Open access peer-reviewed chapter

Biological Synthesis of Nanoparticles Using Endophytic Microorganisms: Current Development

Written By

Omar Messaoudi and Mourad Bendahou

Submitted: 12 February 2020 Reviewed: 25 August 2020 Published: 03 October 2020

DOI: 10.5772/intechopen.93734

From the Edited Volume

Nanotechnology and the Environment

Edited by Mousumi Sen

Chapter metrics overview

1,048 Chapter Downloads

View Full Metrics

Abstract

Nanotechnology is a new emerging interdisciplinary approach created by pairing of engineering, chemical, and biological approaches. This technology produces nanoparticles using different methods of traditional physical and chemical processes; however, the outlook in this field of research is to use ecofriendly, nontoxic, and clean methods for the synthesis of nanoparticles. Biological entities, such as plants, bacteria, fungi, algae, yeast, and actinomycetes, are the best candidate to achieve this goal. Among the biological route, those involve endophtic microorganisms to reduce metallic ions into nanoparticles. This method is considered as an attractive option and can open a new horizon on the interface of biology and nanotechnology. The present chapter highlights the latest research about endophytic microorganisms and their application in the synthesis of nanoparticles, as well as the mechanisms involved in the formation of nanoparticles.

Keywords

  • endophyte microorganisms
  • green nanotechnology
  • nanoparticles

1. Introduction

Nanotechnology is a new emerging interdisciplinary approach of created by pairing of biotechnology, and nanotechnology [1]. This new technology produced nanoparticles of various types (silver, copper, zinc, gold, etc.) at the nanoscale level (less than 100 nm). Three different methods can be employed for the synthesis of nanoparticles, including, chemical, physical and biological methods. These three methods follow either the bottom-up approach, or the top-down approach for the synthesis of nanoparticles [2].

The outlook in this field of research is to use ecofriendly, nontoxic and clean method for the synthesis of nanoparticles [3]. The chemical and physical methods are generally expensive and associated with destructive effects on the environment and human health [4]. In order to counter those limitations, one of the proposed solution is the application of a novel route for producing nanoparticles based on bottom-up method, called ‘green synthesis’, which is regarded as an important tool and gaining great attention in current research. This method is based on the utilization of natural resource, such as plants, fungi, bacteria, actinomycetes, yeast and algae, to reduce the metal ions into metallic nanoparticles [5].

The green synthesis of nanoparticles offers a set number of benefits compared with physical and chemical methods, since this method is cost-effectively, eco-friendly, uses less energy and can provide nanoparticles with better defined size and morphology, with a great compatibility for pharmaceuticals, medical, agronomical and environmental applications [6].

Microbial-mediated biosynthesis of nanomaterials is one of the promising biological-based nanomanufacturing process [7]. Microorganisms can produce nanoparticles by intracellular or extracellular synthesis, according to the location where nanoparticles are formed, through enzymes or biomolecules generated by the cell activities [8]. The use of microorganisms offers different advantages over the biosynthesis of nanoparticles by plants and algae, since microorganism can be easily scale-up, and they offert the possibility to changing culture condition to obtained nanoparticles with desired shape and sizes [9].

One approach that shows immense potential is based on the biosynthesis of nanoparticles using endophytic microorganisms, which is considered as a new potential source, under explored [10]. In this chapter, we present, the latest research about nanoparticles from endophytic microorganisms.

Advertisement

2. Endophytic microorganism: bacteria and fungi

“Endophytes” is a Greek word that mean “within plant”, this term is used for microorganisms (bacteria or fungi) that dwell within plant tissues, without causing any disease, infection, or damage to the plant tissues [11]. Every plant host, intercellularly and/or extracellularly, in various spaces of plant parts including roots, leaves, stems, flowers, and seeds, one to more endophytes microorganisms [12]. To date, endophytes microorganism has been found in all plant species that exist on the earth (nearly 390,000 plants) [13]. Mutualist is the most common relationship between plants and endophytes, however, in some cases and under some conditions, the endophytes can behave as opportunistic pathogens [14].

To have a stable symbiotic relationship, the plant host provides to endophytes the necessary organic nutrient, generated through photosynthesis, for growth and multiplication [14]. On the other side the endophytes offer different beneficial effects to the host plant, this including: (i) nutrient assimilation: by synthesis of iron (Fe)-sequestering siderophores, fixation of atmospheric nitrogen, solubilization of minerals such as phosphorus [15]. (ii) Stimulation of plant growth: by secretion of plant growth regulators (PGRs), such as auxin, cytokinin, ethylene and gibberellin [16]. (iii) Protection of host plants from attack of pathogens microorganisms and insects: through secretion of various bioactive secondary metabolites as well as lytic enzymes [17].

The endophytes microorganisms can be acquired directly from the environment (horizontal transmission), or are vertically transmitted from generation to generation via seed [18]. The majority of endophytes are acquired via the first mechanism of transmission, this was confirmed through the study of the diversity of microorganisms in seeds and seedlings, raised under sterile conditions, which are typically lower than the diversity of microorganisms in plants grown in soil [19].

Endophytes are studied under two categories, bacterial endophytes and fungal endophytes [20]. The structure of the microorganism communities resides inside the plants, depends on several factors, including, the nature of soil and the plant host species [21]. To study the composition in microorganisms of endophytes, the culture-dependent methods do not allow a complete overview of the endophytic population, because the uncultured microorganisms cannot be recovered and identified using this method. However, the use of molecular approaches, including high throughput techniques of next generation sequencing (NGS), confers a rapid analysis of the composition and diversity of plant microbial endophytes communities [22]. According to the study of Hardoim et al., 2014 [14], which analyze the sequences of 16 s DNAr assigned to endophytic bacteria strains, including cultured and uncultured bacteria, he found that, 96% of analyzed sequences belong to four different cultured phyla, which is reported to be dominant in the plant environment, including: 54% Proteobacteria, 20% Actinobacteria, 16% Firmicutes, and 6% Bacteroidetes. However, 19 phyla belong to the non cultured bacteria. Furthermore, 50% of the analyzed sequences, which are the predominant endophytes strains, belong to the genera, Pseudomonas, Enterobacter, Pantoea, Stenotrophomonas, Acinetobacter, and Serratia, all these genera are member within the class of Gammaproteobacteria (Proteobacteria phylum). Other genera are also well represented whithin endophytic bacteria population, this including Streptomyces, Microbacterium, Mycobacterium, Arthrobacter, as well as Bacillus, Paenibacillus, and Staphylococcus.

Endophytic fungi are ubiquitous in plants and are mainly members of Ascomycota or their mitosporic fungi, as well as some taxa of Basidiomycota, Zygomycota, and Mucoromycota [23]. Li et al. [24], examined endophytic fungi associated with the stem and root of 10 halophytic species colonizing the Gurbantonggut desert, they obtained 36 endophytic fungal taxa, dominated by Alternaria eichhorniae, Monosporascus ibericus, and Pezizomycotina sp. 1. However, a total of 56 endophytic fungi was isolated from leave and root segments of Salvia abrotanoides at the three sites by Teimoori-Boghsani et al. [25]. The isolated strains belong to 16 different fungal genera, this including: Penicillium, Paraphoma, Phaeoacremonium, Talaromyces, Aspergillus, Psathyrella, Trichoderma, Alternaria, Thielavia, Acremonium, Fusarium, Talaromyces, Coniolariella, Paecilomyces, Simplicillium, and Monocillium. Among the obtained strains, only two isolates were recovered from the plant’s leaves (Thielavia microspore and Aspergillus sp.), while the remaining isolates were obtained from root samples.

Advertisement

3. The green nanotechnology

Nanotechnology is a rapidly growing field of science, and can be defined as the manipulation of materials at the nanometer scale or one billionth of a meter. It’s become an integral part of the biotechnology and regarded as one of the key technologies [26].

Nanotechnology produces materials which have one dimension less than 100 nm at least, these materials, called nanoparticles, can be produced using different metals, such as: gold (Au), silver (Ag), copper oxide (CuO), zinc oxide (ZnO), iron (Fe2O3), palladium (Pd), platinum (Pt), nickel oxide (NiO), magnesium oxide (MgO), selenium (Se) and titanium dioxide (TiO2) [27].

The synthesis of nanoparticles is based on two approaches: (1) top-down approach and (2) bottom-up approach (Figure 1) [28]. The first approach (top-down approach) is destructive method, based on the decomposition of larger molecule into smaller units, these unit are then converted into appropriate nanoparticles. Several physical methods are applied in this case: mechanical milling, chemical etching, sputtering, laser ablation electro-explosion [29]. The second approach (bottom-up approach), is employed in reverse to the first approach, in fact, in this case, nanoparticles are formed when atoms are self assemble together [30]. The synthesis of nanoparticles using this approach, can be carried out by several physical and chemical methods including: spinning, template support synthesis, plasma or flame spraying synthesis, laser pyrolysis, CVD, atomic or molecular condensation [31]. Biological routes can also be applied to reduce metallic ions into neutral atoms (zero valent atoms) for synthesis of nanoparticles with bottom-up approach, this method is so called green nanotechnology, in this case several biological sources, available in nature, are involved, such as: (i) utilization of microorganism (bacteria, fungi); (ii) utilization of plant extracts; (iii) utilization of microseaweeds; (iv) using enzymes and biomolecules [32, 33].

Figure 1.

Top-down and bottom-up approach.

Biological agents involved in green nanotechnology offer many benefits as compared with physical and chemical syntheses, in fact, these techniques are costly, requires higher utilization of energy, and utilize toxic chemicals that may have a disastrous effect on the environment [34]. In contrast, biological approach has several edges over chemical and physical methods for synthesis of nanoparticles, as it is low cost, eco-friendly, non-toxic, clean and can be scaled up to larger-scale synthesis with ease [35].

Biological nanoparticles, synthesized using different metal, have been applied in many fields, in fact, the silver nanoparticles are widely used in medical fields, for example Al-Sheddi et al. [36], show the potential of silver nanoparticles synthesized using an extract of Nepeta deflersiana against Human Cervical Cancer Cells (HeLA). However, Soliman et al. [37] indicate that the silver nanoparticles synthesized by the pink yeast, Rhodotorula sp. ATL72, isolated from salt marches near mediterranean sea, Egypt, exhibited strong antimicrobial activity against a wide range of Gram positive and Gram negative bacteria as well as fungi with low MIC value. Moreover, zinc and titanium nanoparticles are generally used in cosmetics fields [38]. Biological nanoparticles can also apply as sensors for various biomolecules related to environmental factors and agriculture, as well as they can also use for gene delivery and cell labeling in plants and in medicine [39].

Advertisement

4. Mechanisms of nanoparticle biosynthesis by microorganisms

Although, the number of studies which elucidate the green synthesis of nanoparticles using microorganisms, there is a little work about the mechanism and the biochemical pathway involved behind the synthesis of metal nanoparticles.

Intra and extra cellulary microbial enzymes and secondary metabolites secreted by microorganisms, play a key role in the reduction of metal ions into their respective nanoparticles. In fact, It has been found that the microorganisms when are exposed to metal ion solution, they are responding to this environmental stress by the secretion of enzymes and biomolecules that possess a reducing potential of metal salts, consequently the metal ions are detoxified to less toxic metal nanoparticles [5].

Three steps are involved in the biosynthesis of nanoparticles by microorganisms (Figure 2):

  • In the first step, metallic ions are captured on the surface of microbial cells via electrostatic interaction with the negatively charged cell wall, or they are absorbed inside the microbial cells, through cationic membrane transport systems that normally transport metabolically important cations [5, 40].

  • In the second step, metallic ions (M+) are bioreduced into zero-valent metals (M°). This reaction can be catalyzed by: (i) the active groups, such as the hydroxyl group (C-OH) or the ionized carboxyl (COO-) group, of biomolecules biosynthetized by the microorganisms having reduction capabilities., or (ii) or by microbial enzymes, such as, NADH-dependent nitrate reductase, which catalyze the reduction of silver ions to silver nanoparticles at pH 7.2, using NADH as electron source and 8-hydroxyquinoline as electron shuttle [41, 42]. As results of this reduction, the metal ions are changed from their mono- or divalent oxidation states to reduced metal ions (zero-valent states). Afterward, the nanoparticles joint to form different morphology shapes such as, spheres, hexagons, triangles, cubes, ovale, etc. [43].

  • The third step corresponding to the stabilization of nanoparticles with capping agents, to prevent further growth and agglomeration and controlling the shape and size of the biosynthesized nanoparticles [5].

Figure 2.

Mechanisms of nanoparticle synthesis.

The size of nanoparticles biosynthesize by endophytic microorganisms affect the activity, it has been proved that nanoparticles with small size provide great surface/volume ration and guarantee a good activity [44]. Different physicochemical parameters should be controlled and optimized, such as, temperature, pH, metal salt concentration, incubation period, agitation, nature and concentration of carbon and nitrogen source in culture media, to producing homogeneous nanoparticles in size and shape, with satisfied activity [38].

Advertisement

5. Nanoparticles synthetized by endophytic microorganisms

Biological methods are being a popular trend in the synthesis of metal nanoparticles. Among them, those involving saprophytic microorganisms (bacteria and fungi), which are able to turn the metal ions, from their environment, into metallic nanoparticles through enzymes and secondary metabolites generated by the cell activities. This process provides greater stability and appropriate dimensions of synthesized nonoparticules [37].

Compared with saprophytic microorganisms, the application of endophytic microorganisms has emerged as a novel research area for the green synthesis of nanoparticles. This field of research can open a new horizon, on the interface of biology and nanotechnology, for novel nanomaterials with diverse applications [45].

Different endophytic microorganisms, including fungi, bacteria and actinomycetes, can be used for the biosynthesis of nanoparticles from different metal, such as silver, gold, zinc, copper, etc. Table 1 summarizes the recent researches in this field.

PlantsEndophytesShapesSizeTypes of NPsActivityReferences
Coriandrum sativumBacillus siamensis C1Spherical25–50 nmSilverAntibacterial[46]
Allium sativumPseudomonas poae COSpherical19.8–44.9 nmSilverAntifungal[47]
Mimosa pudicaAneurinibacillus migulanusSpherical, oval, cubic, triangular~ 24.27 nmSilverAntibacterial[48]
Coffea arabicaPseudomonas fluorescens 417Spherical5–50 nmGoldAntibacterial[49]
Raphanus sativusAlternaria sp.Spherical4–30 nm.SilverAntibacterial[35]
Taxus baccataNemania sp.Spherical or ellipsoidal5–70 nmSilverAntibacterial[50]
Erythrophleum fordiiAlternaria tenuissimaSpherical15–45 nm.Zinc oxideAntimicrobial, anticancer and antioxidant[51]
Chonemorpha fragrans.Fusarium solaniSpindle40–45 nmGoldAnticancer[52]
Cinnamomum zeylanicumLasiodiplodia theobromaeSpherical to oval~ 76 nmSilverAntibacterial[53]
Chiliadenus montanusTrichoderma atrovirideSpherical10 to 15 nm.SilverAntibacterial[54]
Madhuca longifoliaPestalotia sp.Angular< 40 nmSilverAntibacterial[55]
Pinus densifloraTalaromyces purpureogenusRound to triangle~ 25 nmSilverAntimicrobial and anticancer[56]
Ocimum tenuiflorumExserohilum rostrata,Spherical10–15 nmSilverAntibacterial, antiinflammatory, and antioxidant[57]
Borszczowia aralocaspicaIsoptericola SYSU 333150Spherical11–40 nmSilverAntibacterial[58]
Oxalis corniculataStreptomyces zaomyceticus Oc-5Spherical~78 nmCopperAntimicrobial, antioxidant and anticancer[59]
Mentha longifoliaStreptomyces sp.Spherical2.3–85 nmSilverAntimicrobial[60]
Convolvulus arvensisStreptomyces capillispiralis Ca-1,Spherical3.6–59 nmCopperAntimicrobial and insecticides[61]
Ocimum sanctumStreptomyces coelicolorSpherical and ellipsoidal~25 nmMagnesiumAntimicrobial[62]

Table 1.

Biosynthesis of nanoparticles from endophytic microorganisms with their respective size and biological activity.

5.1 Nanoparticles synthesized by endophytic bacteria

Some endophytic bacteria, have developed a specific defense mechanism to overcome toxicity of metal ions, this mechanism is based on the precipitation of ions metals at the nanometer scale to produce nanoparticles [63]. It was observed that some of endophytic bacteria could survive and grow even at high metal ion concentrations. Bacteria possess such remarkable ability to reduce metal ions into nanoparticles, can be a good candidate for nanoparticles synthesis [64].

Ibrahim et al. [46, 47] reported the isolation of Bacillus siamensis C1 from Coriandrum sativum and Pseudomonas poae CO from Allium sativum, both strains produce silver nanoparticles with spherical shape and exhibited potential antibacterial, antibiofilm and antifungal activity.

Gold nanoparticles with spherical form and size range from 5 to 50 nm, has been successfully synthesized by the endophytic bacteria, Pseudomonas fluorescens 417, isolated from the plant, Coffea arabica. The synthesized gold nanoparticles show bactericidal activity against a panel of clinically significant pathogens [49]. The same author, Syed et al. [48], use the strain Aneurinibacillus migulanus, isolated from surface sterilized inner leaf segment of Mimosa pudica, for the biosynthesis of silver nanoparticles with different shapes, including, spherical, oval, cubic and triangular shapes. The particle size has been determined by Dynamic Light Scattering (DLS) method, and revealed average size of 24.27 nm. The bactericidal activity of the biosynthesis silver nanoparticles indicates interesting activity against both Gram-positive and Gram-negative pathogenic bacteria. The highest activity was observed against Pseudomonas aeruginosa, which is considered as clinically important bacteria.

5.2 Nanoparticles synthesized by endophytic fungi

In recent years, the utilization of endophytic fungi for the production of metallic nanoparticles has attracted more attention, due to their metal toleration, metal uptake and accumulation capability [65]. Compared with the other microorganisms, fungi are good machines for the synthesis of any type of metallic nanoparticles, and can provide a several advantages, such as: (i) Easy for isolation from soil or plants, compared with rare bacteria and actinomycetes, which required specific enrichment methods for isolation [56]. (ii) Secrete large amounts of metabolites and extracellular enzymes, which facilitate the reduction of metal ions into nanoparticles. (iii) Easy to scale-up, since they have a rapid growth [66] (iv). Most of the fungi have a large range of growth for pH, temperature and Nacl, which facilitate the change of culture conditions in order to produce homogeneous nanoparticles [67].

Clarance et al. [52], reported the isolation of the endophytic fungi, Fusarium solani, from the plant Chonemorpha fragrans, which is used for the biosynthesis of gold nanoparticles. The morphology of synthesized nanomaterials was found to have needled and flower like structures with spindle shape, and showed pink-ruby red colors and high peak plasmon band between 510 and 560 nm. The gold synthesized nanoparticles showed cytotoxic activity against cervical cancer cells (HeLa) (IC50: 0.8 ± 0.5 μg/mL) and human breast cancer cells (MCF-7) (IC50: 1.3 ± 0.5 μg/mL).

Abdelhakim et al. [51], use the culture filtrate of the endophytic fungi Alternaria tenuissima, isolated from Erythrophleum fordii, to produce zinc oxide nanoparticles. The shape of the biosynthesized nanoparticles was spherical and having size diameter ranges between 15 and 45 nm along with significant antimicrobial, anticancer and antioxidant activity.

The endophyte Exserohilum rostrata has been isolated from the plant Ocimum tenuiflorum by Bagur et al. [57], this strain was used for the biosynthesis of spherical silver nanoparticles with a size, range between 10 and 15 nm, and showed significant antimicrobial activity and other biological properties such as, anti-inflammatory, and antioxidant activities.

5.3 Nanoparticles synthesized by endophytic actinomycetes

Actinomycetes are Gram positive bacteria with high G + C, belong to the phylum of Actinobacteria, which is one of the largest taxonomic rank within the domain of Bacteria [68, 69]. This group of microorganisms is known by the production of a wide range of bioactive secondary metabolites. In fact, 70–80% of secondary metabolites in current clinical use, including, antibiotics, antifungals, immunosuppressives, anticancer, insecticides and antivirals, have been isolated and characterized from several species of actinomycetes, particularly from the genus Streptomyces [70].

Nanoparticles from endophytic actinobacteria is an emerging field yet to be established, in fact, when compared with fungi and the other bacteria, only few publications have been reported. Most of the articles about nanoparticles from endophytic actinomycetes, reporting the synthesis of nanoparticles using endophytes belong to the genus of Streptomyces, however, nanoparticles synthesized by rare actinobacteria have been reported in a few papers [60, 62].

The author, Hassan et al. [59, 61], publishes two papers about the utilization of endophytic Streptomyces for the biosynthesis of nanoparticles. In fact, they report the isolation of Streptomyces zaomyceticus Oc-5 and Streptomyces capillispiralis Ca-1, from the plants Oxalis corniculata and Convolvulus arvensis respectively. Both strains were used for the synthesis of copper naoparticles, which exhibited different biological activity, including, antimicrobial, antioxidant and anticancer, and insecticides.

In another study, Dong et al. [58], use a rare actinobacteria, in order to control the disease caused by Staphylococcus warneri which have a significant impact on human health. The researchers use the strain, Isoptericola SYSU 333150, isolated from the plant Borszczowia aralocaspica, for the biosynthesis of silver nanoparticle using photo-irradiation with sunlight exposition for different periods, they obtained spherical nanoparticles with a size range between, 11–40 nm, which exhibit antimicrobial activity against the pathogen S. warneri.

Several others studies confirm that nanoparticles from different metallic natures, sizes and shapes, synthesized by endophytic microorganisms, are attractive options, since they exhibited various pool of biological activities, including, antimicrobial, cytotoxic, antiinflamatory, antioxidant [35, 50, 53, 54, 55, 56, 60, 62].

Advertisement

6. Methods for the isolation of endophytic microorganism and the characterization of synthesized nanoparticles

The isolation methods of endophyte aim to obtained microorganisms reside within plant hosts without causing disease symptoms. The isolation protocol followed depend on several factors such as, the target group of endophyte microorganisms you would like to isolate (bacteria, fungi and Actinobacteria), specie of the host plant, the part of plant tissue, sampling season, culture conditions, etc. [71].

The first step consists on surface sterilization of host plant to remove all the surface-living microorganisms [72]. Several methods can be applied, among them, the plant parts will be immersed sequentially, in several solutions of sterilization, including, 70% ethanol for 5 minutes, followed by (3–10%) of sodium hypochlorite for 2 minutes, and then immersed in hydrogen peroxide (H2O2) for 1 minutes [73]. The final step of sterilization consists to rinse the different plant parts with distilled water three times, and soaked in 10% NaHCO3 to inhibit fungal growth [74].

After surface sterilization, the sterilized tissue samples are cut into small pieces of 1 cm3, under sterile conditions, and then placed on tryptic soy agar plates followed by incubation for 14 days to verify the sterilization effectiveness. Afterwards, the plant segments are grinding in sterile conditions, and then the samples are serially diluted up to 10−3 with sterile water [75]. Aliquots of 100–200 μL of the dilutions will be spread-plated onto a series of appropriate isolation media (depend on the type of endophytic microorganisms). The appeared colonies are transferred to a new culture medium to obtain a pure culture [76]. The endophytic strains are subjected to molecular identification based on sequencing of 16 s rDNA for bacteria, and 18 s r DNA for fungi.

For nanoparticles synthesis, the endophytic strains are culturing in rotating shaker under optimum culture conditions, including: appropriate culture medium, pH, temperature, agitation. After incubation, the culture is centrifuged to separate the biomass from the supernatant [48]. Both supernanant and biomass are tested for nanoparticles synthesize, in fact microorganisms are able to synthesize nanoparticles extracellularly or intracellularly (Figure 3) [77].

Figure 3.

Green synthesis of nanoparticles using endophyte microorganisms.

For extracellular synthesis of nanoparticles, the obtained supernatant is mixed with a filter-sterilized metal salt solution (e.g. AgNo3), the melange is incubated again, the color changing, of the melange after incubation, can indicate the synthesis of nanoparticles [78]. For example, for silver nanoparticles, the color changes from colorless to deep brown, whereas, for gold nanoparticles, it changes from ruby red to a deep purple color. Afterward, the precipitate of nanoparticles formed can be recovered by centrifugation, washed several times with distiled water and collected in the form of a bottom pellet [79].

For intracellular synthesis of nanoparticles, the biomass obtained after centrifugation, is washed several times with distilled water to remove the traces of culture medium, then mixed with a filter-sterilized solution of metal salt [80]. The synthesis of nanoparticles can be monitored by color change after the incubation period [81]. The naoparticules synthesized inside the cell can be released after break down the cell wall by repeated cycles of ultrasonication. The nanoparticles can be purified from cellular debris, after repeated cycles of centrifugation/washing with distilled water [82].

Physicochemical characterization of nanoparticles is performed to determine the morphology, surface area, porosity, particle size and distribution, aggregation, crystal structure (crystallinity), zeta potential, structural properties and others parameters of biosynthetized nanoparticles [40].

In order to analyse the physicochemical properties of nanoparticles, different characterization techniques are applied. This includes the following:

  • The formation of nanoparticles can be confirmed by spectra analysis of absorption in the wavelength range between 200 and 800 nm [83].

  • The morphology, size and distribution of nanoparticles can be determined by Transmission Electron Microscopy (TEM), as well as Scanning Electron Microscopy (SEM), since morphological features significantly affect the activity of nanoparticles [84].

  • The X-ray diffraction (XRD), can be used for the determination of the structural properties of nanoparticles, such as the chemical composition and the crystallinity of synthesized nanoparticles [85].

  • FTIR (Fourier transform infrared) spectroscopy, is performed to identify the functional groups present on nanoparticles [86].

  • Particle size can be estimated using, dynamic light scattering (DLS), which can be used to find the nanoparticles size at extremely low level [85].

  • Surface area characterization, including, stability and surface charge of colloidal nanoparticles are evaluated by zeta potential analysis using a Zetasizer nanomachine [87].

Advertisement

7. Conclusion

Soil microorganisms have been largely explored as a source for nanoparticle biosynthesis; however, few reports are available about the utilization of endophytic microorganisms for synthesizing nanoparticles, and therefore, it is important to focus research in this promising biological route of nanoscience. However, since most of the endophytic microorganisms are uncultivated, it’s important to concentrate researchs in the development of innovating methods for the isolation of this group of microorganisms for further advancement of green synthesis of metal nanomaterials. Additionally, the mechanisms involved in the reduction and stabilization of nanoparticles, using microorganisms, is not well defined, and more elaborated studies are needed to determine all the enzymes and biomolecules involved in the nanoparticle biosynthesis.

References

  1. 1. Porter AL, Youtie J. How interdisciplinary is nanotechnology? Journal of Nanoparticle Research. 2009;11(5):1023-1041. DOI: 10.1007/s11051-009-9607-0
  2. 2. Khan I, Saeed K, Khan I. Nanoparticles: Properties, applications and toxicities. Arabian Journal of Chemistry. 2019;12(7):908-931. DOI: 10.1016/j.arabjc.2017.05.011
  3. 3. Malik B, Pirzadah TB, Kumar M, Rehman RU. Biosynthesis of nanoparticles and their application in pharmaceutical industry. In: Prasad R, Kumar V, Kumar M, editors. Nanotechnology. Singapore: Springer; 2017. pp. 235-252. DOI: 10.1007/978-981-10-4678-0_13
  4. 4. Iravani S. Bacteria in nanoparticle synthesis: Current status and future prospects. International Scholarly Research Notices. 2014;2014:1-18. DOI: 10.1155/2014/359316
  5. 5. Singh J, Dutta T, Kim KH, Rawat M, Samddar P, Kumar P. ‘Green’ synthesis of metals and their oxide nanoparticles: Applications for environmental remediation. Journal of Nanbiotechnology. 2018;16:84. DOI: 10.1186/s12951-018-0408-4
  6. 6. Gour A, Jain NK. Advances in green synthesis of nanoparticles. Artificial Cells, Nanomedicine, and Biotechnology. 2019;47:844-851. DOI: 10.1080/21691401.2019.1577878
  7. 7. Grasso G, Zane D, Dragone R. Microbial nanotechnology: Challenges and prospects for green biocatalytic synthesis of nanoscale materials for sensoristic and biomedical applications. Nanomaterials. 2020;10:11. DOI: 10.3390/nano10010011
  8. 8. Li X, Xu H, Chen ZS, Chen G. Biosynthesis of nanoparticles by microorganisms and their applications. Journal of Nanomaterials. 2011;2011:270974. DOI: 10.1155/2011/270974
  9. 9. Yadav KK, Singh JK, Gupta N, Kumar V. A review of nanobioremediation technologies for environmental cleanup: A novel biological approach. Journal of Materials and Environmental Science. 2017;8:740-757
  10. 10. Rana KL, Kour D, Yadav N, Yadav AN. Endophytic microbes in nanotechnology: Current development, and potential biotechnology applications. In: Kumar A, Singh VK, editors. Microbial Endophytes. Cambridge, MA: Woodhead Publishing; 2020. pp. 231-262. DOI: 10.1016/B978-0-12-818734-0.00010-3
  11. 11. Nath R, Sharma G, Barooah M. Plant growth promoting endophytic fungi isolated from tea (Camellia sinensis) shrubs of Assam. Applied Ecology and Environmental Research. 2015;13:877-891. DOI: 10.15666/aeer/1303_877891
  12. 12. Glassner H, Zchori-Fein E, Yaron S, Sessitsch A, Sauer U, Compant S. Bacterial niches inside seeds of Cucumis melo L. Plant and Soil. 2017;422:1-3. DOI: 10.1007/s11104-017-3175-3
  13. 13. Strobel G, Daisy B. Bioprospecting for microbial endophytes and their natural products. Microbiology and Molecular Biology Reviews. 2003;67:491-502. DOI: 10.1128/MMBR.67.4.491-502.2003
  14. 14. Hardoim PR, Van Overbeek LS, Berg G, Pirttilä AM, Compant S, Campisano A, et al. The hidden world within plants: Ecological and evolutionary considerations for defining functioning of microbial endophytes. Microbiology and Molecular Biology Reviews. 2015;79:293-320. DOI: 10.1128/MMBR.00050-14
  15. 15. Ahemad M, Kibret M. Mechanisms and applications of plant growth promoting rhizobacteria: Current perspective. Journal of King Saud University – Science. 2014;26:1-20. DOI: 10.1016/j.jksus.2013.05.001
  16. 16. Verma A, Kukreja K, Pathak DV, Suneja S, Narula N. In vitro production of plant growth regulators (PGRs) by Azotobacter chroococcum. Indian Journal of Microbiology. 2001;41:305-307
  17. 17. Antoun H, Prévost D. Ecology of plant growth promoting rhizobacteria. In: Siddiqui ZA, editor. PGPR: Biocontrol and Biofertilization. Netherlands: Springer; 2005. pp. 1-38. DOI: 10.1007/1-4020-4152-7_1
  18. 18. Truyens S, Weyens N, Cuypers A, Vangronsveld J. Bacterial seed endophytes: Genera, vertical transmission and interaction with plants. Environmental Microbiology Reports. 2014;7:40-50. DOI: 10.1111/1758-2229.12181
  19. 19. Frank A, Saldierna-Guzmán J, Shay J. Transmission of bacterial endophytes. Microorganism. 2017;5:E70. DOI: 10.3390/microorganisms5040070
  20. 20. Monowar T, Rahman MS, Bhore SJ, Raju G, Sathasivam KV. Silver nanoparticles synthesized by using the endophytic bacterium Pantoea ananatis are promising antimicrobial agents against multidrug resistant bacteria. Molecules. 2018;23:3220. DOI: 10.3390/molecules23123220
  21. 21. Afzal I, Shinwari ZK, Sikandar S, Shahzad S. Plant beneficial endophytic bacteria: Mechanisms, diversity, host range and genetic determinants. Microbiological Research. 2019;221:36-49. DOI: 10.1016/j.micres.2019.02.001
  22. 22. Akinsanya MA, Goh JK, Lim SP, Ting AY. Metagenomics study of endophytic bacteria in Aloe vera using next-generation technology. Genomics Data. 2015;6:159-163. DOI: 10.1016/j.gdata.2015.09.004
  23. 23. Vieira ML, Johann S, Hughes FM, Rosa CA, Rosa LH. The diversity and antimicrobial activity of endophytic fungi associated with medicinal plant Baccharis trimera (Asteraceae) from the Brazilian savannah. Canadian Journal of Microbiology. 2014;60:847-856. DOI: 10.1139/cjm-2014-0449
  24. 24. Li JL, Sun X, Zheng Y, Lü PP, Wang YL, Guo LD. Diversity and community of culturable endophytic fungi from stems and roots of desert halophytes in Northwest China. MycoKeys. 2020;62:75-95. DOI: 10.3897/mycokeys.62.38923
  25. 25. Teimoori-Boghsani Y, Ganjeali A, Cernava T, Müller H, Asili J, Berg G. Endophytic fungi of native salvia abrotanoides plants reveal high taxonomic diversity and unique profiles of secondary metabolites. Frontiers in Microbiology. 2020;10:3013. DOI: 10.3389/fmicb.2019.03013
  26. 26. Abdel-Aziz SM, Prasad R, Hamed AA, Abdelraof M. Fungal nanoparticles: A novel tool for a green biotechnology? In: Prasad R, Kumar V, Kumar M, Wang S, editors. Fungal Nanobionics: Principles and Applications. Singapore: Springer; 2018. pp. 61-87. DOI: 10.1007/978-981-10-8666-3_3
  27. 27. Valavanidis A, Lachogiann T. Engineered nanomaterials for pharmaceutical and biomedical products new trends, benefits and opportunities. Pharmaceutical Bioprocessing. 2016;4(1):13-24
  28. 28. Wang Y, Xia Y. Bottom-up and top-down approaches to the synthesis of monodispersed spherical colloids of low melting-point metals. Nano Letters. 2004;(4):2047-2050. DOI: 10.1021/nl048689j
  29. 29. Priyadarshana G, Kottegoda N, Senaratne A, Karunaratne V. Synthesis of magnetite nanoparticles by top-down approach from a high purity ore. Journal of Nanomaterials. 2015;2015:1-8. DOI: 10.1155/2015/317312
  30. 30. Merkel TJ, Herlihy KP, Nunes J, Orgel RM, Rolland JP, DeSimone JM. Scalable, shape-specific, top-down fabrication methods for the synthesis of engineered colloidal particles. Langmuir. 2010;26(16):13086-13096. DOI: 10.1021/la903890h
  31. 31. Daraio C, Jin S. Synthesis and patterning methods for nanostructures useful for biological applications. In: Silva G, Parpura V, editors. Nanotechnology for Biology and Medicine. Fundamental Biomedical Technologies. New York: Springer; 2012. pp. 27-44. DOI: 10.1007/978-0-387-31296-5_2
  32. 32. Kiranmai M. Biological and non-biological synthesis of metallic nanoparticles: Scope for current pharmaceutical research. Indian Journal of Pharmaceutical Sciences. 2017;79:501-512. DOI: 10.4172/pharmaceutical-sciences.1000256
  33. 33. Saranya S, Vijayarani K, Pavithra S. Green synthesis of iron nanoparticles using aqueous extract of musa ornate flower sheath against pathogenic bacteria. Indian Journal of Pharmaceutical Sciences. 2017;79:688-694. DOI: 10.4172/pharmaceutical-sciences.1000280
  34. 34. Patra JK, Baek KH. Green nanobiotechnology: Factors affecting synthesis and characterization techniques. Journal of Nanomaterials. 2014;2014:219. DOI: 10.1155/2014/417305
  35. 35. Singh T, Jyoti K, Patnaik A, Singh A, Chauhan R, Chandel SS. Biosynthesis, characterization and antibacterial activity of silver nanoparticles using an endophytic fungal supernatant of Raphanus sativus. Journal, Genetic Engineering & Biotechnology. 2017;15:31-39. DOI: 10.1016/j.jgeb.2017.04.005
  36. 36. Al-Sheddi ES, Farshori NN, Al-Oqail MM, Al-Massarani SM, Saquib Q, Wahab R, et al. Anticancer potential of green synthesized silver nanoparticles using extract of Nepeta deflersiana against human cervical cancer cells (HeLA). Bioinorganic Chemistry and Applications. 2018;2018:9390784. DOI: 10.1155/2018/9390784
  37. 37. Soliman H, Elsayed A, Dyaa A. Antimicrobial activity of silver nanoparticles biosynthesised by Rhodotorula sp. strain ATL72. Egyptian Journal of Basic and Applied Sciences. 2018;5(3):228-233. DOI: 10.1016/j.ejbas.2018.05.005
  38. 38. Khandel P, Yadaw RK, Soni DK, Kanwar L, Shahi SK. Biogenesis of metal nanoparticles and their pharmacological applications: Present status and application prospects. Journal of Nanostructure in Chemistry. 2018;8:217-254. DOI: 10.1007/s40097-018-0267-4
  39. 39. Wang JC, Neogi P, Forciniti D. On one-dimensional self-assembly of surfactant-coated nanoparticles. The Journal of Chemical Physics. 2006;125(19):194717. DOI: 10.1063/1.2375091
  40. 40. Ghashghaei S, Emtiazi G. The methods of nanoparticle synthesis using bacteria as biological nanofactories, their mechanisms and major applications. Current Bionanotechnology. 2015;1:3-17. DOI: 10.2174/2213529401999140310104655
  41. 41. Talekar S, Ghodake V, Ghotage T, Rathod P, Deshmukh P, Nadar S, et al. Novel magnetic cross-linked enzyme aggregates (magnetic CLEAs) of alpha amylase. Bioresource Technology. 2012;123:542-547. DOI: 10.1016/j.nanoso.2016.03.002
  42. 42. Velusamy P, Kumar GV, Jeyanthi V, Das J, Pachaiappan R. Bio-inspired green nanoparticles: Synthesis, mechanism, and antibacterial application. Toxicology Research. 2016;32(2):95-102. DOI: 10.5487/TR.2016.32.2.095
  43. 43. Chokkareddy R, Redhi GG. Green synthesis of metal nanoparticles and its reaction mechanisms. In: Kanchi S, Ahmed S, editors. Green Metal Nanoparticles: Synthesis, Characterization and Their Application. Beverly, MA, USA: Scrivener Publishing LLC; 2018. pp. 113-139. DOI: 10.1002/9781119418900.ch4
  44. 44. Niño-Martínez N, Salas Orozco MF, Martínez-Castañón GA, Torres Méndez F, Ruiz F. Molecular mechanisms of bacterial resistance to metal and metal oxide nanoparticles. International Journal of Molecular Sciences. 2019;20:2808-2823. DOI: 10.3390/ijms20112808
  45. 45. Joshi CG, Danagoudar A, Poyya J, Kudva AK, Dhananjaya B. Biogenic synthesis of gold nanoparticles by marine endophytic fungus-Cladosporium cladosporioides isolated from seaweed and evaluation of their antioxidant and antimicrobial properties. Process Biochemistry. 2017;63:137-144. DOI: 10.1016/j.procbio.2017.09.008
  46. 46. Ibrahim E, Fouad H, Zhang M, Zhang Y, Qiu W, Yan C, et al. Biosynthesis of silver nanoparticles using endophytic bacteria and their role in inhibition of rice pathogenic bacteria and plant growth promotion. RSC Advances. 2019;9:29293-29299. DOI: 10.1039/C9RA04246F
  47. 47. Ibrahim E, Zhang M, Zhang Y, Hossain A, Qiu W, Chen Y, et al. Green-synthesization of silver nanoparticles using endophytic bacteria isolated from garlic and its antifungal activity against wheat Fusarium head blight pathogen Fusarium graminearum. Nanomaterials. 2020;10:219. DOI: 10.3390/nano10020219
  48. 48. Prathna TC, Lazar Mathew NC, Ashok M, Raichur AM. Biomimetic synthesis of nanoparticles: Science, technology & amp. In: Amitava M, editor. Applicability, Biomimetics Learning from Nature. Rijeka: IntechOpen; 2010. DOI: 10.5772/8776
  49. 49. Syed B, Prasad NM, Satish S. Endogenic mediated synthesis of gold nanoparticles bearing bactericidal activity. Journal of Microscopy and Ultrastructure. 2016;4:162-166. DOI: 10.1016/j.jmau.2016.01.004
  50. 50. Farsi M, Farokhi S. Biosynthesis of antibacterial silver nanoparticles by endophytic fungus Nemania sp. isolated from Taxus baccata L. (Iranian yew). Zahedan Journal of Research in Medical Sciences. 2018;20(6):e57916. DOI: 10.5812/zjrms.57916
  51. 51. Abdelhakim HK, El-Sayed ER, Rashidi FB. Biosynthesis of zinc oxide nanoparticles with antimicrobial, anticancer, antioxidant and photocatalytic activities by the endophytic Alternaria tenuissima. Journal of Applied Microbiology. 2020;128:1634-1646. DOI: 10.1111/jam.14581
  52. 52. Clarance P, Luvankar B, Sales J, Khusro A, Agastian P, Tack JC, et al. Green synthesis and characterization of gold nanoparticles using endophytic fungi Fusarium solani and its invitro anticancer and biomedical applications. Saudi Journal of Biological Sciences. 2020;27:706-712. DOI: 10.1016/j.sjbs.2019.12.026
  53. 53. Ranjani S, Shariq AM, Mohd A, Senthil KN, Ruckmani K, Hemalatha S. Synthesis, characterization and applications of endophytic fungal nanoparticles. Inorganic and Nano-Metal Chemistry. 2020;27(2):706-712. DOI: 10.1080/24701556.2020.178423
  54. 54. Abdel-Azeem A, Nada AA, O’Donovan A, Kumar TV, Elkelish A. Mycogenic silver nanoparticles from endophytic trichoderma atroviride with antimicrobial activity. Journal of Renewable Materials. 2019;7:171-185. DOI: 10.32604/jrm.2020.08960
  55. 55. Verma SK, Gond SK, Mishra A, Sharma VK, Kumar J, et al. Biofabrication of antibacterial and antioxidant silver nanoparticles (Agnps) by an endophytic fungus Pestalotia Sp. isolated from Madhuca Longifolia. Journal of Nanomaterials & Molecular Nanotechnology. 2016;5:3. DOI: 10.4172/2324-8777.1000189
  56. 56. Xiaowen H, Saravankumar K, Jin T, Myeong-Hyeon W. Mycosynthesis, characterization, anticancer and antibacterial activity of silver nanoparticles from endophytic fungus Talaromyces purpureogenus. International Journal of Nanomedicine. 2019;14:3427-3438. DOI: 10.2147/IJN.S200817
  57. 57. Bagur H, Poojari CC, Melappa G, et al. Biogenically synthesized silver nanoparticles using endophyte fungal extract of Ocimum tenuiflorum and evaluation of biomedical properties. Journal of Cluster Science. 2019;30:1-15. DOI: 10.1007/s10876-019-01731-4
  58. 58. Dong ZY, Narsing Rao MP, Xiao M, Wang HF, Hozzein WN, Chen W, et al. Antibacterial activity of silver nanoparticles against Staphylococcus warneri synthesized using endophytic bacteria by photo-irradiation. Frontiers in Microbiology. 2017;8:1090. DOI: 10.3389/fmicb.2017.01090
  59. 59. Hassan SE-D, Fouda A, Radwan AA, Salem SS, Barghoth MG, Awad MA, et al. Endophytic actinomycetes Streptomyces spp mediated biosynthesis of copper oxide nanoparticles as a promising tool for biotechnological applications. Journal of Biological Inorganic Chemistry. 2019;24(3):377-393. DOI: 10.1007/s00775-019-01654-5
  60. 60. El-Gamal MS, Salah SS, Salem S, Abdullah A. Biosynthesis, characterization, and antimicrobial activity of silver nanoparticles synthesized by endophytic Streptomyces sp. Egyptian Journal of Biotechnology. 2018;56:69-85
  61. 61. Hassan SELD, Salem SS, Fouda A, Awad MA, El-Gamal MS, Abdo AM. New approach for antimicrobial activity and bio-control of various pathogens by biosynthesized copper nanoparticles using endophytic actinomycetes. Journal of Radiation Research and Applied Science. 2018;11(3):262-270. DOI: 10.1016/j.jrras.2018.05.003
  62. 62. El-Moslamy SH. Bioprocessing strategies for cost-effective large-scale biogenic synthesis of nano-MgO from endophytic Streptomyces coelicolor strain E72 as an anti-multidrug-resistant pathogens agent. Scientific Reports. 2018;8(1):3820. DOI: 10.1038/s41598-018-22134-x
  63. 63. Iravani S, Korbekandi H, Mirmohammadi SV, Zolfaghari B. Synthesis of silver nanoparticles: Chemical, physical and biological methods. Research in Pharmaceutical Sciences. 2014;9(6):385-406
  64. 64. Syed B, Prasad MN, Satish S. Synthesis and characterization of silver nanobactericides produced by Aneurinibacillus migulanus 141, a novel endophyte inhabiting Mimosa pudica L. Arabian Journal of Chemistry. 2019;12(8):3743-3752. DOI: 10.1016/j.arabjc.2016.01.005
  65. 65. Moghaddam AB, Namvar F, Moniri M, Tahir PM, Azizi S, Mohamad R. Nanoparticles biosynthesized by fungi and yeast: A review of their preparation, properties, and medical applications. Molecules. 2015;20(9):16540-16565. DOI: 10.3390/molecules200916540
  66. 66. Shah M, Fawcett D, Sharma S, Tripathy SK, Poinern GEJ. Green of metallic synthesis nanoparticles via biological entities. Material. 2015;8:7278-7308. DOI: 10.3390/ma8115377
  67. 67. Guilger-Casagrande M, Lima R. Synthesis of silver nanoparticles mediated by fungi: A review. Frontiers in Bioengineering and Biotechnology. 2019;22(7):287. DOI: 10.3389/fbioe.2019.00287
  68. 68. Ait Barka EA, Vatsa P, Sanchez L, Gaveau-Vaillant N, Jacquard C, Klenk HP, et al. Taxonomy, physiology, and natural products of Actinobacteria. Microbiology and Molecular Biology Reviews. 2016;80:1-43. DOI: 10.1128/MMBR.00019-15
  69. 69. Messaoudi O, Sudarman E, Bendahou M, Jansen R, Stadler M, Wink J. Kenalactams A–E, polyene macrolactams isolated from nocardiopsis CG3. Journal of Natural Products. 2019;82:1081-1088. DOI: 10.1021/acs.jnatprod.8b00708
  70. 70. Messaoudi O, Bendahou M, Benamar I, Abdelwouhid DE. Identification and preliminary characterization of non-polyene antibiotics secreted by new strain of actinomycete isolated from sebkha of Kenadsa, Algeria. Asian Pacific Journal of Tropical Biomedicine. 2015;5:438-445. DOI: 10.1016/j.apjtb.2015.04.002
  71. 71. Lu Y, Chen C, Chen H, Zhang J, Chen W. Isolation and identification of endophytic fungi from Actinidia macrosperma and investigation of their bioactivities. Evidence-based Complementary and Alternative Medicine. 2012;2012:382742. DOI: 10.1155/2012/382742
  72. 72. Passari AK, Misha VK, Gupta VK, Singh BP. Chapter 1: Methods used for the recovery of culturable endophytic actinobacteria: An overview. In: Singh BP, Passari AK, Gupta VK, editors. Actinobacteria: Diversity and Biotechnological Applications: New and Future Developments in Microbial Biotechnology and Bioengineering. Amsterdam: Elsevier; 2018. pp. 1-11
  73. 73. Hallmann J, Berg G, Schulz B. Isolation procedures for endophytic microorganisms. In: Schulz BJE, Boyle CJC, Sieber TN, editors. Microbial Root Endophytes. New York: Springer; 2006. pp. 299-314
  74. 74. Nimnoi P, Pongsilp N, Lumyong S. Endophytic actinomycetes isolated from Aquilaria crassna Pierre ex Lec and screening of plant growth promoters production. World Journal of Microbiology and Biotechnology. 2010;26:193-203. DOI: 10.1007/s11274-009-0159-3
  75. 75. Taechowisan T, Lumyong S. Activity of endophytic actinomycetes from roots of Zingiber officinale and Alpinia galena against phytopathogenic fungi. Annales de Microbiologie. 2003;53:291-298
  76. 76. Passari AK, Mishra VK, Saikia R, Gupta VK, Singh BP. Isolation, abundance and phylogenetic affiliation of endophytic actinomycetes associated with medicinal plants and screening for their in vitro antimicrobial biosynthetic potential. Frontiers in Microbiology. 2015;6:273. DOI: 10.3389/fmicb.2015.00273
  77. 77. Vetchinkina E, Loshchinina E, Kupryashina M, Burov A, Pylaev T, Nikitina V. Green synthesis of nanoparticles with extracellular and intracellular extracts of basidiomycetes. PeerJ. 2018;6:e5237. DOI: 10.7717/peerj.5237
  78. 78. Karthik L, Kumar G, Vishnu-Kirthi A, Rahuman AA, Rao VB. Streptomyces sp. LK3 mediated synthesis of silver nanoparticles and its biomedical application. Bioprocess and Biosystems Engineering. 2014;37:261-267. DOI: 10.1007/s00449-013-0994-3
  79. 79. Singh H, Du J, Singh P, Yi TH. Extracellular synthesis of silver nanoparticles by pseudomonas sp. THG-LS1.4 and their antimicrobial application. Journal of Pharmaceutical Analysis. 2018;8:258-264. DOI: 10.1016/j.jpha.2018.04.004
  80. 80. Ahmad A, Mukherjee P, Senapati S, Mandal D, Khan M, Kumar R, et al. Extracellular biosynthesis of silver nanoparticles using the fungus Fusarium oxysporum. Colloids and Surfaces, B: Biointerfaces. 2003;28:313-318. DOI: 10.1002/cbic.200700592
  81. 81. Abdeen S, Geo S, Sukanya S, Praseetha PK, Dhanya RP. Biosynthesis of silver nanoparticles from Actinomycetes for therapeutic applications. International Journal of Nano Dimension. 2014;5:155-162. DOI: 10.7508/IJND.2014.02.008
  82. 82. Malik P, Shankar R, Malik V, Sharma N, Mukherjee TK. Green chemistry based benign routes for nanoparticle synthesis. Journal of Nanoparticle Research. 2014;2014:302429. DOI: 10.1155/2014/302429
  83. 83. Ingale AG, Chaudhari NA. Biogenic synthesis of nanoparticles and potential applications: An eco-friendly approach. Nanomaterials, Nanotechnology and Nanomedicine. 2013;4(2):165. DOI: 10.4172/2157-7439.1000165
  84. 84. Pal SL, Jana U, Manna PK, Mohanta GP, Manavalan R. Nanoparticle: An overview of preparation and characterization. Journal of Applied Pharmacology. 2011;1(6):228-234
  85. 85. Chauhan RPS, Gupta C, Prakash D. Methodological advancements in green nanotechnology and their applications in biological synthesis of herbal nanoparticles. International Journal of Bioassays. 2012;1(7):6-10
  86. 86. Faraji M, Yamini Y, Rezaee M. Magnetic nanoparticles: Synthesis, stabilization, functionalization, characterization, and applications. Journal of the Iranian Chemical Society. 2010;7(1):1-37. DOI: 10.1007/BF03245856
  87. 87. Otsuka H, Nagasaki Y, Kataoka K. PEGylated nanoparticles for biological and pharmaceutical applications. Advanced Drug Delivery Reviews. 2003;55(3):403-419

Written By

Omar Messaoudi and Mourad Bendahou

Submitted: 12 February 2020 Reviewed: 25 August 2020 Published: 03 October 2020