Introduction

Fruits are widely recognized as a vital part of a healthy diet, and their regular intake may help to prevent a variety of ailments1,2,3. Optimal fruit production, permanent availability worldwide, and affordability are global issues to optimize human´s health. Passion fruit (Passiflora edulis) is an attractive, nutritious fruit crop highly appreciated for fresh consumption and industrial purposes because of its diverse uses for juice, jelly, and ice cream products4. P. edulis is a perennial woody fruit vine that belongs to the Passifloraceae family, native to tropical America (Brazil)5, and bears hermaphrodite, solitary flowers which are located in the leaf axils. The fruit has a stiff, smooth, waxy dark purple or yellow-hued peel with faint, fine white flecks. The fruit is mostly loaded with a fragrant mass of double-walled, membranous sacs holding orange-colored pulpy fluid and up to 250 tiny, hard, dark brown to black pitted seeds on the inside. The fruit has high nutritional and medicinal value. It is a rich source of vitamin A and C and contains fair amounts of iron, potassium, sodium, magnesium, sulfur, and chlorides, and has dietary fiber and protein (reviewed in6). Fruits are eaten fresh or processed into products like jams, squash, juice, cakes, pies, and ice-cream.

Photosynthetic photon flux density (PPFD) sources suitable for indoor cultivation in controlled environments have boosted crop productivity in densely populated areas or plant growth facilities, such as greenhouses7. The spectral properties of irradiances sources must meet the physiological requirements of plants for photosynthesis and photomorphogenic development8. However, for each crop species in its environment, the optimal quality and irradiance sources have to be found, and there is a huge spectrum of physiological processes which respond differently to the irradiances sources in different crop species. Light-emitting diodes (LEDs) have great potential for horticultural applications due to energy efficiency, longevity, and flexibility of their application9. LEDs become more and more suitable in research and commercial agriculture under controlled conditions due to their low radiation, heat, and wide spectral adaptation10.

Brown, et al.11 and Tennessen, et al.12 described the advantage of LED sources for optimal plant growth. The ideal spectral distribution range promotes plant growth with optimum life span and light energy efficiency13. Many studies investigated LED effects on growth, development, morphology, and photosynthesis in different plants14,15,16,17,18, used a combination of fluorescent and LED sources19, replaced fluorescent light tubes with LEDs20, or utilized various LED combinations.

It has been reported that different color ratios (different light spectrums) strongly influence on plants’ physiological and developmental outcomes21,22,23,24. Other researches revealed the effect of light irradiance on plant growth and development23,25,26,27,28,29 and photoperiod23,30. However, little is known about the combined effect of light irradiance, quality, and photoperiod on plants’ growth, development, and physiological response.

In the present study, we used a number of physiological and protective traits of passion fruit (Passiflora edulis var. Golden No. 6) seedlings to optimize their growth under various light regimes. We exposed the seedlings to light from LEDs emitting different wavelengths with three different light irradiances and for 3 light/dark cycles and propose an optimal regime for plant performance.

Results

Growth parameters

Table 1 and Fig. 1 show the effect of the different LED light regimes on the morphology and growth of the passion fruit seedlings. Table 1 demonstrates that the plant height, stem diameter, Number of leaves, internode distance, fresh shoot, and root weights, as well as dry shoot and root weights were the highest for the seedlings treated with the LM5 regime. The lowest values were observed for LM2, except for the root fresh weight. Although not statistically different to the other treatments, the leaf area of the seedlings was the highest with LM7 and the water content of the plants with LM3.

Table 1 Effect of different LED light regimes on plant morphology and growth characteristics of passion fruit seedlings.
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Figure 1
figure 1

Passion fruit seedlings were grown 60 days under different LED light regimes. (Authors need to improve the quality of the superior figure. Images are compressed.

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Table 2 shows the summary of the results based on the orthogonal array design. The optimal growth characteristics in response to the three factors (light irradiance, red-blue light ratio, and duration of LED light regimes) was A2B2C3, which indicated that the optimal light irradiance is 100 µmol m−2 s−1, from light with a R30:B70 ratio, and a photoperiod of 14 h light and 10 h dark. However, the best results for the leaf areas (A2B1C2) and water contents (A1B3C3) were obtained for different conditions.

Table 2 Results of the range and ANOVA of the L9 (33) matrix for the influence of combined irradiances of LEDs light (A), light spectral ratios (B), and photoperiod (C) on growth characteristics of passion fruit seedlings.
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ANOVA analysis of the data is presented in Table 2 and shows that most of the differences are significant (p ˂ 0.05), except for the factor B on stem diameter and leaf area.

Pigments contents

Next, we investigated whether the optimal light conditions obtained for plant growth and development are the same for accumulation of the pigments in the leaves (Fig. 2). As photosynthetic pigments, we assayed Chl a, Chl b, and the total carotenoid pool. Anthocyanin was chosen for a stress-related pigment which accumulates in the vacuole. Treatments with the light regimes LM3- LM7 gave almost identical results for the accumulation of Chl a (Fig. 2a), whereas the amounts of Chl b as well as of the total carotenoid pool were significantly lower under LM7, i.e., high light irradiance applied for a long period of time and with a high R portion (Fig. 2b,d). Since the leaf area under LM7 is the highest, the combination of these two results indicates that plants growing under LM7 can convert the photosynthetic energy quite efficiently into biomass production, which allows them to decrease their Chl b and car levels. Compared with CK treatment, the levels of total chlorophyll in the leaves of seedlings were higher with LM5 than with the other regimes of LED light, with LM2, LM3, LM4, LM6, and LM7 showing no statistical difference (Fig. 3c). The ratio of total chlorophyll to carotenoid was higher with LM7 than the other LED light regimes, while LM9 mode showed the lowest ratio (Fig. 3e).

Figure 2
figure 2

Effect of different LED light regimes on Chl a (a), Chl b (b), total Chl (c), carotenoid (d), ratio of total Chl to carotenoid (e), and anthocyanin contents (f) in leaves of passion seedlings. Each column represents the means of four replicates; different letters on similar columns indicate significant differences using Duncan's multiple range test at p ≤ 0.05.

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Figure 3
figure 3

Effect of modes LED light on CAT (a), POD (b), SOD (c), Total phenols (d), and Flavonoids contents (e) in leaves of passion seedlings. Each column represents the means of four replicates; different letters on similar columns indicate significant differences using Duncan's multiple range test at p ≤ 0.05.

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Furthermore, anthocyanin is a stress pigment31,32, and its accumulation is more efficiently stimulated by cryptochrome than phytochromes33. Consequently, short illuminations with low light irradiances containing a high red-light portion (LM6) lead to the lowest anthocyanin accumulation (Fig. 2f). Moreover, since the amount of anthocyanin accumulating under LM7 is average, this light regime does not induce stress responses.

On the other hand, according to the R-values, the order of influence of the three factors on pigments contents of Passion fruit seedlings was observed in this study (Table 3). Table 3 shows that the order of impact of the three factors on chlorophyll a, chlorophyll b, total chlorophyll, carotenoid, total chlorophyll/carotenoid, and anthocyanin was (A > C > B), (A > B > C), (A > C > B), (C > A > B), (C > A > B), and (A > C > B), respectively.

Table 3 Results of the range and ANOVA of the L9 (33) matrix for the influence of combined irradiances of LEDs light (A), light spectral ratios (B), and photoperiod (C) on Chl contents and antioxidants of passion fruit seedlings.
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Based on the average of pigment contents derived from three factors at each level, the A2B3C1 and A3B1C3 were the best combinations gave the highest chlorophyll a and total chlorophyll/carotenoid, respectively, which indicated that the maximum of chlorophyll a and total chlorophyll/carotenoid presented at (irradiance 200 µmol m−2 s−1 + ratio (R70:G0:B30) + photoperiod 14 h/10 h) and (irradiance 100 µmol m−2 s−1 + ratio (R30:G0:B70) + photoperiod 14 h/10 h), respectively (Table 4). The best combination of different factors with the levels for the highest chlorophyll b and total chlorophyll was A2B2C3, which indicated that the maximum of these parameters presented at (irradiance 100 µmol m−2 s−1 + ratio (R30:G0:B70) + photoperiod 14 h/10 h). In contrast, the highest carotenoid and anthocyanin was A3B3C2, which indicated that the maximum of these parameters presented at (irradiance 200 µmol m−2 s−1 + ratio (R50:G20:B30) + photoperiod 12 h/12 h).

Table 4 Factors and levels of orthogonal experimental design.
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ANOVA (Table 3) showed that these three factors were significant effects on the plant morphology and the growth performance parameters of passion fruit seedlings (p ˂ 0.05), excepted factor B on chlorophyll a, total chlorophyll, and total chlorophyll/carotenoid had no significant effects.

Antioxidant enzymes

The antioxidant enzyme activities for CAT, POD, and SOD, as well as the total phenol and flavonoid contents in leaves of passion fruit seedlings under different LEDs light treatments are shown in Fig. 3. The CAT activity was the highest in seedlings exposed to LM1, followed by LM9, while the activity was the lowest in seedlings exposed to LM2 (Fig. 3a). Interestingly, the results for the POD activity differed substantially: LM5 seedlings showed the highest and LM8 the lowest enzyme activity, and the LM8 treatment was comparable to those with LM2, LM4, and LM9 (Fig. 3b). The SOD activity was the highest in LM9 seedlings (Fig. 3c). The total phenol and flavonoid contents were the highest in LM5 seedlings (Fig. 3d,e). LM4 treatment resulted in the lowest total phenols content (Fig. 3d) and the LM2 treatment in the lowest flavonoids content (Fig. 3e).

Evaluation of the data showed that the three factors have quite different influences on the five antioxidant parameters with CAT (B > C > A), POD (A > C > B), SOD (A > B > C), total phenols (B > A > C), and flavonoids (A > C > B) (Table 4). The highest induction for POD, total phenols, and flavonoids was observed for A2B2C3, i.e. (100 µmol m−2 s−1 light of R30:G0:B70 ratio with a 14 h/10 h photoperiod), while the highest CAT was A1B1C1, which indicated that the maximum of CAT presented at (irradiance 50 µmol m−2 s−1 + ratio (R70:G0:B30) + photoperiod10h/14 h). The A3B3C2 was the best combination gave the highest SOD, which indicated that the maximum of SOD presented at (irradiance 200 µmol m−2 s−1 + ratio (R50:G20:B30) + photoperiod 12 h/12 h). However, when individual enzyme activities and pigment contents were considered, the optimal conditions were quite different from the average value, although ANOVA (Table 4) analyses showed that most of the differences were significant (p ˂ 0.05), excepted factor A and C on CAT, and C on SOD.

Discussion

Light quality has a significant impact on the efficiency of photosynthesis and the morphological and physiological properties of the plant. In this study we tried to find the optimal light quality and quantity for biomass production and development of passion fruit seedlings. A literature survey demonstrates that the optimal light conditions for plants differ substantially34,35. The spectral distribution, illumination period and light irradiance have different effects on the efficiency of photosynthesis36, and the activation of the photoreceptors in different plant species37. The necessity of this study becomes important when our data on passion fruit are compared with those for agriculturally important plant species. In our experiments, passion fruit seedlings responded strongly to LM5 (100 µmol m−2 s−1; R30:G0:B70; 14 h/10 h) with regard to optimal plant height, stem diameter, leaves number, internode distance as well as shoot/root biomass (Table 1). Naznin, et al.38 and Yang, et al.39 investigated in pepper seedlings and Yang et al.40 tomato seedlings, and they found that in particular the red LED light was important for producing strong seedlings. Also, Yousef and coauthors showed that a combination of R and B LED light with a high R portion was effective in producing vigorous grafted tomato seedlings28,29. In most studies a combination of R and B light was more effective in promoting plant growth and development than the use of one LED source alone. For instance, cucumber seedlings grown under equal amounts of R and B light have higher yields compared to seedlings grown under R light only41. Yousef and co-authors extended the study to factory tomatoes and showed that illumination with 100 μmol m−2 s−1 70% R and 30% B resulted in the optimal growth of the plants42. Moreover, the barrier tissue cells in the leaves were particularly well developed and the spongy tissue cells were arranged in an orderly manner43. It appears that blue light is important for passion fruit growth suggesting that activation of the cryptochrome system has a strong influence on its development.

The Chl content affects the photosynthetic ability and reduced carbon production44,45. Moreover, Chl biosynthesis is controlled by the quality of light, and many studies showed the important role of blue light40,46,47,48. Furthermore, ambient light conditions and stress can have profound effects on the Chl a and b levels. Our results showed that LM6 was the best light treatment for Chl a accumulation, followed by LM4, LM7, and LM5 treatments (Fig. 2a), whereas LM5 was optimal for Chl b, and LM9 for carotenoid and anthocyanin accumulation. This is in agreement with the findings of Yang et al.40 and Yousef et al.42,49 with tomato and pepper seedlings38,39. Furthermore, the authors observed that a mixture of red and blue LED lights induced higher levels of these pigments than white fluorescent light.

The benefits of light sources with enriched red and blue light were repeatedly shown for Chl accumulation, photosynthetic enzyme activity, stomatal aperture, and carbohydrate biosynthesis in plants50,51,52,53. Bondada et al.50 showed that red light increased the total Chl content and promoted photosynthesis rates but restricted the transport of carbohydrates from the leaves to the roots. In contrast, several studies showed that photomorphogenesis was more promoted by blue light, which increased Chl a/b ratios and facilitated stomatal opening47,53,54. Li et al.55 showed that besides increased photosynthesis per unit leaf area and a higher Chl a/b ratio, blue light also stimulated ribulose-1,5-bisphosphate carboxylase and phosphoenolpyruvate carboxylase activities, and promoted stomatal opening. Therefore, the red-blue light ratio has a strong influence on morphogenesis and ultimately biomass production. Red light facilitated cell division and expansion, resulting in increased leaf area and root elongation, while blue light inhibited these effects and reduced the leaf area and root elongation56,57. Besides light quality, also the irradiance and duration of illumination is important for yield; reduced photon irradiance in LM2 might be the main reason for the reduced leaf area and biomass production.

Besides photosynthetic parameters, the antioxidant status of the plant is important for fitness and agricultural yields. Antioxidants are involved in biotic and abiotic stress, including defense, oxidative damage, and free-radical scavenging58. Also, light stress plays a crucial role in the production, turnover, and destruction of antioxidants59,60,61. Red light increased the antioxidant activity in pea62 and Dendrobium officinale seedlings63, but also in Eleutherococcus senticosus somatic embryos64. However, the range in which different antioxidant enzymes react to stress differs substantially under different light conditions. Also Naznin, et al.38 showed that the antioxidant capacity of lettuce, spinach, cabbage, Ocimum basilicum, and Capsicum annuum was stimulated by red light, although various cultivars of the same plant can respond quite differently to different light situations42,65. Mengxi, et al.66 showed that blue light promoted antioxidant enzyme activities in Oncidium. Considering that plants have to decide to either invest in growth (photosynthesis) or defense, depending on environmental conditions, including light stress, optimal light sources for plants should balance these responses. Therefore, comparison of the effect of the different light regimes on photosynthesis-related and antioxidant-related responses is important for long-term benefits for the plant.

Plants can accumulate oxidative active chemicals under conditions with insufficient use of light energy during photosynthesis67. Antioxidant enzymes eliminate reactive oxygen species generated during (a)biotic stress including light stress, pathogen attack or senescence68,69. SOD removed H2O2 and O2- generated during oxidative stress and lipid peroxidation; POD and CAT can remove H2O2 from peroxisomes and cytoplasm70,71. The highest antioxidant activities were found with LM1 (CAT; 50 µmol m−2 s−1; R70: G0: B30; 10 h/14 h), LM5 (SOD; 100 µmol m−2 s−1; R30:G0:B70; 14 h/10 h), and LM4 (POD, 100 µmol m−2 s−1; R70:G0:B30; 12 h/12 h) treatments. However, comparison with the other treatments suggest that neither the irradiance of LED light, the red-blue light ratio, nor the photoperiod caused high light stress to the passion fruit seedlings that resulted in an unusual upregulation of the antioxidant enzyme activities.

UV-B light stress affected polyphenol and flavonoid biosynthesis, since they absorb both visible and UV light to protect mesophyll cells from photooxidation72,73. This is important for plants in the field, but not under LED light.

In plants, there has been an increased biosynthesis of phenol and polyphenol compounds to help them cope with the multifarious abiotic and biotic stresses such as salinity, heavy metal, drought, temperature, UV lights, disease progression, etc.74. Cryptochromes and phytochromes, activated by blue, red and far-red LEDs have been intensively studied because they stimulate phenol and flavonoid accumulation in diverse plant species during the germination of sprouts75,76, in adult plants77,78,79, or during postharvest storage80,81. However, the effect of monochromatic LEDs for the induction of these secondary metabolites is dependent on numerous factors and has to be optimized for each plant species and growth condition. White, blue and red light stimulated the activities of the key enzymes of the shikimate and phenylpropanoid pathways, such as phenylalanine ammonia lyase82, chalcone isomerase and synthases, or the leucoanthocyanidin dioxygenase, flavanol synthase, dihydroflavonol 4-reductase and stilbene synthase involved in anthocyanin and flavonoid biosynthesis83,84,85. Not only biosynthesis genes, but also transcriptional activators and repressors play a role in the production of these phenolic compounds and respond to light86. Furthermore, greater production of phenylalanine rather than tryptophan was found to enhance the synthesis of phenolic compounds. This indicates that LEDs can regulate total phenol and total flavonoid concentration by promoting the expression of genes involved in the biosynthesis of the secondary compounds well as indirectly by boosting the precursor molecule79. In this study, the highest contents of total phenols and flavonoids was found with LM5 (100 µmol m−2 s−1; R30:G0:B70; 14 h/10 h light/dark cycles). Literature survey shows that only blue and red light sources were active, whereas green light was less effective78,82,87 or completely ineffective81. Loi, et al.81 did not find a significant increase in phenolic compounds in broccoli with green light, while Ouzounis, et al.88 found a stimulation under higher light irradiance, demonstrating that light irradiance is critical79,89. In general, higher light irradiances were more effective in activating light-responsive genes and the polyphenol content than lower light irradiances. Nonetheless, the findings are strongly dependent on the investigated plant species77,90, cultivars91,92, and timing of LED exposure88. Most notably, each polyphenolic compound reacts differently to different light qualities75. We also found that the CAT, SOD and POD activities responded differently to the different light regimes. Thus, a detailed analyses of the accumulation of antioxidant compounds is required for each plant species and cultivars, in particular when LEDs are used93.

Material and methods

Growth conditions and plant materials

All experiments were conducted in LED light chambers at Fujian Agriculture and Forestry University, Fuzhou, Fujian, China. The manufacturer of the tested LED lamps is Kedao Technology Corporation (Huizhou, China) with the type of UH-BLDT0510. Our studies were complied with the relevant institutional, national, and international guidelines and legislation. The growth chambers at an optimum temperature, i.e., 27 ± 2 °C Day/23 ± 2 °C night, relative humidity was maintained at 65 ± 5% during the entire experimental procedures, and LED light's spectrum distribution as shown (Fig. 4).

Figure 4
figure 4

The treatments of LED light's spectrum distribution.

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The seeds were provided by the Fruit Research Institute, Fujian Academy of Agricultural Sciences. In August 2020, the fruits from the mature passion fruit variety ‘Golden No. 6’ was harvested, the seeds were cleaned with gauze bag, dried in a natural shade, and sealed in a Ziplock bag. To improve germination rate, the seeds were washed with distilled water, wrapped in wet gauze, placed in a Petri dish, and stored in an incubator at 35 °C. After 7 to 9 days, the percentage of germination is approximately 80%. The passion seeds were sown in 50-cell plug trays (28 cm width × 54 cm length × 8 cm height, Luoxi Plastic Products Co., Shandong, China) that was filled with commercial growing substrate (N1:P1:K1 ≥ 3%, organic matter ≥ 45%, pH 5.5–6.5). In total, 100 seedlings were grown in each box. Irrigation was provided for the seedlings daily or as required.

Seedlings were fertilized with water-soluble fertilizers (compound of fertilizer "N20: P20: K20 + TE", Ruierkang Co., Russia, and Stimufol Amino (compound fertilizers “N 25%, P 16%, K 12%, Fe 0.17%, amino acids 2%, Mo 0.001%, B 0.044%, Cu 0.085, Zn 0.03%, Mg 0.02%, Mn 0.085%, Co 0.01%, and EDTA”, Shoura Co., Egypt.)) two times per week through irrigation. Fertilization started one week after planting.

Multiple-factor experiment design

The Orthogonal Experimental design method was used to analyze three factors with three levels each. As shown in Table 4, from the possible 27 treatments, 9 treatments (and a white fluorescent light control) were performed. Three light irradiances (50, 100, 200 μmol m−2 s−1; A1-A3) were given with red (R), green (G), and blue (B) LEDs filters (B1-B3) in 3 combinations (R:G:B in %: 70:0:30, 30:0:70, and 50:20:30 Fig. 4), and three photoperiods (C1-C3) (10/14 h, 12/12 h, and 14/10 light/dark cycles).

Measurements and calculations

Measurement of growth and biomass parameters

Growth performance was estimated 60 days after sowing. We used a ruler to measure the plant height and the distance between nodes (cm), and a vernier caliper to measure the stem diameter (mm). The plant height was measured from the ground surface to the plant growth point; the stem diameter at the base of the stem; the node spacing between the 4th and 5th leaves. Leaf area (the third leaf below the top of the plant) was measured by LA-S Wanshen Plant Image Analyzer (Wanshen Testing Technology Co., Ltd., Hangzhou, China). The determination of the leaf dry material was obtained weighing the fresh leaves (washed and rinsed with deionized water), and the material was oven-dried (YH-9203A, Qingdao Yosion Labtech Co. Ltd., China) at 105 °C for 20 min, and drying continued at 70 °C, until a constant weight was reached.

Measurement of chlorophyll (Chl) content

Sixty days after sowing, the total Chl and carotenoid contents were determined from fresh medium-aged leaves with excluded the edges and veins of leaves (Fifth leaf from the top). Tissues of fresh leaves (0.2 g) were cut, ground well, suspended in 5 ml of 95% ethanol and filtered. The filtrate was made up to 25 ml by adding 95% ethanol. Absorbance of the filtered solution for Chl (Chl) a, Chl b, and carotenoid at 665 nm, 649 nm and 470 nm, respectively, was measured using a spectrophotometer (UV-5100B, Unico. Shanghai, China), while the Chl content was determined using the following equations94:

Chl a (mg g−1 FW) = (13.95 OD665 − 6.88 OD649) V/200 W

Chl b (mg g−1 FW) = (24.96 OD649 − 7.32 OD663) V/200 W

Total Chl (mg g−1 FW) = Chl a + Chl b

Car (mg g−1 FW) = (1000 OD470 − 2.05 Chl a − 114.80 Chl b) V/ (245 × 200 W)

Chl/Car ratio = (Chl a + Chl b) / Car


Where (Chl a) = chlorophyll a, (Chl b) = chlorophyll b, (Car.) = carotenoid, and (ToCh/Car.) = Total chlorophyll/ Carotenoid; (V) = volume (25 ml.) and (W) = sample weight (g).

Determination of anthocyanin

Sixty days after sowing, anthocyanin content was determined from fresh medium-aged leaves (Fifth leaf from the top) after removal of the veins. The plant material was cut into small pieces. To 0.1 g material, 5 mL 1% HCL-methanol solution was added, the solution was poured into a 5 mL centrifuge tube. The extraction took place in the dark until the tissue became white. The absorbance was measured at 530 and 600 nm and the anthocyanin content in leaves was calculated according to Cao, et al.95. The difference between the absorbance values at 530 nm and 600 nm represents the anthocyanin content, i.e. (OD530-OD600)/g.

Measurement of antioxidant enzyme activities

The superoxide dismutase (SOD) activity was determined by the nitrogen blue tetrazole (NBT) method of96. 0.1 g of frozen leaf (fresh medium-aged leaves Fifth leaf from the top) powder was weighed, 5 mL of phosphoric acid buffer (pH7.8) was added, and the slurry was centrifuged at 4000 rpm at 4° for 10 min. The supernatant was used for the enzyme assays. One unit of SOD caused inhibition of the photoreduction of NBT by 50%. The superoxide dismutase (SOD) activity was measured in the same extract by the increase in absorbance at 470 nm due to guaiacol oxidation activity and was quantified according to the method described by García-Triana, et al.97.

The peroxidase (POD) activity was determined by the guaiacol method98. 0.1 g of frozen leaf (Fifth leaf from the top) powder was weighed, resuspended in 10 mL phosphoric acid buffer (pH5.5) at 4 °C and centrifuged at 3000 rpm for 10 min. 0.1 mL enzyme extract was added to either 0.05 mol/L phosphoric acid buffer (2.9 mL), 2% H2O2 (1.0 mL), and 0.05 mol/L guaiacol (1.0 mL). Heat-treated extract (5 min) was used as control. The solution was incubated at 37 °C for 15 min, and then quickly transferred to an ice bath. 2.0 mL of 20% trichloroacetic acid was added to terminate the reaction. After centrifugation at 5000 rpm for 10 min, the absorbance was read at 470 nm according to Wang, et al.99.

The catalase (CAT) activity was determined by the ultraviolet absorption method100. 0.1 g of frozen fresh leaf (Fifth leaf from the top) powder was weighed and resuspended in 5 mL pre-cooled phosphoric acid buffer (pH 7.8, 1% polyvinylpyrrolidone). After accurate temperature adjustment to 5 °C for 10 min, the suspension was centrifuged at 4000 rpm for 15 min. The supernatant was used for the CAT assay by measuring the absorbance at 240 nm. All enzymes’ activities were expressed as unit’s min−1 g−1 sample.

Determination of total phenols and flavonoids

The total phenol and flavonoid contents were determined as previously described by Pourmorad, et al.101. To 0,1 g of frozen leaf (Fifth leaf from the top) powder 20 mL of 1% HCL-methanol solution was added to extract the pigments at 4 °C in the dark for 20 min. Total phenol and flavonoids content was determined by absorbance measurements at 280 and 325 nm, respectively.

Statistical analysis

The Orthogonal Experimental design method was used to determine the number of experiments to be conducted. All the data were subjected to one-way analysis of variance (ANOVA). Duncan's multiple range tests102 was used to test the significant difference between the means at 0.05 significance level using SPSS software (Version 16 SPSS Inc. Chicago, Illinois). The importance of the three factors for the measured parameters was assessed according to the effectiveness of each factor103 by the range value (R) using Excel 365 (v16.0). The most important impact factor has the greatest R-value. Adobe Illustrator software package version 23.0.3 was used to improve the quality of the images.

Conclusion

Artificial light is very important for countries that do not have natural sunlight, especially LED light, because it consumes less electricity, produces less heat, and has a longer lifetime. In our research, we studied the effect of different combinations of light irradiances and qualities with different photoperiods on plant growth parameters, pigments contents, and some antioxidants. The best results were achieved with a mixture of red and blue light and a long photoperiod (either 12 h/12 h or 14 h/10 h light/dark cycles). The variation among the studied parameters underlines the importance of this study to understand which light regime is optimal for growth and development of passion fruit seedlings to balance growth and stress responses.