Characterization, antioxidant and anticoagulant properties of exopolysaccharide from marine microalgae

The sulfated exopolysaccharide extracted from marine microalgae attracted considerable attention from both the nutraceutical and pharmaceutical industries. In the present study biomass of five marine microalgae were screened to find strains with high capacity for the production of sulfated exopolysaccharides. The anticoagulant and antioxidant activities of extracted sulfated polysaccharides were evaluated using activated partial thromboplastin time (aPTT), prothrombin time (PT), DPPH and ABTS assays, respectively. The sulfated polysaccharides extracted from Picochlorum sp. showed a strong DPPH scavenging effect with 85% antioxidant activity. The sulfated polysaccharides of Chlorella sorokiniana, Chlorella sp. (L2) and Chlorella sp. (D1) scavenged more than 90% of the ABTS radicals. However, the sulfated polysaccharide extracted from Chlorella sorokiniana, and Chlorella sp. (N4) showed anticoagulant properties. The dual anticoagulant-antioxidant activities in Chlorella sorokiniana could be explained by the combination of various factors including sulfate content and their binding site, monosaccharide residue and glycoside bond which are involved in the polysaccharide’s bioactivity. Sulfated exopolysaccharides (sPS) were extracted from marine green microalgae by the heated acid extraction method. sPS with the higher sulfate/sugar ratio presented potent ABTS radical scavenging activity. Some of the sPS revealed anticoagulant effects in activated partial thromboplastin time (aPTT) and prothrombin time (PT) assays. Sulfated exopolysaccharides (sPS) were extracted from marine green microalgae by the heated acid extraction method. sPS with the higher sulfate/sugar ratio presented potent ABTS radical scavenging activity. Some of the sPS revealed anticoagulant effects in activated partial thromboplastin time (aPTT) and prothrombin time (PT) assays.


Introduction
There is a remarkable focus on the development of value-added functional food products with healthpromoting properties and improved nutrition from the new natural marine resources (Galasso et al. 2019;Bernaerts et al. 2019). The wide diversity in the biochemical composition of marine organisms represents a rich source of valuable metabolites. Marine valuable bioactive compounds such as microalgae exopolysaccharides (EPS) are known as novel and interesting resources for the pharmaceutical and food industry (Liu et al. 2018;Zhang et al. 2019). The various biological activity of EPS is due to a complex interaction of multiple structural patterns including molecular weight, the sugar residue composition, types of glycosidic bonds, the monosaccharides nature, and the presence of some Mousavian et al. AMB Express (2022) 12:27 non-sugar units (sulfates, methyl, organic acid, amino acids, or amine) in the polysaccharide backbone (Berthon et al. 2017;Pierre et al. 2019). Certainly, the most common structural pattern of EPS consists of sulfate esters attached to glycosides and their sulfation level play an important role in biological applications (Zhang et al. 2019). Sulfate content between the sulfated polysaccharides (sPS) extracted from the various strains of microalgae are different (De Jesus Raposo et al. 2013). The content of sulfate sPS has a strong effect on physiochemical characterization and biological activity (Zhang et al. 2019;Jiao et al. 2011).
Recently, the importance of microalgal sPS in cosmetics, food, medical and pharmacological industries has grown significantly (Zhang et al. 2019;Minhas et al. 2016). They have shown antibacterial, antiviral (De Jesus Raposo et al. 2013;Wu et al. 2013), anti-inflammatory (Wu et al. 2015), antioxidant, anti-tumor and lowering cholesterol activities (Bernaerts et al. 2019; Barkia et al. 2019;Amaro et al. 2013). They are used to block the adhesion of pathogenic microorganisms such as Helicobacter pylori on epithelial cells as an anti-adhesive agent (Guzman-Murillo and Ascencio 2000; Ascencio et al. 1993).
The pharmaceutical and food industries have shown rapid interest in the development of natural, safe and new multi-target bioactive compounds like antioxidants and anticoagulants especially of marine origin (Chu 2011;Burg and Oshrat 2015). Marine algal sPS possess potent antioxidant activities through scavenging effects on the free radicals with direct or indirect interaction. In the continuing search for new and natural resources of bioactive compounds for anticoagulant activity, microalgae sulfated polysaccharides with hemi-ester sulfate group in sugar units have been introduced. Algal sPS have an anticoagulant activity similar to heparin as a natural highly sulfated mucopolysaccharide (Mišurcová et al. 2015).
The anionic nature of sPS due to the existence of the sulfate group makes them suitable candidates for bioapplications such as antioxidant and anticoagulant agents. Microalgae sPS as a glycosaminoglycan containing sulfate ester in their various sugar units can be an interesting candidate for medical applications (Marques et al. 2016).
In the present study, the sPS production and characterization in terms of yield, total carbohydrate and sulfate contents of the five isolated microalgae strains from the Persian Gulf are described. Upon our knowledge, this study represents the first description of isolated microalgal strains [Chlorella sorokiniana, Chlorella sp. (L 2 ), Chlorella sp. (D 1 ) , Chlorella sp. (N 4 ) and Picochlorum sp.] from these habitats for sPS production. The strains containing the sPS with the most potent antioxidant and anticoagulant activities have been evaluated and presented.

Morphological and molecular characterization
During the culturing process capsule's microalgae were identified by observation of morphological characteristics under a light microscope with negative staining. After elementary identification, the molecular analysis was further confirmed by sequencing of the 18S ribosomal RNA gene.

Determination of sPS total carbohydrates
Total carbohydrates of EPS were analyzed by the phenolsulfuric acid method as described by Dubois et al. (1956). It is based on the production of furfural derivatives due to the dehydration of hydrolyzed saccharides with concentrated sulfuric acid. Thereafter, 5% phenol was added to the solution and incubated in the water bath for 10 min at 90 °C. After cooling to room temperature, the plate was read using a UV-Visible spectrophotometer (BioTek, Epoch, Gen5) at 490 nm. The calibration curve was created using known concentrations of D-glucose (0-0.2 mg/mL) and heparin sodium stock solution (0-5 mg/mL) as a reference standard.

Determination of sPS sulfate content
The sulfate content measurement was carried out according to a BaCl 2 gelatin method with some modifications (Dodgson and Price 1962). Briefly, the samples were hydrolysis in N-hydrochloric acid 1 M at 105-110 °C for 5 h. Then, 3% (w/v) trichloroacetic acid and barium chloride-gelatin reagent were added to the mixture, which was kept for 15-20 min at room temperature. The solution absorbance was measured at 360 nm (BioTek, Epoch, Gen5). The calibration curve was obtained using K 2 SO 4 as a standard (55-550 µg/mL). sPS extraction yield (%) = Dried crude sPS weight g /Powder weight g × 100%

HPLC and infrared spectroscopic analysis of sPS
The samples were hydrolyzed in 0.07% HCl for 4 h in 90 °C. The monosaccharides in the microalgae extract were quantified by HPLC on Eurokat H column (8 mm × 30 cm), using sulfuric acid 0.01 N (pH: 2.15) as the mobile phase (flow rate 0.6 mL/min) and refractive index detector, as described by Dokhani et al. (1988). The IR spectra of the microalgae extracts samples were recorded on Bruker Tensor 27 FTIR spectrometer between 400 and 4000 cm −1 (Baky et al. 2013).

Antioxidant activity DPPH radical scavenging assay
The 2, 2 diphenyl-1-picrylhydrazyl (DPPH) radicals were used to investigate the scavenging activity of sPS. The assay was carried out in a 96 well microplate with 200 µL of DPPH (2 Mm at ethanol) solution and sample. Different concentrations (0.5-2 mg/mL) were tested for each sample in triplicate. The plate was then covered and kept for 30 min in the dark at room temperature and then absorbance was read at 517 nm using a microplate reader (BioTek, Epoch, Gen5). The percentage of DPPH scavenging activity was calculated (Romano et al. 2009).

ABTS radical cation scavenging assay
The capability of sPS scavenging activities of 2,20-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical cation was determined with the method reported by Liu et al. with some modifications. After preparation of ABTS solution (absorbance: 0.7 ± 0.05 at 734 nm), the samples solutions (2, 1, 0.5, 0.1, and 0.05 mg/mL) were mixed with ABTS diluent. Then this mixture was kept in dark at room temperature for 6 min and the absorbance was measured at 734 nm in a microplate reader (BioTek, Epoch, Gen5). The scavenging rate (%) was used to evaluate the ABTS scavenging capacity of different sPS ).

Anticoagulant activity
Anticoagulant activities of EPS samples were evaluated using prothrombin time (PT) and activated partial thromboplastin time (APPT) assay. Control plasma samples were mixed with various EPS concentrations (0.05-2 mg/mL) and incubated at 37 °C for 60 s. The mixture and pre-warmed aPTT assay reagent were incubated at 37 °C for 2 min. Finally, pre-warmed calcium chloride (0.25 mol/L) was added and clotting time was recorded. In prothrombin time (PT) assay, control plasma was mixed with EPS samples in different concentrations (0.025-0.2 mg/mL). Then prewarmed PT assay reagent was added and clotting time was recorded (Li et al. 2016). The heparin was used as standard (0-0.05 mg/mL).

Statistical analysis
The carbohydrate and sulfate content data for microalgal strains were performed using a one-way analysis of variance (ANOVA, p < 0.05) with applying the Minitab 18 software. Another statistical analysis was carried out using excel 2019. All experiments were performed at least in triplicate and data were represented as mean ± standard deviation.

Microalgae growth monitoring
The microalgae growth was determined by optical density, cell counting and dry weight. The exponential and linear phases of growth occurred between 12 and 16th day. The highest growth percentage was observed at the exponential phase and then the growth decreases. The cultivation process was monitored up to 28 days and the stationary phase of isolated microalgae occurred between the 16th and 28nd day (Fig. 1). The cultivation period has been extended till 28 days because EPS is produced in the stationary phase.

Microalgae morphological and molecular characterization
Morphological characters such as the presence of mucilaginous capsules surrounding microalgae cells were observed using light microscopy. The isolated microalgae were identified based on molecular studies using 18S rRNA analysis to phylogenetically identify EPS-producing microalgae strains. The partial sequences of the 18S rRNA gene of L 1 , N 4 , D 1 , and L 2 (816 bp, 850 bp, 980 bp and 1216 bp) were submitted to GenBank, respectively. The result of the BLAST analysis of the rRNA sequence was shown in Table1.

Carbohydrate and sulfate estimation
As presented in Fig. 2, C. sorokiniana and Chlorella sp. (L 2 ) showed the highest carbohydrate production. In this study yields of crude EPS produced by the microalgae strains ranged from 14 to 19% (w/w) using heated acid in 4 h at 90 °C.
The carbohydrate contents in the EPSs were also found to vary greatly, ranging from 67 mg/g dry mass of Picochlorum sp. strain to 103 mg/g dry mass of Chlorella sp. content of the EPS sugar (103 mg/g dry extract) as compared to 95 mg/g dry mass of C. sorokiniana. In all the studied species, the EPSs with different sulfate contents were obtained ranging from about 35 mg/g dry biomass produced by Picochlorum sp. to about 93 mg/g dry biomass produced by C. sorokiniana (Fig. 3).
As shown in Fig. 4, the highest sulfate content of sPS from C. sorokiniana, and Chlorella sp. (D 1 ) were reported to 93 and 76 mg/g dry mass, respectively.
Also, in this study carbohydrate and sulfate content of the algal extract were evaluated and compared with heparin sodium, as standard. A comparative data for total carbohydrate and sulfate content was presented in Table2.
In this respect, Chlorella sp. (N 4 ) and C. sorokiniana with 768 ± 18 and 709 ± 50 carbohydrate content equivalent heparin sugar mg/g dry biomass, presented the highest sugar content. But C. sorokiniana and Chlorella sp. (D 1 ) contained more equivalent heparin sulfate. For example, the carbohydrate content in 1 g of C. sorokiniana dry extract was equivalent to 0.7 g heparin sugars content. According to the results, the sugar content of heparin equivalent in sulfated polysaccharides extracted from the studied strains was estimated to be 50-77% (Table 2). The sugar content of sPS was measured also using D-glucose as standard.

Fourier transform infrared (FT-IR) characterization and monosaccharide composition of the sPS
The FTIR spectra characters of polysaccharides and heparin sodium as standard was presented in Fig. 5. A total of 11 monosaccharides (mannose, glucosamine, trehalose, glucose, galactose, xylose, fructose and ribose) and oligosaccharides (sucrose, maltose and raffinose) were used as standard. The HPLC chromatogram of the crude sPS exhibited in Table 3.

Radical scavenging activities
The DPPH and ABTS colorimetric methods were used to assess the possible antioxidant potential of sPS. The scavenging DPPH radical's activity of sPS was determined. As shown in Fig. 6 some sulfated polysaccharides samples revealed apparent inhibition activities on DPPH radicals. Our results exhibited that the DPPH scavenging activity of Picochlorum sp. sulfated polysaccharides was significantly higher than other extracted polysaccharides (p < 0.05).
The ABTS radical scavenging activities of sPS extracted from five microalgae strains at different concentrations (0.05-2 mg/mL) were evaluated (Fig. 7). The ABTS radical scavenging of sPS of all strains except Chlorella sp. (N 4 ) may be due to the least sulfate/sugar ratio, reached to higher than 50% activity at 1 mg/mL.

Anticoagulant activities
The anticoagulant activity of sPS and heparin as control were measured using PT and aPTT assay. As shown in Table 4, C. sorokiniana sPS prolonged clotting time more than 38 s at 10 µg/mL in aPTT test. The PT activity by C. sorokiniana and Chlorella sp. (N 4 ) sPS at 200 µg/mL increased clotting time (up to 14 s).
sPS extracted from Chlorella sp. (N 4 ) with the lowest sulfate/sugar ratio showed the highest PT activity, but despite high sulfate/sugar ratio in Chlorella sp. (D 1 ) sPS, no anticoagulant activity was observed.

Discussion
Five microalgae strains isolated from the Persian Gulf were evaluated for biomass, polysaccharides production and their biological activities. The production of microalgal EPSs generally is related to the microalgae cultivation condition and is different from species to species (Delattre et al. 2016). Also, the extraction method has a significant effect on the extraction yields of microalgae polysaccharides (Yuan et al. 2020). According to our data the heated acid hydrolysis extraction method of Chlorella sp. polysaccharide yields ranged from14 to 19% which is in agreement with that (18%) of 80-90 °C water extraction method from the Chlorella source (Lai and Sun 2017). Also, Sui et al. (2012) study showed an extracted polysaccharide yield ranged from 13 to 19% from Chlorella sp. with hot water incubation (90 °C, 30 min). While the other study reported a crude polysaccharide yield of approximately 9.62 ± 0.11% dry weight of Chlorella-Arc in the 88 °C and 3 h incubation (Song et al. 2018). The significant effect of the temperature on polysaccharide yield is related to the breaking of the internal and external hydrogen bonds of biopolymer and increasing the solubility of polysaccharides and their diffusion in water (Kumar and Fotedar 2009).
Likewise, the acid heated extraction EPS yield (19%) for C. sorokiniana in this study remained higher than those obtained by Suárez et al. for the C. sorokiniana (15%) by using hot water extraction (Suárez et al. 2005). The highest rate of sulfate/sugar, 0.98 and 0.96 were observed   (Nishino and Nagumo 1992). HPLC analysis of extracted EPS under 0.07% acid hydrolysis at 90 °C indicated that it is composed of different sugars in the form of monomer (glucose), dimer (sucrose), or trimer (raffinose). Sucrose was dominant in the sulfated polysaccharide extracted from C. sorokiniana acid hydrolysate. Glucosamine was the most abundant monosaccharide in the Chlorella sp. (L 2 ) and Chlorella sp. (N 4 ), respectively. Detection of amino sugar in Chlorella vulgaris cell wall was also reported previously by Ortiz-Tena et al. (2016). In addition, they revealed that detected glucosamine in microalgae is most probably part of chitin-like polymer available as N-acetyl glucosamine in the cell wall (Ortiz-tena et al. 2016). In our study small amount of raffinose were observed in C. sorokiniana extracellular sugar. According to our knowledge, only one study reported accumulation of raffinose in unicellular Chlorella vulgaris after cold shock (Salerno and Pontis 1989). The culture condition and hydrolysis procedure including acid concentration, hydrolysis temperature and incubation time affect the microalgae monosaccharide's profile. The effect of culture conditions and polysaccharides hydrolysis procedure including acid concentration, temperature and incubation time, on the microalgae monosaccharides profile was confirmed previously (Schulze et al. 2017).
The absorbance at wavenumbers 3440 cm −1 OH and 1200-800 cm −1 shows the IR spectrum of carbohydrates (McCann et al. 1992
The correlation of the polysaccharide structures with their biological function fulfilled the bioactivity of the exopolysaccharides produced by these strains. The maximum DPPH scavenging activities (85%) were observed at the concentration of 2.0 mg/mL for Picochlorum sp. sPS. The hydrogen atom in the hydroxyl group available in Picochlorum sp. sPS (FTIR data) leads to the stronger hydrogen atom-donating capacity in DPPH scavenging assays. Many researchers have investigated the in vitro and in vivo antioxidant activities of microalgae polysaccharides. The 16-polysaccharide extracted from C. pyrenoidosa by Hu et al. (2007) displayed significant anti-radical activities, varying from 29.67 ± 0.29% to 54.16 ± 4.49% at 10 mg/mL (Hu et al. 2007). In our study notable antioxidant activity was not observed in sPS extracted from microalgae C. sorokiniana (C. pyrenoidosa) at tested concentrations (0.05-2 mg/mL). Our finding was in keeping with many reports on the antioxidant activities of sPS extracted from algae. The evaluation of antioxidant activities of exopolysaccharides from Chlorella zofingiensis (EPS-CZ), C. vulgaris (EPS-CV) and C. pyrenoidosa (EPS-CP) demonstrated DPPH radical scavenging activities. At the concentration of 3.0 mg/ mL, the EPS-CV and EPS-CZ inhibited 59.6% and 71.5% of DPPH radicals, respectively. The EPS-CP had 55.2% of DPPH radical scavenging activity at the concentration of 2.0 mg/mL (Zhang et al. 2019). According to Zhang et al. (2013) report water and alkali extracted polysaccharides from Enteromorpha linza showed over 83 and 89% DPPH scavenging activity, respectively at 3.61 mg/mL concentration. The high DPPH scavenging activity, 73%, at 160 µg/mL of extracted sPS from Gracilaria corticate and the IC 50 value of 32 µg/mL for Nostoc carneum exopolysaccharide has been reported (Seedevi et al. 2016;Mervat et al. 2015). Also, the DPPH radical scavenging effect of crude polysaccharide from C. pyrenoidosa in concentration 10mg/mL was reported as 54.16 ± 4.49% (Hu et al. 2007). The result of the present study indicated that due to the high electrons donating ability of sulfated polysaccharides of C. sorokiniana, Chlorella sp. (L 2 ) and Chlorella sp. (D 1 ), the ABTS radical scavenging activity was increased to > 82% at the concentration of 1 mg/mL. It is interesting to determine the chemical constituents and scavenging activity relationship for sPS extracted from microalgae. The sulfated polysaccharides from Chlorella sp. (L 2 ) and Picochlorum sp. with similar sulfate/sugar ratio showed potent radical scavenging activities 91% in ABTS and 85% in DPPH scavenging activity, respectively.
The hypothesis of the relationship between the free radical scavenging capability of EPS and the existence of functional groups such as C=O, -COOH, -O-and -OH in its structure due to donating electron activity is well accepted (Sun et al. 2015).
Based on the FTIR spectrum result, it is possible that high ABTS radical scavenging in C. sorokiniana, Chlorella sp. (L 2 ) and Chlorella sp. (D 1 ) sPS samples were due to the existence of the carbonyl group of a carboxylic acid group of uronic acid and the hydrogen atom in the hydroxyl group. Evaluating the results acquired for sPS extracted from four Chlorella species, sPS C. sorokiniana, Chlorella sp. (D 1 ) and Chlorella sp. (L2) showed higher antioxidant activity than Chlorella sp. (N 4 ). The sPS extracted from chlorella strains except for Chlorella sp. (N 4 ) had relatively strong ABTS radical trapping, and the scavenging activity was 90% when the polysaccharide concentration was 2 mg mL −1 . Since the electron transfer reaction in polysaccharides provides the hydrogen or electrons required to form stable molecules from free radicals (Wang et al. 2022). This result suggested that ABTS scavenging capacity may be due to the presence of the broad peak vibrations of the OH group (3200-3500 cm −1 ) in C. sorokiniana, Chlorella sp. (D 1 ) and Chlorella sp. (L2). Low potency of the Chlorella sp. (N 4 ) strain to inhibit free radicals was associated with the lack of this spectrum (FTIR spectrum data). Therefore since the ABTS assay evaluated non-physiological free radicals (Wang et al. 2022), it may be indicated sPS extracted from C. sorokiniana, Chlorella sp. (D 1 ) and Chlorella sp. (L2) may directly scavenge free radicals.
ABTS scavenging activity of sPS extracted in the current study was higher than the scavenging activity of the previously reported study. According to Chen et al. (2018) study, the concentration of 4 mg/mL of AnPS polysaccharide fraction extracted from Ascophyllum nodosum had the highest ABTS radical scavenging activity (70%) among three different fractions.
Antioxidant activity is related to the molecular weight, sulfate content and position of a sulfate group, different type of the major sugar unit, glycosidic branching and glycoprotein residuals of polysaccharides Wang et al. 2018;Chu, 2011;Qi et al. 2005). There is a correlation between uronic acids, the reducing and nonreducing end contents and antioxidant activities in polysaccharides Wang et al. 2018).
It was observed that aPTT and PT activity of C. sorokiniana and Chlorella sp. (N 4 ) sPS were lower than heparin. Heparin quickly increased the aPTT and PT times; the clotting time was more than 60 s at 5 µg/mL for aPTT and 13.69 s at 25 µg/mL for PT. Therefore, position to obtain the same effect as with heparin high concentration of sPS were required. By our results, five times lower anticoagulant activity in aPTT assay was reported for sPS purified from Arthrospira platensis than heparin (Majdoub et al. 2009). Also, the anticoagulant activity of two sPS extracted from Monostroma nitidum was reported to be weaker than heparin (Mao et al. 2008).
According to some research, in addition to sulfate concentration, the differences in the structural variation of sPS such as the distribution pattern and position of sulfate and chemical composition mainly the monosaccharide units could affect the sPS anticoagulant activity (Li et al. 2015;Yang et al. 2002;De Jesus Raposo et al. 2013). As can be seen from previous studies, the abundance of glucuronic acid branches in Cladosiphon okamuranus fucoidan, adversely affected the aPPT assay (Cumashi et al. 2007).
Conceptually, polysaccharides with in vitro low anticoagulant effects could be assumed as antithrombotic agents (Liet al. 2015;Mourão, 2015). In this regard, the tested sPS with poor anticoagulant activity may exhibit antithrombin activity in bleeding disorder which requires further study.
In total, the difference between the sulfate heteropolysaccharides extracted from the three chlorella strains in this study lies in their performance. For the anticoagulant effect, C. sorokiniana and Chlorella sp. (N 4 ) showed higher activity than other chlorella strains. One explanation for this may be due to similar carbohydrate content equivalent heparin sugar (mg)/g dry biomass in sPS extracted of C. sorokiniana and Chlorella sp. (N 4 ). Moreover, the content of sulfate esters plays an important role in sPS bioactivities. Interestingly, Chlorella sp. (N 4 ) with a lower sulfate/sugar ratio (0.41) showed lower antioxidant activity. Whereas Chlorella sp. (D1) with sulfate/sugar ratio 0.53 following C. sorokiniana and Chlorella sp. (L2) with sulfate/sugar ratios 0.98 and 0.94, respectively, presented a high antioxidant effect. As a result, the finding of this study, suggest that antioxidant and anticoagulant activity of sPS was related to the sulfate ester content. This result indicates that some of the sPS could be a potential resource of natural antioxidants for further investigation in the food industry. So commercial development of this natural product can lead to the extension of functional food additives. Meanwhile, the C. sorokiniana sPS with anticoagulant and antioxidant activities could be a promising anticoagulant candidate with lower bleeding risk in stroke and heart ischemic disease.