricultural Sciences, Autonomous University of Baja California, Carretera a Delta/Oaxaca s/n, Ejido Nuevo León, Valle de Mexicali, Mexicali 21100, Baja California, Mexico
2
Faculty of Engineering and Business San Quintin, Autonomous University of Baja California, San Quintín 22930, Baja California, Mexico
3
Department of Medical and Life Sciences, Cienega University Center (CUCIÉNEGA), University of Guadalajara, Av. Universidad 1115, Lindavista, Ocotlán 47820, Jalisco, Mexico
4
Desert Research and Extension Center, University of California, 1004 E Holton Rd., Holtville, CA 92250, USA
5
Department of Research and Postgraduate in Food, University of Sonora, Blvd Luis Encinas y Rosales S/N, Col. Centro, Hermosillo 83000, Sonora, Mexico
*
Authors to whom correspondence should be addressed.
Horticulturae 2023, 9(3), 344; https://doi.org/10.3390/horticulturae9030344
Submission received: 27 December 2022 / Revised: 26 February 2023 / Accepted: 28 February 2023 / Published: 6 March 2023

Abstract

:
The availability of water and nitrogen in the soil affect the metabolism of onion bulbs. The synthesis of metabolites and bioactive compounds are the most affected, along with the quality of the onion bulbs However, it is necessary to know the effects of different water levels and nitrogen fertilization to optimize the quality of the onion. The objective of this research was to study the effects of the different conditions of hydric stress and nitrogen fertilization during the development of onion (Allium cepa L.) crop, regarding its physicochemical and bioactive properties. Onions were grown using four available irrigation regimes (25, 50, 75 and 100%) and four doses of nitrogen fertilization (100, 150, 200 and 250 kg N ha−1). Onion without any treatment was considered as a control. The treatments low in irrigation and nitrogen fertilization increased the pH level (5.7 to 5.9) and bulb coloration in bright white/yellowish tones. An increase was observed compared to control in titratable acidity (0.13%) just in the nitrogen content, ascorbic acid (46%) and antioxidant capacity with DPPH (12.3%) and ABTS (93.7%). A decrease was shown in soluble solids (14.6%), firmness (3.5 kg cm−2), dry matter (6.6%), total phenols (50%) and FRAP (33.2%) values. Pyruvic acid remained constant (1.5 µmol g−1 FW). The onion bulb extracts showed an erythroprotective effect with a hemolysis inhibition percentage higher than 95%. Finally, the onions had low pungency, and were soft and extra sweet. The treatments with 25% usable humidity and nitrogen fertilization of 150 and 250 kg ha−1, favored the physical, chemical and bioactive quality of the onion bulb.

Graphical Abstract

1. Introduction

The onion (Allium cepa L.) is one of the most important and most widely grown commercial crop products in the world [1], with a global production of about 100 million tons annually [2]. Onion consumption is generalized in almost every tradition and culture, as a complement in culinary preparations due to its nutritional properties as well as for medicinal uses [3]. Among the nutritional properties of this crop are a wide source of A and C vitamins, and minerals such as iron, thiamine, niacin and manganese [4]. Onion is also known to have large amounts of antioxidant compounds due to the synthesis of phenolic elements and flavonoids [5]. Flavor and pungency are biochemical attributes due to several of its bioactive organosulfur and phenolic compounds [6]. In addition to sulfur compounds such as sulfoxides, mono, di and trisulfurs, onion contains phytonutrients such as terpenoids, tannins, alkaloids, thiosulfinates and fructoligosaccharides [7].
Onion owes its biological properties to its flavonoids, phenolic acid content and organosulfur compounds, which are very important in treating and preventing a series of chronic diseases [8,9]. These properties have antimicrobial, antidiabetic, analgesic, anti-inflammatory, hypolipidemic, antihypertensive, immunoprotecting and antioxidant effects [10,11,12]. Thus, onions are a natural source of antioxidants [13]. The measuring of antioxidant activity in onions has been estimated using a series of in vitro testing that includes 2,2′-acid azyno-bis-(3-ethylbenzoathiazoline-6-sulfonic) (ABTS), 1,1-diphenyl-2-pycrylhydrazyl (DPPH), ferric reducing antioxidant power (FRAP), lipid peroxidation, oxygen radical absorbance capacity (ORAC) and total antioxidant capacity (TAC), as well as Trolox equivalent antioxidant capacity (TEAC) [14]. Some of the factors that influence the antioxidant activity in onions are related to the variety, agronomical management, storage conditions, extraction methods and processing technologies applied to onions [15,16,17,18,19].
On the other hand, some authors mention that plants grown under abiotic stress conditions biosynthesize secondary metabolites, including a wide array of bioactive compounds acting as functional molecules for crop adaptation, but which are also of great interest to human health [20]. Among the types of abiotic stress, hydric stress is the main factor responsible for the high metabolite content in plants [21]. Likewise, limited nitrogen supply has been associated with high levels of phenolic compounds in crops [22]. The amount of irrigation water and application of nitrogen in onions not only affects performance, but also their biochemical qualities [23].
Some research reports that quality attributes, such as firmness and color, can be influenced by onion genetic makeup, agronomic practices and water management [24] and [25]. Similarly, ref. [26] mentions that the chemical composition of the onion is determined by genetic factors, while the changes in the concentration of substances, such as organic acids [27], could be determined by the environment and agricultural practices. As a result, this study intends to analyze the effect of different hydric stress conditions and nitrogen fertilization during the development of onion (Allium cepa L.) crop in terms of physicochemical and bioactive properties in an arid environment.

2. Materials and Methods

2.1. Study Site

Field studies were conducted during the period of January to May 2021 in the experimental area of the Institute of Agricultural Sciences of the Autonomous University of Baja California (32°24′34″ N, 115°11′16″ W). The climate, according to the Köppen classification, is hot desert with scarce precipitation in winter (BW [h’] hs [x’] [e’]) [28]. The environmental conditions that occurred during the experimental period are shown in Table 1. The soil properties were clayey texture, EC 5.2 ds m−1, SAR 1.7, pH 8.0, chlorine 1063 ppm, bicarbonate 732 ppm, magnesium 388.8 ppm, calcium 240.5 ppm, sodium 181 ppm, potassium 78 ppm, sulfate 2.39 ppm and nitrate 2.28 ppm.

2.2. Crop Establishment and Management

The white onion variety Sierra Blanca hybrid of intermediate photoperiod was transplanted on January 1st, when the seedlings presented from 3 to 4 leaves. The seedlings were planted in double rows with a spacing of 80 × 20 × 15 cm between furrow, row and plants, respectively. The water without fertilizer was applied weekly through a drip irrigation system during the first 30 days of the crop (before the beginning of bulb formation). Water contained 0.9 ds m−1 and a pH of 8.01. Weeds were controlled manually.

2.3. Treatments and Experimental Design

At the beginning of the onion bulb formation, treatments were applied. Four nitrogen fertilization dosages (100, 150, 200 and 250 Kg N ha−1) as well as four levels of available soil moisture (25, 50, 75 and 100%) were analyzed. The combination of both factors can be seen in Table 2. Onion without any treatment was considered as a control. The available soil moisture was established based on the soil water characteristic curve of clayey texture. Soil moisture regimes were determined with a watermark sensor to a depth 30 cm. A reading of 10 ± 5 cb corresponded to a 100% Aw, 35 ± 5 cb to 75% Aw, 70 ± 5 cb to 50% Aw, 70 ± 5 cb to 50% Aw and 110 cb to 25% Aw. The experiment was conducted in 4 × 4 split plot in randomized complete block design (RCBD) with three repetitions.

2.4. Physicochemical Parameters

These parameters were studied using the Association of Official Agricultural Chemists (AOAC) [29] methodology. Ten grams of fresh onion tissue was homogenized in a commercial Osterizer blender with 50 mL of distilled water (pH 7.0). The extract was filtered and used to determine pH, titratable acidity (%) and total soluble solids (°Brix). The color was measured in two planes opposite the equatorial section of the onion, using a chroma meter CR-410 (Konica Minolta, Inc., Tokyo, Japan) (Figure 1). Color values were expressed using a tridimensional coordinate system L* a* b*, where the vertical axis L* is the luminosity (black = 0 and white = 100), the horizontal axis a* is the trend from red to green and b* is the trend from blue to yellow. Additionally, the values of C* (Chroma) and h (hue) were determined [30]. In addition to this, firmness (expressed in Newton (N)) was measured using a digital Chatillon DFE-100 texture meter (AETEK Inc., New Taipei, Taiwan) with a cylindrical 8 mm point. Finally, we determined the dry matter percentage by placing the bulb cut up into pieces in a drying stove at 60 °C for a period of 72 h [31].

2.5. Pyruvic Acid Determination

This was quantified by using the method proposed by Anthon and Barret [32]. Five grams of vegetable tissue were homogenized with 5 mL of distilled water. After 10 min at room temperature, the mixture was filtered by using 2 layers of organza fabric. The filtrate was centrifuged at 3000 rpm at 4 °C for 10 min. An aliquot of 25 µL of the supernatant was taken and combined with 1 mL of deionized water and 1 mL of 2,4-dinitrophenylhydrazine (DNPH 0.25 g L−1 in HCl 1 M) solution. The mixture was incubated at 37 °C in a water bath for 10 min, and 1 mL of NaOH (1.5 M) was added. Afterwards, the absorbance at 515 nm was recorded and the triplicated results were calculated through a pyruvate pattern curve and expressed in µmol·g−1 of fresh weight.

2.6. Ascorbic Acid Determination

The ascorbic acid contents were determined by using Tillman’s method, which is also known as the 2,6-dichlorophenolindophenol volumetric method. This is based on the reduction of 2,6-dichlorophenolindophenol by the ascorbic acid. Five grams of fresh tissue was homogenized with 50 mL of oxalic acid at 5%. Afterwards, an aliquot of 5 mL was taken and treated with Tillman solution until a permanent pink color was visible for 1 min. The triplicated results were calculated by comparing to a standard curve using pure ascorbic acid and expressed in mg of ascorbic acid 100 g−1 of fresh weight [29].

2.7. Preparation of Onion Extracts

The extraction was carried out according to Downes et al. [33] with some modifications. The onion samples were previously dehydrated at 32 °C (150 ± 0.5 mg) for 48 h, pulverized and filtered by using a 30-mesh sieve (0.595 nm). Samples were dissolved in 3 mL of acidified methanol composed of 70:29.5:0.5 (v/v/v) methanol (reactive grade): water (Milli Q): HCl (reactive grade). Afterwards, the samples were placed in a water bath at 35 °C for 90 min, shaking every 15 min during the extraction. After they cooled down, the samples were centrifuged at 10,000 rpm for 15 min and adjusted at 0.06 g mL−1. Then, they were stored at −20 °C until they were analyzed. The extracts were used to determine total phenols, antioxidant activity and erythroprotective activity.

2.8. Total Phenol Determination

Total phenols were determined by using the Folin–Ciocalteu technique [34]. An aliquot of 10 µL of the extract was added to 25 µL of Folin solution 1 N. After 5 min at room temperature, 25 µL of Na2CO3 solution at 20% and 140 µL of distilled water were added to reach a final volume of 200 µL. The absorbance was determined after 39 min at 760 nm. A calibration curve was produced between 0 and 1 mg mL−1 by using gallic acid as a standard. Assays were performed in triplicate. All results were expressed in milligrams of gallic acid equivalent per gram of sample (mg GAE g−1).

2.9. Antioxidant Capacity Determination

2.9.1. Ferric Reducing Antioxidant Power (FRAP)

The antioxidant power due to reduction from a ferric to ferrous ion was determined by using the Rubio et al. [35] methodology with a few modifications. Firstly, an acidified stock solution of a sodium acetate buffer (300 mmol L−1, pH 3.6) was prepared. In addition, a second solution containing a TPTZ iron complex (2,4,6-tripyridyl-s-triazine) using 20 mmol of FeCl3·6H2O in a TPTZ solution in 40 mmol of HCl was mixed. Once the stock solutions were prepared, a FRAP work solution was made in a 10:1:1 relation (Buffer: FeCl3·6H2O: TPTZ·HCl). In a plate of 96 wells, 20 µL of extract and 280 µL of the FRAP solution were added. Absorbance was determined 30 min later with a Thermo Fisher Scientific Inc. Multiskan GO, NY, USA microplate reader. Ferric ion reduction was determined through a change in color from yellow to blue. A Trolox standard curve was produced in a concentration range from 0 to 200 µM. The results were expressed as µM ET g−1 of sample.

2.9.2. DPPH (2,2-Diphenyl-2-Pycrylhydrazyl)

This step was conducted with 1.5 mg of the DPPH• radical dissolved in 50 mL of methanol. This solution was adjusted to 0.7 ± 0.01 at 515 nm [36]. A total of 200 µL of DPPH• radical was mixed with 20 µL of extract. The sample was kept in darkness for 30 min, and the absorbance at 515 nm was determined. A Trolox standard curve was made (0 to 200 µM) and the results were expressed in µM of Trolox equivalents per gram of sample (µM TE g−1).

2.9.3. ABTS (acid 2,2′-Azyno-bis-3 Ethylbenzothiazoline-6-Sulfonic)

This step was conducted following the Re et al. [37] methodology. The radical was prepared by dissolving 19.3 mg of ABTS in 5 mL of distilled water. Independently, potassium persulfate (0.0378 g) was dissolved in 1 mL of water. A total of 88 µL of the persulfate solution was added to the ABTS solution and left in the dark for 12 h. This last solution was adjusted to 0.7 ± 0.05 at 734 nm. Subsequently, the prepared ABTS•+ cationic radical solution (270 µL) was added to 20 µL of the sample, and after 30 min at room temperature, the absorbance at 734 nm was determined. A Trolox calibration curve was made between 0 and 1 mg mL−1. The results were expressed in µM of Trolox equivalents per gram of sample (µM ET g−1).

2.10. Erythroprotective Activity

When cells (erythrocytes) are exposed to free radicals, they attack the phospholipids of the membranes, causing their destruction or hemolysis. The presence of ascorbic acid and phenolic compounds contributes to the protection of erythrocytes against free radicals [38]. For this analysis, erythrocytes were obtained through the venipuncture technique following the Mexican regulations (NOM-253-SSA1-2012) [39]. Erythrocytes (O blood group Rh+) were extracted from healthy subjects who signed their respective informed consent forms. Blood was deposited in a sterile vial containing anticoagulant (EDTA). Erythrocyte suspension was prepared at 10% with a saline solution containing phosphate (PBS) pH 7.4. It was centrifuged at 2000× g for 10 min at 4 °C and washed three times. The red blood cell packs (erythrocytes) were recovered, and after that, an erythrocyte suspension in PBS was prepared with a 5:95 (v/v) ratio, respectively. The erythroprotective effect was measured by quantifying the anti-hemolytic activity of the extract. Firstly, hemolysis was induced by using AAPH (2,2′-azobis(2-methylpropionamidine), which generates free radicals in the erythrocyte membrane. In order to conduct the analysis, we proceeded to use 100 µL of erythrocytes + 100 µL of the AAPH + 100 µL of each extract (0.06 g mL−1). We considered the erythrocyte suspension and the AAPH with erythrocytes as controls. Following this, we incubated at 37 °C for 3 h, shaking continuously (30 rpm), and we added 1 mL of PBS prior to centrifuging at 2000× g for 10 min at 4 °C. The supernatant was read at 540 nm in a 96-well microplate. The hemolysis inhibition percentage was obtained by using Equation (1):
% Hemolysis inhibition = (AAPH − HS)/AAPH × 100
where AAPH is the hemolysis absorbance caused by the AAPH, and HS is the absorbance of the hemolysis inhibition for each treatment according to the Lu et al. [40] methodology.

2.11. Statistical Analysis

The data from each variable of the study were subjected to analysis of variance (ANOVA) and Tukey’s multiple comparison test (p ≤ 0.05), using the statistical software SAS 9.4. Principal component analysis was used to identify grouping variables in the treatments.

3. Results and Discussions

3.1. Physicochemical Parameters

Table 3 shows the physicochemical parameters of onion regarding available soil moisture and nitrogen fertilization. The levels of pH varied because of the available moisture (p < 0.05) and nitrogen fertilization (p < 0.05). However, this difference was minimal between the untreated sample and those with the different treatments maintaining an acid pH (5.7–5.9). This behavior was similar to that reported by Wakchaure et al. [41] in white onions under severe hydric stress or excessive irrigation, recording pH values of 5.8 to 5.6. However, Venâncio et al. [42] reported that, regarding the soil fertilization and salinity, the pH of the bulbs did not record any significant differences. It is likely that the pH variation of the bulb relies on the agronomical management of the crop, cultural practices and environmental conditions, as indicated by Klunklin and Savage [43].
Titratable acidity was a characteristic which showed a response to irrigation (p < 0.05) and fertilizers (p < 0.05). Treatment with 100% moisture and 250 Kg N ha−1 obtained the highest acidity, registering 0.135%. With a difference in pH, there was a slight increase in titratable acidity in the treatments of 75 and 100% available moisture, whereas in fertilization, the same increase appeared in the 150 kg N ha−1 treatment. Acidity measures both free protons as well as those connected, as opposed to pH, which measures only free protons. Therefore, pH remained with a constant number of free protons in the different treatments while acidity did not. This might be because onion bulbs have different organic acid contents. Organic acids are distributed unevenly in onion bulbs with higher levels of malate in the external scales and citrate in the internal ones [44].
Total soluble solids showed a decrease of about 14.6% compared to untreated onion, showing no significant differences in 25% available moisture and in 100 kg N ha−1 of fertilizer. Similar results were reported by Pejic et al. [45] and Ghodke et al. [46]. Yoo et al. [47] mention that the crop used in this research (“Sierra Blanca”) is sweet. On the other hand, Chávez-Mendoza et al. [48] indicated that it contains 12.9± 0.8 °Brix, a similar amount to that obtained in our research (12.3 °Brix). Regarding color, particularly at 0 and 25% of available moisture, “L*” showed values close to 100, which indicates higher color clarity; “b*” showed a slighter tendency more towards a yellow color; and “C*” high brightness in the bulb surface. The value a*, since it is too small, tends to be white in color. The values of h obtained indicate white/yellow hues. It is possible that the 0 and 25% treatments of usable humidity showed a higher whiteness, luminosity and brightness in the bulbs due to restricted irrigation conditions. Plants under hydric stress protect themselves by reducing the photosynthesis rate [46,49] and the production of chlorophyl or color [50], redirecting most of the energy from the plant to the production of more proline (40%) and phenols (26%), thus promoting its special coloration [51].
Firmness was slightly higher in untreated samples of onion (4.5 kg cm−2) compared to treated bulbs (3.5 kg cm−2). Mallor et al. [24] and Agnieszka et al. [25] mention that the quality attributes such as firmness can be influenced by agronomical practices and water management. Randle [52] indicates that high doses of nitrogen in crops can produce soft bulbs and decrease the useful post-harvest life. On the other hand, Di Miceli et al. [53] reported higher firmness (8.44 kg cm−2 and 7.94 kg cm−2) in onions with high nitrogen concentrations (160 and 220 kg N ha−1, respectively). These controversies among researchers suggest that the genetic composition of the onion is related to the firmness of the bulb.
The onion dry matter (Figure 2) had a significant response to soil moisture and fertilization (p < 0.05). The highest dry weight (Figure 2A) was recorded in the control treatment (12.7%), followed by 25 and 50 usable humidity percentage (6.6% and 5%, respectively). The 75 and 100% levels of humidity recorded less dry matter and showed no significant differences. We observed a similar trend in fertilization treatments (Figure 2B) with 0 nitrogen (12.7%), 100 (5.3%) and 150 (5%) kg N ha−1. Hence, in both factors, there was a decrease of about 40–48% dry matter in comparison to the control. Fatideh and Asil [54] and Abdelkhalik et al. [55] reported that the maximum production of dry matter in onions was recorded with minimum humidity treatments, a behavior which was similar to our results. Khokhar [56] mentioned that too much nitrogen can not only reduce the amount of dry matter, but it can also cause an excessive vegetative growth and delayed maturity, among other variables.
The interaction that presented the highest percentage of dry matter was that of the treatments of 25% available soil moisture and 100 Kg N ha−1, registering 7.4%, followed by the interaction of 25% moisture and 150 Kg N ha−1, with 6.9% for these variables.

3.2. Pyruvic Acid Content

This parameter is directly related to the pungency of the onion bulb. The “Sweet Onion Industry” in Georgia (USA), indicates the scale of pyruvic acid values varying from 0 to 18 µmol g−1 FW. When values are between 0 and 3, they are considered to be low-pungency onions, between 3 and 7 is considered to be medium pungency and if they are higher than 7, they are considered to be high-pungency onions. Another more specific scale is the one presented by “Vidalia Labs International” in Georgia (USA, 2005), where the scale is between the values of 0 and 10 µmol g−1 FW. If the pyruvic acid values are lower than 3, they are considered to be weak flavored onions, those between 3 and 5.5 are classified as being slightly pungent, those between 5.5 and 6 are pungent and if the value is higher than 6, they are considered very pungent. Therefore, onions with a level of pyruvic acid lower than 3.5 are called extra sweet onions, those between 3.6 and 5.5 are sweet onions and those with values higher than 5.6 are hot onions [24]. All samples had 1.5 µmol g−1 FW of pyruvic acid. Therefore, they fall within the classification of low pungency, weak flavored and extra sweet onions. Similar amounts have been reported by Abdissa et al. [57] in red Bombay onions, and by Ghodke et al. [46] and Gonçalves et al. [58] in sweet onions.

3.3. Ascorbic Acid Content

Ascorbic acid content held a significant relation with irrigation and fertilizers (p < 0.05). Ascorbic acid contents increased compared to the control (Figure 3). From 50% to 100% available soil moisture levels, there was an approximate increase of 46% of ascorbic acid. There were no significant differences between treatments (Figure 3A). In terms of fertilization response, the level of 200 kg N ha−1 recorded higher ascorbic acid contents (15.13 mg/100 g FW) with a 47.4% increase compared to the control (Figure 3B). As opposed to other bioactive compounds, the effect of hydric deficit on the accumulation of ascorbic acid in agricultural crops is, in some cases, inconsistent [59]. For example, there was an increase in ascorbic acid reported by Wichrowska et al. [60] and Golubkina et al. [61] in ‘Efekt’ onions when growing with hydric deficit. However, Ncayiyana et al. [62] reported no significant differences in the ascorbic acid content of red and white onions at different nitrogen fertilization doses. Ascorbic acid is considered an antioxidant that induces responses related to plant growth to cope with stress. Stress increases the level of cell oxidation state, which induces an increase in the synthesis of antioxidants to counteract the effects of that oxidation. This may explain the ascorbic acid increase in the different treatments applied to the onions.

3.4. Total Phenols

Phenolic compounds showed a decrease with the different treatments compared to the control both in available soil moisture as well as with the use of nitrogen fertilization (Table 4). The more the doses of the treatments increased, the lower the number of phenolic compounds in the onion bulbs, thus showing a negative correlation (r2 = −0.8227). It has been reported that the proportion of phenols in onions varies depending on the color. Red and yellow onions have the main polyphenols: gallic and ferulic acids, particularly quercetin as QDG (quercetin-3,4′-diglucoside) and Q4′G (quercetin-4′-glucoside) [63]. However, even though phenols protect cells from potential oxidative damage caused by oxidative stress [41], this time, this role was mitigated by ascorbic acid, which showed an increase in the different treatments, and also has functions similar to those of phenolic compounds. On the other hand, this behavior could be due to environmental or genetic crop factors [64].

3.5. Antioxidant Capacity

The potential of a substance or compound to inhibit or hinder the oxidation of a substrate is known as antioxidant capacity. There are two main mechanisms to carry this out: by electron transfer (SET) or by proton transfer (HAT). The test to obtain FRAP is about an SET electron transfer reaction based on the reduction of a yellow complex of ferric tripyridyl triazine or Fe3+-TPTZ (2,4,6-trypyridyls-triazine) to the blue-colored reduced ferrous complex Fe2+-TPTZ by an acid medium antioxidant [35]. According to the results, the reducing antioxidant power in onions also decreased with the different treatments compared to the control (Table 4). This could have been due to the decrease in the number of phenolic compounds, since there was a positive correlation between phenolic compounds and the FRAP (r2 = 0.8742), indicating that most of the reducing power was due to this type of compound. Pulido et al. [65] state that quercetin has a higher capacity than ascorbic acid to reduce Fe3+ in the FRAP test. The amounts obtained in the present research (66.8 µM TE g−1) were higher than those reported by Gorinstein et al. [66] in white onions (15.44 a 23.39 µM TE g−1).
On the other hand, DPPH and ABTS are synthetic free radicals that help us measure antioxidant activity known as antiradical activity. Free radicals are unstable molecules since they have one or more unpaired electrons, which can cause the oxidation of other molecules, thus inducing cellular damage and cellular death, which is why it is so important to study them [16,36]. In this research, onion bulb extracts showed an increase in the inhibition of both radicals in all the treatments studied compared to the control (Table 2). Even in ABTS, there was double the activity in the treatments at 25% of available moisture and 100 kg N ha−1. Phenolic compounds and ascorbic acid showed a high positive correlation in both radicals DPPH (r2 = 0.9124 and r2 = 0.8843, respectively) and ABTS (r2 = 0.9424 and r2 = 0.9043, respectively) indicating that both groups of compounds present in the onion bulb have an antiradical activity. Ibrahim et al. [67] mention that low levels of nitrogen fertilization could be related to antioxidant activities higher than those exposed to more favorable conditions due to the accumulation of polyphenolic compounds in vegetable tissues. This behavior was proven in the antiradical activity with DPPH and ABTS.

3.6. Erythroprotection Effect

Cellular membranes (such as those of erythrocytes) formed by phospholipids are widely susceptible to oxidation and damage by free radicals. For this reason, the ability of antioxidants present in onions to prevent hemolysis of erythrocytes was evaluated in this study [38]. The AAPH (2,2′-azobis(2-methylpropionamidine)) compound is an inductor of peroxyl (ROO•) radicals in the erythrocyte membrane causing lipidic peroxidation and, consequently, hemolysis. Therefore, in this study, onion bulb extracts were used to inhibit this hemolysis. Both in treatments with available soil moisture as well as those with nitrogen fertilization, there was an increase in the hemolysis percentage compared to the control (Figure 4). Treatments starting at 50% available moisture showed a hemolysis percentage higher than 90% (Figure 4A), whereas in conditions starting at 100 kg N ha−1, percentages higher than 85% were observed (Figure 4B). According to correlations conducted with ascorbic acid and the number of phenolic compounds with regard to the hemolysis percentage, we observed a higher correlation of both compounds (r2 = 0.9362 and r2 = 0.9643, respectively), thus indicating that both groups of compounds contribute to the protection of erythrocytes against free radicals.
In this context, with this technique, it is possible to also attribute an antioxidant capacity because it neutralizes peroxyl radicals. It is generally through the HAT mechanism because of the transfer of a hydrogen atom (H•) from a phenol (Ar-OH) or any other antioxidant compound of the radical ROO•, thus neutralizing this radical and avoiding hemolysis [14]. Among the phenolic compounds in onions (quercetin and its glucosides, kaempferol, isorhamnetin, myricetin, gallic acid, ferulic acid) [6,68], quercetin has a high antiradical activity and acts as a strong antioxidant due to its structural properties [69]. Therefore, onion bulb extracts with the different treatments generate compounds that may have erythroprotective properties.

3.7. Combined Variable Analysis with Principal Components

In the principal component analysis of the irrigation regime and nitrogen fertilization combination, it was found that 69% of the treatments variation is associated with the first two principal components (PC). PC1 contributed 55.48 % and PC2 with 13.72 %. The most important variables in PC1 were pH, dry matter (%), light (L), phenols and FRAP. In PC2, color parameters (a, h) and DPPH were the outstanding ones.
The treatments dispersion according to CP1 and CP2 (Figure 5), shows that in PC1 the treatment 1 (control: without water and nitrogen fertilizer) was outstanding in dry matter percentage, phenols production, FRAP and in color the luminosity. In descending order, treatments 2, 3, 4 and 5 were identified as those with the highest expression of the aforementioned variables. In these treatments, the minimum irrigation regime condition was maintained in combination with different nitrogen doses. In the rest of the treatments a similar behavior is maintained. Based on these results, it is evident that the minimum moisture condition has a greater impact on the physicochemical and bioactive levels in the onion.
Regarding CP2, it is identified that treatments 1, 6, 10, 14 and 16, present numerically lower values in the attributes of color (a) and tonality (h). There is an intermediate group integrated by 2, 4, 7, 11, 12, 13 and 15. Another group that can be distinguished is the format for treatments 3, 5 and 8, which registered the highest values. The same behavior was observed in DPPH.
In the joint analysis of CP1 and CP2, treatments 3 and 5 were identified as the best for producing good quality onions in physicochemical and bioactive properties. In both treatments an irrigation regime of 25% available soil moisture and nitrogen fertilization of 150 and 250 kg ha−1, respectively are maintained. With these results it is evident that water stress condition improves the bulb quality, although the risk of inducing a reduction in yield due to water availability.

4. Conclusions

The factors available soil moisture and nitrogen fertilization mainly had an influence on the increase in titratable acidity, ascorbic acid and antioxidant capacity by DPPH and ABTS. In contrast, these factors influenced the reduction in pH, soluble solids, firmness, dry matter, total phenol levels and FRAP reducing power. Pungency was not affected by any of the treatments, leaving onions in a low-pungency classification, weak flavored and extra sweet. However, the extracts from the onion bulbs have a good erythroprotective effect and high antioxidant capacity to prevent lipidic peroxidation, which can benefit consumers, giving it added value, and with this property, they can prevent cellular damage and prevent chronic degenerative diseases. The treatments with 25% usable humidity and nitrogen fertilization of 150 and 250 kg ha−1, favored the physical, chemical and bioactive quality of the onion bulb.
Therefore, this study provides the necessary basis to continue carrying out and delving into more studies on the bioactive properties of onions, manipulating their composition and other factors besides soil moisture and nitrogen content such as lighting and some others. In general terms, most of the measured parameters were mainly fostered by low soil moisture (50%) and nitrogen (100 kg N ha−1) levels, which are a financially and environmentally feasible advantage for onion crops.

Author Contributions

Conceptualization, R.D.I.-G. and R.F.D.-M.; methodology, R.S.-O., Á.M.S.-H. and D.G.-M.; formal analysis, R.I.G.-V.; resources, J.D.-R. and A.M.G.-L.; writing—original draft preparation, S.M.B.-H.; supervision, C.L.D.-T.-S.; project administration, O.G.-J.; graphical abstract, C.L.D.-T.-S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was carried out in accordance with the Declaration of Helsinki of 1975. The clinical laboratory is accredited by ISO-IEC 17.025 (NMX-EC-17025) and ISO 15.189 prepared by the technical committee ISO/TC 212 (Clinical Laboratory Testing and In vitro Diagnostic Systems) taking as reference the ISO/IEC 17.025 and ISO 9001 standards.

Informed Consent Statement

All subjects gave their informed consent for inclusion in the study prior to their participation.

Data Availability Statement

The original contribution data presented in this research are included in the article; further inquiries can be directed to the corresponding authors.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples are available from the corresponding authors.

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Figure 1. Measurement of onion color using a chroma meter CR-410 (Konica Minolta, Inc., Japan).
Figure 1. Measurement of onion color using a chroma meter CR-410 (Konica Minolta, Inc., Japan).
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Figure 2. Onion dry matter at different (A) soil moistures and (B) nitrogen fertilization. Different letters indicate significant difference (p < 0.05). Media ± standard deviation of three repetitions.
Figure 2. Onion dry matter at different (A) soil moistures and (B) nitrogen fertilization. Different letters indicate significant difference (p < 0.05). Media ± standard deviation of three repetitions.
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Figure 3. Onion ascorbic acid content at different (A) soil moistures and (B) nitrogen fertilization. Different letters indicate significant difference (p < 0.05). Media ± standard deviation of three repetitions. FW = fresh weight.
Figure 3. Onion ascorbic acid content at different (A) soil moistures and (B) nitrogen fertilization. Different letters indicate significant difference (p < 0.05). Media ± standard deviation of three repetitions. FW = fresh weight.
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Figure 4. Erythroprotective effect reported in percentage inhibition of hemolysis of onion bulb extracts from different (A) soil moistures and (B) nitrogen fertilization. Different letters indicate significant difference (p < 0.05). Media ± standard deviation of three repetitions.
Figure 4. Erythroprotective effect reported in percentage inhibition of hemolysis of onion bulb extracts from different (A) soil moistures and (B) nitrogen fertilization. Different letters indicate significant difference (p < 0.05). Media ± standard deviation of three repetitions.
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Figure 5. Principal component analysis (PCA) of physical, chemical and bioactive characteristics of the onion bulb.
Figure 5. Principal component analysis (PCA) of physical, chemical and bioactive characteristics of the onion bulb.
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Table 1. Environmental conditions recorded during the experimental period between January and May 2021. Average monthly values of meteorological data recorded with an automatic weather station.
Table 1. Environmental conditions recorded during the experimental period between January and May 2021. Average monthly values of meteorological data recorded with an automatic weather station.
VariableJanuaryFebruaryMarchAprilMay
Accumulated precipitation (mm)8.900.100.000.000.00
Total solar (Cal cm−2)259.37357.70456.14526.70581.27
Minimum air temperature (°C)3.485.726.6711.6714.12
Maximum air temperature (°C)21.3724.1525.5732.7735.83
Average air temperature (°C)12.1014.9116.3222.8225.48
Minimum relative humidity (%)28.2918.0617.9312.7310.52
Maximum relative humidity (%)88.8184.2783.6374.7282.27
Average relative humidity (%)58.7946.8245.6137.8139.83
Average dew points (°C)2.291.362.224.397.40
Average wind speed (m s−1)1.251.551.641.761.81
Average soil temperature (°C)12.8113.7415.2419.8523.00
Table 2. Description of treatments of nitrogen fertilization and soil moisture in onion cultivation.
Table 2. Description of treatments of nitrogen fertilization and soil moisture in onion cultivation.
TreatmentAvailable Soil Moisture (%)Nitrogen Fertilization Dosage (Kg ha−1)
100
225100
325150
425200
525250
650100
750150
850200
950250
1075100
1175150
1275200
1375250
14100100
15100150
16100200
17100250
Table 3. Physicochemical parameters of onion bulbs (Allium cepa L.) in response to available soil moisture and nitrogen fertilization.
Table 3. Physicochemical parameters of onion bulbs (Allium cepa L.) in response to available soil moisture and nitrogen fertilization.
Color
Available Soil Moisture (%)pHTitratable Acidity (%)TSS *
(°Brix)
L*a*b*C*hFirmness
(kg cm−2)
05.9 ± 0.1 a0.12 ± 0.0 b14.4 ± 0.3 a95.7 ± 1.0 a−1.0 ± 0.6 a15.0 ± 1.4 a14.6 ± 0.8 a93.7 ± 2.0 b4.5 ± 2.0 a
255.7 ± 0.0 b0.12 ± 0.0 b12.3 ± 0.0 b91.3 ± 1.4 b−1.8 ± 1.9 b12.6 ± 0.5 b12.7 ± 0.5 b96.9 ± 2.2 a3.4 ± 1.0 b
505.7 ± 0.0 b0.12 ± 0.0 b12.3 ± 0.0 b90.0 ± 0.2 c−1.5 ± 0.2 ab11.1 ± 0.8 c11.0 ± 0.8 c97.7 ± 1.3 a3.6 ± 0.0 b
755.7 ± 0.0 b0.13 ± 0.0 a12.2 ± 0.0 b89.5 ± 0.8 c−1.5 ± 0.7 ab11.0 ± 1.4 c11.1± 1.5 c97.5 ± 2.5 a3.8 ± 1.5 b
1005.7 ± 0.0 b0.13 ± 0.0 a12.3 ± 0.0 b89.7 ± 1.4 c−1.4 ± 0.6 ab10.4 ± 1.2 c10.6 ± 1.2 c97.7 ± 2.2 a3.7 ± 0.1 b
Color
Nitrogen (kg N Ha−1)pHTitratable Acidity (%)TSS *
(°Brix)
L*a*b*C*hFirmness
(kg cm−2)
05.9 ± 0.1 a0.12 ± 0.0 b14.4 ± 0.3 a95.7 ± 1.0 a−1.0 ± 0.6 a15.0± 1.4 a14.6 ± 0.8 a93.7 ± 2.0 b4.5 ± 2.0 a
1005.7 ± 0.0 b0.12 ± 0.0 b12.3 ± 0.0 b90.3 ± 1.4 b−1.5 ± 1.9 ab11.0 ± 0.5 b11.1 ± 0.5 b96.4 ± 2.2 a3.6 ± 1.0 b
1505.7 ± 0.0 b0.13 ± 0.0 a12.3 ± 0.0 b90.1 ± 0.2 b−1.5 ± 0.2 ab11.4 ± 0.8 b11.5 ± 0.8 b97.5 ± 1.3 a3.6± 0.0 b
2005.7 ± 0.0 b0.13 ± 0.0 a12.2 ± 0.0 b90.1 ± 0.8 b−1.6 ± 0.7 ab11.0 ± 1.4 b11.2± 1.5 b97.9 ± 2.5 a3.7 ± 1.5 b
2505.7 ± 0.0 b0.13 ± 0.0 a12.2 ± 0.0 b90.0 ± 1.4 b−1.6 ± 0.6 b11.7 ± 1.2 b11.7 ± 1.2 b97.9 ± 2.2 a3.5 ± 0.1 b
Media ± standard deviation. Different letters in each column indicate significant difference (p < 0.05). * TSS: total soluble solids. The color values were expressed using a tridimensional coordinate system L* a* b*, where the vertical axis L* is the luminosity (black = 0, and white = 100), the horizontal axis a* is the trend from red to green, and b* is the trend from blue to yellow. C* and h correspond to chroma and hue, respectively.
Table 4. Total phenol content and antioxidant activity (FRAP, DPPH and ABTS) in onion bulbs (Allium cepa L.) grown at different levels of available soil moisture and nitrogen fertilization.
Table 4. Total phenol content and antioxidant activity (FRAP, DPPH and ABTS) in onion bulbs (Allium cepa L.) grown at different levels of available soil moisture and nitrogen fertilization.
Available Soil Moisture (%)Total Phenols
(mg GAE g−1 DW)
FRAP
(µM TE g−1 DW)
DPPH
(µM TE g−1 DW)
ABTS
(µM TE g−1 DW)
025.40 ± 0.1 a66.78 ± 0.0 a37.91 ± 1.2 e32.89 ± 0.3 e
2517.52 ± 0.7 b50.08 ± 0.1 b42.57 ± 0.1 a63.74 ± 0.2 a
5015.99 ± 0.2 c48.45 ± 0.2 c41.88 ± 0.1 b55.58 ± 0.2 b
7514.78 ± 0.1 d47.57 ± 0.3 d41.47 ± 0.1 c51.97 ± 0.0 c
10011.86 ± 0.7 e43.61 ± 0.3 e38.53 ± 0.4 d49.86 ± 1.4 d
Nitrogen Fertilizer
kg N ha−1
Total Phenols
(mg GAE g−1 DW)
FRAP
(µM TE g−1 DW)
DPPH
(µM TE g−1 DW)
ABTS
(µM TE g−1 DW)
025.40 ± 0.1 a66.78 ± 0.0 a37.91 ± 1.2 c32.89 ± 0.3 d
10015.16 ± 0.7 bc46.17 ± 0.1 d40.94 ± 0.1 b57.57 ± 0.2 a
15016.09 ± 0.2 b47.61 ± 0.2 c41.35 ± 0.1 a56.38 ± 0.2 b
20014.94 ± 0.1 cd48.32 ± 0.3 b40.87 ± 0.1 b56.71 ± 0.0 b
25013.97 ± 0.7 d47.61 ± 0.3 c41.29 ± 0.4 a50.50 ± 1.4 c
Values are the mean ± standard deviation of three replicates. All samples were significant (p < 0.0001). Total phenols determined with Folin–Ciocalteu method (mg GAE g−1); FRAP: iron reducing/antioxidant power; TE: Trolox equivalent; DPPH (1,1-diphenyl-2-picrylhydrazyl); ABTS (2,2-azinobis (3-ethylbenzothiazoline 6-sulfonic acid)); DW: dry weight. Different letters indicate significant difference (p < 0.05).
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Barrales-Heredia, S.M.; Grimaldo-Juárez, O.; Suárez-Hernández, Á.M.; González-Vega, R.I.; Díaz-Ramírez, J.; García-López, A.M.; Soto-Ortiz, R.; González-Mendoza, D.; Iturralde-García, R.D.; Dórame-Miranda, R.F.; et al. Effects of Different Irrigation Regimes and Nitrogen Fertilization on the Physicochemical and Bioactive Characteristics of onion (Allium cepa L.). Horticulturae 2023, 9, 344. https://doi.org/10.3390/horticulturae9030344

AMA Style

Barrales-Heredia SM, Grimaldo-Juárez O, Suárez-Hernández ÁM, González-Vega RI, Díaz-Ramírez J, García-López AM, Soto-Ortiz R, González-Mendoza D, Iturralde-García RD, Dórame-Miranda RF, et al. Effects of Different Irrigation Regimes and Nitrogen Fertilization on the Physicochemical and Bioactive Characteristics of onion (Allium cepa L.). Horticulturae. 2023; 9(3):344. https://doi.org/10.3390/horticulturae9030344

Chicago/Turabian Style

Barrales-Heredia, Susana Marlene, Onécimo Grimaldo-Juárez, Ángel Manuel Suárez-Hernández, Ricardo Iván González-Vega, Jairo Díaz-Ramírez, Alejandro Manelik García-López, Roberto Soto-Ortiz, Daniel González-Mendoza, Rey David Iturralde-García, Ramón Francisco Dórame-Miranda, and et al. 2023. "Effects of Different Irrigation Regimes and Nitrogen Fertilization on the Physicochemical and Bioactive Characteristics of onion (Allium cepa L.)" Horticulturae 9, no. 3: 344. https://doi.org/10.3390/horticulturae9030344

APA Style

Barrales-Heredia, S. M., Grimaldo-Juárez, O., Suárez-Hernández, Á. M., González-Vega, R. I., Díaz-Ramírez, J., García-López, A. M., Soto-Ortiz, R., González-Mendoza, D., Iturralde-García, R. D., Dórame-Miranda, R. F., & Del-Toro-Sánchez, C. L. (2023). Effects of Different Irrigation Regimes and Nitrogen Fertilization on the Physicochemical and Bioactive Characteristics of onion (Allium cepa L.). Horticulturae, 9(3), 344. https://doi.org/10.3390/horticulturae9030344

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