*Corresponding Author:
S. Nayaka
Department of Botany, Karnatak University, Dharwad, Karnataka 580003, India
E-mail: [email protected]
Date of Received 20 July 2021
Date of Revision 11 December 2021
Date of Acceptance 15 September 2022
Indian J Pharm Sci 2022;84(5):1178-1188  

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The current study investigated about the biogenic synthesis and evaluation of biological activities of Amycolatopsis sp. strain MN235945 fabricated silver nanoparticles and their characterization by ultraviolet-visible spectroscopy, fourier transform infrared spectroscopy, high resolution-transmission electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffractometry and zeta potential analysis. The most potent isolate Amycolatopsis sp. strain MN235945 was identified by morphological and genotypic characterization and biological activity of silver nanoparticles was studied via antimicrobial and anticancer activity assays. The synthesized silver nanoparticles with spherical shape and polydispersed nature showed ultraviolet visible spectroscopy, absorption maximum at 417 nm with the smallest size of 19.40 nm. The presence of various biological functional groups and different elemental composition of silver nanoparticles were determined along with zeta potential value of -34.8 mV; whereas, the X-ray diffractometry analysis revealed the specific Bragg’s diffraction peaks for metallic silver. The silver nanoparticles with increased antimicrobial activity significantly inhibited cervical adenocarcinoma HeLa and human breast cancer MCF-7 tumour cells with IC50 values of 81.12 and 235.45 μg/ml respectively. These encouraging results obtained via low-cost green synthesis of silver nanoparticles from marine Amycolatopsis sp. strain MN235945 provide helpful information for further research and designing an anticancer agent in coming years using Amycolatopsis sp. strain MN235945 mediated silver nanoparticles with minimal side effects.


Marine Amycolatopsis sp., silver nanoparticles, antimicrobial, anticancer activity, reactive oxygen species

Nanotechnology is an essential field in recent days, where it is dealing with many research like synthesis, characterization and different shapes, sizes (1-100 nm) of the nanoparticles. Several studies regarding the synthesis of biological nanoparticles using various microorganisms like fungi, Actinomycetes, bacteria, viruses and different plant parts are investigated. It shows promising potential for controlling different pathogens. With multiple applications, nanoparticle research plays a vital role in the fields such as cancer study[1], larvicidal and insecticidal activity[2] and plant disease control in agricultural sciences[3]. Biological activities like antibacterial, antifungal, anticancer[4], anti-inflammatory, antiviral, cardioprotection[5], wound healing[6], and biosurfactants[7] helped nanotechnology to gain enormous popularity within a short time.

Silver nanoparticles (AgNPs) have been used in various applications like cosmetics, solar cells, catalysts, ceramics, gas sensors, anti-bacterial properties, energy sector plastics, environmental protection[8], drug delivery and bioimaging, textiles, probes, commercial products such as pastes, food packaging, soaps, optical and electrical properties, toxicity against cancer cells[9,10]. There are varieties of methods like physical, chemical and biological approaches to synthesize AgNPs and biological synthesis of AgNPs is more opted[11,12]. The AgNPs synthesis using various microorganisms are well documented in Streptomyces rochei MHM13[13], Aspergillus tamarii[14], Penicillium atramentosum KM[15], Acinetobacter baumannii[16], Gordonia amicalis HS11[17], and Escherichia coli[18], Lactobacillus plantarum TA4[19] and from Enhalus acoroides[20].

Actinomycetes are unicellular, gram-positive bacteria; it belongs to the order Actinomycetales. This group is widely distributed in the environment and found in various habitats like plants, soil, freshwater, marine, and soil, etc. and well known for producing many antibiotics. The present investigation focuses upon the formation of AgNPs by Amycolatopsis sp. which is a reducing agent. Amycolatopsis sp. has many antibiotics like balhimycin, tolypomycin, vancoresmycin and nogabecin[21].

In present days, cancer is among the reasons for the highest number of mortality worldwide, as mentioned in one out of six deaths across the globe[22]. Among the various types of cancers in humans, cervical and breast carcinoma are observed in the highest percentage of incidence[21]. These cells spread in the blood and lymph system through the entire body; despite chemotherapy, radiotherapy is the most common type of cancer treatment, these protocols causing side effects. These advantages are cost-effective for the synthesis of nanoparticles for cancer treatment. At present, AgNPs are used as anticancer agents to treat several types of cancers such as epithelial carcinoma (A549), hepatocellular carcinoma (HepG2)[23], cervical adenocarcinoma (HeLa)[24] and human breast cancer (MCF-7)[25].

Meanwhile, AgNPs have been recognized as innovative materials and have found their applications in different fields, starting from antimicrobials to cancer therapy[26]. The present study is carried out for the first time using Amycolatopsis sp. strain MN235945 for the synthesis of AgNPs and their cytotoxic activity against HeLa and MCF-7 cell lines.

Materials and Methods

Sample collection and isolation of Actinomycetes:

The sediment samples were collected from different locations of Maravanthe beach, Kundapur, Udupi, Karnataka, India. The samples were used to isolate Actinomycetes on starch casein agar media using the spread plate method. Later, the pure cultures of Actinomycetes strains were screened for antagonistic activities by perpendicular streak method and the isolate showing good inhibition activity was selected for AgNPs synthesis.

Preparation of cell free extract and biosynthesis of AgNPs:

The isolated marine Actinomycetes were cultured in a 250 ml conical flask containing 100 ml of starch casein broth medium at pH 7.2 with the following composition starch 1 g, casein 0.03 g, calcium carbonate 0.002 g, ferrous sulphate 0.001 g, potassium nitrate 0.2 g, magnesium sulphate 0.005 g and sodium chloride 0.2 g. The incubation of the inoculated flasks was done at 33° for 5 d. After incubation, cultures were centrifuged at 8000 RPM for 15 min to obtain the culture supernatant and the same was mixed with an aqueous solution of 1 mM silver nitrate (100 ml) at pH 8.0. The mixture was incubated in the dark for 5 d to allow the formation of AgNPs and observed for the colour change in the reaction mixture.

Characterization of synthesized AgNPs:

The bio-reduction of silver ions (Ag+) to elemental silver (Ag0) was monitored in the scanning range between 300 to 700 nm by using a double beam Ultra-Violet Visible (UV-Vis) spectrophotometer (METASHUV-9000 A). The Fourier-Transform Infrared (FTIR) spectroscopy was performed to detect possible bio-reductants by scanning in the range of 4000 to 400 cm-1 with 4 cm-1 resolution using FTIR instrument (Nicolet 6700, USA). The AgNPs were observed under Scanning Electron Microscope (SEM) equipped with Energy Dispersive X-Ray (EDX) analyzer (JSM-IT 500LA) to determine morphology and elemental composition. The shape and size of the biosynthesized AgNPs were determined by High Resolution Transmission Electron Microscopic (HR-TEM) analysis (FEI, TECNAI G2, F30) with an accelerating voltage of 100 kV. The particle size and surface morphology of nanoparticles were evaluated using Image J 1.45 software. The crystal structure and particle size were studied by X-Ray Diffraction (XRD) (Rigaku Miniflex Smart Lab SE, 600) instrument and operating at 40 kV and 30 mA. The size and surface charge values were measured with the help of the zeta potential instrument (Horiba Scientific) and the thermal stability of AgNPs was studied by Thermo-Gravimetric Analysis (TGA) from room temperature to 600° using TGA instrument (TA instruments, SDT Q 600 and DSC Q20, USA).

Genotypic characterization of potent isolate:

Genomic DNA was isolated from the selected strain and 16S rRNA genes were amplified and sequenced using the Sanger sequencing method (Applied Biosystems, 3500 series genetic analyzer). The obtained gene sequence was deposited to the National Center for Biotechnology Information database via nucleotide BLAST (BLASTn) web portal. The DNA sequence was aligned and the taxonomical hierarchy was studied by constructing neighbour joining the phylogenetic tree using MegAlign Pro 17 (DNASTAR Lasergene) software.

Antimicrobial activity of AgNPs:

Antimicrobial activity of AgNPs fabricated by Amycolatopsis sp. strain MN235945 was tested against pathogenic microorganisms like Pseudomonas aeruginosa (MTCC424), Staphylococcus aureus (MTCC6908), Enterococcus faecalis (MTCC6845), Escherichia coli (MTCC40), Fusarium oxysporum (MTCC2087), Candida glabrata (MTCC3814), Alternaria alternata (MTCC2060) and Candida albicans (MTCC227) were procured from National Collection for Industrial Microorganisms, Pune, India and sub-cultured on nutrient broth media before incubating at 37° for 48 h. For the agar well diffusion method, the bacterial and fungal cultures were spread on Mueller-Hinton agar plate using a sterile cotton swab. The wells were loaded with 25, 50, 75, 100 µl of AgNPs suspension (1 mg/ml stock) and 50 µl of distilled water was used as negative control; whereas 50 µl of (25 µg/ml) streptomycin and fluconazole were taken as standards for bacteria and fungi, respectively.

Evaluation of Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC):

The inhibitory action of AgNPs was further tested using MIC and MBC studies on bacterial pathogens to find out the minimum concentration of AgNPs that inhibit the growth of bacterial strains. The tests were carried out according to the methods described in Clinical and Laboratory Standards Institute (CLSI) and conducted on 96-well microtiter plates for MIC by taking resazurin as indicator with streptomycin as standard; and the MBC test was conducted on Mueller-Hinton agar plates. For MIC the bacterial inoculum concentration of 106 Mcfarland standards was taken along with 100 μl of AgNPs (500 μg/ml) from the stock solution.

Column 1 with only medium and column 2 with medium and bacterial inoculum were taken as negative and positive controls, respectively. Further, 30 μl of resazurin was added in each well and the plate was incubated at 37° for 24 h. Similarly, the MBC test was performed by spreading the suspension from each well of microtiter plate on Mueller-Hinton agar plates and incubated at 37° for 48 h. Finally, the concentration at which the bacterial growth was not observed was taken as MIC and MBC values.

In vitro anticancer activity of AgNPs:

Cell viability (3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide (MTT)) assay: The cytotoxicity of AgNPs was tested against HeLa and MCF-7 cell lines using MTT cell viability assay. The cancer cell lines were procured from the National Centre for Cell Science, Pune, India, and sub-cultured on Dulbecco Modified Eagle Medium (DMEM-#AL111, Himedia). Both cancer cell lines were separately plated in 96 well plates (Corning, USA) at a density of 20 000 cells per well without AgNPs (control). The cells were allowed to grow for 24 h inside a 5 % CO2 incubator (Healforce, China), and then the desired concentrations of AgNPs (6.25, 12.5, 25, 50 and 100 µg/ml) were added along with 0.5 mg/ml of MTT reagent (#4060, Himedia) and 4.3 μg/ml (HeLa) and 3.48 μg/ml (MCF-7) camptothecin (#C9911, Sigma) as standard. After incubating for 24 h at 37° in a 5 % CO2 atmosphere, the spent media was removed from the plates. Further, 100 μl of Dimethyl Sulfoxide (DMSO-#PHR1309, Sigma) was added after removing the MTT reagent. The absorbance was read on an Enzyme Linked Immunosorbent Assay (ELISA) reader to determine the change in colour intensity at 570 nm using 630 nm as a reference wavelength.

Reactive Oxygen Species (ROS) assay: HeLa and MCF-7 cells were cultured on DMEM medium in a 96-well plate with 10 000 cells/200 μl cell density and incubated in a CO2 incubator at 37° for 24 h. The spent medium was aspirated and washed with 100 μl of 1X Phosphate Buffer Saline (PBS) and then treated with H2O2 of 100 μM concentration and test compounds with IC50 concentrations except for cell control in 200 μl of culture medium before keeping the cells for 24 h incubation.

Then, the medium was removed and washed with PBS. For staining, 2',7'-dichlorodihydrofluorescein diacetate (H2DCFDA) stock solution (4 mM) was diluted into Dulbecco’s Phosphate Buffered Saline (DPBS, #TL1006, Himedia) to make 10 μM fresh working solution. Finally, the cells were stained with H2DCFDA and kept for incubation for 2 h at 37° under dark. Further, the cells were observed under a confocal microscope at different time intervals (0 to 120 min) at excitation and emission wavelengths of 488 nm and 535 nm, and images were analyzed by Image J software and recorded.

Results and Discussion

The green synthesis of AgNPs by Amycolatopsis sp. strain MN235945 was primarily indicated by the colour change of the reaction mixture from colourless to brown after adding AgNO3. The UV-Vis spectrum showed an absorption maximum at 417 nm after the incubation period confirming the synthesis of biogenic AgNPs (fig. 1A and fig. 1B). The previous studies reported that the change in the colour of the reaction mixture after adding AgNO3 was due to the excitation of surface plasmon resonance phenomenon of metallic silver. Further, AgNPs synthesis was confirmed by UV-Vis. spectrum because of the optic response of AgNPs of marine Streptomyces rochei MHM13 and Streptomyces sp. GUT 21 indicated a strong surface plasmon resonance band at 410 nm[13,27].


Fig. 1: (A) Visual observation of colour of reaction mixture before and after synthesis; (B) UV-Vis. absorption spectrum of AgNPs synthesized by Amycolatopsis sp. strain MN235945.

The FTIR spectrum of AgNPs revealed absorption bands at 3290, 2930, 1726, 1635, 1351, 1026, 823, 463 and 429 cm-1, respectively (fig. 2). The strong intensity band at 3290 cm-1 was characteristic of O=H bonded alcohols, and the strong, intensive peak at 2930 cm-1 corresponded to C-H stretching alkanes. Similarly, the band at 1726 cm-1 was attributed to C=O aldehyde; 1635 cm-1 to N-H bending primary and secondary amines, and the peak at 1351 cm-1 corresponded to S=O sulfones, sulfates, and sulfonyl chlorides. The medium intensity peak at 1026 cm-1 assigned to the C-O bonded ethers, esters, and carboxylic acids. The weak intensity peak at 823 cm-1 was correlated to C-H bending aromatics, and the other weak intensity peak at 463 cm-1 corresponded to C-X bonded bromide or iodide. Similar results were observed stating the role of biological materials in the reduction and synthesis of AgNPs, where proteins and other biomaterials were present along with AgNPs as capping and stabilization components. Also the data indicated that amines, alcohols, alkanes, alkynes, amino acids, and carboxylates residues involved in the synthesis, capping and stabilization of AgNPs[28,29].


Fig. 2: FTIR spectrum analysis of AgNPs synthesized by Amycolatopsis sp. strain MN235945.

The biosynthesized AgNPs were elucidated with HR-TEM to determine the surface morphology and size of the AgNPs. HR-TEM micrograph showed polydispersed, spherical-shaped AgNPs with the smallest size of 19.40 nm (fig. 3A). The previous studies on HR-TEM analysis of biosynthesized AgNPs from Streptomyces sp. and Nocardiopsis alba supported our results, where the synthesized AgNPs size ranged from 10 to 20 nm and 20 to 60 nm, respectively. The synthesis of AgNPs from microbes depends on the concentration of metal ions and incubation period provided[30,31].


Fig. 3: Characterization of Amycolatopsis sp. strain MN235945 AgNPs; (A): HR-TEM; (B): EDX; (C): XRD and (D): Zeta potential.

The elemental composition of Amycolatopsis sp. strain MN235945 synthesized AgNPs was obtained by EDX analysis. An intense signal at 3 keV in the metallic silver region was observed as the confirmation for the AgNPs synthesis. EDX determines the abundance and distribution of specific elements present in the nanoparticles. A trace elemental mapping of AgNPs by EDX pattern was obtained for Carbon (C) (40.09 %), Oxygen (O) (38.72 %), Sodium (Na) (3.34 %), Chlorine (Cl) (5.67 %), Potassium (K) (1.82 %), and Silver (Ag) (10.37 %), as shown in fig. 3B. The strong signal energy peaks in the range of 2 to 4 keV. Similar results suggested about metallic AgNPs, which typically depicted a strong signal peak at 3 keV due to surface plasmon resonance and the weaker signals for C, O, K, and silicon, the other biomolecules that are involved in the capping of AgNPs. They also suggested that, among the different signals, the C, K and other signals may probably be due to X-ray emission from proteins, enzymes, and carbohydrates in extracts[32,33].

X-ray diffraction analysis of Amycolatopsis sp. strain MN235945 synthesized AgNPs revealed well-defined peaks for metallic crystal silver with the crystalline nature of AgNPs. The XRD pattern showed the main reflection planes at the 2? degrees of 32.16°, 46.13°, 57.36° and 76.60° respectively, corresponding to the (111), (200), (220), and (311) facets of the Bragg’s planes, suggesting the Face-Centered Cubic (FCC) nature (fig. 3C). Similarly, the XRD data showed that the AgNPs fabricated by endophytic Actinomycetes showed particle size from 19 to 35 nm with the peaks indicating the Bragg’s scattering of crystalline AgNPs with spiral structures and depicted the crystalline nature of the synthesized AgNPs[34,35].

The stability of the biosynthesized AgNPs was analyzed by zeta potential peak at -34.8 mV (fig. 3D), which suggested that the surface of the AgNPs was negatively charged and well dispersed in the medium. The higher negative values indicated higher stability of AgNPs, and zeta analysis indicated the high dispersivity and well-defined colloidal nature of the AgNPs. The obtained results agreed with the previous study, which also reported higher negative values of zeta potential and these values confirmed the repulsion among the particles and proved that they were very stable[36].

The genomic DNAwas extracted from the isolated strain, and the 16S rRNA was amplified with the help of 27F forward (5'-AGAGTTTGATCCTGGCTCAG-3') and 1492R reverse (5'-GGTTACCTTGTTACGACTT-3') primer.

The genomic 16S rDNA and the amplified 16S rDNA in comparison with the standard ladder are represented in fig. 4A and fig. 4B, respectively. The obtained sequence of 985 base pairs was submitted to the gene bank with accession number MN235945. Finally, to validate the reproducibility, the phylogenetic tree was constructed by the bootstrap analysis method using MegAlign Pro (DNASTAR Lasergene) software (fig. 5A). The colony of Amycolatopsis sp. strain MN235945 was having an ovoid structure with a rough surface and was monosporous (fig. 5B). Likewise, the biosynthesis of AgNPs from Streptomyces rochei MHM13[13], where the potent isolate was identified based on 16S rRNA gene sequencing followed by the analysis of phylogenetic tree of the isolate along with the most similar sequences obtained via BLASTn.


Fig. 4: Agarose gel electrophoresis image of Amycolatopsis sp. strain MN235945; (A) Genomic 16S rRNA gene with 1 kilobase ladder and (B) Amplified 16S rRNA gene with 1 kilobase ladder.


Fig. 5: Genotypic and Morphological characterization, (A) Phylogenetic tree and (B) SEM Image shows spore formation of Amycolatopsis sp. strain MN235945.

The antagonistic activity of synthesized AgNPs were investigated against both bacteria and fungi organisms using well diffusion method (fig. 6). The results documented that among the selected bacterial pathogens, Escherichia coli exhibited 19 mm, 19 mm, 21 mm and 22 mm of inhibition zones for 25, 50, 75, and 100 μl of AgNPs suspension; whereas, among the fungal pathogens, Alternaria alternata was found to be the most sensitive with inhibition zones of 18 mm, 19 mm, 19 mm, and 20 mm for 25, 50, 75, and 100 μl of AgNPs suspension, respectively. However, Staphylococcus aureus and Fusarium oxysporum were found to be least sensitive to the biosynthesized AgNPs among the tested microbial pathogens. The ability of the AgNPs to inhibit all tested organisms suggested that, these nanoparticles contained potential antimicrobial activity against infectious pathogens. They also suggested that the AgNPs attach to the microbial cell wall and interact with lipopolysaccharides and disrupt them. The AgNPs binds to enzymes, proteins, and DNA upon entering into the bacterial cell and lead to cell death by disrupting the cellular biochemical reactions and DNA replication mechanism of the microbial pathogens[37,38].


Fig. 6: Antimicrobial activity of AgNPs synthesized by Amycolatopsis sp. strain MN235945 against pathogenic microorganisms;

The synthesized AgNPs exhibited considerable MIC and MBC values against all the tested bacterial pathogens by inhibiting the growth of pathogenic bacteria even at low concentrations. The biogenic AgNPs showed significant bactericidal activity against pathogens and the results were showed in Table 1. Similar results from previous studies on MIC and MBC activities of microbial mediated AgNPs reported that the biological AgNPs displayed high inhibitory activity against bacterial pathogens even at low concentrations. They concluded that the AgNPs with smaller sizes provide a larger surface area for interaction with the microbial cell membrane, adding to the alterations in some primary functions of bacteria, such as permeability and cell respiration[39,40].

S No. Name of the Pathogen Std. (µg/ml) MIC (µg/ml) MBC (µg/ml)
1 Staphylococcus aureus 10±0.5 128±1.0 128±1.0
2 Enterococcus faecalis 7±0.5 64±0.57 64±0.57
3 Pseudomonas aeruginosa 10±0.76 32±1.0 64±0.76
4 Escherichia coli 5±0.36 48±1.52 48±1.0

Table 1: MIC and MBC Values of AGNPS Synthesized by Amycolatopsis Sp. Strain MN235945 against Pathogenic Microorganisms.

In vitro anticancer activity of AgNPs against HeLa and MCF-7 cell lines and the morphological changes of HeLa and MCF-7 cell lines on the addition of different concentrations of AgNPs and standard drug camptothecin were recorded using a confocal microscope. The synthesized AgNPs had dose-dependent cytotoxic effects on HeLa and MCF-7 cells in vitro (fig. 7A-fig. 7G and fig. 8A-fig. 8G) with   exhibiting   IC50 concentrations of 81.12 µg/ ml and 235.45 µg/ml against HeLa and MCF-7 cells, respectively. Similarly, previous studies conducted on the anticancer activities of AgNPs against selected cell lines reported that the AgNPs showed dose-dependent activity. The AgNPs treated cells were different from the untreated cells in cell shape, size, and other morphological details and the morphological changes in the cells including rounding or shrinking at varying degrees was a clear indication of cytotoxicity[41,42].


Fig. 7: MTT anticancer activity of Amycolatopsis sp. strain MN235945 AgNPs on HeLa cell line; (A) Untreated; (B) Standard; (C) 6.25µg/ml; (D) 12.5 µg/ml; (E) 25 µg/ml; (F) 50 µg/ml and (G) 100 µg/ml of AgNPs treatment.


Fig. 8: MTT anticancer activity of Amycolatopsis sp. strain MN235945 AgNPs on MCF-7 cell line; (A) Untreated; (B) Standard; (C) 6.25µg/ml; (D) 12.5 µg/ml; (E) 25 µg/ml; (F) 50 µg/ml and (G) 100 µg/ml of AgNPs treatment.

The ROS production was coupled with AgNPs and potentially induced cell death in HeLa and MCF-7 cell lines and untrea cells (fig. 9A-fig. 9G and fig. 10A-fig. 10G) after treatment of AgNPs at different time intervals from 0 to 120 min. The notable increase in the ROS expression level was observed with increase in concentration of AgNPs through elevating fluorescent intensity and the appearance of dissembled gaps between neighbouring cells were characteristics of apoptosis. Whereas  the fluorescent green coloured cells represented the presence of AgNPs absorbed by the cancer cells. According to the previous reports, ROS are free radicals that play a vital role in the living system by causing cell damage and cell death. AgNPs treated cells were different from the untreated cells in case of cell shape, size and other morphological details. The treated cells were somewhat granular shaped with less well-defined colony morphology and the rapidly increased ROS generation was due to the nature of surface, size, shape, and intensity of AgNPs. The overproduction of ROS induces apoptosis in several types of cancers, and cell death occurs due to an imbalance between pro and anti-oxidants levels inside the tumour cells[43-45].


Fig. 9: ROS-mediated anticancer activity of Amycolatopsis sp. strain MN235945 AgNPs on HeLa cell line, (A) 0 min; (B) 5 min; (C) 15 min; (D) 30 min; (E) 60 min; (F) 90 min and (G) 120 min of treatment time.


Fig. 10: ROS-mediated anticancer activity of Amycolatopsis sp. strain MN235945 AgNPs on MCF7 cell line, (A) 0 min; (B) 5 min; (C) 15 min; (D) 30 min; (E) 60 min; (F) 90 min and (G) 120 min of treatment time.

The present work illustrated an environmental friendly and cost effective synthesis procedure of small sized AgNPs using marine Actinomycete Amycolatopsis sp. strain MN235945. UV-Vis observation of Amycolatopsis sp. AgNPs shown absorption maximum at 417 nm, FTIR analysis revealed the presence of biomolecules involved in the capping and stabilization, and TEM data confirmed that the particles were polydispersed and spherical in shape with 19.40 nm being the smallest particle size. The EDX confirmed the elemental analysis of AgNPs; whereas, zeta potential of biosynthesized AgNPs was found at -34.8 mV and the crystalline nature was determined by XRD analysis. The microbial synthesized AgNPs showed increased antimicrobial and anticancer activity with increase in concentration. Based on these findings, the Amycolatopsis sp. strain MN235945 AgNPs may be used for valuable applications in various fields such as medicine, clinical and could also be used as anticancer agents after successful clinical test and other in vivo studies.


The authors would like to thank University Scientific Instrumentation Center (USIC), Karnatak University Dharwad, for extending instrumentation facilities and the work was supported by the University Research Scholarship (URS), Karnatak University, Dharwad .

Author contributions:

SN designed the concept and supervised the experiments. PSS carried out experimental analysis and wrote the manuscript. MPB wrote and edited the manuscript.

Statement on the welfare of animals:

This article does not contain any studies with human participants or animals performed by any of the authors.

Informed consent:

Informed consent was obtained from all individual participants included in the study.

Conflicts of interest:

The authors declare no conflict of interest.