The silver nanoparticles were biosynthesized using fungal isolates as well as their mixed cell free filtrate acting as a consortium namely, DS-2 (Penicillium oxalicum), DW-8 (Fusarium hainanense) and DSW-28, respectively. The UV-Visible spectra determined the surface plasmon resonance at 438, 441 and 437 nm for the silver nanoparticles synthesized by DS-2, DW-8 and DSW-28, respectively. The Tauc’s plot analysis disclosed the band gap energy between 2.21 eV to 2.24 eV which depicted their ability to act as a semiconductor. The TEM imaging revealed the spherical shape along with the average particle size of DS-2 as 11.14 ± 2.39 nm and DW-8 as 7.59 ± 1.31 nm whereas that of DSW-28 as 5.73 ± 0.4 nm. Thus, the silver nanoparticles synthesized by DSW-28 were smaller in size than the individual isolates. The XRD pattern of the silver nanoparticles exhibited the crystalline structure corresponding to their peaks. The FTIR spectra indicates the presence of different functional groups on the surface of the synthesized silver nanoparticles. The broad-spectrum antimicrobial activity was exhibited by silver nanoparticles synthesized by DSW-28 against Gram positive, Gram negative bacteria and plant pathogen Fusarium oxysporum than the individual fungal isolates. The DSW-28 synthesized silver nanoparticles also acts as an effective antioxidant by depicting their radical scavenging activity against DPPH. Moreover, the silver nanoparticles synthesized by DSW-28 also inhibited the growth of 4th instar larvae of Aedes aegypti and Culex quinquefasciatus more efficiently than DS-2 and DW-8 in a dose-dependent method. The impressive bioactivity of the silver nanoparticles synthesized by the mixture of cell free filtrate of various fungi acting as a consortium recommends their prospective use in agriculture as well as in biomedical as an antimicrobial, antioxidant and larvicidal agents in future.
Research Article
Biogenic Synthesis of Silver Nanoparticles Mediated by the Consortium Comprising the Marine Fungal Filtrates of Penicillium Oxalicum and Fusarium Hainanense Along With Their Antimicrobial, Antioxidant and Larvicidal Potency
https://doi.org/10.21203/rs.3.rs-1115139/v1
This work is licensed under a CC BY 4.0 License
Version 1
posted 03 Dec, 2021
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Penicillium oxalicum
Fusarium hainanense
Consortium
Antioxidant activity
Antimicrobial activity
Larvicidal activity
- First report on green synthesis of silver nanoparticles using consortium developed using two marine derived fungi Penicillium oxalicum and Fusarium hainanense.
- Biosynthesized silver nanoparticles were stable at room temperature for more than 6 months.
- Antibacterial effect of nanoparticles on three Gram-positive and two Gram-negative bacteria due to their synergistic effects.
- Antifungal effect of nanoparticles against plant pathogenic fungi Fusarium oxysporum
- Antioxidant activity of silver nanoparticles using DPPH.
- Larvicidal activity of silver nanoparticles against 4th instar larvae of Aedes aegypti and Culex quinquefasciatus
Nanoscience explicit a prospering field offering a better future which deals with the nano-sized material within the range of 1-100 nm with varied properties conceding them immense potentials that can be utilized in diverse applications like agriculture, pharmaceutical, healthcare and medicine [1]. Amidst all metallic nanoparticles, silver nanoparticles are significantly utilized for their broad-spectrum antimicrobial, antioxidative, anticancer as well as larvicidal potentiality [2, 3, 4]. Synthesis of silver nanoparticles by chemical and physical techniques pose several drawbacks such as utilizing high raw materials, requiring high temperature and discharging toxic by-products which can be considered hazardous for both human health as well as agriculture [5, 6]. Moreover, the production of silver nanoparticles by biological method using natural sources such as plants, fungi, bacteria, algae, archaea etc. provides an easy, cost-effective and ecologically non-perilous alternative for their large-scale synthesis. This technique imparts stability and facilitates the fabrication of silver nanoparticles with desired size and morphology [4, 7].
Fungi tends to be more ideal for the biogenic synthesis of silver nanoparticles as they are easy to handle and harvest in bulk amount, possess high tolerance towards the metal, secrete higher amount of the unique extracellular proteins and other biomolecules which acts as a reducing as well as capping agents responsible for the stability nanoparticles [6, 8]. Besides this, the development of a consortium using cell free filtrate from different fungal strains provides a novel and unique approach for the biological synthesis of the silver nanoparticles. The utilization of mixed cell free filtrate from different fungi enhances the biofabrication of silver nanoparticles efficiently than the individual isolates with better stability, smaller particle size and higher bioactivity as they possess variety of biomolecules from different fungal sources [9, 10].
In the present study, the fungal isolates were screened out for the synthesis of silver nanoparticles. The cell free filtrate of two best screened out fungi namely DS-2 (Penicillium oxalicum) and DW-8 (Fusarium hainanense) were utilized in equal volumes as a consortium DSW-28 for the production of silver nanoparticles. The biosynthesized silver nanoparticles using both the individual fungal isolates (DS-2, DW-8) as well as mixed filtrate (DSW-28) were further characterized by UV-Visible and FTIR spectroscopic analysis, TEM imaging and XRD. The Antimicrobial activity of the synthesized silver nanoparticles was carried out against the three-Gram positive, the two-Gram negative bacteria as well as the plant pathogenic fungi namely Fusarium oxysporum. Furthermore, the antioxidant and the larvicidal activity of the synthesized silver nanoparticles were also carried out considering them as an effective antimicrobial as well as mosquitocidal agents in future.
Biosynthesis of Nanoparticles
The fungal isolates Penicillium oxalicum (DS-2) and Fusarium hainanense (DW-8) (GenBank accession number: MT647130 and MT647137) were grown in potato dextrose broth in shaking condition (120 rpm) for 96 h at 28 ºC. Harvested Biomass (6 g) was filtered through Whatman® filter paper no. 42 followed by washing with Milli-Q water and resuspended in 100 mL of Milli-Q water for 24 h at 60 ºC. The biomass was again filtered using Whatman® filter paper no. 42. The acquired cell free filtrate (CFF) was further utilized for the biogenesis of silver nanoparticles (AgNPs). For the biosynthesis of silver nanoparticles (AgNPs), 10 mL of CFF from each fungal strain (DS-2 and DW-8) and their mixture (DSW-28) in ratio of 1:1 v/v; (pH-9.0) was reacted with 90 mL of 10 mM silver nitrate solution (AgNO3, M.W. 169.87, HiMedia) at 60 ºC in the water bath. The experiment was carried out in dark condition to avoid any photochemical reactions.
Characterization of mycosynthesized silver nanoparticles
Characterization of synthesized nanoparticles from monocultures (DS-2 and DW-8) and their consortium (DSW-28) were carried out using UV-Visible, X-ray diffraction (XRD), Attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) and Transmission electron microscopy (TEM). Biosynthesis of silver nanoparticles was analyzed using UV–Vis spectrophotometer (Shimadzu, UV-1800 series) and absorption spectra were measured in the range of 300 nm to 700 nm. Morphological study (Shape and size) of the synthesized AgNPs were analyzed by TEM. The surface chemistry of the sample was studied using ATR-FTIR. Analysis of diffraction patterns were carried out using X-ray diffractometer. CuKα radiation with a wavelength of 1.5406 nm was recorded in the 2θ range from 0º to 90º and operated at 30 kV and 100 mA. Band gap energy (Eg) of nanoparticles was calculated by using Tauc’s plot.
Antimicrobial activity of silver nanoparticles (AgNPs)
Antimicrobial activity of synthesized AgNPs was carried out against three Gram-positive (B. subtilis, B. megaterium and S. aureus), two Gram-negative bacteria (P. aeruginosa and E. coli) and the Plant pathogenic fungi Fusarium oxysporum. The antibacterial activity was carried out via a well diffusion method. Bacterial strains were grown in nutrient broth at 37 ºC for 24 h and were adjusted to 0.5 as per McFarland standards. 100 µL of bacterial suspension was spread on a nutrient agar plate using a glass spreader under sterile conditions. A 12 mm diameter well was punched on the nutrient agar plate using a cork borer and the synthesized AgNPs and AgNO3 were inoculated in each well. Similarly, 100 μL of ampicillin (1 mg/mL) served as a positive control. All the plates were incubated at 37 °C for 24 h and the antibacterial activity was evaluated by measuring the diameter of the inhibition zone using zone scale (HiMedia). Antifungal activity of AgNPs was performed using plant pathogenic fungal strain Fusarium oxysporum. Fungal suspension (106 spores/mL) was spread on potato dextrose agar plate and a 12 mm diameter well was punched on the agar plate using a cork borer and the synthesized AgNPs and AgNO3 were inoculated in each well. Similarly, 100 μL of fluconazole (1 mg/mL) served as a positive control. The plates were incubated at 28 °C for 72 h and the antifungal activity was evaluated by measuring the diameter of the inhibition zone using zone scale (HiMedia) [11].
Antioxidant activity by 2,2-diphenyl-1- picrylhydrazyl (DPPH) method
The antioxidant potency of synthesized AgNPs was tested using the method described by [12] with minor modifications. The DPPH test was used to assess the radical scavenging activity of AgNPs. Various concentrations (10, 20, 30, 40, 50, 75, and 100 µg/mL) of 1 mL AgNPs were vortexed with 1 mL of freshly prepared 1 mM DPPH solution. The solution was then maintained in the dark for 30 min at room temperature. At 517 nm, the absorbance was measured. As a control, DPPH with all reagents except the sample was utilized, and methanol was used as a blank.
Mosquito rearing and Larvicidal activity of AgNPs
Aedes aegypti and Culex quinquefasciatus were collected from ICMR- National Institute of Malaria Research, Nadiad, Gujarat, India in February - 2021 and have been maintained under aseptic and suitable environmental conditions (relative humidity: 80 ± 10%, temperature: 28 ± 1ºC, photoperiod: 16:8 h light/dark cycle) in insectarium. The larvae were hatched until reaching the 4th instar and then were used for larvicidal activity. 25 4th instar larvae were placed in 200 mL of the test solution with various concentrations of silver nanoparticles (10, 25, 50 and 100 ppm) under preceding conditions. During this time period, no food supplements were provided and mortality was determined 24 h after the initiation of each bioassay. Larvae were termed as dead when the larvae either did not move, showed slow movement or were unable to rise to the surface of medium.
Statistical analysis
Statistical analysis was accomplished using IBM SPSS Statistics 23. All the experimental values were expressed as a mean ± SE. Significance level also indicated after performing 1 way ANOVA analysis. All the graphical representations were prepared in Origin 2021 (9.8) and MedCalc (version 20.015) [4, 10].
Penicillium oxalicum (DS-2) and Fusarium hainanense (DW-8) were isolated from soil and water sample, respectively, collected from the sea coast of Diu, India (20°42'17.3" N 70°54'55.8" E), and were subjected to AgNPs biosynthesis (Fig. 1). The CFF of Penicillium oxalicum (DS-2), Fusarium hainanense (DW-8) and their consortium (DSW-28) was reacted with 10 mM AgNO3 solution in a 9:1 (v/v) ratio. The addition of AgNO3 to the CFF of Penicillium oxalicum (DS-2), Fusarium hainanense (DW-8) and their consortium (DSW-28) resulted in an immediate change in solution color from colorless to light yellow, followed by a change to light brown at 12 h and a dark brown solution at 36 h as the reaction progressed, as shown in Figure 2.
UV-Visible spectroscopic analysis
A UV–Visible spectrophotometer was used to monitor the continuous formation of AgNPs. The synthesized CFF reduced AgNPs that had shown a unique absorption peak attributing to their surface plasmon resonance [13]. The absorption peak for DS-2, DW-8, and DSW-28 in the UV–visible spectrum of an aqueous medium containing silver nanoparticles was with 438, 441, and 437 nm, respectively. With the increasing incubation time, the intensity of the absorption peaks was increased. Even after 72 hours of incubation, there has been no change in the location of the absorption peak (Table 1), indicating that the AgNPs have a uniform particle shape [14]. Furthermore, it is proven that the synthesis of highly dense nanoparticles is responsible for enhancing the intensity of absorption peaks [15]. The results have been found to be consistent with the findings of many other researchers around the world. Figure 3 indicates that the SPR of synthesized AgNPs has not shown any change after 6 months (stored at room temperature).
Band gap energy by Tauc’s plot
A semiconductor's band gap energy describes the amount of energy required to excite an electron from the valence band to the conduction band. The Tauc’s plot proposed using optical absorption spectra was to estimate the band gap energy of amorphous semiconductors in 1966 [16]. The band gap energy (Eg) of all the three synthesized AgNPs was then estimated by extrapolating linear section of the curve (UV-Visible spectra) from Tauc's plot. The AgNPs of DS-2, DW-8, and DSW-28 achieved band gap energies of 2.21, 2.24, and 2.21 eV, respectively, in Figure 4. As a semi-conductive material, these particles with enormous band gap energies can be employed in advanced optoelectronic devices, batteries, and sensors. The band gap value is quite comparable to what has previously been reported in the literature, and it is possible that this value is attributable to the quantum confinement effect [4, 17].
Fourier-transform infrared spectroscopic (FTIR) analysis
Figure 5 depicts the FTIR spectrum of synthesized AgNPs, which shows absorption peaks in the 4000 cm-1 to 500 cm-1 range. The absorption bands in the FTIR spectra of DS-2 were found to be 3265 cm-1, 2127 cm-1, 1661 cm-1, and 760 cm-1. Absorption bands observed for DW-8 were at 3298 cm-1, 2135 cm-1, 1662 cm-1, and 745 cm-1, whereas the absorption bands observed for their mixed CFF (DSW-28) were at 3266 cm-1, 2093 cm-1, 1660 cm-1, and 744 cm-1. The FTIR peaks at various location in the region of 4000 cm-1 to 500 cm-1 indicate the presence of capping and stabilizing biomolecules on the nanoparticles' surface. Dr. Friedrich Menges' software SpectraGryph (version 1.2) was used to analyze ATR-FTIR spectra. Table 2 shows the peaks and their corresponding functional groups, which concurred with the research results of several researchers throughout the world.
At optimum conditions, the incorporation of silver salt into CFF solution results in immediate binding of silver ions with the protein and other molecules present in CFF solution with functional groups such as –OH and C=C being captured, resulting in conformational changes in proteins that represent its hydrophobic residues to the aqueous phase, resulting in infiltration of reducing agents from CFF solution and thus providing capping to silver ions with the formation of stable nanoparticles [18, 19]. Assuming the CFF of the marine fungi Penicillium oxalicum and Fusarium hainanense used in this study, it is conceivable that alkyne, sulfurous and phenolic compounds, proteins, alcohol and other water-soluble biomolecules contributed as reducing and stabilizing agents to the silver nanoparticles [5, 20].
X-ray diffraction analysis
Figure 6 depicts the distinct XRD patterns of mycosynthesized AgNPs by DS-2, DW-8 and DSW-28. XRD pattern of DS-2 exhibited diffraction peaks corresponding to [111], [200], [220] and [311] appearing at 2θ representing the value of 37.89°, 44.19°,64.22° and 77.11°, respectively. XRD pattern of DW-8 exhibited diffraction peaks corresponding to [110], [111], [200] and [220] appearing at 2θ representing the value of 33.18°, 37.76°,46.74° and 66.12°, respectively. The XRD pattern of consortium DSW-28 exhibited diffraction peaks corresponding to [110], [111], [200]and [311] appearing at 2θ representing the value of 33.31°, 38.11°, 44.2° and77.6°, respectively. In accordance with COD ID no. 1100136, these peaks represent crystallographic planes of face-centered cubic (fcc) Ag. The Debye-Scherrer formula was used to calculate the mean particle size of AgNPs [21].
Where,
D represents the crystalline size (nm),
Λ indicates the wavelength of X-ray (0.1541 nm),
β specifies the angular line full width at half maximum (FWHM) of the peak (in radians) and
θ displays the Braggs angle (in radians)
As indicated in Table 3, the mean size of the silver nanoparticles was estimated to be from 14.19 ± 3.14 nm, 8.87 ± 2.31 nm, and 5.14 ± 0.99 nm for DS-2, DW-8, and DSW-28, respectively. The nanocrystalline nature of the mycosynthesized NPs is attested by the extensive pattern of the XRD diffraction peaks [7].
Transmission Electron Microscopic (TEM) analysis
As shown in Figure 7, TEM analysis demonstrated the synthesis of nanocrystalline silver particles. AgNPs with a spherical morphology and uniform size of 11.14 ± 2.39 nm, 7.59 ± 1.31 nm, and 5.73 ± 0.4 nm of DS-2, DW-8, and DSW-28, respectively, were observed. Particles of larger sizes were found in the sample in exceptional cases, although in small proportions. The presence of lattice fringes in the TEM images of synthesized AgNPs demonstrated their crystalline structure, with the 'd' spacing values correlating to the X - ray diffraction patterns. Furthermore, the selected area electron diffraction (SAED) pattern exhibited ring patterns with single spots in a ring (Fig. 7) that are consistent with the XRD patterns. Figure 8 shows the TEM-derived size distribution curve. The nanoparticles with the size range of 5.19 to 21.3 nm for DS-2, 3.04 to 13.5 nm for DW-8, and 1.5 to 17.3 nm for DSW-28 were obtained according to TEM analysis. Until now, a larger size range of AgNPs produced employing various fungus and plant extracts has also been described [13, 22, 23].
Antimicrobial activity of AgNPs
The antimicrobial potential of AgNPs was assessed by measuring the inhibition zone diameter and the observations are shown in Table 4 and Table 5. In this study, the highest zone of inhibition had been observed against Gram-positive bacteria compared to the Gram-negative bacteria. The prospect of employing these AgNPs as a broad-spectrum antimicrobial agent was clearly recognized by these results. This experiment is in correspondence with the view of Mistry et al. (2021) [4] that the probable antimicrobial potential of AgNPs is because of their higher surface-to-volume ratio and their crystalline structure [24]. The AgNPs have been found to rupture the cell membrane, resulting in the generation of reactive oxygen species (ROS) that damage the DNA and proteins, followed by the microorganism's destruction [25]. Many previous studies have reported that AgNPs are more hazardous to the Gram-negative bacteria than Gram-positive bacteria since they have a thinner peptidoglycan layer through which AgNPs can infiltrate and disrupt their proteins and DNA, ultimately leading to microbial death. Conversely, higher amount of nanoparticles are required to show antibacterial potency against gram positive bacteria as they contain thicker peptidoglycan layer [26]. As a consequence, AgNPs aren't highly effective against Gram-positive microorganisms. However, AgNPs synthesized by DS-2, DW-8 and DSW-28 showed very effective results against Gram-positive bacteria (Table 4). Fusarium oxysporum is a plant pathogenic fungus known to cause wilt in many ecologically important plants like cumin, banana that leads to yield loss [27, 28]. To overcome this issue, Fusarium oxysporum was treated by AgNPs synthesized from DS-2, DW-8 and DSW-28. Results obtained after incubation period of 72 h has shown intensive antifungal potential of AgNPs. Zone of inhibition of mixed CFF DSW-28 was higher (19 ± 0.32 mm) in comparison of DS-2 (13 ± 0.33 mm), DW-8 (15 ± 0.31 mm), standard fluconazole (12 ± 0.17 mm) and 10 mM AgNO3 solution (11 ± 0.35 mm) (Table 5). In this study interestingly, AgNPs derived from mixed CFF of marine fungi Penicillium oxalicum and Fusarium hainanense were found to be impressively effective against Gram-positive as well as Gram-negative bacteria and plant pathogenic fungal strain in compare of their individual CFF (DS-2 and DW-8). In mixed CFF, presence of various precious biometabolites from both the fungi could be responsible for higher bioactivity towards human as well as plant pathogens. This characteristic of mycosynthesized AgNPs will contribute in the advancement of broad-spectrum antimicrobial activity [5].
Antioxidant capacity of CFF derived AgNPs
DPPH is a stable molecule that can be reduced by admitting hydrogen or electrons, and it has been extensively utilized to assess antioxidant properties of the silver nanoparticles. In this experiment, various concentrations of biosynthesized AgNPs were reacted with DPPH reagent to assess their antioxidative potency. As a result, AgNPs synthesized by marine fungal cell free filtrate DS-2 and DW-8 and their consortium DSW-28 have shown effective antioxidant potential as their radical scavenging ability was increasing with the increment in their concentration. Figure 9 shows the antioxidant activity of the AgNPs. Their IC50 value was calculated in Microsoft excel-2019 which was about 71.33 (µg/mL) for DS-2, 61.30 (µg/mL) for DW-8 and DSW-28 was about 42.56 (µg/mL). Above mentioned results confirmed that the AgNPs synthesized by mixing their CFF have more antioxidative properties than AgNPs synthesized using their individual CFF which were DS-2 and DW-8 as they possess lower IC50.Antioxidative potential of the silver nanoparticles is due to the adsorption of fungal constituents from CFF on the silver nanoparticle [12]. Metal nanoparticles produced by marine fungi exhibit a wide range of biological activities, including antioxidant, antibacterial, and antimalarial properties. Marine fungus like Aspergillus brunneoviolaceus and Cladosporium cladosporioides have recently been found to produce AgNPs with excellent antioxidant activity. The findings significantly support the use of AgNPs as natural antioxidants for health protection against a wide range of oxidative stressors associated with degenerative diseases. This antioxidant validation is essential for synthesized AgNPs before their utilization against experimental models such as mice or against humans [4, 24, 29, 30].
Larvicidal activity of silver nanoparticles
The synthesized AgNPs from DS-2, DW-8 and DSW-28 were exposed against 4th instars larvae of Aedes aegypti and Culex quinquefasciatus at various concentrations (10–100 µg/mL) for 24 h. Amongst all, the AgNPs synthesized from mixed CFF of DS-2 and DW-8 which is DSW-28 had exhibited potent larvicidal activity. Figure 10 depicts the dose response plot of AgNPs against larvae of Aedes aegypti and Culex quinquefasciatus. The maximum mortality rate observed for DSW-28 was 88% and 92% with LC50 values of 35.37 and 13.35 µg/mL against Aedes aegypti and Culex quinquefasciatus, respectively (Fig-10). Distilled water was taken as a control. No mortality of any larvae was observed in control groups. The mortality rate was significantly augmented with an increasing dose-dependent manner where the highest mortality rate was observed with the increasing concentrations of synthesized AgNPs. This difference in lethal concentrations might be due to differences in secondary metabolites present in the fungi. It has been reported that AgNPs are responsible for impeding the process of food consumption development in mosquito young instar resulting in their death. Furthermore, AgNPs can easily penetrate into the exoskeleton of larvae and attach to the sulfur or phosphorus containing biomolecules like proteins, DNA and RNA which leads to the quick denaturation of organelles and enzymes which could be the possible reason for the death of mosquito larvae. Due to the disturbance in proton motive force important for ATP construction and decreased permeability of membrane by AgNPs, cellular functions may not work properly and cell will die [31, 32, 33]. AgNPs synthesized from DSW-28 had shown highest rate of mortality against both the larvae. Reason behind that characteristic of DSW-28 could be synergistic effect of both the fungal metabolites present and attached on the surface of nanoparticles [10].
A novel approach of synthesizing silver nanoparticles using the mixture of cell free filtrate of different fungi has been demonstrated in this study. The biogenic silver nanoparticles were spherical in shape with the average particle size of 5.73 ± 0.4 nm displaying maximum surface by volume ratio exhibiting better biopotentials compared to the silver nanoparticles synthesized by individual isolates. The broad-spectrum antimicrobial activity of the synthesized nanoparticles against bacteria as well as plant pathogenic fungi revealed their potentiality in both medicine as well as agriculture. The synthesized silver nanoparticles displayed their efficient antioxidative potentiality against DPPH and also larvicidal activity by ceasing the growth of 4th instar larvae of Aedes aegypti and Culex quinquefasciatus. Thus, the study unfolds the unique perspective of using the mixture of cell free filtrate of different fungi for the effective synthesis of silver nanoparticles with desired size and bio-potentialities in diverse fields.
Acknowledgements
The Authors highly acknowledge the Department of Biotechnology and Department of Life Sciences for providing the research facilities.
Funding
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Contribution
Rashmi Thakor: Conceptualization, Validation, Writing-review and editing, Writing-original draft
Harsh Mistry: Writing-review and editing, Writing-original draft, Data curation, Formal analysis
Hitesh Patel: Methodology, Resources
Himanshu Bariya: Methodology, Writing-original draft, Project administration, Investigation
Corresponding author
Correspondence to Himanshu Bariya
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Table 1 UV–visible spectroscopy data
|
s/n |
Time of incubation |
DS-2 |
DW-8 |
DSW-28 |
Color change |
|||
|
Peak intensity (Abs.) |
λ max (nm) |
Peak intensity (Abs.) |
λ max (nm) |
Peak intensity (Abs.) |
λ max (nm) |
|||
|
1 |
24 h |
0.975 |
437 |
1.179 |
441 |
1.529 |
438 |
Light yellow to light brown |
|
2 |
48 h |
1.102 |
438 |
1.323 |
441 |
1.640 |
436 |
Light brown to dark brown |
|
3 |
72 h |
1.131 |
437 |
1.476 |
440 |
1.754 |
439 |
Dark brown |
|
4 |
96 h |
1.191 |
439 |
1.567 |
441 |
1.868 |
437 |
Dark brown |
|
5 |
185 days |
1.224 |
438 |
1.602 |
441 |
1.902 |
437 |
Dark brown |
Table 2 Fourier-transform infrared spectroscopy (FTIR) interpretation
|
s/n |
DS-2 |
DW-8 |
DSW-28 |
Stretching/Bond |
Functional group |
Reference |
|
Wave number (cm-1) |
Wave number (cm-1) |
Wave number (cm-1) |
||||
|
1 |
3265 |
3298 |
3266 |
O-H stretching |
Alcohol/Phenol |
Thirunavoukkarsu et al. 2013 |
|
2 |
2127 |
2135 |
- |
C≡C stretching |
Alkyne |
Saravanan et al. 2018 |
|
3 |
- |
- |
2093 |
C=S stretching |
Sulfur compound |
Kumar et al. 2014 |
|
4 |
1661 |
1662 |
1660 |
C-C/ C-N stretching |
Alkene or amines |
Koyyati et al. 2014 |
|
5 |
760 |
745 |
744 |
C-H bending |
alkane |
Jyoti et al. 2016 |
Table:3 X-ray diffraction interpretation
|
AgNPs |
s/n |
2θ |
θ |
FWHM |
Crystallite Size D(nm) |
D nm (Average) |
(hkl) |
|
DS-2 |
1 |
37.89 |
18.945 |
0.73 |
11.50 |
14.19 ± 3.14 |
111 |
|
2 |
44.19 |
22.095 |
1.1 |
7.79 |
200 |
||
|
3 |
64.22 |
32.11 |
0.63 |
14.88 |
220 |
||
|
4 |
77.11 |
38.555 |
0.45 |
22.57 |
311 |
||
|
DW-8 |
1 |
33.18 |
16.59 |
1.41 |
5.85 |
8.87 ± 2.31 |
110 |
|
2 |
37.76 |
18.88 |
0.72 |
11.61 |
111 |
||
|
3 |
46.74 |
23.37 |
0.62 |
13.88 |
200 |
||
|
4 |
66.12 |
33.06 |
2.28 |
4.15 |
220 |
||
|
DSW-28 |
1 |
33.31 |
16.655 |
1.76 |
4.71 |
5.14 ± 0.99 |
110 |
|
2 |
38.11 |
19.055 |
1.28 |
6.56 |
111 |
||
|
3 |
44.2 |
22.1 |
3.4 |
2.52 |
200 |
||
|
4 |
77.6 |
38.8 |
1.5 |
6.79 |
311 |
Table: 4 Antibacterial activity of AgNPs against Gram-positive and Gram-negative bacteria
|
S/n |
Microorganisms |
DS-2 (100 µL) |
DW-8 (100 µL) |
DSW-28 (100 µL) |
Ampicillin (1 mg/mL) |
AgNO3 (10 mM, 100 µL) |
|
ZOI* (mm) |
ZOI* (mm) |
ZOI** (mm) |
ZOI* (mm) |
ZOI** (mm) |
||
|
1 |
B. subtilis |
13 ± 0.30 |
14 ± 0.31 |
16 ± 0.21 |
10 ± 0.30 |
9 ± 0.29 |
|
2 |
S. aureus |
12 ± 0.32 |
13 ± 0.30 |
15 ± 0.20 |
12 ± 0.33 |
11 ± 0.24 |
|
3 |
P. aeruginosa |
14 ± 0.31 |
14 ± 0.28 |
16 ± 0.24 |
13 ± 0.32 |
9 ± 0.30 |
|
4 |
E. coli |
14 ± 0.28 |
15 ± 0.29 |
17 ± 0.20 |
10 ± 0.30 |
8 ± 0.32 |
|
5 |
B. megaterium |
12 ± 0.25 |
12 ± 0.26 |
19 ± 0.22 |
14 ± 0.31 |
8 ± 0.25 |
Average value with standard error (p < 0.05) of three set of experiments. Experiment performed in triplicate. ** indicate highly significance at p<0.05 and * indicate significant at p<0.05.
Table 5 Antifungal activity of AgNPs against plant pathogenic fungi Fusarium oxysporum
|
S/n |
Microorganisms |
DS-2 (100 µL) |
DW-8 (100 µL) |
DSW-28 (100 µL) |
Fluconazole (1 mg/mL) |
AgNO3 (10 mM, 100 µL) |
|
ZOI* (mm) |
ZOI* (mm) |
ZOI** (mm) |
ZOI* (mm) |
ZOI** (mm) |
||
|
1 |
Fusarium oxysporum |
13 ± 0.33 |
15 ± 0.31 |
19 ± 0.32 |
12 ± 0.17 |
11 ± 0.35 |
Average value with standard error (p < 0.05) of three set of experiments. Experiment performed in triplicate. ** indicate highly significance at p<0.05 and * indicate significant at p<0.05.
