Thidiazuron-enhanced biosynthesis and antimicrobial efficacy of silver nanoparticles via improving phytochemical reducing potential in callus culture of Linum usitatissimum L.
Authors Anjum S, Haider Abbasi B
Received 11 December 2015
Accepted for publication 16 January 2016
Published 22 February 2016 Volume 2016:11 Pages 715—728
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Prof. Dr. Thomas J. Webster
Sumaira Anjum, Bilal Haider Abbasi
Department of Biotechnology, Quaid-i-Azam University, Islamabad, Pakistan
Abstract: Green synthesis of silver nanoparticles (AgNPs) by using plants is an emerging class of nanobiotechnology. It revolutionizes all domains of medical sciences by synthesizing chemical-free AgNPs for various biomedical applications. In this report, AgNPs were successfully synthesized by using whole plant extract (WPE) and thidiazuron-induced callus extract (CE) of Linum usitatissimum. The phytochemical analysis revealed that the total phenolic and flavonoid contents were higher in CE than that in WPE. Ultraviolet-visible spectroscopy of synthesized AgNPs showed a characteristic surface plasmon band in the range of 410–426 nm. Bioreduction of CE-mediated AgNPs was completed in a shorter time than that of WPE-mediated AgNPs. Scanning electron microscopy showed that both types of synthesized AgNPs were spherical in shape, but CE-mediated AgNPs were smaller in size (19–24 nm) and more scattered in distribution than that of WPE-mediated AgNPs (49–54 nm). X-ray diffraction analysis confirmed crystalline nature (face-centered cubic) of both types of AgNPs. Fourier-transform infrared spectroscopy revealed that the polyphenols and flavonoids were mainly responsible for reduction and capping of synthesized AgNPs. Energy dispersive X-ray analysis further confirmed the successful synthesis of AgNPs. Moreover, the synthesized AgNPs were found to be stable over months with no change in the surface plasmon bands. More importantly, CE-mediated AgNPs displayed significantly higher bactericidal activity against multiple drug-resistant human pathogens than WPE-mediated AgNPs. The present work highlighted the potent role of thidiazuron in in vitro-derived cultures for enhanced biosynthesis of chemical-free AgNPs, which can be used as nanomedicines in many biomedical applications.
Keywords: silver nanoparticles, Linum usitatissimum L., in vitro cultures, thidiazuron, antimicrobial, multidrug-resistant bacteria
Synthesis of metallic nanoparticles is a gigantic and an expanding area due to their potential applicability in numerous fields such as electronics, optoelectronics, functional biology, drug delivery, antimicrobials, and biosensors.1 Numerous research techniques for the production of metallic nanoparticles through different physical and chemical methods are presented by the scientists. However, these synthetic methods, involving different chemicals, are expensive and may lead to the presence of noxious chemical species tangled on the surface of nanoparticles, which may have adverse effects in various biological and biomedical applications.2,3 This increases the growing need to develop environment-friendly procedures for synthesis of metallic nanoparticles through “green synthesis” and other new biological approaches.4 Synthesis of metallic nanoparticles by plant extracts is the most implemented method of green, eco-friendly fabrication of nanoparticles and also has a distinctive advantage that plants are extensively distributed, easily accessible, less biohazardous, and act as a source of numerous metabolites.5,6 Among the metallic nanoparticles, silver nanoparticles (AgNPs) represent one of the most comprehensively studied nanomaterials and the most favorite target of the aforementioned “green” methods, which fascinate scientists due to their distinctive antimicrobial properties.7 Due to the emergence of infectious diseases and antibiotic resistance in pathogenic microorganisms, pharmaceutical industries and scientists are looking for new antimicrobial agents, and AgNPs are the most promising contenders for antimicrobial action. Broad-spectrum bioactivities of AgNPs make them promising agents not only in fighting infections but also in tackling serious issues of tumors and, particularly, multidrug-resistant cancer cells.8
Plant extracts are believed to act as reducing and capping agents in the synthesis of nanoparticle due to the presence of bioactive compounds. The nature of plant extract affects the kind of nanoparticles synthesized in a highly critical manner, with the source of plant extract being the most vital factor affecting the morphology of synthesized nanoparticles.9 Interestingly, this is so because different plant extracts contain different amounts of biochemical reducing agents.10 Use of extracts from various plant parts, such as fruits, stems, bark, seeds, and latex, has been reported for the green synthesis of AgNPs.4,11–13 Unfortunately, very few reports are available on the role of in vitro-derived cultures of plants in the synthesis of AgNPs.14–16
The exploitation of plants in in vitro cultures is an opportunity to diversify these sources of biochemical reducing agents, which are either produced in limited quantities in wild plants or difficult to synthesize commercially in laboratories.17 Different plant growth regulators (PGRs) are used in in vitro cultures of plants to stimulate the production of phytochemicals.18,19 Among the different PGRs, thidiazuron (TDZ) is comparatively a better bioregulator of plant morphogenesis and is of immense importance since it has shown a dual activity of auxins and cytokinins.20,21 TDZ has a significant stimulatory effect on the enhancement of phytochemicals, which act as reducing and stabilizing agents.22
Linum usitatissimum L., is one of the oldest cultivated annual crops, which is not only commercially important but also has a long history of medicinal uses due to the presence of bioactive components, such as phenolic acids, flavonoids, polyunsaturated fatty acids, dietary fiber, and proteins.23,24 The bioactivity of L. usitatissimum is mainly due to lignans (polyphenols), which are an important class of plant secondary metabolites and have been linked to the prevention and treatment of cardiovascular disorders, hypercholesterolemia, diabetes, diarrhea, and breast and colon cancers.25–29 In the present study, a novel approach for the synthesis of AgNPs has been described by using silver nitrate solution (SNS) in the presence of two different types of in vitro-derived extracts of L. usitatissimum, that is, whole plant extract (WPE) and callus extract (CE). The major goal of this study was to develop a rapid and safe method for biosynthesis of AgNPs. Synthesized AgNPs were further characterized by different techniques, and their antibacterial efficacy was evaluated against multiple drug-resistant human pathogens (Escherichia coli, Klebsiella pneumoniae, and Staphylococcus aureus). Furthermore, we have also explored the potential role of TDZ in in vitro-derived cultures in the biosynthesis of AgNPs. To the best of our knowledge, this is the first study that utilizes the in vitro-derived cultures of L. usitatissimum for the biosynthesis of AgNPs.
Materials and methods
Seed germination and collection of plantlets
Seeds of L. usitatissimum L. (brown variety) were collected and provided by Dr Nisar Ahmad, Assistant Professor at University of Swat, Pakistan. Seeds were surface sterilized according to the method of Ali and Abbasi,30 with some modifications. Briefly, seeds were washed with running tap water and then immersed in 1% mercuric chloride solution for 1 minute and in 70% ethanol for 2 minutes, followed by washing three times with autoclaved distilled water. Then, the seeds were carefully dried on sterilized filter papers inside a laminar flow bench and placed onto Murashige and Skoog basal medium (MS0)31 containing 30 g L−1 sucrose and 8 g L−1 agar as solidifying agent. The pH of all media was adjusted to 5.6, and the media were autoclaved at 121°C for 20 minutes. Inoculated flasks were placed in a growth chamber at 25°C±2°C for a 16 hours light/8 hours dark photoperiod with light intensity of 40 μmol m−2 s−1. After 25 days of inoculation, we collected in vitro-derived plantlets of L. usitatissimum for extract preparation and stem explants for callus induction.
Establishment of callus culture
For callus induction, ~1–2 cm of stem explants lacking nodules were inoculated on MS31 media containing 30 g L−1 sucrose and 8 g L−1 agar, along with varying concentrations (0.5 mg L−1, 1.0 mg L−1, 2.0 mg L−1, 3.0 mg L−1, 4.0 mg L−1, and 5.0 mg L−1) of TDZ. The pH of the media was adjusted to 5.6–5.7 prior to autoclaving, and the cultures were maintained at 25°C±2°C for 16/8 hours photoperiod in the growth chamber. For each concentration of TDZ, three explants were placed in a conical flask as one replicate, and the whole experiment was performed with three replicates. Callus induction frequencies were recorded on a weekly basis, and the calli emerged from the explants were collected after 5 weeks of inoculation for extract preparation.
Approximately 10 g of each in vitro-derived whole plantlets and callus obtained in response to 2.0 mg L−1 TDZ (yielding the highest phytochemical contents) culture of L. usitatissimum were separately mixed with 100 mL of distilled water and boiled for 15 minutes in a 500 mL Erlenmeyer flask. The extracts thus formed were cooled down to room temperature and filtered through a filter paper, and the volume of the filtrates was adjusted to 100 mL with distilled water (Figure 1) and stored at 4°C for further use.
Determination of total phenolic and flavonoid content
Total phenolic content (TPC) was determined using Folin–Ciocalteu’s reagent according to the method described by Velioglu et al.32 Absorbance was measured at 725 nm using ultraviolet–visible (UV–vis) HALO DB-20 spectrophotometer (Dynamical Ltd, Victoria, Australia). The calibration curve (0–50 μg mL−1, R2=0.968) was plotted using gallic acid as standard. All determinations were performed in triplicate, and the TPC was expressed as mg g−1 gallic acid equivalents of dry weight (DW). Total flavonoid content (TFC) was determined using aluminum chloride colorimetric method as described by Chang et al.33 Absorbance of the reaction mixtures was measured at 415 nm by using UV-Vis HALO DB-20 spectrophotometer. The calibration curve (0–40 μg mL−1, R2=0.998) was plotted using quercetin as standard. The TFC was expressed as quercetin equivalents g−1 of DW.
WPE- and CE-mediated biosynthesis of AgNPs
Aqueous extracts (WPE and CE) of L. usitatissimum were mixed separately with SNS (1 mM) in different ratios (1:1 v/v, 1:2 v/v, 1:5 v/v, and 1:10 v/v) to find out the appropriate concentrations of SNS for optimal AgNP biosynthesis. Briefly, 100 μL of each extract was mixed separately with 100 μL of SNS (1:1 ratio) and subsequent mixtures were prepared by increasing the SNS volume up to 1,000 μL. These mixtures were prepared in 1.5 mL Eppendorf tubes, and the reactions were allowed to progress at room temperature for different time periods. The bioreduction of silver ions was observed by change in the color of the reaction mixtures during different time intervals (0 minute, 10 minutes, 20 minutes, 30 minutes, 1 hour, 2 hours, 6 hours, 12 hours, and 24 hours). All experiments were carried out in triplicates and representative data are presented here.
Characterization of AgNPs
AgNP biosynthesis was monitored by recording UV–vis spectra (λ= 300–750 nm) as a function of time on a HALO DB-20 spectrophotometer. The reaction mixtures showing optimal biosynthesis of AgNPs were further ensued by pelleting and washing AgNPs to remove unreacted SNS and plant extracts. Briefly, 1 mL of each reaction mixture was centrifuged at 12,000 rpm for 10 minutes at room temperature. Supernatants were discarded, and the AgNPs pellets were resuspended in 1 mL of distilled water, followed by centrifugation at 12,000 rpm for 10 minutes. This process of washing was repeated three times, and the resulting AgNPs were air-dried to evaporate excessive liquid and used for further characterization.
Fourier-transform infrared spectroscopy
Fourier-transform infrared (FTIR) spectra of the WPE- and CE-mediated AgNPs were recorded using Perkin–Elmer model in the transmittable mode at the range of 3,500–500 cm−1 in potassium bromide (KBr) pellets to find out the possible functional groups involved in the reduction and stabilization of AgNPs. Each sample was recorded with KBr pellets on an FTIR spectroscope at room temperature.
X-ray diffraction analysis
The crystalline structures of the synthesized AgNPs were investigated by X-ray diffraction (XRD). Powdered samples were used, and the diffraction patterns were recorded in the scanning mode on a Shimadzu-Model XRD 6000 operated at 40 kV with a current of 30 mA and Cu/Kα radiation in the range of 20°–80° in 2θ angles. The average particle size of the synthesized AgNPs was calculated using the Debye–Scherrer equation.34
where k is the shape factor (0.94), λ is the X-ray wavelength (λ=1.5418 Å), β is the full width at half maximum in radians, and θ is the Bragg’s angle.
Scanning electron microscopy and energy dispersive X-ray analyses
The morphology of both types of synthesized AgNPs (WPE and CE mediated) was observed by scanning electron microscopy (SEM) by using the SIGMA model (MIRA3; TESCAN Brno, s.r.o., Brno, Czech Republic) operated at an accelerating voltage of 10 kV. The samples were prepared on a carbon-coated copper grid by simply dropping a very small amount of the samples on the grid. The film was then allowed to dry under a mercury lamp for 5 minutes, and the SEM images were collected at different magnifications. For elemental analysis, the AgNPs were dried and drop-coated onto carbon film. Energy dispersive X-ray (EDX) analysis was then performed using the EDX detector attached with SEM.
Antimicrobial activities of AgNPs against multiple drug-resistant bacteria
S. aureus (ATCC-6538), E. coli (ATCC-15224), and K. pneumoniae (ATCC-4619), obtained from the American Type Culture Collection (ATCC), Manassas, VA, USA, were used for this experiment. This study was approved by the ethical committee of the Department of Biotechnology, Quaid-i-Azam University, Islamabad, Pakistan. The in vitro antibacterial activity was analyzed out with WPE- and CE-mediated AgNPs by well diffusion method. Briefly, the dried AgNPs were weighed (10 mg mL−1) and dissolved in sterile distilled water and used immediately. Three highly multiple drug-resistant bacterial strains, namely, E. coli, K. pneumoniae, and S. aureus, were used for assessing the antibacterial activity. The inoculums were prepared by growing a single colony overnight in nutrient broth. The nutrient agar plates were swabbed with bacterial strain broth, and 15 μL of each synthesized AgNPs (10 mg mL−1), 1 mM SNS (positive control), commercial antibiotic as standard (ampicillin disk, 10 mg), WPE, and CE (negative control) were added in the wells. The plates were incubated at 37°C for 24 hours in an incubator, and the zone of inhibition (mm) was measured. Data were collected from three independent experiments for each strain, and each experiment was repeated three times.
All experiments were conducted in triplicate unless otherwise specified. Mean values of various treatments were subjected to analysis of variance, and significant difference was separated using Duncan’s multiple range test.35 SPSS (Windows Version 7.5.1, SPSS Inc., Chicago, IL, USA) was used to determine the significance at P<0.05.
Results and discussion
L. usitatissimum is known to be a rich source of bioactive compounds (flavonoids and phenolics) that might play a substantial role in the reduction and stabilization of AgNPs. Phytochemical analysis of WPE and CE of L. usitatissimum revealed significant variations in TPC and TFC. In the case of CE, maximum levels of TPC (5.10 mg g−1 DW) and TFC (2.72 mg g−1 DW) were found in response to 2.0 mg L−1 TDZ, whereas lower levels of TPC and TFC were found in response to all other applied concentrations of TDZ (Figure 2). Therefore, callus induced by 2 mg L−1 TDZ which accumulated higher levels of phenolic and flavonoid content, was used for biosynthesis of AgNPs. However, in the case of WPE, the TPC (3.42 mg g−1 DW) and TFC (1.61 mg g−1 DW) were found to be significantly lower than those of CE. This might be due to the young mass of cells with different ploidy levels in the callus, which may be metabolically active to produce various types of phytochemicals responsible for the bioreduction of metal atoms.8,14 Additionally, TDZ is an important PGR, which had been reported for the production of important bioactive compounds in many plant species.20,21 The variation in the production of these phytochemicals in response to different concentrations of TDZ can be due to the activation or the inhibition of key enzymes phenylalanine ammonia lyase and tyrosine ammonia lyase, which are crucial for biosynthetic pathways of these phytochemicals.36
WPE- and CE-mediated biosynthesis of AgNPs
Many studies have shown that the bioactive compounds, such as flavonoids, tannins, phenolics, amides, and proteins, present in plants act as reducing and capping agents.3,4,6,37,38 Since the WPE- and TDZ-induced CE of L. usitatissimum contain high levels of polyphenols and flavonoids, we expect that they will serve as reducing and capping agents for the biosynthesis of AgNPs. Therefore, we synthesized AgNPs using WPE- and TDZ-induced CE to find out the better reducing source. The formation of AgNPs in aqueous extracts can be monitored visually by color change from yellowish brown to dark brown. In our initial experiments, 1,000 μL each of WPE and CE was mixed separately with 1 mM SNS in different v/v ratios (1:1, 1:2, 1:5, and 1:10; extract/SNS). The reaction mixtures started turning brown immediately as they were mixed and continued turning darker with the passage of time. These reaction mixtures were kept at room temperature for 24 hours, but no further change in color was observed after 6 hours, suggesting that the color attained by all reaction mixtures was stable (Figure 3A and B). However, no color change was observed with WPE, CE, or SNS alone under the same conditions. In case of WPE-mediated biosynthesis of AgNPs, the only reaction mixture with 1:10 ratio (WPE/SNS) turned darker more rapidly compared to the rest of WPE/SNS reaction mixtures (Figure 3B). However, in the case of CE-mediated biosynthesis of AgNPs, the reaction mixtures with 1:2, 1:5, and 1:10 ratios turned brown more rapidly than other reaction mixtures (Figure 3A), indicating that TDZ-induced CE is a better reducing source than WPE. This also showed that higher concentrations of SNS speed up the biosynthesis of AgNPs, which is in agreement with a previous study involving Agrimoniae herba extract as a reducing agent.39 The highest color intensity was observed in CE-mediated AgNP reaction mixture of 1:10 ratio. The change in color is the preliminary indication of biosynthesis of AgNPs, and this color change is due to the strong absorption of visible light due to excitation of surface plasmon resonance, which may affect the size and shape of AgNPs.16,39
UV–vis spectroscopic characterization of AgNPs
UV–vis spectroscopy is one of the vital techniques used for analyzing the formation and stability of AgNPs in aqueous solution. It is reported in the literature that AgNPs exhibit a characteristic surface plasmon resonance peak in the range of 400–480 nm wavelength.8,40 As shown in Figure 4, the WPE and CE mixed with SNS in different ratios showed a characteristic surface plasmon resonance between 410 nm and 426 nm, indicating the presence of AgNPs in the solution. However, the 1:1 ratio of both types of reaction mixtures did not show any characteristic peak of AgNPs (Table 1). Highest absorbance with comparatively narrow peaks was observed when both extracts (WPE and CE) were mixed separately with SNS in 1:10 ratio, indicating higher yield of nanoparticles. The increase in absorbance intensity is due to increasing number of AgNPs formed as a result of reduction of silver ions.16,41 It is well known that the absorbance intensity mainly depends on the size and shape of AgNPs, and in general, absorbance peak decreases as the size of the nanoparticles increases.42
Effect of reaction time on synthesis and stability of AgNPs
To find out the reduction time of silver ions in the reaction mixtures, we investigated the absorbance intensities and wavelength peaks of reaction mixtures at different time intervals (10 minutes to 24 hours) by using UV–vis spectrophotometer. In the case of WPE/SNS reaction mixtures, an expansion of reaction time was accompanied with an obvious increase in the absorbance intensity before 6 hours, but no significant enhancement was found after 6 hours. This showed that the reduction of silver ions in WPE/SNS reaction mixtures was completed within 6 hours, with no further increase in absorption (Figure 5A). Similar results were also reported in the synthesis of AgNPs using the extract of Chrysanthemum indicum.34 However, in the case of TDZ-induced CE/SNS reaction mixtures, reduction of silver ions was completed within 2 hours, resulting in high yield of nanoparticles within a short time (Figure 5B). Among all the tested ratios of WPE and CE with SNS, 1:10 ratio of CE/SNS showed the highest absorbance intensity at 418 nm with a comparatively narrow peak and shorter reduction time. This might be due to enhancement of phytochemical reducing agents (TPC and TFC) in TDZ-induced CE as compared to WPE, resulting in rapid biosynthesis of AgNPs by speeding up the reduction of silver ions. These results are in agreement with those reported by Sheshadri et al43 who described the role of melatonin in the biosynthesis of AgNPs. Since 1:10 ratios of both types of reaction mixtures showed high absorption peak and complete reduction in lesser time period, we further proceeded with only these two reaction mixtures (1:10 ratio of WPE/SNS and CE/SNS). The stability of the synthesized AgNPs was examined by keeping the reaction mixtures at room temperature for 2 months, and it was found that the reaction mixtures showed peaks at the same wavelength with similar absorption intensity, which confirmed the stability of synthesized AgNPs (Figure 6). This showed that the phytochemicals present in the extracts not only act as reducing agents but also stabilize the synthesized AgNPs by preventing them from agglomeration. Similar results were also reported in the synthesis of AgNPs using the extract of A. herba.39
FTIR spectroscopy analysis of AgNPs
FTIR measurements were carried out to determine the possible interfacial phytochemicals involved in the reduction, capping, and stabilization of AgNPs. The results showed intense absorption peaks at ~3,691.10 cm−1, 3,601.23 cm−1, 3,003.58 cm−1, 2,934.07 cm−1, 1,811.83 cm−1, 1,714.03 cm−1, 1,323.34 cm−1, 1,241.13 cm−1, 1,096.44 cm−1, 1,065.14 cm−1, 958.68 cm−1, 860.01 cm−1, 730.54 cm−1, 653.07 cm−1, and 624.01 cm−1 for CE-mediated AgNPs (Figure 7A) and sharp absorption peaks at ~3,699.92 cm−1, 3,600.82 cm−1, 3,003.76 cm−1, 2,942.92 cm−1, 1,811.87 cm−1, 1,713.96 cm−1, 1,580.98 cm−1, 1,407.93 cm−1, 1,323.50 cm−1, 1,182.37 cm−1, 1,141.01 cm−1, 1,095.08 cm−1, 1,065.07 cm−1, and 958.01 cm−1 for WPE-mediated AgNPs (Figure 7B). The absorption peaks in the region of 3,774.38–3,601.23 cm−1 were assigned to strong –OH stretching in alcohols, flavonoids, and phenolic compounds.3 The intense bands in the region of 2,934.07–2,891.01 cm−1 correspond to O–H stretching of carboxylic groups, while the broad band appearing at 1,714.03 cm−1 may be due to C=O stretching of carbonyl group. The absorption band at 1,241.13 cm−1 corresponds to C–N stretching of aliphatic amines, and the band at 1,065.14 cm−1 indicated =C–H bending of alkenes.39,40 The peak around 653.07 cm−1 region represents the –OH bending of the phenolic group.34 These results showed that both types of synthesized AgNPs shared some common peaks in the region of 3,600–1,350 cm−1 but clearly different peaks in the region of 1,300–620 cm−1, suggesting the presence of some additional phytochemicals in CE (due to TDZ-induced stress) compared to WPE. The present data strongly indicated the involvement of polyphenols, flavonoids, aliphatic amines, and carbonyl compounds in the reduction and capping of AgNPs. Our results are in good agreement with other reports available in the literature, suggesting the involvement of aforementioned groups in the biosynthesis of AgNPs.11,13,15,16,41
Figure 7 FTIR spectra of AgNPs.
XRD analysis of AgNPs
The crystalline nature of both types of synthesized AgNPs was confirmed by XRD analysis. XRD pattern of CE-mediated AgNPs (Figure 8A) showed four distinct diffraction peaks at 38.31°, 44.37°, 65.41°, and 77.29°, which can be attributed to 111, 200, 220, and 311 crystallographic planes of the face-centered cubic (FCC) crystalline silver.39 Similarly, the WPE-mediated AgNPs also showed four characteristic peaks at 38.13°, 44.23°, 64.53°, and 77.39° attributed to 111, 200, 220, and 311 crystalline planes of FCC crystalline structure of metallic silver (Figure 8B).3 Some unidentified crystalline peaks were also observed at 32.33°, 46.37°, and 68.93°, which are also apparent in many other works in which the XRD pattern includes the relevant 2θ range.44 These peaks might be due to the presence of bioactive compounds on the surface of AgNPs, which are responsible for their capping. The average size of AgNPs was calculated by using the Debye–Scherrer equation by determining the full width at half maximum of the Bragg’s reflection corresponding to the (111) crystalline plane of both types of synthesized AgNPs.45 The average crystalline sizes were calculated to be ~19.61 nm for CE-mediated AgNPs and 54.19 nm for WPE-mediated AgNPs, which are in good agreement with the sizes calculated by SEM. These results clearly showed that both types of synthesized AgNPs exhibit the same crystalline structure (FCC) but vary in their sizes. CE-mediated AgNPs are smaller in size, compared to WPE-mediated AgNPs, and hence are believed to be more efficient in their antimicrobial action because the smaller size makes the particles to penetrate more easily into the cells.46
Figure 8 XRD patterns of AgNPs.
SEM and EDX analyses of AgNPs
SEM technique was used to determine the size and morphology of synthesized AgNPs. SEM images (Figure 9A and B) clearly depict that both types of synthesized AgNPs were bead-like spherical in shape. However, the CE-mediated AgNPs were more dispersed than WPE-mediated AgNPs. Size calculation by SigmaScan Pro software attached with SEM showed that both types of synthesized AgNPs were clearly distinguishable owing to their size differences: 19–24 nm (CE-mediated AgNPs) and 49–54 nm (WPE-mediated AgNPs). These results revealed that the CE-mediated AgNPs were smaller in diameter and more scattered in distribution than that of WPE-mediated AgNPs.16 The SEM images also showed that the large bioactive compounds are attached to the surfaces of small AgNPs, making them stable by preventing agglomeration. The presence of metallic silver in the synthesized AgNPs was further confirmed by the EDX analysis. The EDX spectra (Figure 10A and B) showed strong peaks of metallic silver in the range of 3.0–4.0 keV. Metallic silver nanocrystal usually showed strong absorption spectra in the range of 2.5–4.0 keV, and similar results were also reported earlier.44–47
Figure 9 SEM images of AgNPs.
Figure 10 EDX spectra of AgNPs.
Possible mechanism involved in biosynthesis of AgNPs
The probable mechanism involved in the biosynthesis of AgNPs by plant metabolites is still largely unexplored.48 FTIR analysis of WPE- and CE-mediated AgNPs revealed that polyphenols, flavonoids, and carbonyl compounds are chiefly responsible for the reduction and stabilization of nanoparticles. Some important compounds of phenolic and flavonoid classes, which might be involved in the reduction of silver ions, are shown in Figure 11A. Determination of TPC and TFC showed that the WPE- and TDZ-induced CE are rich in phenolic and flavonoid contents, which are also in agreement with FTIR results. We, therefore, hypothesize the mechanism of reduction by showing the reduction of Ag+ to Ag0 by the flavonoid standard compound (quercetin) through a redox reaction (Figure 11B). Additionally, the plant active compounds from extracts were also responsible for the capping and stabilization of AgNPs (Figure 11C), as FTIR spectra of both WPE- and CE-mediated AgNPs showed the presence of almost similar functional groups. This proposed mechanism of AgNP biosynthesis is in good agreement with a previous report.3
Antibacterial activities against multiple drug-resistant bacteria
The antimicrobial efficacy of WPE- and CE-mediated AgNPs was examined against three highly multiple drug-resistant bacterial strains (E. coli, K. pneumoniae, and S. aureus) by using a standard antibiotic (ampicillin), positive control (SNS), and negative control (WPE and CE). WPE, CE, and SNS alone showed minimal levels of bactericidal activity as compared to both types of synthesized AgNPs (Figure 12). The zone of inhibition was measured in mm (Table 2), showing that all bacterial strains were more susceptible to CE-mediated AgNPs than to WPE-mediated AgNPs, which showed a moderate level of susceptibility. Surprisingly, both types of synthesized AgNPs demonstrated prominent results against S. aureus (11.1 mm and 13.5 mm) when compared to ampicillin (1.11 mm). These results (Figure 12 and Table 2) clearly showed that the CE-mediated AgNPs were more potent in their antibacterial action as compared to WPE-mediated AgNPs, suggesting the possible role of differences in their sizes. Similar potent antibacterial activity was reported by AgNPs, greenly synthesized by leaf and CE of Sesuvium portulacastrum.16 The size and shape of the synthesized nanoparticles play an important role in biomedical applications.34 Smaller sized nanoparticles are considered to be more efficient in their antimicrobial action because they can penetrate more easily into the cells.46 The smaller sized CE-mediated AgNPs (19–24 nm) showed enhanced zone of inhibition against the tested bacterial strains as compared to the larger sized WPE-mediated AgNPs (49–54 nm). The mechanism behind the antibacterial activity of AgNPs is not yet fully explored. Probably, the AgNPs exhibit the bactericidal activity by interacting with bacterial cell wall, deactivating the cellular enzymes, and causing disruptions in plasma membrane permeability. This disruption may result in the release of reactive oxygen species that can damage the DNA and proteins, eventually leading to the death of bacterial cells.49
In the present study, a novel protocol has been developed for rapid, safe, and cost-effective biosynthesis of AgNPs, demonstrating the potential role of PGRs in the enhancement of phytochemicals in in vitro-derived cultures of plants. These phytochemicals act as reducing and capping agents in the biosynthesis of AgNPs, thus avoiding the use of hazardous chemicals. Present results clearly indicated the superiority of TDZ-induced CE over WPE for rapid biosynthesis of AgNPs. The CE-mediated AgNPs were smaller in size, more scattered in distribution, synthesized in short time, and possess high bactericidal activity than that of WPE-mediated AgNPs. The present study has opened new possible ways of utilizing in vitro-derived cultures for synthesis of AgNPs. These chemical-free synthesized AgNPs can be used in many biomedical applications and also for the successful development of drug delivery in future.
The authors report no conflicts of interest in this work.
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