EXOPOLYSACCHARIDES PRODUCED BY THE SYMBIOTIC NITROGEN-FIXING BACTERIA OF LEGUMINOSAE ( 1 )

The process of biological nitrogen fixation (BNF), performed by symbiotic nitrogen fixing bacteria with legume species, commonly known as α and β rhizobia, provides high sustainability for the ecosystems. Its management as a biotechnology is well succeeded for improving crop yields. A remarkable example of this success is the inoculation of Brazilian soybeans with Bradyrhizobium strains. Rhizobia produce a wide diversity of chemical structures of exopolysaccharides (EPS). Although the role of EPS is relatively well studied in the process of BNF, their economic and environmental potential is not yet explored. These EPS are mostly species-specific heteropolysaccharides, which can vary according to the composition of sugars, their linkages in a single subunit, the repeating unit size and the degree of polymerization. Studies have showed that the EPS produced by rhizobia play an important role in the invasion process, infection threads formation, bacteroid and nodule development and plant defense response. These EPS also confer protection to these bacteria when exposed to environmental stresses. In general, strains of rhizobia that produce greater amounts of EPS are more tolerant to adverse conditions when compared with strains that produce less. Moreover, it is known that the EPS produced by microorganisms are widely used in various industrial activities. These compounds, also called biopolymers, provide a valid alternative for the commonly used in food industry through the development of products with identical properties or with better rheological characteristics, which can be used for new applications. The microbial EPS are also able to increase the adhesion of soil particles favoring the mechanical stability of aggregates, increasing

levels of water retention and air flows in this environment.Due to the importance of EPS, in this review we discuss the role of these compounds in the process of BNF, in the adaptation of rhizobia to environmental stresses and in the process of soil aggregation.The possible applications of these biopolymers in industry are also discussed.Index terms: Exopolysaccharides, nodules, environmental stress, soil aggregation, rhizobia.

INTRODUCTION
Nitrogen (N) is a constituent of various cellular components, such as amino acids, proteins, enzymes, nucleic acids and chlorophyll.Numerous fundamental biochemical reactions involve the presence of N, which is the fourth most-consumed nutrient of cultivated plants.In the case of some plants in the Leguminosae family, N can be fully or partially provided through the symbiosis of the legume plants with nodulating N 2 -fixing bacteria, commonly known as rhizobia.
Rhizobia belong to a particular group of microorganisms that have an enzyme complex called nitrogenase, responsible for the reduction of atmospheric nitrogen (N 2 ) to ammonia (NH 3 ).This process is known as Biological Nitrogen Fixation (BNF) and it is an important N source in agricultural systems, consequently reducing the requirements of N fertilization of legume crops.In Brazil, the best example of BNF application is the inoculation of soybean (Glycine max.(L.) Merrill) with strains of the genus Bradyrhizobium, making N fertilization completely unnecessary and ensuring greater competitiveness of this commodity in the international market (Vargas et al., 1982;Moreira & Siqueira, 2006).
The rhizobia synthesise signaling molecules that are responsible for the nodule development after the stimulation of flavonoids exuded from the roots of legumes in the soil (Broughton et al., 2000;Shorupska et al., 2006).These signaling molecules, called Nod factors, are lipochitooligosaccharides that have various chemical substitutions.Nod factors are responsible for initiating root hair curling, infection thread formation and activation of cellular division of cortical cells, resulting in the formation of the nodules (Schulze et al., 1998).Within these nodules, the bacteria differentiate into bacteroids that perform the BNF process.In response, the plants provide carbohydrates as carbon and energy source for these bacteria.Nod factors are not the only bacterial signals necessary for the establishment of a successful symbiosis.As in other interactions between bacteria and plants or animals, surface polysaccharides (SPS) are also involved.These molecules act as important signals in symbiotic processes and are present in Gramnegative bacteria as cyclic glucans, lipopolysaccharides (LPS), capsular polysaccharides (KPS) and exopolysaccharides (EPS), (Spaink, 2000;Fraysse et al., 2003;D'Haeze et al., 2004).
The cyclic glucans are usually concentrated in the periplasmic space, where they are important regulatory compounds involved in the osmotic adaptation of bacteria (Breedeveld et al., 1993).The LPS are anchored in the bacterial outer membrane and consist of three parts: lipid A, the core polysaccharide and the O-antigen polysaccharide (Madigan et al., 2004).The KPS are surface polysaccharides that form a cohesive layer adhered to the bacterial cell surface, while EPS refers to polysaccharides with little or no cell association (Fraysse et al., 2003;Lepek & D'Antuono, 2005;Shorupska et al., 2006) (Figure 1).This review is focused on the EPS and their function in the process of symbiotic BNF and the adaptation of rhizobia to environmental stresses.Brief considerations of the potential industrial applicability of these bacteria in the production of gums and the importance of these compounds in soil aggregation are also presented.
Both α and β proteobacteria are able to produce EPS that can be classified as homo and heteropolysaccharides.Homopolysaccharides are generally neutral glucans, whereas heteropolysaccharides are mostly polyanionic compounds, due to the presence of uronic acid.The EPS produced by rhizobia are mostly species or strain-specific heteropolysaccharides and are formed from repeat units of hexose residues such as glucose, galactose, mannose, rhamnose, and galacturonic and glucuronic acids with pyruvate, acetyl, succinyl and hydroxybutanoic substitutions (Lepek & D'Antuono, 2005).The EPS produced by rhizobia are highly diverse, varying in the type of sugars and their linkage in the single subunit, repeat unit size and polymerization degree, as well as non-carbohydrate decoration (van Workun et al., 1998;Laus et al., 2005;Fraysse et al., 2003;Shorupska et al., 2006).Figure 2 shows the primary structure of EPS from different rhizobia species.Among the genera of known αrhizobia, the EPS composition has only been characterized for Rhizobium, Bradyrhizobium, Sinorhizobium and Azorhizobium so far.
The chemical composition of EPS produced by other species of the Rhizobium genus has also been described, such as the EPS of R. tropici CIAT899 T (Figure 2d) composed of subunits consisting of glucose and galactose sugars at a ratio of 6:2 (Gil-Serrano et al., 1990) and the EPS produced by Rhizobium sullae strain KYGT207, which is formed from monomers of glucose, galactose and mannuronic acid at a ratio of 2:1:1 (Kaci et al., 2005).Rhizobium huakuii isolated from nodules of Astragalus sinicus produces EPS composed of glucose, galactose, ribose and glucuronic acid at a ratio of 5:1:1:1 (Hisamatsu et al., 1997) and Rhizobium sp.N613 produces a homogenous β-glucan which consists of β-D-(1-4)-glucose and β-D-(1-6)glucose at a ratio of 2:1 (Zhao et al., 2010).
Among the best-known EPS produced by rhizobia is succinoglycan (EPS I), produced by strains of Sinorhizobium meliloti (Figure 2g).This EPS is composed of an octasaccharide of repeat units containing one galactose and seven glucoses (Leigh et al., 1985;Reinhold et al., 1994).S. meliloti also has the ability to synthesise another exopolysaccharide, galactoglucan (EPS II), which is synthesized under low-phosphate conditions or when mutations in genes related to EPS I synthesis occur (Zhan et al., 1989;Zhan et al., 1991;Keller et al., 1995).EPS II is a disaccharide with repeat units composed of one glucose and one galactose (Zhan et al., 1989;Her et al., 1990) (Figure 2h).Both EPS I and II may be secreted in two different fractions, high or low molecular weight.The high molecular weight fractions of EPS I and II have hundreds to thousands of monomeric units (10 6 -10 7 Da), while the low-molecular-weight fractions consist of monomers, dimers and trimers in the case of EPS I and oligomers (15 to 20 units) in the case of EPS II (Gonzalez et al., 1996;Gonzalez et al., 1998;Wang et al., 1999;Shorupska et al., 2006).
The EPS produced by Azorhizobium caulinodans strain ORS571 T , different from other EPS produced by species of rhizobia, is a linear homosaccharide The β-rhizobia genus Burkholderia contains both associative and symbiotic species.The EPS structure of the N 2 -fixing strains of the symbiotic species B. caribensis MWAP71 is composed of glucose and thalose in a 2:1 ratio (Vanhaverbeke et al., 2001).As an example of the EPS described for associative species of N 2 -fixing Burkholderia, we can cite the B. kuruensis strain M130, which produces two distinct EPS, EPS A and EPS B. EPS A is composed of rhamnose, glucose and glucuronic acid at a ratio of 2:2:1, whereas EPS B is a mixture of two polymers of hepta or octasaccharide repeat units composed of rhamnose, galactose, glucuronic acid and glucose at a ratio of 2:2:2:1 or 2:2:2:2 (Mattos et al., 2001;Hallack et al., 2010).B. tropica Ppe8 is not actually a valid species, but a study of the composition of its EPS revealed that it is formed by subunits composed of rhamnose, glucose and glucuronic acid at a ratio of 2:2:1 (Serrato et al., 2008).
A wide variety of chemical structures of different rhizobia species were described, however, the chemical composition of the EPS of some genera such as Mesorhizobium have not been determined yet.The chemical characterization of the EPS of other rhizobia species is still needed, since the characterization of these compounds is highly relevant from an economic and agricultural point of view.It should also be emphasized that these studies dealt mainly with strains from temperate regions, which are adapted to quite different weather and soil conditions from those in tropical regions.
adhesion to root surface, root hair curling, infection thread formation (in root hairs), formation of nodule meristem, nodule development and differentiation, release of rhizobia from infection threads, their division and differentiation into bacteroids, development of nitrogenase, biochemical and physiological functions associated with N 2 fixation and maintenance of nodule function (Sprent, 1989).
The biological functions of EPS in rhizobiumlegume symbiosis are related to different stages of plant infection by the bacterium.It has already been shown that these compounds are essential for the effective establishment of the symbiosis between Rhizobium sp.NGR234 and Leucaena leucocephala or Macroptilium atropurpureum.Mutant strains deficient in EPS production were unable to promote the formation of efficient nodules on these different hosts, and the ability to induce functional nodules with these mutants was restored by adding purified EPS from the parental strain (Djordjevic et al., 1987).EPS production is also indispensable in the nodule formation process by M. tianshanense, and no nodules were formed when EPS mutant strains were inoculated on roots of Glycyrrhiza uralensis (Wang et al., 2008).
A mutation in R. leguminosarum bv.trifolii 24.1 for EPS production (exo -mutants) formed inefficient nodules in Trifolium pratense plants (Skorupska et al., 1995), and the EPS of R. leguminosarum bv.viciae ANU843 was necessary to induce root hair curling and infection thread formation in V. sativa (van Workun et al., 1998).Inoculation with exo -mutants of R. leguminosarum RBL5523 on the roots of V. sativa subsp.nigra also blocked the infection thread formation, which was aborted soon after initiation of the infection process (Laus et al., 2004(Laus et al., , 2005)).The co-inoculation of mutant exo -Nod + mutants with exo + Nod -mutants restored the nodule development process in Rhizobium bacteria, demonstrating the importance of EPS in the nodulation process (van Workun et al., 1998;Laus et al., 2005).
The influence of EPS on root hair curling and bacteria invasion into the nodule was assessed with different strains mutated for EPS production (exo -), using S. meliloti Rm1021 symbiosis with Medicago sativa plants.Strains with the exo -phenotype were not capable of nodulating these plants efficiently (Leigh et al., 1985;Battisti et al., 1992;Urzainqui & Walker, 1992).The addition of small EPS quantities produced by wild strains during inoculation with exo -mutants allowed the formation of functional nodules.The addition of low-molecular weight EPS I (succinoglycan) at the moment of inoculation of exo -mutants of S. meliloti Rm1021 led to the formation of a nodule morphology similar to the wild type strain, with the presence of a large quantity of bacteroids (Battisti et al., 1992;Urzainqui & Walker, 1992).
A mutant of S. meliloti Rm2011 unable to produce EPS I only induced the formation of pseudonodules that did not contain an infection thread or bacteroids in M. sativa (Niehaus et al., 1993).An intact structure of the EPS I of S. meliloti Rm1021 is required for the initial infection thread formation and elongation (Cheng & Walker, 1998), suggesting that the EPS functions as a signaling molecule that recognizes complex receptors present in plants.A EPS I mutant of S. meliloti CXM1-118 inoculated into M. sativa and M. trunculata plants formed small, irregularly shaped and inefficient nodules that were formed three to four days after those induced by the parental strain (Zatovskaya et al., 2007).Electron microscopy analysis of these nodules revealed the presence of highly vacuolated cells that contained a reduced number of bacteroids.
In the case of S. meliloti Rm1021, EPS II is also involved in the formation of nodules that fix N 2 efficiently, overcoming the symbiotic defects of strains deficient in the production of EPS I, which are able to functionally replace succinoglycan (Glazebrook & Walker, 1989;Gonzalez et al., 1996).Moreover, the addition of low-molecular-weight EPS II to mutants deficient in the production of EPS I and II enabled the process of N 2 fixation, producing nodules morphologically indistinguishable from those produced by the wild type strain (Gonzalez et al., 1996).Also, the symbiotically active fraction of EPS II (lowmolecular-weight fraction) is shown to be a critical factor for biofilm formation and root colonization.Thus, the ability of S. meliloti Rm1021 to properly attach to root surfaces and form biofilms conferred by the synthesis of EPS may embody the main function of these symbiotically essential molecules (Rinaudi & González, 2009).
The EPS also play a fundamental role in the initial stages of the symbiotic interaction between Bradyrhizobium japonicum 110spc4 and Glycine max in preventing the defense response of the host plant.EPS mutant strains (exo -) of B. japonicum stimulated the accumulation of phytoalexins (defense substances produced by plants) in the early stages of interaction with Glycine max.After 72 h of incubation, the levels of phytoalexins produced by the plants were 10-fold higher than in plants inoculated with the wild type strain (Parniske et al., 1993(Parniske et al., , 1994)).
Exo -mutants of S. meliloti Rm2011, when inoculated on M. sativa, formed pseudonodules that induced an alteration in the defense response of the plants, with increased wall thickness of the cortical cells and an accumulation of phenolic compounds in the cells of these nodules (Niehaus et al., 1993).In the symbiosis of R. leguminosarum bv.trifolli 24.1 with T. pratense, EPS-deficient mutants induced the accumulation of phenolic compounds and necrosis in the cortical cells of the host plant, which indicates a plant defense reaction in response to the infection process (Shorupska et al., 1995).In mutants that produced small amounts of EPS, the defense reaction of the plant was not as strong; infection threads were formed, but resulted in the development of irregularly shaped bacteroids and an electron-dense cytoplasm, which are both signs of degeneration (Bialek et al., 1995).
In the Azorhizobium caulinodans ORS571 T -Sesbania rostrata symbiosis, mutants deficient in EPS production were unable to penetrate the tissues of the host plant due to the loss of protection by EPS upon exposure to H 2 O 2 , produced by Sesbania rostrata as a defense mechanism (D' Haeze et al., 2004).
The function of EPS in the determination of rhizobia-host plant specificity is still very controversial (Shorupska et al., 2006).Van Workun et al. (1998) demonstrated that exo -mutants of R. leguminosarum bv.viciae RBL5523 inoculated into V. sativa can overcome the lack of EPS production when homologous EPS (structurally similar), but not heterologous EPS (structurally different) are added, suggesting that there are some structural requirements for EPS to function as a signaling molecule in the process of symbiosis.A hybrid strain of Rhizobium sp NGR234 containing the genes of S. meliloti for the production of EPS I was capable of inducing the formation of nodules in L. leucocephala plants, which however were not able to fix N 2 , indicating that the EPS structure is essential for the formation of efficient nodules (Gray et al., 1991).
In co-inoculation experiments using the RBL5833 exo -strain of R. leguminosarum with other species of EPS-producing bacteria (Agrobacterium tumefaciens LBA4301, Rhizobium NGR234, R. leguminosarum bv.trifolii ANU845 and LPR5045, R. tropici CIAT899 T , S. meliloti RCR2011) in V. sativa roots, nodules were formed only on roots inoculated with rhizobia producing EPS homologs (R. leguminosarum bv.trifolii ANU845 and LPR5045) and with rhizobia producing similar EPS (R. tropici CIAT899 T ).However, the transformation of heterologous strains with the symbiotic pRL1J1 Sym plasmid of R. leguminosarum enabled these strains to form efficient nodules in V. sativa plants, which indicates that the specificity of N 2 -fixing bacteria is not determined exclusively by the EPS structure (Laus et al., 2005).
Considering that a limited number of rhizobia species deficient in EPS production were investigated for co-inoculation with non-homologous EPS-producing species, the hypothesis that EPS are involved in specificity to the host plant cannot be confirmed.Therefore, it is not possible to relate EPS with specificity of N 2 -fixing bacteria and legumes.

EXOPOLYSACCHARIDES IN THE PROCESS OF RHIZOBIA ADAPTATION TO LIMITING ENVIRONMENTAL CONDITIONS
For the establishment of the symbiosis between rhizobia and legumes, in addition to the requirements for recognition of specific chemical signals between the symbionts, the environmental conditions must be adequate for the development of this interaction.In tropical regions it is common to find highly acidic soils associated with toxic Al, salinity, low levels of Ca and P, high temperatures, and other types of stresses.Most arable soils have low pH (< 5.0) contributing to reduction in nutrient availability such as Ca 2+ and Mg 2+ and increasing the concentrations of toxic elements such as Al 3+ and Mn 2+ (Ribeiro et al., 1999).Phosphorus rarely exceeds 5.0 mg dm -3 , generally ranging from 1.2 to 1.5 mg dm -3 (Mello et al., 1983).According to the classes of interpretation of P availability, these levels are very low (Ribeiro et al., 1999).Moreover, the soil surface layer can reach temperatures of around 40 °C (Hafeez et al., 1991).Soils with these characteristics may not only limit plant growth, but the survival of rhizobia in the soil, its infection of the plant and the process of BNF as well.
As described above, the EPS produced by rhizobia are very diverse in composition and chemical structure.Besides, under normal cultivation conditions, there is great variability in the production of EPS by rhizobia strains, both quantitatively and qualitatively.The strains with high levels of EPS production tend to be more tolerant to acidic conditions and salinity than strains that produce low EPS levels (Cunningham & Munns, 1984;Eaglesham et al., 1987;Xavier et al., 1998;Freitas et al., 2007;Xavier et al., 2007).In the case of saline stress, the EPS surrounds the bacterial cells, decreasing the cell surface contact with the saline medium and increasing cell resistance to the osmotic effect (Elsheikh & Wood, 1990).
The strains BR 29 and SEMIA 587 of Bradyrhizobium elkanii, recommended as soybean inoculants, produce greater amount of EPS when grown in acidic conditions than when cultivated at a neutral pH (Barberi et al. 2004;Miguel & Moreira, 2001).The same trend of increased production of EPS under acidic conditions and with limited Ca 2+ was observed in the strain USDA 3187 of Bradyrhizobium sp.(Macció et al., 2002).
The limitation of some nutrients, e.g., Ca and P, can also lead to increased EPS production by certain rhizobia strains.In these cases, the increased EPS production is considered an adaptation mechanism of these bacteria (Barberi et al., 2004;Macció et al., 2002).Thus, the EPS synthesis by rhizobia can also be regulated by the culture conditions.
As previously mentioned, Sinorhizobium meliloti produces two types of EPS, and the concentration of phosphate in the medium regulates the production of one type of EPS at the expense of the other.Under low-phosphate conditions EPS II predominates, and the colonies of these bacteria have a more mucoid morphology.Under normal conditions, S. meliloti produces EPS I, with less mucoid colonies (Zhan et al., 1991;Mendrygal & Gonzalez, 2000).
However, abiotic stresses do not always induce greater production of EPS by rhizobia strains.This was observed for S. meliloti strains grown under acidic conditions at low Ca 2+ concentrations.Under these conditions, the limitation of Ca 2+ in the culture medium drastically reduced the production of EPS by the strains (Dilworth et al., 1999;Delavechia et al., 2003).
The different rhizobium genera differ in EPS production when the strains are cultivated under different environmental conditions, causing alterations in the production and chemical composition of these compounds.The species or strain-specific EPS substances are essential for the establishment and effectiveness of the symbiosis between rhizobia and legumes, and it is important to understand the influence of these characteristics on the nodulation process.
Studies on EPS I and II produced by S. meliloti were performed in order to determine the function of these two compounds during nodulation of M. sativa.It was observed that EPS I is more efficient in mediating the invasion processes, although both EPS act in the process of M. sativa nodulation (Pellock et al., 2000).These authors report that the ability of S. meliloti to produce two types of EPS and their nodulation process represents a competitive advantage of this strain, since even under limiting environmental conditions the process of nodulation and N 2 fixation is not affected.
Due to their predominantly anionic nature, the EPS have the capacity to strongly interact with metal cations and play an important role in the sequestration or immobilization of these ions in the environment (De Philippis & Vincenzini, 1998).Despite the increase in EPS production in response to heavy metals studied in other bacterial species, few studies on rhizobia have been performed (Santamaría et al., 2003).EPS produced by Bradyrhizobium (Chamaecytisus) BGA-1 and Bradyrhizobium japonicum USDA 110 in the presence of solutions of Fe 3+ , Al 3+ and Th 4+ form a gelatinous precipitate composed of EPS bound to these metals (Corzo et al., 1994;Santamaría et al., 2003;Diaz-Marrero et al., 2004).The EPS of Rhizobium etli is also able to bind to metal ions, and is able to rapidly adhere to Mn 2+ and Pb 2+ (Foster et al., 2000).The complexation of Cd 2+ by the bacterium S. meliloti can be also the result of the attachment of this ion to extracellular polymeric substances and the amount of Cd 2+ bound to the EPS increases at high Cd 2+ concentrations (Slaveykova et al., 2010), suggesting a potential application of this biopolymer in the field of bioremediation.

OF RHIZOBIUM EPS
EPS produced by some microorganism species are widely used in various industrial activities.These compounds, also called biopolymers, are hydrosoluble gums with the ability to form gels and viscous solutions in an aqueous medium.
Microbial biopolymers vary greatly in their composition and consequently in their physical and chemical properties.Due to this wide diversity in both structure and physical properties (high viscosity, networks of intermolecular cohesive properties) the applications of these compounds is broad in the food, pharmaceutical, petroleum, cosmetic, textile, paint industry and agricultural products (Bryers, 1993).
Dextran, xanthan and gellan produced by the bacteria Leuconostoc spp., Xanthomonas spp.and Sphingmonas elodea respectively, are still among the few microbial polysaccharides marketed on a large scale, and these compounds are very important in the gum market.The structure of these polysaccharides is rather varied.Xanthan is composed of glucose, mannose and glucuronic acid at a ratio of 2:2:1.Dextran is a homopolysaccharide composed of glucose molecules, while gellan is a heteropolysaccharide consisting of glucuronic acid, glucose and rhamnose with glycerate and acetate groups in its structure.Economically, xanthan is the most important microbial polysaccharide, with a worldwide production of about 40 to 50 thousand tons/year and a value of about 270 million U.S. dollars annually.The annual demand is estimated to increase at a continuous rate of 5 to 10 % (Pradella, 2006).Table 2 shows the main examples of bacterial EPS applied in various industrial activities.
It is economically attractive to search for new polysaccharide-producing microorganisms.The production of large quantities is a challenge being met by several research groups, as microbial biopolymers can be produced in large quantities and fermentation offers the advantage of controlled production.This eliminates the problems found in the production of polymers by plants and algae, e.g., problems with harvesting, climate conditions or marine pollution (Sutherland, 2001).
The atmospheric N 2 fixing bacteria (NFB) can be found as both free-living organisms and in association or symbiosis (e.g.rhizobium-legumes).Studies on commercial EPS applications are more advanced for the free-living NFB, e.g., clairana produced by Beijerinckia sp.(Moreira et al., 2003) and the alginate produced by Azotobacter vinelandii (Garcia-Cruz et al., 2008).
Since there are no studies on the commercial production of gum by rhizobia, these can be considered unexplored sources of microbial polysaccharides, highly promising for industrial applications.These bacteria have high morphological, physiological, genetic and phylogenetic diversity, which can be a valuable source for the screening of strains with target properties.Furthermore, they are not pathogenic and produce large amounts of EPS.In figure 3 we illustrate the appearance of colonies characterized by R. Bras. Ci. Solo, 35:657-671, 2011 aggregation process is related to several factors, such as the physical properties, climatic conditions and biological activities in the soil (Materechera et al., 1994;Bezzate et al., 2000).
The action of microorganisms, notably fungi and bacteria, in the process of soil particle aggregation is principally related to the EPS production by these organisms (Alami et al., 2000).Microbial EPS can increase the adhesion of soil particles to plant roots and the mechanical stability of rhizospherical soils, besides increasing the level of water retention in this environment (Chenu & Roberson, 1996;Amellal et al., 1998).
The inoculation of wheat (Triticum durum L.) with the associative bacterium Paenibacillus polymyxa, selected by its ability to fix N 2 , resulted in a 57 % increase of the soil mass that adhered to the roots and an increased frequency of aggregates with sizes between 0.2 and 2 mm due to EPS production (levan), which contributed to the aggregation of this soil (Gouzou et al., 1993;Bezzate et al., 2000).The same effect on wheat was also observed after inoculation with other associative species.Inoculation of wheat seedlings in soil with 24 % water content with Pantoea aglomerans resulted in an increase in the adhesion of soil particles to the roots: 140 mg of soil adhered to 1 mg of roots in the inoculated treatment compared to 90 mg of soil that adhered in the control treatment.There was also a significant increase in the macroporosity of the inoculated soil (diameters of 10 to 30 μm) compared to the uninoculated control (Amellal et al., 1998).
The effect of inoculation of clay soils with the diazotrophic cyanobacterium Nostoc spp.resulted in an increased incidence of porosity in the inoculated soils (30 %) compared with the control soil without inoculation (5 %).Electron microscopy analysis allowed the visualization of the primary soil aggregation that resulted from the interaction of the secreted EPS with soil particles (Falchini et al., 1996).These cyanobacteria can establish symbiosis with species of fungi, bryophytes, gymnosperms, and high gum production on solid medium, and the precipitation of EPS from strains of Mesorhizobium plurifarium BR3804 and R. tropici CIAT899 T , recommended by MAPA (Ministério da Agricultura, Pecuária e Abastecimento) as inoculants for the species Chamaecrista ensiformis and Phaseolus vulgaris, respectively, demonstrating the high potential of these strains for the production of these biopolymers.

ROLE OF EPS IN SOIL AGGREGATION
Soil aggregation is essentially related to suitable physical conditions underlying plant growth.The  angiosperms or live freely in the soil.The EPS of Nostoc ssp.contributes not only to the soil biochemical properties but also to soil fertility, once the EPS produced by this cyanobacterium increases the soil C pool as carbohydrates (Maqubela et al., 2009).Also, the water retained in the EPS matrix reduces evaporation losses and potentially increases the waterholding capacity of the soil (Mager, 2010).
Some studies relating the production of EPS by strains of rhizobia and soil aggregation have also been described.Inoculation of a Rhizobium sp.strain into Triticum durum L. plants significantly increased the percentage of aggregates with a diameter of 1.6 to 2 mm, and the water stability in this fraction was 42 ± 5 % in the inoculated treatments compared with 30 ± 4 % in the control (Kaci et al., 2005).Another strain of Rhizobium sp., promoting growth of Helianthus annuus L. provided a significant increase in the volume of macro pores (diameter from 12 to 60 μm) in soil inoculated with this bacterium.Under water stress, the soil structure around the root system changed, which avoided negative effects of water deficit on the growth of the inoculated plants (Alami et al., 2000).In another study it was observed that EPS synthesis in Rhizobium sp.YAS34 is also decisive for the colonization of the basal part of the root system and that it increases the stability of root-adhering soil on Arabidopsis thaliana and Brassica napus roots (Santaella et al., 2008).
Conformational studies of the structure of EPS from Burkholderia caribensis MWAP71 demonstrated that this strain produces an EPS responsible for aggregation by the adsorption capacity to mineral surfaces and the adhesive properties of this biopolymer (Vanhaverbeke et al., 2003).
Although little attention has been paid to the influence of microorganisms in the process of soil aggregation, particularly to bacteria-producing EPS, microbial EPS are important biological factors that influence the soil structure formation.These compounds contribute to the stability and aggregation of particles and are potential agents for improving the structural quality of agricultural soil.Thus, the magnitude of such effects should be quantified, to evaluate the feasibility of its management for improving soil physical conditions.

FINAL CONSIDERATIONS
The BNF process based on the legume-Rhizobium symbiosis leads to a high sustainability of agricultural systems.BNF increases soil fertility and organic matter levels and reduces the need for N fertilization, resulting in both economic and environmental benefits.Despite all data available in the literature about the possible roles of EPS in the symbiosis establishment and functioning, the exact role of these compounds in the process is not yet completely understood, and further studies on the signaling mechanisms is required.Previous research of the role of EPS in nodulation and BNF based on the study of mutant strains for EPS production was focused mainly on the genera Rhizobium and Sinorhizobium, while the understanding of these processes in other species is scarce or absent.Thus, research and comparisons among the wide range of other genera are necessary.
Although there is evidence of strain-and speciesspecificity, EPS production by rhizobia is regulated by environmental conditions which, in some cases, increases the ability to adapt to various stress conditions.Thus, studies related to the role of EPS in the process of adaptation of these bacteria to various edaphic and climate conditions are particularly important, since EPS affect the survival and functionality of the rhizobia strains.
In recent years, the industrial demand for bacterial EPS (biopolymers) has grown significantly.These compounds are widely applicable in various fields, due to their diverse structural and physico-chemical properties.Bacterial EPS offer several advantages, such as the potential for controlled, high-speed production with higher yield and greater purity and consistency than alternative sources.Nevertheless, information on rhizobial EPS is not available, representing a wide range of unexploited possibilities.
EPS also offer a potencial application in agriculture due to it adhesive properties and it ability to form gels that promote the adhesion of soil particles, forming stable aggregates that contribute to better plant growth and development.Although the role of bacterial EPS in soil aggregation is recognized, little information is available in the literature about the specific action of known bacteria and possible methods of management.
Considering that none of the α and β-rhizobia were shown to be pathogenic so far, they can be generally characterized as an unexplored source of microbial EPS with great potential in industrial applications and as stabilizing soil agents.Furthermore, the role of these compounds in stress adaptation may be an important criterion for the selection of inoculant strains to raise plant productivity by BNF under different soil and climatic conditions.The biodiversity of rhizobia in tropical soils represents a vast and unexplored field calling for research in this area.

Figure 3 .
Figure 3. (a) Colonies of the M. plurifarium BR3804 strain, grown in 79 medium with bromothymol blue; (b) the biopolymer produced by M. plurifarium BR3804 after precipitation with ethanol (1.44 g dry weight EPS/L of medium) after 72 h of culture; (c) colonies of R. tropici CIAT899 T strain, grown in 79 medium with bromothymol blue; (d) biopolymer produced by R. tropici CIAT899 T after precipitation with ethanol (3.0 g dry weight EPS/L of medium) after 72 h of culture.