Fagonia indica is an important medicinal plant species used traditionally against a variety of diseases. In this study, we initiated callus cultures from healthy stem explants. We observed maximum callus induction frequency (88%) on MS media supplemented with Thidiazuron (1.0 mg/mL). We also examined the callus cultures to determine the impact of iron-doped zinc oxide nanoparticles (Fe-ZnO-NPs) in concentrations (15.62 to 250 µg/mL) on biomass accumulation, secondary metabolism, and antioxidative potential in callus cultures of F. indica. Our results showed that maximum callus biomass (FW = 13.6 g and DW = 0.58 ± 0.01) was produced on day 40 when the media was supplemented with 250 µg/mL Fe-ZnO-NPs. Similarly, maximum TPC (268.36 µg GAE/g of DW) was detected in 40 days old callus added with 125 µg/mL Fe-ZnO-NPs. Maximum TFC (78.56 µg QE/g of DW) was observed in 20 days old callus grown in 62.5 µg/mL Fe-ZnO-NPs containing media. Maximum total antioxidant capacity (390.74 µg AAE/g of DW) was observed in 40 days old callus with 125 µg/mL Fe-ZnO-NPs treated cultures, respectively. The antioxidant potential was in correlation with the TPC. These results showed that Fe-ZnO-NPs elicitors can increase the biomass and activate secondary metabolism in F. indica cells.
Research Article
Iron-doped zinc oxide nanoparticles-triggered elicitation of important phenolic compounds in cell cultures of Fagonia indica.
https://doi.org/10.21203/rs.3.rs-314389/v1
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Callus culture
Fagonia indica
elicitation
Iron-doped Zinc oxide nanoparticles
total phenolic content
In vitro cultures of plants provide a model platform for studying their potential as factories for important medicinal compounds. In vitro cultures, including plant cell and callus cultures, can serve as factories of phytochemicals/secondary metabolites that can be produced in uniform quality for the fight against many threatening diseases, including infectious diseases such as the currently pandemic Covid-19 (Khan et al., 2020b). The in vitro culture-based production of phytochemicals has an additional benefit of consistency in yield and quality (Khan et al., 2016). Different medicinal plant species are considered for developing cell cultures according to their pharmaceutical uses. These plants have analgesic, astringent, antioxidant, antitumor, prophylactic, and febrifuge activities. F. indica is such an important species of the genus Fagonia. Numerous reports are available on its anticancer activity, fever, toothache, asthma, kidney diseases, urinary discharge, and stomach problems (Eman et al., 2010). However, inconsistency in clinical trials and lack of sustainable harvest strategies from field-grown wild plants cause problems in consistently producing phytochemicals. The establishment of the plant in vitro cultures can circumvent many issues in biomass production (Yousaf et al., 2019). Elicitation has been proved a handy tool for improved secondary metabolites' production in different medicinal plants in vitro cultures (Khan et al., 2019a). The role of nanoparticles as abiotic elicitors for producing secondary metabolites from the in vitro cultures is a new frontier in metabolic engineering approaches (Khan et al., 2020a). These nanoparticles execute oxidative stress in the plant cells grown via in vitro culture techniques, which activate their metabolism and enhance antioxidant activities (Javed et al., 2018). Nanoparticles have a smaller size (0-100nm) and large surface to volume ratio, due to which they reveal remarkable unique features. Nanobiotechnology has also found new applications in agriculture and plant biotechnology (Khan et al., 2019b). Nanomaterials can help in speedy plant germination and increase resistance to various abiotic and biotic stresses. They can improve plants' growth with lesser ecological influences compared to traditional methods (Alharby et al., 2016; Ali et al., 2019). Among various nanoparticles, zinc oxide nanoparticles (ZnO-NPs) have received more importance (Srivastava et al., 2013). Zinc oxide (ZnO) performs an active role in various regulatory functions and is involved in plants' response to abiotic stresses. It has been identified that Zinc has a vital role in the protection of plant cells against oxidative stresses and the management of reactive oxygen species (ROS) (Alharby et al., 2016). Studies have shown that Iron-doped Zinc oxide nanoparticles (Fe-ZnO-NPs) have a high surface area and maximum catalytic activity than pure ZnO and Fe2O3 systems (Hassan et al., 2012). Therefore, this study was designed to assess the physiological and biochemical effects of Fe-ZnO-NPs on callus cultures of F. indica. This study aimed to evaluate the impact of the addition of Fe-ZnO-NPs on the biomass accumulation and production of medicinal metabolites in callus cultures of F. indica.
2.1 Plant material and culture conditions
The seeds of F. indica were sterilized by treating them with 0.1 % mercuric chloride solution. According to Khan et al., the seeds were dried on filter paper for 3-5 minutes before nicking the seeds speedy and efficient germination (Khan et al., 2016). Murashige and Skoog (MS) media were used to grow plants such that 2.2 g of MS media was added with 15 g of sucrose and 4 g of agar in 500 mL distilled water. The pH of the media was optimized to 5.2-5.8 before the optimization of pH. After media preparation, 35 mL of the media was transferred to flasks covered with cotton and aluminum foil and were autoclaved and kept overnight for further use. Seeds were then transferred to media per flask, and the flasks were plugged with cotton and covered with aluminum foil properly to avoid contamination. The cultured flasks were transferred to a growth chamber (BioBase, BJPX-A1500C, Ltd. China) for germination. The growth conditions were maintained such that humidity was 70 %, temperature 25 ± 2 ˚C, and an illumination of 16-hour light/8-hour dark.
2.2 Callus culture initiation
For initiation of callus cultures, the media was added with Thiadizuron (TDZ @ 1 mg/mL) according to Khan et al. (Khan et al., 2016). The plant stem was cut into pieces (5 mm in length), transferring two stem cuttings to each flask. The culture flasks were transferred to the growth chamber to initiate callus (BioBase, BJPX-A1500C, LTD CHINA). The conditions in the growth chamber were such that (humidity was 70 %, temperature 25 ± 2 ˚C, and a photoperiod (16-hour light/8-hour dark) to produce the biomass of callus.
2.3 Dispersion and supplementation of media with Iron-doped Zinc Oxide Nanoparticles:
Fe-ZnO-NPs were prepared and characterized by different concentrations of Fe-ZnO-NPs for the MS media (250, 125, 62.5, 31.25, and 15.62 µg/mL) were prepared in distilled water. The Fe-ZnO-NPs were properly dispersed in-stock solution by sonication (Power sonic 405, Korea) for an hour. After preparing the final concentration for 250 µg/mL Fe-ZnO-NPs, serial dilution was used to prepare the other concentrations. Afterward, approximately 0.4 g of callus was transferred to each flask containing 35 mL media with the different concentrations of Fe-ZnO-NPs (250, 125, 62.5, 31.25, and 15.62 µg/mL). Callus without Fe-ZnO-NPs in the media was used as a control. The flasks were then transferred to allow the callus' growth in a growth chamber (BioBase, BJPX-A1500C, Ltd China). The callus culture samples were harvested on day 10, day 20, and day 40 from the initial callus transfer date. The fresh weight of callus was recorded after each harvest by an Analytical balance (AW 120, Electronic balance). The callus was then kept in a dry heat oven overnight at 35 ºC for recording the dry weight. The callus was then ground to fine powder, which was stored for further analysis.
2.4 Analysis of the accumulation of secondary metabolites
Total phenolic content and Total flavonoid content assays were used to determine the accumulation of secondary metabolites in response to Fe-ZnO-NPs. For the determination of TPC, 20 µL of sample and 90 µL of Folin-Ciocalteu reagent were added by a multi-channel micropipette to a 96 wells microplate. Then 90 µL of sodium carbonate was added. Gallic acid concentrations (25, 20, 15, 10, and 5 µg/mL) were used as a positive control for the process. For the determination of TFC, 20 µL of the sample, 10 µL of Potassium acetate, 10 µL of Aluminium Chloride, and 160 µL of distilled water were added to a 96 well microplate. After this, incubation of the microplate for 30 minutes. Quercetin final concentrations, (40, 20, 10, 5, and 2.5 µg/mL) were used positive control for the process. The absorbance of samples was recorded for TPC and TFC analysis through a microplate reader (TSx800Absorbance Reader, BioTek Inc., USA). All the experiments were carried out in triplicate. All the experiments were carried out in triplicate.
2.6. Determination of antioxidative potential in response to Fe-ZnO-NPs
The antioxidant activities were determined by the Diphenyl picryl hydrazyl (DPPH) assay. The DPPH free radicle scavenging activity was performed such that 20 µL of sample and 180 µL of DPPH reagent were added to wells of microplate and then incubated for an hour. Ascorbic acid (40, 20, 10, and 5 µg/ml) used as a positive control for the assay. Similarly, the phosphomolybdenum method was used to determine the total antioxidants capacity of the sample. First, 180 µL of total antioxidants capacity reagent (TAC) and 20 µL of the sample extract were added to the 96 wells microplate. The mixture was then incubated in a water bath at 95 ºC for 90 min. After this, the sample was cooled down at room temperature. For drawing standard curve, 40, 20, 10, and 5 µg/mL of ascorbic acid was used as a positive control for the assay. The absorbance of samples was recorded through a microplate reader (TSx800 Absorbance Reader, BioTek Inc., USA). All the experiments were carried out in triplicate.
2.7. HPLC-UV characterization
HPLC-UV characterization and quantification were carried out according to a reported method (Zeb, 2015). Briefly, 1-gram powdered sample for cell cultures was added water and methanol in equal ratio, and the mixture was subject to heating in a water bath at 70˚C for 1 hour. The mixture was then spun for 10 minutes at 4000 rpm and was ultimately filtered (Whatman filter paper 11 μm).
The Agilent-1260 infinity High-performance liquid chromatography (HPLC) system was employed to identify and quantify phenolic compounds. The HPLC system's essential parts were a quaternary pump, an auto-sampler, a degasser, an ultraviolet array detector (UVAD), and a C18 column (Agilent-Zorbax-Eclipse column). The solution (B and C) gradient was such that solvent B was a mixture of acetic acid: methanol: deionized water (20: 100: 180 v/v), and solvent C was a mixture of acetic acid deionized water: methanol (20: 80: 900) v/v. The solvents were provided as gradient such that they started and gradually decreased the solvent in concentration. Solvent B was given in volume 100%, 85%, 50%, and 30% at 0, 5, 20, and 25 minutes, finally giving way to 100% solvent C from 30 minutes onwards till 40 minutes. Elution was recorded after 25 minutes. The ultraviolet array detector (UVAD) was set at wavelength 320 nm to analyze phenolic compounds, and the chromatograms were recorded from 190-500 n. The quantification of antioxidants was measured by formula:
Where As= Standard peak area; Ax= Sample peak area; Cs= Standard concentration (0.09 µg/ml); and Cx= Sample concentration.
2.7. Statistical Analysis
We have performed the experiments for this study according to a completely randomized design. The experiments were repeated twice, with three replicated during each experiment for statistical accuracy. We have used linear regression analysis to determine the significant mean difference (P < 0.05). We used Origin 8.5 pro for the preparation of all the figures.
3.1 Growth and morphological attributes of callus cultures
Callus was obtained using healthy stem cutting as explant (5 mm approx.) from a 30-day old plantlet (Figure 1). Approximately 400 mg callus was sub-cultured in 35 mL MS media with TDZ (1.0 mg/mL), a plant growth regulator, and Fe-ZnO-NPs as elicitors. The callus response was slow in the initial stages, but it improved with time. Fresh green and friable callus were obtained on days 10 and 20, while yellowish-green callus after 40 days of a culture grown under different concentrations of Fe-ZnO-NPs compared to control (Figure 1). The interactions of NPs with the callus changed their color from light green to yellowish-green because metallic nanoparticles, including metal oxides and pure metals, have been recently studied to affect various plants' progress. Various developmental constraints verified in plants, such as propagations, development, biomass-accumulation, and biochemical events, have been observed in response to these metallic NPs in diverse plants. Various impacts of NPs in plants range from helpful to destructive and from deceptive physiological to veiled biochemical deviations (Khan et al., 2019c).
The fresh weight of the culture was measured on days 0, 10, 20, and 40. The results showed that at day 10, callus with the highest FW (2.43±0.41 g) was observed in the group supplemented with 31.25 µg/mL Fe-ZnO-NPs, while the lowest FW (1.50±0.06 g) was observed in the group supplemented with 15.62 µg/mL Fe-ZnO-NPs as compared to control group (1.98±0.31 g). On day 20, the control group exhibited the highest FW (6.39±0.49 g) compared to the different concentrations of Fe-ZnO-NPs (Table 1). On day 20, the lowest FW (3.19±0.41 g) was observed in the group grown under the effect of 250 µg/mL Fe-ZnO-NPs. Increasing the concentration of Fe-ZnO-NPs, decrease in the FW of callus was observed such that the FW was 5.80±1.23, 4.77±0.80, 4.39±1.11, and 3.87±1.91 g at a concentration of 15.62, 31.25, 62.5, and 125 µg/mL, respectively. The reason for decreasing FW with increasing concentration of Fe-ZnO-NPs seems to be because high Zn concentrations are toxic to the plants. For instance, Broadley et al. (2007) showed that Zn phytotoxicity becomes apparent at a concentration higher than 300 mg/kg in leaves. However, in a nano form, zinc aided by Fe affects biomass accumulation positively once the callus cells get enough time to get acclimatized. Our results show that 40 days, the highest FW (13.6±0.24 g) was observed in callus grown in 250 µg/mL Fe-ZnO-NPs, while the lowest FW (8.39±0.59 g) was observed in 62.5 µg/mL as compared to the control group where the FW was (13.0±0.49 g). When dry weight was recorded, after 10 days, the highest DW (0.13±0.02 g) was recorded in callus grown under the effect of 31.25 µg/mL Fe-ZnO-NPs. In comparison, the lowest DW after 10 days (0.08±0.01 g) was observed in callus grown in 15.62 µg/mL Fe-ZnO-NPs compared to the control group (DW = 0.11±0.31 g). Similarly, on day 20, the highest DW (0.29±0.02 g) was recorded in the control group compared to the different concentrations of Fe-ZnO-NPs. It was observed that on day 20, the DW decreased with increasing the concentrations of Fe-ZnO-NPs in the media (Table 1). It seems like the cells of F. indica got acclimatized to the application of Fe-ZnO-NPs with time. It is evident from the results such that the highest FW and DW were recorded because of supplementation of 250 µg/mL Fe-ZnO-NPs. Metallic nanoparticles have been observed to impact plants' various developmental processes, such as propagations, development, biomass-accumulation, and biochemical events. Different impacts of NPs in plants range from helpful to destructive and from deceptive physiological to veiled biochemical deviations (Khan et al., 2019c). Fe-ZnO-NPs are inorganic nanoparticles that offer more significant material properties with functional flexibility [9]. There are numerous methods to change the dielectric and other metal oxide nanostructure properties in doping. In this study, Fe-ZnO-NPs seems to act as a multi-pronged tool having the nutrient supplementation capability in the form of essential supplements like Iron (Fe) and Zinc (Zn) (Xie et al., 2019). Conversely, these are provided as nanomaterial with an enhanced delivery to cells where they play their crucial role in growth and development as micronutrients (Cabot et al., 2019). For instance, studies have shown that these NPs improved germination and rate of growth. The NPs may also prove poisonous for the plants by increasing ROS production and changing the plants' genetic and anatomical performances. For instance, Zinc oxide nanoparticles have been observed to boost progress in terms of rate of seed germination, seedling potency, initial flowering, and improved chlorophyll content in different plants such as cucumber, green pea, peanut, and Glycine max L (soybean) (Khan et al., 2019c).
3.2 Phytochemical analysis of callus under Fe-ZnO-NPs stress
3.2.1 Production of total phenolic content
The TPC at days 10, 20, and 40 of the callus subcultures was determined. The highest TPC (268.79±11.44 µg GAE/g of DW) was produced in 40-days old callus cultures when supplemented with 125 µg/mL Fe-ZnO-NPs. Generally, at day 10, TPC was the high in quantity (239.56±3.46 µg GAE/g of DW) when the callus cultures were supplemented with 15.62 µg/mL Fe-ZnO-NPs as compared to the control group (TPC = 230.44 ± 3.46 µg GAE/g of DW). While the lowest TPC (178.34±6.54 µg GAE/g of DW) was recorded in the 10 days old callus when supplemented with 250 µg/mL Fe-ZnO-NPs. In 10 days, old callus, the TPC decreased compare to control when the media was having higher than 15.62 µg/mL Fe-ZnO-NPs (Figure 2). A more inadequate response in terms of TPC with increasing concentration of Fe-ZnO-NPs seems to be because of the cells' inability to cope with the excess nanomaterial in the media. This response correlates with the lower response of biomass accumulation at day 10 (Table 1). This lower biomass might be because chemically synthesized nanomaterial proves toxic to cells, making them unable to cope with or acclimatize to them. The NPs may also prove poisonous for the plants by increasing ROS production and changing the plants' genetic and anatomical performances (Kim et al., 2017). DNA breakage was also detected due to ZnO-NPs toxicity in Allium cepa (Rastogi et al., 2017). However, increasing the concentration of nanoparticles up to 125 µg/mL increased TPC compared to the control group. On day 20, the TPC was highest (232.84 ± 7.85 µg GAE/g of DW) when media was supplemented with 62.5 µg/mL Fe-ZnO-NPs. In comparison, the TPC observed in the control group after 20 days were 225.89±12.67 µg GAE/g of DW. A higher TPC concentration was produced in numerous plant species in response to different environmental strains (Hussain et al., 2019).
3.4.2 Production of flavonoids in response to Fe-ZnO-NPs supplementation
The TFC in 10, 20, and 40 days of callus establishment was recorded. The highest TFC (78.56±0.12 µg QE/g of DW) was recorded on day 20 was recorded in callus derived from media supplemented with 62.5 µg/mL Fe-ZnO-NPs. Generally, at day 10, the TFC was high in quantity (44.26±3.35 µg QE/g of DW) in media with 62.5 µg/mL Fe-ZnO-NPs, while the lowest (27.01±5.80 µg QE/g of DW) when the concentration of Fe-ZnO-NPs in media reached 250 µg/mL compared to the control group with TFC = 33.30±1.59 µg QE/g of DW. Similarly, for the other concentrations, the TFC increasing with increasing the concentrations of Fe-ZnO-NPs in the media. TFC derived from callus grown with 15.62, 31.25, and 125 µg/mL Fe-ZnO-NPs produced 53.11±4.47, 59.16±3.98, and 63.20 µg QE/g of DW, respectively as compared to the control group with TFC = 29.36±4.56 µg QE/g of DW. More specifically, the TFC increased with increasing concentration of Fe-ZnO-NPs up to 62.5 µg/mL. At higher concentrations, the production of TFC declined. This can be seen in figure 3 such that, with 125 µg/mL, the highest TFC recorded was 63.20 µg QE/g of DW in 20 days old callus followed by 59.86±2.89 µg QE/g of DW in 40 days old callus (Figure 3). In this study, it was observed that Fe-ZnO-NPs, in higher concentrations, caused toxicity to callus. In low concentration, it induces better impacts on the production of secondary metabolites in callus culture. The NPs in higher concentrations were observed to enter the plant and plasma membrane cell wall and network with the various plant processes (Rastogi et al., 2017).
In general, essential micronutrients aid in plant health by directly activating enzymes that produce defense metabolites like flavonoids. Although no specific mechanism has been established, Zinc plays a vital role in plant immune responses (Cabot et al., 2019). Besides Zn, Fe plays a crucial role in mediating an oxidative burst via the production of H2O2 (Greenshields et al., 2007), which leads to the production of scavenging secondary metabolites. This seems to be one reason for triggering the production of phenolics and flavonoids in callus cultures of F. indica by Fe-ZnO-nanomaterials loaded with both Fe and Zn.
3.4.3 Antioxidant defense system triggered by Fe-ZnO-NPs supplementation
According to the % DPPH scavenging capacity of 10-, 20- and 40-days old callus, the antioxidant activities were determined. On day 10, the highest antioxidant activity was recorded (67.78 %) in callus obtained from media with 31.25 µg/mL Fe-ZnO-NPs. The lowest activity (49.01 %) was produced in the control group (Figure 4). Furthermore, FRSA of 54.34, 56.86, 51.51, and 49.07 % was observed in callus derived from 15.62, 62.5, 125, and 250 µg/mL Fe-ZnO-NPs, respectively. On day 20, the highest antioxidants activity (75.27 %) was produced in callus obtained at 15.62 µg/mL Fe-ZnO-NPs. In comparison, the lowest activity (58.83 %) was produced in callus derived from media with 250 µg/mL Fe-ZnO-NPs. Furthermore, there was a decrease in FRSA with increasing nanoparticle concentration in the media such that 69.41, 65.73, and 59.18 % FRSA was recorded in callus grown at 31.25, 62.5, and 125 µg/mL Fe-ZnO-NPs, respectively compared to the control group with 64.77 % activity. On day 40, the highest antioxidant activity (93.02 %) was observed in callus derived from media having 15.62 µg/mL Fe-ZnO-NPs. In comparison, the lowest activity (52.95 %) was recorded in 125 µg/mL Fe-ZnO-NPs. Fe and Zn are showed to induce ROS-dependent antioxidant defense mechanisms. Metal accumulation in plant cells triggers the antioxidant defense system by activating superoxide dismutase, catalase, or other detoxification-related enzymes such as acid phosphatase (ACP) and alkaline phosphatase (AKP) (Khan et al., 2019d). Besides, phenolic and flavonoids are recognized to have antioxidant activity, and these compounds of the extract are responsible for these activities (Rebaya et al., 2014). Plants defend themselves by scavenging free radicals with phytochemicals, which act as antioxidants. Another essential and recently defined factor that supports the Zn-mediated defense of plant cells is Zinc finger protein (ZFP). ZFPs play a crucial role in plant growth and development phytohormone response and stress tolerance (Noman et al., 2019).
The importance of Fe-ZnO-NPs is further evident in their role in enhancing the total antioxidants capacity of cells of F. indica. The TAC in 10, 20, and 40 days after callus subculture was recorded. On day 10, the highest TAC (327.96±7.46 µg AAE/g of DW) was recorded in callus grown under the effect of 125 µg/mL Fe-ZnO-NPs, while the lowest TAC (157.57±1.33 µg AAE/g of DW) was recorded in callus supplemented with 250 µg/mL Fe-ZnO-NPs. A TAC of 228.06±7.60, 238.15±8.77, and 230.07±8.99 µg AAE/g of DW was seen in 15.62, 31.25, 62.5 µg/mL Fe-ZnO-NPs, respectively compared to the control group (TAC = 216.23±9.61 µg AAE/g of DW). On day 10, the TAC increased compare to control at 15.62, 31.25, 62.5, and 125 µg/mL Fe-ZnO-NPs, respectively. However, there was no significant difference in TAC at the medium concentrations of Fe-ZnO-NPs. On day 20, the highest TAC, i.e., 313.92±2.10 µg AAE/g of DW, was recorded in callus grown with 62.5 µg/mL Fe-ZnO-NPs, while the lowest TAC (199.64±8.17 µg AAE/g of DW) was recorded from callus grown on media with 31.25 µg/mL Fe-ZnO-NPs as compared to the control group with TAC 230.84±6.41 µg AAE/g of DW (Figure 5). At day 40, the highest TAC (390.74±5.56 µg AAE/g of DW) was observed in callus derived from 125 µg/mL Fe-ZnO-NPs containing media, while the lowest TAC, i.e., 241.35±6.97 µg AAE/g of DW was recorded in control. Further, TAC = 247.38±2.71, 265.14±7.29, 246.51±3.54, and 317±10.10 µg AAE/g of DW was recorded in callus derived from media with 15.62, 31.25, 62.5, and 250 µg/mL Fe-ZnO-NPs, respectively. On day 40, the TAC increased with increasing concentration of Fe-ZnO-NPs. The Phosphomolybdenum quantitative technique was used to study the TAC changes of the F. indica callus under Fe-ZnO-NPs concentrations. The results indicate that Fe-ZnO-NPs supplementation increases the TAC. These results demonstrated a significant increase in callus antioxidant activity in response to in vitro Fe-ZnO-NPs supplementation. The role of Fe-ZnO-NPs as abiotic elicitors in callus physiology and secondary metabolites production from the callus of F. indica is a new frontier in abiotic stress elicitation. These nanoparticles execute oxidative stress to the callus tissues, which activates their metabolism and enhances all antioxidant activities. However, the callus' growth and antioxidant activities are alleviated because higher Fe-ZnO-NPs cause lethality to plant ultimately (Javed et al., 2018).
3.4.4. HPLC analysis of Fe-ZnO-NPs based elicited cultures:
HPLC analysis of our samples revealed that Fe-ZnO-NPs supplementation had a marked effect on the production of phenolic compounds in cell cultures of F. indica. A total of seven antioxidant phytochemicals/compounds were identified in plant extracts (Table 2).
There was variation in terms of quantity as well as the uniqueness of production of secondary metabolites in cell cultures triggered by Fe-ZnO-NPs in media (Figure S1-S3). For instance, the control group, i.e., cell cultures devoid of Fe-ZnO-NPs, produced Malic acid in quantities equivalent to 18.56 µg/ml, which was enhanced to 23.90 µg/ml in cell culture extract supplemented with 31.25 µg/ml Fe-ZnO-NPs. Interestingly, however, the increase in Fe-ZnO-NPs concentration (250 µg/ml) caused a decline in malic acid production to 6.43 µg/ml.
Similarly, the quantities of Ellagic acid, Morin, Mandelic acid, and Pyrogallol were enhanced in Fe-ZnO-NPs supplemented cell cultures compared to control (Table 2). Furthermore, it has been observed that Fe-ZnO-NPs (250 µg/ml) triggered the production of Epigallocatechin gallate (6.65 µg/ml), which was absent in the control group. One of the reasons for this could be the fact that Iron (Fe) is a transition metal that forms chelates and complexes with phenolic plant secondary metabolites. It has been observed that epigallocatechin gallate acts as a robust Iron chelator (Md Nesran et al., 2020). In our case, the supplementation of iron in the form of Fe-ZnO-NPs might have triggered the production of enhanced quantities of this compound to reduce the toxic effects of Iron and Zinc given in excess amounts (250 µg/ml). Epigallocatechin gallate is a Catechin. The results observed above could be validated through another exciting observation that the amount of Catechin hydrate reduced a bit in Fe-ZnO-NPs based samples. This hint toward the possibility that Catechin hydrate might have contributed to an ester's formation with gallic acid, i.e., Epigallocatechin gallate.
On the other hand, the control, i.e., callus cultures devoid of Fe-ZnO-NPs, produced Rutin (0.69 µg/ml) which was not present in cell cultures supplemented with Fe-ZnO-NPs. The quantification and identification of each phenolic compound with its particular peak position and retention time (Rt) are presented in Table 2. The representative chromatograms are given in the supplementary information (ES1-3).
Conclusively, Fe-ZnO-NPs proved to be very efficient regulators of physiology and biochemical parameters of F. indica callus cultures. These results showed that Fe-ZnO-NPs could prove as a vital elicitor of plant cell metabolism. The Fe-ZnO-NPs elicited callus cultures exhibited higher levels of phenolics, flavonoids, and antioxidants activity. Doped form of nanomaterials could prove as a new frontier in applying different strategies for producing novel secondary metabolites in the cells of medicinal plants. The findings of the current study suggest that nanoparticles, especially Fe-ZnO-NPs, possess a strong potential to enhance biomass production and yield of total phenolic, total flavonoids, antioxidants activity, and total antioxidant capacity compounds in callus cultures of F. indica.
Acknowledgments: The authors acknowledge the role of the Department of Biotechnology, University of Malakand, in providing resources to perform this research.
Funding: Part of the research supplies for the project's execution was provided through the Higher Education Commission research project, NRPU 6649.
Disclosures
Conflicts of interest/Competing interests:
The authors declare no conflict of interests.
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Table 1: Comparison of physiological parameters in 10, 20, and 40 days old callus produced from the stem of F. indica in MS medium supplemented with TDZ and different concentrations of Fe-ZnO-NPs.
|
Concentrations of Fe-ZnO-NPs (µg/mL) |
Day 0 |
Day 10 |
Day 20 |
Day 40 |
|||||||||
|
FW(g) |
FW (g) |
DW (g) |
Callus color |
Callus texture |
FW (g) |
DW (g) |
Callus color |
Callus texture |
FW (g) |
DW (g) |
Callus color |
Callus texture |
|
|
Control |
0.4 |
1.98±0.31b |
0.11±0.01ab |
Y/G |
Friable |
6.39±0.49a |
0.29±0.02a |
Y/G |
Friable |
13.0±0.49ab |
0.52±0.02ab |
Y/G |
Friable |
|
15.62 |
0.4 |
1.50±0.06c |
0.08±0.01b |
Y/G |
Friable |
5.80±1.23b |
0.26±0.02ab |
G |
Friable |
13.2±0.17ab |
0.46±0.02b |
Y/G |
Friable |
|
31.25 |
0.4 |
2.43±0.41a |
0.13±0.02a |
Y/G |
Friable |
4.77±0.80c |
0.22±0.01bc |
Y/G |
Friable |
12.6±0.13b |
0.41±0.03bc |
Y/G |
Friable |
|
62.5 |
0.4 |
2.19±0.20ab |
0.11±0.01ab |
Y/G |
Friable |
4.39±1.11cd |
0.23±0.02b |
Y/G |
Friable |
8.39±0.59d |
0.35±0.03c |
G |
Friable |
|
125 |
0.4 |
1.96±0.30b |
0.11±0.01ab |
G |
Friable |
3.87±1.91d |
0.21±0.07bc |
Y/G |
Friable |
8.90±1.44c |
0.32±0.03cd |
Y/G |
Friable |
|
250 |
0.4 |
2.02±0.17ab |
0.11±0.01ab |
Y/G |
Friable |
3.19±0.41e |
0.16±0.01c |
G |
Friable |
13.6±0.24a |
0.58±0.01a |
Y/G |
Friable |
FW = Fresh weight, DW = Dry Weight, Y = Yellow, G = Green
Table 2: HPLC based quantification of phenolic compounds triggered as a result of Fe-ZnO-NPs in cell cultures of Fagonia indica.
|
Sample Extract |
No. of Peak |
Retention time (min) |
Phenolic compounds Identity |
HPLC-UV λmax (nm) |
Peak Area of sample |
Peak Area of standard |
Concentration (µg/ml) |
Identification Reference |
|
Control |
1 |
2.6 |
Malic acid |
320 |
74.81 |
40.32 |
18.56e |
Reference Standard |
|
2 |
12.4 |
Morin |
320 |
32.90 |
20.0 |
16.45f |
Reference Standard |
|
|
3 |
16.5 |
Ellagic acid |
320 |
97.98 |
319.24 |
3.07i |
Reference Standard |
|
|
4 |
20.5 |
Catechin hydrate |
320 |
385.32 |
78.0 |
49.4c |
Reference Standard |
|
|
5 |
22.7 |
Rutin |
320 |
156.79 |
2241.2 |
0.69k |
Reference Standard |
|
|
6 |
27.7 |
Pyrogallol |
320 |
1878.23 |
1.014 |
18522.97bc |
Reference Standard |
|
|
7 |
30.2 |
Mandelic acid |
320 |
20.96 |
72.0 |
2.91j |
Reference Standard |
|
|
40-1
|
1 |
2.6 |
Malic acid |
320 |
96.32 |
40.32 |
23.90de |
Reference Standard |
|
2 |
8.3 |
Epigallocatechin gallate |
320 |
18.27 |
72.6 |
2.52j |
Reference Standard |
|
|
3 |
12.4 |
Morin |
320 |
55.11 |
20.0 |
27.55d |
Reference Standard |
|
|
4 |
16.5 |
Ellagic acid |
320 |
237.34 |
319.24 |
7.43g |
Reference Standard |
|
|
5 |
20.5 |
Catechin hydrate |
320 |
56.04 |
78.0 |
7.18g |
Reference Standard |
|
|
6 |
27.7 |
Pyrogallol |
320 |
1968.24 |
1.014 |
19410.65a |
Reference Standard |
|
|
7 |
30.2 |
Mandelic acid |
320 |
129.91 |
72.0 |
18.04e |
Reference Standard |
|
|
40-2 |
1 |
2.6 |
Malic acid |
320 |
25.90 |
40.32 |
6.43h |
Reference Standard |
|
2 |
8.3 |
Epigallocatechin gallate |
320 |
48.33 |
72.6 |
6.65h |
Reference Standard |
|
|
3 |
12.4 |
Morin |
320 |
85.66 |
20.0 |
42.83c |
Reference Standard |
|
|
4 |
16.5 |
Ellagic acid |
320 |
233.46 |
319.24 |
7.31g |
Reference Standard |
|
|
5 |
20.5 |
Catechin hydrate |
320 |
346.95 |
78.0 |
44.48c |
Reference Standard |
|
|
6 |
27.7 |
Pyrogallol |
320 |
1885.61 |
1.014 |
18595.75b |
Reference Standard |
|
|
7 |
30.2 |
Mandelic acid |
320 |
19.41 |
72.0 |
2.69j |
Reference Standard |
40-1 = Cell cultures supplemented with 31.5 µg/ml Fe-ZnO-NPs for 40 days;
40-2 = Cell cultures supplemented with 250 µg/ml Fe-ZnO-NPs for 40 days
- Electronicsupplementaryinformation.docx
Figure S1: Representative chromatogram of phenolic compounds detected in extract devoid of Fe-ZnO-NPs. Figure S2: Representative chromatogram of phenolic compounds detected in extract supplemented with 31.25 µg/ml Fe-ZnO-NPs. Figure S3: Representative chromatogram of phenolic compounds detected in extract supplemented with 250 µg/ml Fe-ZnO-NPs