Plants require a great number of elements (mac-ronutrients: N, P, K, Ca, Mg, S, C, O, H and mic-ronutrients: Fe, B, Cl, Mn, Zn, Cu, Mo, Ni) and their com-pounds for growth and development. Those elements are used to create and maintain the cells and the necessary life processes such as growth, reproduction, respiration and photosynthesis. As a part of photosynthesis, plants create various forms of polysaccharides, lipids, proteins and other organic molecules (Kirkby, 2012). For normal functioning, the plant absorbs various chemical elements from the soil, which in combination with water and carbon-dioxide form compounds (White, 2012).

Numerous elements are widespread in the soil in forms that plants cannot assimilate. Because of that, the basic precondition for a plant to uptake certain element is its bioavailability (White, 2012). Water and nitrogen are considered to be the most important factors for development of a plant (Gonzalez-Dugo et al., 2010). Plants are only able to absorb nitrogen in the form of nitrate and ammonia, while molecular form from the air remains unavailable to them. When the level of nitrogen in the plants is low vegetation is limited, leading to reduced productivity (Hassen et al., 2016). Besides that, phosphorus usually originates from insoluble phosphate rock formations, and in spite of a large amount of phosphorus in the soil (400-1200 mg/kg), only a small part of it is available to the plant for plant metabolism processes. Phosphorus deficiency may cause slower growth of the plant and reduced leaf biomass (Cakmak, 2002; Avdalovic et al., 2015). Similarly, potassium regulates enzymatic reactions, salt stress resistance, stomata functions, photosynthesis and carbohydrate transport (Perrenoud, 1990). Lack of potassium in soil may cause plant functions disorder, resulting in poor crop quality (Lawton & Cook, 1954; Wang et al., 2013). And furthermore, plant productivity is significantly influenced by the presence of other elements and plant hormones, thus, it is quite clear that every plant should be supplied with a sufficient amount of every nutrient. The long-term practice of enriching the soil through the use of chemical fertilizers has proven to be quite unfavorable for the environment and has led us to alternative solutions that will provide plants with the necessary compounds (Zaidi et al., 2015). One of the more popular approaches is the use of microorganisms that promote plant growth, and their incorporation into microbial fertilizers which, when applied to seeds, plant itself or incorporated in the ground may provide all the nutrients plant need (Mrkovacki et al., 2012).

As previously stated, PGPMs naturally inhabit the rhizosphere, favorably affect the plant, improving its productivity and resistance to pathogens (Mrkovacki et al., 2012). Some of the PGPMs, which in general can be divided into bacteria and fungi, include the following strains: A zospirillum, Azotobacter, Rhizobium, Pseudomonas, Enterobacter, Bacillus, Paenibacillus, Klebsiella, Flavobacterium, Gluconobacter, Penicillium, Trichoderma and Streptomyces (Nadeem et al., 2015). Microorganisms such as Rhizobium, Klebsiella, Clostridium, Bacillus megaterium, Penicillium sp ., Trichoderma viride im-prove growth and crop yield, while Pseudomonas au-reofaciens, Trichoderma, Streptomyces sp. may act as biocontrol agents against pests and plant disease (Abhilash et al., 2016).

Based on their interaction with the plant, plant growth promoting bacteria (PGPB) can be divided into symbiotic or free-living bacteria (Zaidi et al., 2015). They can further be divided into extracellular and intracellular. Extracellular PGPBs inhabit the space of the rhizosphere, the root surface or the intracellular space of the root cells, while the intracellular PGPBs inhabit the root cells, penetrate the cell wall and integrate with the plant, forming new organ on the plant tissue – nodule, that provides optimal conditions for the bacteria (Kiprovski, 2012; Owen et al., 2015). On the other hand, plant growth promoting fungi include arbuscular mycorrhizas (AM), ectomycorrhizae (EcM) and root fungi such as Penicillium, Trichoderma and Aspergillus. They produce organic acids and enzymes that inhibit pathogens or dissolve insoluble compounds (Owen et al., 2015).

Knowing that every plant has a defense system against pathogens, it is interesting to discuss the way plants actually detect and distinguish beneficial microbes from a pathogenic kind. It is believed that every plant has a receptor with microbe-associated molecular patterns which are the key elements in a plant-microbe communication (Finkel et al., 2017). In that process, different signaling mechanisms are involved (chemoattraction, initiation of the nodulation process, release of volatile compounds etc.) and a variety of chemical compounds (organic acids, sugar, flavonoids, volatiles) are released. Presence of a certain compound is actually signal for starting off root colonization or nodule forming process. After colonizing the plants root, bacteria start to show their beneficial effects (Lugtenberg, 2015). Beneficial effects are various and depend on a particular plant and microorganism applied (Table 1).

There is a wealth of literature covering different possibilities of inoculation of wide range of plants, even in horticulture and fungiculture (Rainey, 1991; Qin et al., 2016). Rhizobia is used by great number of commercialized fertilizers designed for legume crops, although some studies show other choices might be successful as well (Marks et al., 2015). For example, Pseudomonas aeruginosa was used to promote growth of faba beans and common beans at the same time preventing root rotting caused by Fusarium culmorum (Haddoudi et al., 2017). Cereals inoculation have been particularly studied as well. Numerous researches show that inoculation of maize or wheat provides excellent results. Different species have been tested out ( Burkholderia capacia, Bacillus subtilis Azotobacter sp ., Azospirillum sp ., Pseudomonas sp.) in a form of a single or mixed inoculum showing significant growth promotion in terms of plant's dry weight, root length and yield (Boddey et al., 1986; Bevivino et al., 1998; Gholami et al., 2009; Sachin, 2009; Yazdani et al., 2009; Rojas-Tapias et al., 2012; Kavamura et al., 2013; Mumtaz et al., 2017). Accomplished results may differ based on the potting medium used. Earlier study (Bevivino et al., 1998) shows that sand-peat/manure mixture gave better results in terms of fresh plant weight, when compared to the soil which is original bacterial inhabitant. This indicates the importance of choosing a suitable carrier and delivery system, which will be discussed later in the review.

PGPMs affect plants by increasing crop yield and plant resistance to stressful environmental conditions and pathogens (Garcia-Fraile et al., 2015). These bacteria can directly affect the plant by producing substances that can regulate growth and improve the yield. Besides, they can increase water uptake, nutrient uptake and essential elements uptake, all of them having a beneficial effect on the plant (Zhao et al., 2010; Rojas-Tapias et al., 2012; Grobelak et al., 2015; Owen et al., 2015). Indirect mechanisms include the inhibition of pathogens through the production of antibiotics and enzymes. Among that, PGPMs increase the availability of micronutrients (uptake of Fe, Zn, Se) through the processes of solubilization chelating and oxidation/reduction reactions in the soil (Abhilash et al., 2016). An overview of the mechanisms of action of certain PGPMs is shown in Table 2.

Direct PGPM mechanisms of action

The main mechanisms PGPMs use to contribute to the increase of nutrients in the soil are nitrogen fixation and phosphate solubilization, along with solubilization of other minerals. After photosynthesis, nitrogen fixation is the most important biological process in nature, enabling the circulation of nitrogen in the biosphere (Wani et al., 2016). Symbiotic bacteria from the group Rhizobium and Frankia, and non-symbiotic bacteria such as Azospirlillum sp., Azotobacter sp. and Acetobacter sp. have the ability to assimilate N ₂ from the atmosphere and convert it into NH ₃ ^- as part of a mechanism well-known as nitrogen fixation (Szilagyi-Zecchin et al., 2016). Nitrogen fixation is controlled through the amount of oxygen and the availability of nitrogen and is carried out with the help of the nitrogenase, enzyme produced by bacteria (Vijayabharathi et al., 2016). The transformation of nitrogen takes place through ammonification, nitrification, nitrogen fixation and denitrification (Bjelic, 2014).

The conversion of insoluble forms of phosphorus into forms that are more available to the plant in the rhizosphere is achieved by means of bacteria called phosphate-solubilizers (Szilagyi-Zecchin et al., 2016). Some of the PGPMs, including Pseudomonas sp., Bacillus sp., Burkholderia sp., Rhizobium sp. and Flavobacterium sp., have the ability to solubilize some insoluble phosphate compounds. The usage of these bacteria as a part of bioinoculants may enhance the assimilation of phosphate and offers numerous advantages to the direct stimulation of plant growth (Hassen et al., 2016). In some cases, bacteria from the group of Bacillus, Pseudomonas, Serratia and Streptomyces can take part in the solubilization and mineralization at the same time (Miloševic & Govedarica, 2001; Gopalakrishnan et al., 2014). Ibarra-Galeana et al. (2017) proved that Sinorhizobium meliloti, Bacillus flexus and Bacillus megaterium have the possibility to solubilize tricalcium phosphate and hydroxyapatite. During that process, some extracellular enzymes (various phosphatases) and important compounds (pH lowering organic acids, siderophores and hydroxyl ions) are released in order to dissolve the minerals. While substrate is being degraded, phosphorus is delivered into the soil (Sharma et al., 2013; Souza et al., 2015; Basu et al., 2017).

Knowing the importance of other macro- and micronutrients, it is important to research strains that will enhance their absorption from the soil. It has been recently reported (Mumtaz et al., 2017) that inoculation with Zn-solubilizing bacteria can help to enhance Zn nutrition by plants, therefore improving the growth of plant. In this particular study Bacillus aryabhattai and B. subtilis were used to inoculate maize, which resulted in better growth of the plant. On the other hand, Azosprillium brasilense is proved to be Fe-solubilizing bacteria increasing the Fe and biomass content in cucumber plants (Pii et al., 2015), which is attributed to production of siderophores and will be discussed in next section of this review.

PGPMs are also able to make phytohormones which stimulate plant growth, thus the mechanism of their activity is known as biostimulation. Some of the most important phytohormones are auxins, cytokinins, gibberellins and abscisic acid (Gopalakrishnan et al., 2014).

Auxins are plant hormones with a cardinal role to modulate the development of a plant. As much as 80% of the PGPMs can synthesize the indole acetic acid (IAA), which has an important role in the stimulation of cellular division and differentiation (Mrkovacki et al., 2012). IAA induces the occurrence of lateral roots among dicotyledons and adventive roots among monocotyledons, improves secondary thickening of the walls and an increase in xylem cells, which results in better minerals and water uptake (Hassen et al., 2016; Vijayabharathi et al., 2016). Azospirillum sp., fluorescent Pseudomonas sp., and several other PGPMs secrete IAA (Hassen et al., 2016; Tabatabaei et al., 2016).

Gibberellins take part in cellular elongation and division, as well as the internodium elongation. The mechanisms which improve plant growth through gibberellins are as yet unknown (Vijayabharathi et al., 2016). Some authors believe that gibberellins increase the density of the absorbent hairs on the root that soak up water and nutrients, which contributes to the formation of greater sized fruits, an increased number of buds, prevents the dormant stage of the bulb and stimulates parthenocarpy. The lack of gibberellins is responsible for the occurrence of dwarf plants (Gopalakrishnan et al., 2014).

Cytokinins stimulate cellular division in some plants and in some cases the development of the root and absorbent hairs on the root (Gopalakrishnan et al., 2014). In addition, they take part in the growth of plant callus and help the differentiation of the shoots (Vijayabharathi et al., 2016). Ninety percent of rhizosphere microorganisms have the ability to produce and release cytokinins, while approximately 30 compounds from the group of cytokinins that promote growth have a microbial origin. Existing data indicates that Rhizobium sp. produces cytokinins ( Gopalakrishnan et al., 2014).

Abscisic acid regulates the physiological processes in plant (Vijayabharathi et al., 2016). In part, it is synthesized in the chloroplasts, while its entire biosynthesis primarily takes place in the leaves, initiated by the stressful environmental conditions such as a lack of water and low temperatures (Gopalakrishnan et al., 2014). It helps the germination of the seed, the closing of stomata and tolerance to environmental stress (Vijayabharathi et al., 2016).

Indirect PGPM mechanisms of action

Various pathogenic bacteria, fungi and nematodes may infect the plant and thus reduce crop yield to a great extent. As previously indicated, PGPMs significantly influence the induction of plant resistance to pathogens by synthesizing various antibiotics, siderophores, cyanides or lytic enzymes (Bjelic, 2014).

One of the main mechanisms for the control of pathogens is the ability to synthesize one or more antibiotics. Many PGPMs with the ability to synthesize antibiotics also produce cyanide, which in most cases has a synergistic effect when combined with antibiotics (Glick, 2015). Furthermore, with the aim to prevail over the restricted supply of iron in the soil, some PGPMs are able to produce siderophores. Siderophores are low molecular mass organic compounds with strong chelating affinity towards ions of iron (Fe ⁺³). In presence of oxygen, most of the iron particles are only partly soluble and thus are not completely available to the living organisms (Gopalakrishnan et al., 2014). Bacterial siderophores have a positive effect on the growth of plants, functioning as a source of iron that is readily usable to the plant (Hassen et al., 2016). Certain studies have indicated that Pseudomonas, which produces siderophores, influences antifungal activity towards different pathogenic fungi (Manwar et al., 2004), while Bacillus cereus has a potential in biocontrol of rice fungi (Etesami & Alikhani, 2017). Pseudomonas strains have been studied way back in 1984 when it was proved that they inhibit growth of six fungi by virtue of siderophore production (Lockwood & Schippers, 1984). Pseudomonas putida efficiently controlled tomato foot and root tor caused by Fusarim oxysporum in laboratory experiments as well as at industrial level (Validov et al., 2009).

In addition, PGPMs have a positive effect on the characteristics of the soil itself and their consortiums are successfully used in the processes of bioremediation. This is how nutrient poor and polluted soil becomes arable and available to agricultural production, since a transformation occurs in the hydrocarbons and other pollutants into less detrimental forms (Beškoski et al., 2012). Microorganisms that effectively break down hydrocarbons and oil-based pollutants include Nocardia sp., Pseudomonas sp., Acinetobacter sp., Flavobacterium sp., Micrococcus sp., Arthrobacter sp., Corynebacterium sp., Mycobacterium sp., Bacillus sp., etc. (Milic et al., 2009; Beškoski et al., 2011). AM fungi are also studied in the phytoremediation processes, indicating their role in improving soil conditions and enhancing plant tolerance to heavy metals (Barea et al., 2005). Some studies have shown that commonly known PGPM ( Bacillus sp., Pseudomonas sp., Agrobacterium sp., etc) not only improve the plant growth, but also reduce uptake of heavy metals by plants (Ahemad, 2015; Ullah et al., 2015). For example, Microbacterium sp. successfully prevented chromium toxic effect on pea by simply reducing its bioavailability in soil (Soni et al., 2014). On the other hand, Pseudomonas putida is capable of simultaneously degrading naphthalene in soil, protecting the seed and the plant from possible lethal effect (Lugtenberg & Kamilova, 2009).

The choice of culture depends primarily on the objective of the formulation of fertilizers, that is, the effects that should be achieved, as well as the plants on which they will be applied. In addition, it is necessary to consider the complexity of the procedure for replicating the desired culture and to consider whether the final product will consist of a pure or mixed culture (Herrmann & Lesueur, 2013).

Research has shown that the greatest benefit for the plant is achieved by using mixed inoculants (Yazdani et al., 2009; García de Salamone et al., 2012; Hajnal-Jafari et al., 2012; Mrkovacki et al., 2012). The idea to study mixed inoculants came from a fact that the natural habitat of microorganisms consists of various species living at the same place. This, in turn, is connected to their close relationship with the plant and other microorganisms included in the natural processes of defense and struggle for location and/or nutrients (Owen et al., 2015). The advantage of using a mix of cultures when compared to individual strains is also demonstrated in the processes of cleaning up the environment using microorganisms through a process of bioremediation. Namely, both in the laboratory and at the industrial level, microbial units have proven to have a significantly greater effect and longer life-span in contaminated soil (Beskoski et al., 2011; Gojgic-Cvijovic et al., 2012). Moreover, mixed inoculants also participate in some of the key processes such as the humidification of anthropogenically contaminated terrains, which is how microorganisms practically prepare the soil for cormophyte growth (Miletic et al., 2014).

The medium for microbial growth and multiplication needs to be cheap, easily available and should contain the necessary nutrients. In most cases, fermentation is initiated on a liquid surface, while solid-state fermentation is usually used for producing fungi (Shaikh & Sayyed, 2015). The medium used for fermentation should be sterile. High temperatures during the process of sterilization could affect some of the thermo-degradable compounds, which could change the content of the medium and the outcome of the fermentation (Doran, 2013). To prevent this from happening continuous monitoring is required during the whole process in order to ensure the desired quality (Glick, 2015). Some of the most commonly used substrates are glucose and sucrose (as a source of carbon) and ammonium sulfate (as a source of nitrogen). Besides that, most of the bacteria require the presence of some trace elements and vitamins. For example, in the case of B. subtilis thiamine is required to start the sporulation, while addition of calcium enhances the sporulation process (Monteiro et al., 2014). When it comes to cell viability, addition of different compounds ( e.g.: polyvinylpyrrolidone – PVP or carboxymethyl cellulose – CMC) have also proven very efficient. Namely, it has been found that in many cases lysis of cells and reduction of the number of cells in the fermentation broth occurs, which is regulated by the addition of the mentioned substances (Leo Daniel et al., 2013). That is why many researchers prefer to use a chemically defined medium (Table 3) which allows them to adjust the ratio of specific substances and achieve the best result with the desired microorganism (Zhang & Greasham, 1999). Besides that, in recent years different agriculture waste materials have been applied into systems based on solid-state fermentations. It has been suggested that this method provides best quality spores at a low price and it is expected that people will soon take advantage of its potential (Vassilev et al., 2015).

Irrespective of the type of fermentation, oxygen is added to the bioreactor (usually in the form of sterile air), anti-foaming agents, as well as acids and bases for the regulation of pH values (Glick, 2015). Oxygen concentration should be on a specific level during the whole fermentation process and it is necessary to permanently provide a sufficient amount of oxygen for the growth of aerobic bacteria. Still, importation of oxygen into the bioreactor can create bubbles which can affect the cellular growth and lower the volumetric mass transfer coefficient (Garcia-Ochoa & Gomez, 2009). Since gas content is highly affected by agitation and type of gas distributor, this problem can be solved using an appropriate stirring speed (Kielbus-Rapala & Karcz, 2011). An effective sporulation and higher biomass concentration are achieved when there is an excess of oxygen. In environment limited in oxygen concentration, supplied with essential nutrients, B. subtilis has the ability to produce bioactive compounds which are highly active against phytopathogenic bacteria. In anaerobic conditions, this microorganism does not show growth, except in the case of the addition of pyruvate, when it comes to growth through fermentation and anaerobic respiration (de Carvalho et al., 2010).

Mixing is very important in every fermentation process for a variety of aspects of fermentation. Effective mixing will fasten the process, enhance mass transfer and reduce the hydraulic retention time (Kielbus-Rapala & Karcz, 2011). Mixing is also necessary to prevent thermal stratification, maintain the desired pH values, to increase contact between the substrate and microbial culture, prevent foaming and to provide uniform distribution of the substrate and microorganisms (Liu, 2012). Besides that, good mixing can prevent the accumulation of toxic metabolites in the areas of the bioreactor which are characterized by weaker mixing (Glick, 2015). Successful mixing is easily accomplished in bioreactors of a smaller size, but it represents the main problem when the extent of the fermentation rises. Large-scale operations require additional researches, since the results can vary depending on the volume of bioreactor (AL-Mashhadani et al., 2015). Adequate mixing is also providing the effective control of the oxygen concentration in the reactor (de Carvalho et al., 2010). An overview of the research related to cultivation of various PGPBs is given in Table 4.

The commercial application of microbial fertilizers depends on the development of formulations with sustainable carriers which can enable the longer viability of the applied microorganism. "Primitive" inoculants, bacterial cultures without supplemental carriers, are rarely used commercially and they can only be seen during starting experiments, since they are easy to use (Bashan et al., 2014). Considering the fact that the formulations represent the final form of the product which will be sold on the market, their function is to stabilize the microorganism, help its release onto the desired plant, protect the microorganism and increase its functionality (Shaikh & Sayyed, 2015). The choice of carrier depends on desired viability of microorganism as well as on the type of application (liquid, powder or seed coating) (Nakkeeran et al., 2005). Bacteria can also be subjected to lyophilization and stored without carriers, albeit with the application of cryoprotectants such as mannitol or microcrystalline cellulose. The addition of a carbon source or cellular protectant can increase the life span and effectiveness of the fertilizer. Glucose, sucrose, maltose, trehalose, molasses and glycerol are some of the cellular protectors that are often used (Garcia-Fraile et al., 2015). An ideal carrier should be resistant to the external environment, biodegradable, economic and easily available. It should extend the lifespan of the formulation and have a good buffer capacity (Leo Daniel et al., 2013; Garcia-Fraile et al., 2015).

In general, carriers can be divided into organic and inorganic, based on the nature of their composition. Based on their state, formulations can be liquid or solid (Nakkeeran et al., 2005). Microorganisms can be formulated in the form of concentrated dry or wet dust, granules and briquettes which are easy to store, transport and apply. Dry powder and dry granules are the best choices for spore forming microorganisms, while wet dust and granules contain metabolically active microorganisms (Ramadan et al., 2013; Mishra & Arora, 2016). On the other hand, liquid formulations contain different compounds apart from microorganisms. Those compounds protect the cell and support prolonged cellular life and resistance to environmental conditions (Herrmann & Lesueur, 2013). Liquid formulations are typically water-based, oil-based on polymer products. Polysaccharides such as resin, CMC and polyvinyl alcohol derivatives are often used to change the characteristics of the fluid in liquid formulations (Shaikh & Sayyed, 2015).

When it comes to organic carriers, peat and compost are used the most. When peat and microorganisms are mixed, microorganisms maintain their metabolic activity and in some cases continue to multiply during storage (Bashan et al., 2014; Figueiredo et al., 2016). Similar shortcomings can be cited for plant waste material which is generally not used for commercial purposes. On the other hand, sawdust and other waste material from the wood-woodworking industry have found wide application in other forms of biotechnological processes which include the use of microorganisms, such as bioremediation, where they function as carriers, but also as an alternative source of carbon and energy (Ramadan et al., 2013). Furthermore, compost can be considered as a possible carrier, especially for the production processes that include specific cells. For example, the addition of diazotrophs or phosphate-solubilizing bacteria in the compost increases the amount and availability of the nitrogen and phosphorus in the final product (Malusá et al., 2012).

Polymers are new materials among carriers for microbial fertilizers which encapsulate or "immobilize" microorganisms and release them gradually in the process of degradation (Herrmann & Lesueur, 2013). Even though they offer numerous advantages, the viability of the inoculant is still an issue. This is why the addition of nutrients into inoculant is being studied and tested to enable the prolonged life span of the microorganism (Díaz-Barrera et al., 2011). Among them, hetero copolymers excite great interest. They are the result of grafting natural products such as microbial produced levan and polystyrene, which combine the best features of both types of material, and where the final product has better features than the initial components with an increased biodegradability (Kekez et al., 2016).

Even though many researches confirm the beneficial effect of PGPMs on plants and there is an abundance of tested inoculums with various combinations of microorganisms (some of them commercially available), the results are not always consistent and in some cases unexpected (Shaikh & Sayyed, 2015; Abhilash et al., 2016; Keswani et al., 2016). Study taken in Belgium during the 1999-2000 season, tested out inoculation of winter wheat with Azospirillum brasilense and Azospirillum iraknse. Although early studies during growth season proved positive effect in terms of plant and root dry weight and number of shoots, the ultimate result was not that encouraging. At the end of the season, due to bad weathering conditions, final yield of winter wheat didn't reach its full potential. Similar results have been witnessed in Mexico, implying the main barrier to commercial application of PGPMs (Dobbelaere et al., 2001).

Experience has proven that microbial fertilizers are not accepted to a great extent by agricultural producers because it is not easy to replicate their effect on the field. It is obvious that if the inoculant is not made or applied in the appropriate manner, the useful features of the fertilizer will not be manifested (Mishra & Arora, 2016). Reduced number of viable cells and bad colonization of the root have been noted in the case of many biofertilizers available on sale. A contamination of the inoculant was also noted in many of commercially available products, which leads to a lack of trust in microbial fertilizers and influences their commercial potential (Vassilev et al., 2015). Handling these products requires attention wherefore improper use represents the main reason that such a large number of microorganisms give good results in laboratory conditions, but not in the field, and pretty much explains why the commercialization of these products is not easy (Bashan et al., 2014).

There is a proposal to determine the natural microbiome of each plant and to design microbial fertilizer especially for that specific plant, based on its needs and environment (Chebotar et al., 2015). A study about inoculation of wheat with Azospirillum sp. clearly indicates that strains isolated from wheat roots performed better in the experiment when compared to strains isolated from other places (Boddey et al., 1986). Certain authors have given a suggestion for developing fertilizers that will be enriched with different metabolites along with microorganisms, according to plants requirements (Marks et al., 2015). Also, it is considered that the biofertilizers will have a greater application in the future if we are able to develop inert material that can increase product stability, lengthen its life span and its effectiveness in the field itself (Abhilash et al., 2016). One of the ways in which these problems could be overcome is the development of the so-called "tailor-made" products, which will be structured according to the needs of the buyers and can lead to a greater price of the final product (Shaikh & Sayyed, 2015). In addition, it is interesting to note that most or researches are mainly focused on the characterization of microorganisms that are suitable for plants as well as on the further application in the soil-plant system in controlled conditions. Processes of mass multiplication and formulating procedures have been studied to a much smaller extent, even though they have the most significant importance for the effectiveness of the product (Vassilev et al., 2015).