Sustainable Exopolysaccharide Production by Rhizobium viscosum CECT908 Using Corn Steep Liquor and Sugarcane Molasses as Sole Substrates

Microbial exopolysaccharides (EPS) are promising alternatives to synthetic polymers in a variety of applications. Their high production costs, however, limit their use despite their outstanding properties. The use of low-cost substrates such as agro-industrial wastes in their production, can help to boost their market competitiveness. In this work, an alternative low-cost culture medium (CSLM) was developed for EPS production by Rhizobium viscosum CECT908, containing sugarcane molasses (60 g/L) and corn steep liquor (10 mL/L) as sole ingredients. This medium allowed the production of 6.1 ± 0.2 g EPS/L, twice the amount produced in the standard medium (Syn), whose main ingredients were glucose and yeast extract. This is the first report of EPS production by R. viscosum using agro-industrial residues as sole substrates. EPSCSLM and EPSSyn exhibited a similar carbohydrate composition, mainly 4-linked galactose, glucose and mannuronic acid. Although both EPS showed a good fit to the Herschel–Bulkley model, EPSCSLM displayed a higher yield stress and flow consistency index when compared with EPSSyn, due to its higher apparent viscosity. EPSCSLM demonstrated its potential use in Microbial Enhanced Oil Recovery by enabling the recovery of nearly 50% of the trapped oil in sand-pack column experiments using a heavy crude oil.

Microbial EPS, which can be produced from renewable resources, exhibit less environmental impact when compared with synthetic polymers, and their production is faster than those obtained from plants. Furthermore, they usually display excellent rheological properties, stability at a wide range of environmental conditions, and a broad variety of chemical structures, which provides them different physicochemical properties [3,6,[10][11][12][13][14]. Microbial EPS usually exhibit remarkable biological activities (e.g., antitumor, antimicrobial, antioxidant, anti-inflammatory, immunomodulatory or prebiotic activity) that are not present in synthetic polymers [1,7,9,15]. Therefore, some of them could be incorporated The EPS-producing strain R. viscosum CECT908 was stored at −80 • C in a synthetic medium supplemented with glycerol (15%, v/v). The composition of the synthetic medium was as follows (g/L): glucose, 25; yeast extract, 3; K 2 HPO 4 , 2; MgSO 4 .7H 2 O, 0.1; and pH 7 [30]. Erlenmeyer flasks (500 mL) containing 200 mL of synthetic medium were incubated at 28 • C and 180 rpm for 168 h after inoculation with 1% (v/v) of a pre-culture prepared from frozen stocks (grown for 24 h under the same conditions). In order to evaluate EPS production, bacterial growth and sugars consumption, samples were taken every 24 h. The apparent viscosity of the samples was measured as described in the following sections. In some cases, the EPS produced was recovered and quantified, as Polymers 2023, 15, 20 3 of 15 described below. Bacterial growth was determined by the plate count technique. Serial dilutions of culture samples were performed in a saline buffer (9 g NaCl/L) supplemented with Tween 80 (0.1 g/L) and plated in MA medium, with the following composition (g/L): glucose, 20; peptone, 5; malt extract, 3; yeast extract, 3; agar, 20; and pH 7. The plates were incubated at 28 • C and the number of cells was expressed as Log 10 colony-forming units (CFU) per mL. Sugars concentration was determined through HPLC, as described below. All experiments were performed at least in triplicate.

Alternative Culture Media
Sugarcane molasses and corn steep liquor (CSL), provided by local industries, were evaluated as low-cost substrates for EPS production. Different culture media were prepared containing different concentrations of both substrates. All media were adjusted to pH 7 using 6 M HCl or 10 M NaOH, and cultures were performed as described in the previous section. EPS production, bacterial growth and sugar consumption were evaluated as described for the synthetic medium. All assays were performed in triplicate.

Recovery and Purification of Exopolysaccharides
The culture broth samples were centrifuged (9400× g, 30 min) for cell separation. Whenever required, viscous samples were diluted with demineralized water (between three and five times) in order to reduce their viscosity before centrifugation and allow the sedimentation of the cells. The crude EPS was precipitated through the addition of hexadecyltrimethylammonium bromide (CTAB) to the cell-free supernatants, and subsequently purified as described by Novak and co-workers [31]. The purified EPS was freeze-dried, weighed, and stored at −20 • C for further studies.

Analytical Techniques
A Discovery HR1 rheometer (TA Instruments, New Castle, DE, USA), provided with a cone-plate geometry (diameter 60 mm; angle 2.006 • ; gap 0.064 mm), was used to measure the apparent viscosity (η, mPa s) and shear stress (τ, mPa) of culture broth samples, EPS and xanthan gum (Sigma-Aldrich Co., Saint Louis, MO, USA) solutions at different shear rates ( . γ, 0.1-300 s −1 ). The measurements were performed at 25 • C, and the viscosity values presented correspond to a shear rate of 1.4 s −1 , unless indicated otherwise. Each sample was analyzed in triplicate.
The concentration of sugars and lactic acid in the cell-free supernatants was determined using an HPLC system equipped with an Aminex ® HPX-87H (300 × 7.8 mm, Bio-Rad, Des Plaines, IL, USA) column coupled to an UV detector (K-2501, Knauer, Highwood, IL, USA) and a refractive index detector (RI-2031 Plus, JASCO, Oklahoma City, OK, USA). H 2 SO 4 (5 mM) was used as mobile phase (flow rate 0.6 mL/min), and the column temperature was set at 35 • C. Calibration curves prepared using pure compounds were used to calculate the concentration of different sugars and lactic acid. Chromatograms were analyzed using the software Varian Star 6 Chromatography Workstation (Varian, Palo Alto, CA, USA).

Sugars Analysis
Neutral sugars were released from EPS samples by treatment with 72% (w/w) H 2 SO 4 (3 h, room temperature), followed by hydrolysis (2 M H 2 SO 4 , 1 h, 120 • C) using a heating block. The sugars were then derivatized to their alditol acetates and analyzed using a gas chromatograph equipped with a flame ionization detector (GC-FID PerkinElmer-Clarus 400) and provided with a DB-225 column [32,33]. Samples were analyzed in duplicate.
Uronic acids (UA) were determined using a colorimetric method according to a modification [34] of the method proposed by Blumenkrantz and Asboe-Hansen [35]. Samples were prepared by pre-hydrolysis (72% (w/w) H 2 SO 4 , 3 h, room temperature) followed by hydrolysis (1 M H 2 SO 4 , 1 h, 100 • C) using a heating block. A calibration curve was prepared using D-galacturonic acid as standard. Samples were analyzed in triplicate.

Linkage Analysis of Carbohydrates
Methylation analysis was used to identify glycosidic linkages following a protocol described by Reis and co-workers [36]. Briefly, EPS were methylated using CH 3 I, dissolved in CHCl 3 :MeOH (1:1, v/v), and dialyzed against 50% EtOH. Subsequently, methylated EPS were carboxyl-reduced in order to identify the uronic acid derivatives. The obtained product was completely dried and reduced with LiAlD 4 (lithium aluminum deuteride) in dried tetrahydrofuran at 65 • C for 4 h. EtOH and water were used to destroy the remaining reagent, the pH was adjusted to neutral value (2 M H 3 PO 4 ), and further extraction was performed using CHCl 3 :MeOH (2:1, v:v). After solvent evaporation, the product obtained was hydrolyzed (trifluoroacetic acid 3 M), reduced (NaBD 4 (sodium borodeuteride)) and acetylated. The partially methylated alditol acetates (PMAAs) obtained were analyzed by gas chromatography-mass spectrometry (GC-qMS) according to Reis and co-workers [36]. For that purpose, a Shimadzu GCMS-QP2010 Ultra (Shimadzu Co., Tokyo, Japan), equipped with a HT5 (Trajan Scientific, Victoria, Australia) capillary column (30 cm length × 0.25 mm i.d., 0.1 µm film thickness), was used. Samples were dissolved in 70 µL of anhydrous acetone, and injection was performed in split mode (split ratio 2.0) with the injector operating at 250 • C. The initial temperature was set at 80 • C, and a linear increase (7.5 • C/min up to 140 • C) was applied. After standing for 5 min at 140 • C, a linear temperature increase (0.2 • C/min up to 143.2 • C) was applied, followed by a linear increase up to 250 • C (15 • C/min), standing 5 min at this temperature. Helium was used as a carrier gas (flow rate 1.84 mL/min), with a column head pressure of 124.1 kPa. The GC was connected to an Agilent 5973 mass quadrupole selective detector, operating with an electron impact mode at 70 eV, and scanning the range m/z 50-700 in a 1 s cycle in a full scan mode acquisition.

Acetylation Degree
Methyl and acetyl groups were quantified as methanol and acetic acid, respectively, as described by Nunes et al. [37]. Briefly, EPS samples (1 mg) were dissolved in water (250 µL) and sonicated (10 min) in a water bath at room temperature. 1-propanol (50 µL, 0.2%) was added to the samples as internal standard. Subsequently, 100 µL of 2 M NaOH were added to the samples and saponification was promoted by incubation at 25 • C for 1 h. The reaction was stopped by the addition of 150 µL of 2 M HCl, and the solution was filtered (0.2 µm nylon filter). Finally, the filtrate was injected in a Hewlett-Packard 5890 series II GC-FID, equipped with a DB-Wax column (J&W) (30 cm length × 0.53 mm i.d. × 1.0 mm film thickness). Hydrogen was used as the carrier gas (flow rate 6 mL/min). Calibration curves were prepared using pure compounds at concentrations between 100 and 500 mg/L. Estimated concentrations were determined by comparing the obtained peak areas with the area of the known concentration of the internal standard. Samples were prepared in duplicate, and each run was performed twice.

Oil Recovery Assays
Sand-pack columns were used to evaluate the performance of the EPS produced by R. viscosum CECT908 (grown in the optimized alternative culture medium) in MEOR. The columns, the sand and the methodology used were the same as the ones described in our previous work [2]. The viscosity of the crude oil used (η 40 • C = 496 ± 54 mPa s) was determined using a hybrid rheometer (Discovery HR1, TA Instruments, USA). Control assays were performed by injecting demineralized water or xanthan gum (Sigma-Aldrich Co., USA) solutions, instead of EPS. All assays were performed at 40 • C in triplicate.

Exopolysaccharide Production by Rhizobium viscosum CECT908 Grown in Synthetic Medium
When R. viscosum was grown in the synthetic medium, the highest apparent viscosity (3560 ± 96 mPa s) was achieved after 144 h (Figure 1), corresponding to the production of 3.0 ± 0.2 g EPS/L. The number of cells increased fast in the first 48 h, and after that remained almost stationary, achieving 8.3 × 10 9 -1.0 × 10 10 CFU/mL between 96 and 144 h. A slight decrease was observed in the pH of the culture medium along the fermentation, dropping from 7.0 to values around 6.5. After 144 h of growth, 11.3 ± 1.2 g/L of residual glucose remained in the culture medium, corresponding to a glucose consumption rate of 54.8%. However, reducing the initial concentration of glucose from 25 to 20 g/L resulted in lower apparent viscosity values (2595 ± 81 mPa s) and a lower EPS production (2.2 ± 0.3 g/L). This is in agreement with previous studies performed with R. viscosum CECT908, where the highest EPS production was achieved using 25 or 30 g/L of carbon source (glucose or xylose) [30,31]. The presence of a high concentration of residual sugar in the culture medium is in accordance with previous reports [16,18,38,39]. Contrarily, other EPS-producing strains exhibit sugar consumption rates higher than 90% [8,17,19,22,24,25].

Exopolysaccharide Production by Rhizobium viscosum CECT908 Grown in Synthetic Medium
When R. viscosum was grown in the synthetic medium, the highest apparent viscosity (3560 ± 96 mPa s) was achieved after 144 h (Figure 1), corresponding to the production of 3.0 ± 0.2 g EPS/L. The number of cells increased fast in the first 48 h, and after that remained almost stationary, achieving 8.3 × 10 9 -1.0 × 10 10 CFU/mL between 96 and 144 h. A slight decrease was observed in the pH of the culture medium along the fermentation, dropping from 7.0 to values around 6.5. After 144 h of growth, 11.3 ± 1.2 g/L of residual glucose remained in the culture medium, corresponding to a glucose consumption rate of 54.8%. However, reducing the initial concentration of glucose from 25 to 20 g/L resulted in lower apparent viscosity values (2595 ± 81 mPa s) and a lower EPS production (2.2 ± 0.3 g/L). This is in agreement with previous studies performed with R. viscosum CECT908, where the highest EPS production was achieved using 25 or 30 g/L of carbon source (glucose or xylose) [30,31]. The presence of a high concentration of residual sugar in the culture medium is in accordance with previous reports [16,18,38,39]. Contrarily, other EPSproducing strains exhibit sugar consumption rates higher than 90% [8,17,19,22,24,25].

Sugarcane Molasses as an Alternative Carbon Source for Exopolysaccharide Production
To reduce the production costs of the R. viscosum EPS, glucose was replaced by sugarcane molasses in the synthetic medium. Sugarcane molasses, which is commonly used as a carbon source in different biotechnological processes, is a residue from sugar refineries, whose exploitation is economically unfavorable [40]. The molasses used in this work contained sucrose (435 ± 8 g/kg), glucose (119 ± 5 g/kg) and fructose (51 ± 2 g/kg). Besides carbohydrates, sugarcane molasses contains metal ions (calcium, cooper, iron, magnesium, manganese, phosphorous, potassium and sodium), vitamins, organic acids and amino acids, which improve bacterial growth [8,22,38,40].

Sugarcane Molasses as an Alternative Carbon Source for Exopolysaccharide Production
To reduce the production costs of the R. viscosum EPS, glucose was replaced by sugarcane molasses in the synthetic medium. Sugarcane molasses, which is commonly used as a carbon source in different biotechnological processes, is a residue from sugar refineries, whose exploitation is economically unfavorable [40]. The molasses used in this work contained sucrose (435 ± 8 g/kg), glucose (119 ± 5 g/kg) and fructose (51 ± 2 g/kg). Besides carbohydrates, sugarcane molasses contains metal ions (calcium, cooper, iron, magnesium, manganese, phosphorous, potassium and sodium), vitamins, organic acids and amino acids, which improve bacterial growth [8,22,38,40].
Different culture media were prepared containing different concentrations of molasses (40-80 g/L). The cultures were performed as described for the synthetic medium, and EPS production was determined by measuring the apparent viscosity of the culture medium at different time intervals ( Figure 2).
As can be seen in Figure 2, the lowest concentration of molasses tested (40 g/L) resulted in a rapid increase in the apparent viscosity of the culture medium when compared with the other media, achieving its maximum after 48 h of growth (576 ± 87 mPa s). However, after that point, the apparent viscosity decreased. As the concentration of molasses increased, the time necessary to achieve the highest apparent viscosity value also increased, probably due to an adaptation of the microorganism to the substrate (precultures were performed in the synthetic medium, which contains glucose as carbon source, whereas sugarcane molasses contains glucose, fructose and sucrose, with sucrose being the most abundant sugar). With the media containing 50 and 60 g molasses/L, similar apparent viscosity values to those obtained with the synthetic medium were achieved after 144 h of growth (3389 ± 154 mPa s and 3854 ± 122 mPa s, respectively). The media containing 70 and 80 g molasses/L led to worse results, i.e., lower values of apparent viscosity. According to these results, a concentration of 60 g/L of sugarcane molasses (which corresponded to 26.1 ± 0.9 g sucrose/L, 7.2 ± 0.6 g glucose/L and 3.1 ± 0.3 g fructose/L) was selected to perform the following studies.
Polymers 2023, 15, x FOR PEER REVIEW Different culture media were prepared containing different concentrations of ses (40-80 g/L). The cultures were performed as described for the synthetic medium EPS production was determined by measuring the apparent viscosity of the cultu dium at different time intervals (Figure 2). As can be seen in Figure 2, the lowest concentration of molasses tested (40 g sulted in a rapid increase in the apparent viscosity of the culture medium when com with the other media, achieving its maximum after 48 h of growth (576 ± 87 mPa s) ever, after that point, the apparent viscosity decreased. As the concentration of mo increased, the time necessary to achieve the highest apparent viscosity value a creased, probably due to an adaptation of the microorganism to the substrate (pre-cu were performed in the synthetic medium, which contains glucose as carbon s whereas sugarcane molasses contains glucose, fructose and sucrose, with sucrose the most abundant sugar). With the media containing 50 and 60 g molasses/L, simi parent viscosity values to those obtained with the synthetic medium were achieve 144 h of growth (3389 ± 154 mPa s and 3854 ± 122 mPa s, respectively). The media co ing 70 and 80 g molasses/L led to worse results, i.e., lower values of apparent vis According to these results, a concentration of 60 g/L of sugarcane molasses (which sponded to 26.1 ± 0.9 g sucrose/L, 7.2 ± 0.6 g glucose/L and 3.1 ± 0.3 g fructose/L selected to perform the following studies. Molasses from sugar beet and sugarcane were identified as suitable carbon s for the production of xanthan gum, gellan gum, welan gum, pullulan and panto Xanthomonas campestris, Sphingomonas spp., Alcaligenes spp., Aureobasidium pullula Pantoea sp. [8,15,21,22,38,41]. Other alternative carbon sources used for the produc different EPS are summarized in Table 1. However, some of those substrates requ pretreatment (e.g., acid or enzymatic hydrolysis) to hydrolyze disaccharides or co Molasses from sugar beet and sugarcane were identified as suitable carbon sources for the production of xanthan gum, gellan gum, welan gum, pullulan and pantoan by Xanthomonas campestris, Sphingomonas spp., Alcaligenes spp., Aureobasidium pullulans and Pantoea sp. [8,15,21,22,38,41]. Other alternative carbon sources used for the production of different EPS are summarized in Table 1. However, some of those substrates required a pretreatment (e.g., acid or enzymatic hydrolysis) to hydrolyze disaccharides or complex carbohydrates into monosaccharides [13,15,18,38]. In other cases, inhibitory compounds (e.g., heavy metals, organic acids, phenolic compounds or furan aldehydes) present in those substrates had to be removed before their use as carbon source [18,38,40]. On the contrary, in our case, sugarcane molasses was used as carbon source without any previous treatment, which is crucial from an economic perspective, in order to lower production costs.

Corn Steep Liquor as an Alternative Nitrogen Source for Exopolysaccharide Production by Rhizobium viscosum CECT908
CSL, the main residue of corn starch production, was evaluated as an alternative nitrogen source for EPS production by R. viscosum. CSL is rich in proteins, amino acids, vitamins and trace elements, making it a great nutritional supplement for numerous biotechnological processes and an inexpensive substrate when compared with yeast extract [12,19,42,43]. The CSL used in this work also contained glucose (28 ± 2 g/L) and fructose (29 ± 1 g/L). In the synthetic medium containing 60 g/L of molasses instead of glucose, yeast extract was replaced by different concentrations of CSL (10,20,30,50 and 100 mL/L). As in the previous assays, EPS production was assessed by measuring the apparent viscosity of the culture medium at different time intervals. Regarding the media containing 50 and 100 mL CSL/L, the apparent viscosity did not increase during the fermentation (even after 168 h of growth), indicating that there was no production of EPS. In the media containing 20 and 30 mL CSL/L, the highest apparent viscosity values (6925 ± 128 mPa s and 4675 ± 172 mPa s, respectively) were achieved after 144 h of growth. The best result was obtained using 10 mL CSL/L, leading to a viscosity of the culture medium of 10,531 ± 292 mPa s after 144 h of growth (almost three times the value obtained using the synthetic medium).
Finally, a simplified low-cost culture medium (CSLM), containing CSL (10 mL/L) and sugarcane molasses (60 g/L) as sole ingredients, was evaluated. In this case, the apparent viscosity values obtained after 144 h of growth were similar to those achieved with the same culture medium supplemented with K 2 HPO 4 and MgSO 4 (10,697 ± 326 mPa s (Figure 3)), and the amount of EPS produced was 6.1 ± 0.2 g/L. Despite the higher EPS production achieved, the bacterial growth profile and CFU/mL obtained using this medium were similar to those observed in the synthetic medium (Figures 1 and 3). Regarding the pH, it exhibited an opposite tendency when compared with the synthetic medium, with a slight increase along the bacterial growth. After 144 h, 13.0 ± 0.7 g/L of residual sucrose remained in the culture medium, whereas the concentration of glucose and fructose was almost zero (total sugars consumption rate 64.7%). As can be seen in Table 1, EPS yields were almost the same in the synthetic and the low-cost (CSLM) medium.  The applicability of CSL as an alternative nitrogen source for the production of EPS by different microorganisms has been previously reported. CSL was successfully used to replace yeast extract in the culture medium used for the production of gellan gum by Sphingomonas paucimobilis [4], and offered the best results among different agro-industrial wastes evaluated as alternative nitrogen sources for the production of pullulan by A. pullulans RBF 4A3 [12,19]. Similar to the results herein reported for R. viscosum CECT908, concentrations of CSL higher than 1-2% were detrimental to EPS production, which was attributed to its high lactic acid content [12,19,39]. According to the HPLC analysis, the CSL used in this work contained 123 ± 18 g lactic acid/L, which is in agreement with previous reports [43].
EPS titers between 0.29 and 100 g/L have been reported for different microorganisms, with productivities between 0.19 and 100 g/(L × day) [  K 2 HPO 4 and MgSO 4 are crucial for the proper production of EPS by R. viscosum. This was demonstrated by growing R. viscosum in a synthetic medium without these salts. When MgSO 4 was removed from the synthetic medium, no significant increase in the apparent viscosity of the culture medium was observed, indicating that there was no production of EPS; the bacterial growth was lower, and the pH exhibited a similar profile when compared with the synthetic medium (data not shown). In the synthetic medium without K 2 HPO 4 , a similar bacterial growth was observed, in comparison to the synthetic medium, and the apparent viscosity achieved 2170 ± 142 mPa s after 144 h of growth; however, the pH dropped to approximately 5 (data not shown). The fact that EPS production in the low-cost medium was not affected by removing K 2 HPO 4 and MgSO 4 may be due to the presence of those elements in CSL or sugarcane molasses [38,40,42]. Phosphate is required for the activation of sugars during EPS synthesis, whereas magnesium is a co-factor of enzymes involved in the metabolism and transport of carbohydrates. Furthermore, K 2 HPO 4 acts as buffering agent [15,17,40].
The applicability of CSL as an alternative nitrogen source for the production of EPS by different microorganisms has been previously reported. CSL was successfully used to replace yeast extract in the culture medium used for the production of gellan gum by Sphingomonas paucimobilis [4], and offered the best results among different agroindustrial wastes evaluated as alternative nitrogen sources for the production of pullulan by A. pullulans RBF 4A3 [12,19]. Similar to the results herein reported for R. viscosum CECT908, concentrations of CSL higher than 1-2% were detrimental to EPS production, which was attributed to its high lactic acid content [12,19,39]. According to the HPLC analysis, the CSL used in this work contained 123 ± 18 g lactic acid/L, which is in agreement with previous reports [43].

Rheological Properties
The rheograms obtained for aqueous solutions (1 g/L) of EPS Syn (EPS produced in the synthetic medium), EPS CSLM (EPS produced in the alternative low-cost medium) and xanthan gum showed a non-Newtonian pseudoplastic behavior, characterized by a non- linear relationship between shear rate and shear stress, and an inverse relationship between apparent viscosity and shear rate (Figure 4).

Rheological Properties
The rheograms obtained for aqueous solutions (1 g/L) of EPSSyn (EPS produced in the synthetic medium), EPSCSLM (EPS produced in the alternative low-cost medium) and xanthan gum showed a non-Newtonian pseudoplastic behavior, characterized by a non-linear relationship between shear rate and shear stress, and an inverse relationship between apparent viscosity and shear rate (Figure 4).  Typically, other EPS have been reported to have this behavior. At low shear rates, EPS solutions exhibit high viscosity values because EPS molecules are arranged in intricate and intertwined aggregates. However, as the shear rate moves from low to high values, the apparent viscosity decreases as those aggregates are disorganized and EPS molecules organize themselves along the flow direction [6,8,16,20,24]. The Herschel-Bulkley model describes the relationship between shear stress and shear rate (Equation (1)): Typically, other EPS have been reported to have this behavior. At low shear rates, EPS solutions exhibit high viscosity values because EPS molecules are arranged in intricate and intertwined aggregates. However, as the shear rate moves from low to high values, the apparent viscosity decreases as those aggregates are disorganized and EPS molecules organize themselves along the flow direction [6,8,16,20,24]. The Herschel-Bulkley model describes the relationship between shear stress and shear rate (Equation (1)): where τ represents the shear stress (Pa), τ 0 is the yield stress (Pa), . γ is the shear rate (s −1 ), K is the flow consistency index (Pa s n ) and n is flow behavior index (dimensionless).
EPS CSLM and EPS Syn exhibited a good fit to the Herschel-Bulkley model (R 2 = 0.9996), and similar flow behavior indexes (0.4547 and 0.4766, Figure 4A,B). Pseudoplastic fluids are characterized by flow behavior indexes lower than 1. As expected, xanthan gum also showed a pseudoplastic behavior (n = 0.4746, Figure 4C). EPS CSLM exhibited a higher flow consistency index when compared with EPS Syn , as a result of its higher viscosity, and higher apparent viscosity values than xanthan gum at the same shear rates (Figure 4).

Exopolysaccharides Characterization
Sugars analysis showed a similar carbohydrate composition for EPS Syn and EPS CSLM , with higher amounts of galactose, followed by glucose and uronic acids, with the proportion of 1.3:1.0:0.5 (EPS CSLM ) and 1.3:1.0:0.7 (EPS Syn ) ( Table 2). R. viscosum was previously reported to produce an anionic extracellular heteropolysaccharide, whose carbohydrate composition was the same regardless of the carbon source used [26,31]. However, the ratios herein obtained are slightly different from those reported for the EPS produced by R. viscosum NRRL B-1973 grown in starch-derived sugars, which possessed an equimolar proportion of these carbohydrates [26]. When R. viscosum NRRL B-1973 was grown in glucose, xylose or xylan hydrolysate, similar molar percentages to EPS CSLM and EPS Syn were found, especially when using a xylan hydrolysate as the carbon source (1.2:1.0:0.7) [31]. This polysaccharide was previously reported to contain between 20 and 30% of the dry weight of O-acetyl groups, depending on the carbon source used [26][27][28]31]. The quantification of acetic acid ( Table 2) showed that the acetyl groups accounted for 18.4% and 21.3% of EPS CSLM and EPS Syn total weight, respectively. Table 2. Sugars composition of polysaccharides produced by Rhizobium viscosum CECT908 grown in synthetic (EPS Syn ) and low-cost medium (EPS CSLM ), and acetic acid released from them. The residues of arabinose and xylose found in EPS CSLM and mannose found in EPS Syn can be derived from the culture media, as CSL has been previously reported to contain arabinoxylans [45], and the synthetic medium contains mannoproteins from a yeast extract [46]. Methylation analysis (Table 3) demonstrated that the EPS produced have a backbone composed of (1→4)-linked-galactosyl residues, which accounts for about 50% of the glycosidic linkages, (1→4)-linked-glucosyl residues (13% for EPS CSLM and 14% for EPS Syn ) and (1→4)-linked-mannuronosyl residues (11% for EPS CSLM and 17% for EPS Syn ). This structure is in accordance with the literature, as the EPS produced by R. viscosum was previously reported to have a linear structure consisting predominantly of repeating trisaccharide units: O-(D-mannopyranosyl uronic acid-(β1→4)-O-(D-glucopyranosyl-(β1→4)-D-galactose [28]. The quantified branched residues may result from the acetyl groups that still resisted the alkaline media during methylation analysis, showing acetylation pattern mainly in glucose residues at position O-6.

Sample
The similar carbohydrate composition of EPS CSLM and EPS Syn (Table 2) does explain their different viscosities ( Figure 4A,B). The viscosity of xanthan gum is attributed to its high molecular weight (2-20 × 10 6 Da), and the rigid and ordered helical conformation of xanthan gum chains in solution [10,21,25]. The high viscosity of EPS CSLM ( Figure 4B) can be explained because anionic linear EPS molecules tend to adopt more extended conformations, due to repulsion forces between negative charges, when compared with neutral EPS. Furthermore, high acetylation degrees ( Table 2) have been associated with high viscosities [24,31].

Economic Analysis
The use of expensive nutrients (e.g., yeast extract, peptone, glucose) for EPS production results in high production costs. In order to make the production process economically viable, it is necessary to find alternative low-cost carbon and nitrogen sources. The alternative low-cost culture medium (CSLM) developed in this work for EPS production by R. viscosum CECT908, contains CSL and sugarcane molasses as the only ingredients, without additional supplements. Furthermore, both substrates were used without the need of any pretreatment, which is beneficial from an economic perspective. Table 4 shows an analysis of the EPS production costs using the synthetic and the low-cost medium. As can be seen, the use of the alternative medium reduced the cost of the nutrients necessary for the production of 1 kg of EPS more than 30 times when compared with the synthetic medium.

Oil Recovery Assays
The applicability of the EPS produced by R. viscosum CECT908 in the alternative low-cost medium (EPS CSLM ) in MEOR was assessed in sand-pack column assays using a heavy crude oil (η 40 • C = 496 ± 54 mPa s). In order to study the effect of the viscosity of the solution injected in the efficiency of the oil recovery process, aqueous solutions of EPS CSLM and xanthan gum, with apparent viscosities around 50 and 100 mPa s, were prepared. In this case, the apparent viscosity values presented correspond to a shear rate of 9.2 s −1 , as shear rates between 6 and 10 s −1 are commonly used as reference for oil reservoirs [5,6]. The sand-pack columns (280 mL) were first saturated with demineralized water, and after that with crude oil. The amount of oil retained into the columns (OOIP) was between 89 and 96 mL in the different assays, which represents between 95% and 100% of the pore volume of the columns. After the water flooding process (secondary recovery), around 50% of the OOIP was recovered ( Table 5). The residual oil entrapped into the columns (between 43 and 50 mL) was the target of the tertiary oil recovery process. EPS CSLM or xanthan gum solutions (200 mL) were injected into the columns, followed by 200 mL of demineralized water. In the control assays, the columns were flooded with 400 mL of demineralized water. As can be seen from the results obtained (Table 5), in the control assays no additional oil was recovered. However, in the assays performed with EPS CSLM , almost 50% of the entrapped oil (25-26% of the OOIP) was recovered, regardless of the viscosity of the solution injected. That could be due to the formation of a stable oil displacement front with the lowest EPS CSLM concentration tested (corresponding to an apparent viscosity of 50 mPa s), whose efficiency was not improved by increasing the viscosity of the solution injected up to 100 mPa s. Furthermore, taking into account that around 50% of the entrapped oil was recovered in these assays, in order to recover additional oil, it may be necessary to use of a combination of EPS with surfactants/and or alkalis, in order to reduce the interfacial tension of the oil/sand/water system and change the wettability of the substrate from oil-wet to water-wet [6,20,23,24]. It is important to highlight that EPS CSLM demonstrated a higher efficiency than xanthan gum at the same conditions (Table 5), which is in agreement with previous reports [2]. The shear thinning behavior of EPS CSLM makes it appropriate for use in MEOR. When it is injected into the oil well at high flow rates, it exhibits a low apparent viscosity, which reduces the injection pressure and energy consumption. Inside the oil reservoir, as the flow rate decreases, the apparent viscosity increases again, improving the sweep efficiency [2,5]. EPS CSLM performed well in terms of oil recovery when compared with other EPS. In our previous work, in sand-pack column assays performed using a heavy oil (η 40 • C = 167 ± 41 mPa s), the EPS produced by R. viscosum CECT908 grown in a synthetic medium allowed the recovery of 38% of the entrapped oil, whereas xanthan gum recovered between 30% and 32% [2]. Xu and co-workers [23] studied the applicability of welan gum in MEOR. Using a heavy oil (458 mPa s), tertiary recoveries between 34.5% and 35.7% (corresponding to final recoveries between 71% and 75%) were obtained [23]. The EPS diutan gum produced by Sphingomonas sp. allowed tertiary oil recoveries between 20% and 25% (final recoveries 60%-64% of OOIP) in assays performed using a crude oil with a viscosity of 274 mPa s [11]. In the case of WL gum (an EPS produced by Sphingomonas sp. WG) a tertiary recovery of 14.5% was achieved in sand-pack column assays (oil viscosity 300 mPa s), similar to the results obtained with HPAM (13.3%) and xanthan gum (14.8%), resulting in final recoveries between 70% and 75% [5]. Jang and co-workers [10] studied the applicability of xanthan gum in MEOR, in comparison to HPAM. Using a heavy oil (450 mPa s), final recoveries between 67% and 69% were obtained with xanthan gum, whereas in the case of HPAM, they were around 62% [10]. Table 5. Results of sand-pack column assays performed with the exopolysaccharide produced by Rhizobium viscosum CECT908 grown in the low-cost medium (EPS CSLM ) and xanthan gum. The apparent viscosity was measured at 40 • C and the values presented correspond to a shear rate of 9.2 s −1 . The results represent the average of three independent experiments ± standard deviation.

Conclusions
A low-cost culture medium was developed for EPS production by R. viscosum CECT908, using sugarcane molasses (60 g/L) and CSL (10 mL/L) as sole substrates. The amount of EPS produced using the low-cost medium (EPS CSLM ) was around 6 g/L, almost twice the amount produced using the conventional synthetic medium (EPS Syn ), which contains glucose and yeast extract. As a result, the cost of the substrates necessary to produce 1 kg of EPS was reduced almost 30 times. Although EPS CSLM and EPS Syn displayed a similar carbohydrate composition, EPS CSLM exhibited a higher viscosifying activity when compared with EPS Syn . Consequently, more studies are necessary to understand their different properties. Finally, the applicability of EPS CSLM in MEOR was demonstrated in laboratory sand-pack column assays using a heavy crude oil, where it allowed the recovery of approximately 50% of the entrapped oil, showing a better performance than xanthan gum.