Effect of extraction method on the chemical profiles and bioactivities of soybean hull polysaccharides

Abstract The yields, properties, and bioactivities of polysaccharides extracted by three methods from soybean hulls (SSCPs) were evaluated: hot water extraction (H‐SSCP), microwave‐assisted ammonium oxalate extraction (A‐SSCP), and microwave‐assisted sodium citrate extraction (S‐SSCP). A‐SSCP gave the highest yield of polysaccharides (9.3 ± 0.5%) although all three products had similar physicochemical characteristics and FT‐IR spectra. A‐SSCP and S‐SSCP produced polysaccharides with lower molecular weight distributions and higher total reducing power and scavenging ability for ABTS+• and DPPH• free radicals. Furthermore, the effect of SSCPs on carbon tetrachloride (CCl4)‐induced liver injury was investigated in the mice. When compared with H‐SSCP and S‐SSCP, A‐SSCP significantly decreased the levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), malondialdehyde (MDA), and reactive oxygen (ROS) to normal (p < .05) and increased the level of glutathione (GSH) to normal (p < .05). A‐SSCP was the most effective polysaccharide, yielding an approximately normal hepatic appearance with well‐preserved cytoplasm, obvious cell boundaries, with legible nuclei and nucleoli. This study indicates that polysaccharides extracted from soybean hulls via microwave‐assisted ammonium oxalate extraction have the potential to be developed as a new functional food contributing to the alleviation of liver damage.

Some natural plant polysaccharides with low cytotoxicity have been investigated as novel antioxidants in the food and pharmaceutical industries. Numerous studies have found that carbon tetrachloride (CCl 4 ) exposure induces several alterations in liver tissues and that natural plant polysaccharides protect liver cells from such oxidative stress (Bargougui et al., 2019;Mahmoud et al., 2012).
Soybean, a species of legume, is one of the major sources of energy and nourishment for the world's population. Soy hulls are the seed coats of soybeans (~8% by weight) obtained as a by-product of the soybean processing industry. Most are discarded or used in animal feeds (Kim et al., 2015); however, some studies have indicated that antioxidant components are present in plant hulls (Asamarai et al., 1996;Duh et al., 1992;Lai et al., 2010). The insoluble carbohydrate fraction of hulls consists of approximately 30% pectin, 20% cellulose, and 50% hemicellulos (Gnanasambandam & Proctor, 1999). Soy hulls have been considered as a source of novel polysaccharides. Soluble polysaccharides from soybean meal have been shown to have free radical scavenging activity and may be considered as good radioprotective agents (Mateos-Aparicio et al., 2010;Yao et al., 2011). However, no information is available on the bioactivity of soy hull polysaccharides (SSCP).
Our research group previously extracted SHSP with ammonium oxalate coupled with microwave treatment, concluding that SHSP consists mainly of galactose, xylose, galacturonic acid, arabinose, rhamnose, and glucose and that Mg 2+ can induce the gelation of these polysaccharides (Liu et al., 2013). The aim of this study was to investigate the effects of various extraction methods on the yield of these polysaccharides. The chemical properties of SSCPs were characterized by high-performance gel filtration chromatography (HPGFC), ion chromatography (IC), Fourier-transform infrared spectroscopy (FT-IR), and scanning electron microscopy (SEM). In addition, in vitro antioxidant activities and the in vivo hepatoprotective potential of SSCPs against CCl 4 -induced tissue damage were evaluated. This information will be helpful in both exploiting a novel antioxidant and maximizing the utilization and value of soybean hulls.

| Hot water extraction
Fifty g of the soybean hull samples were broken into powder and discolored with ethanol solution (1%) in a ratio of 1:10 (m/v). The dried soybean bean hull samples were extracted with a ratio of soybean powder to water of 1:20 (m/v), 85℃ heating for 4 hr. After cooling and filtering, the extract was centrifuged at 4,500 × g for 10 min, the supernatant was collected and concentrated, and its pH was adjusted to 4.0 with 1 M HCl. The polysaccharide was precipitated by addition of 2 volumes of pure ethanol and dried at 65℃ for 6 hr, thus obtaining H-SSCP samples.

| Microwave-assisted ammonium oxalate/ sodium citrate extraction
After discoloring with 1% ethanol solution, 50 g of the soy hull samples were extracted in 20 times volumes of 0.6% (w/v) ammonium oxalate/sodium citrate (analytical reagent) with 85℃ microwave heating for 20 min at 480 W. After cooling and filtering, the extracts were centrifuged at 4,500 × g for 10 min, the supernatant was collected and concentrated, and its pH was adjusted to 4.0 with 1 M HCl. Then, crude A-SSCP/S-SSCP were obtained by a series of procedure including ethanol precipitation and drying at 65℃.

| Determination of carbohydrate, protein, sulfate, uronic acids, and acetyl group contents in SSCPs
The polysaccharide content can be quantified by phenol-sulfuric acid method (Cuesta et al., 2003). Coomassie Brilliant Blue G-250 is used for investigating protein content (Georgiou et al., 2008). The sulfate content was determined by barium chloride-gelatin method (Kawai et al., 1969). Uronic acid units can be quantified by a colorimetric determination after treatment with concentrated sulfuric acid and carbazole (Li et al., 2007). The acetyl groups on the SSCPs are converted into a ferric-acetohydroxamic complex that is quantitated using UV-Vis spectrophotometer (Metcalfe, 2019).

| Molecular weight determination
The molecular weight of soybean hull polysaccharides was determined by using Waters 1525 HPGFC equipped with 2,414 differential refractive detector and Empower3 workstation. The soybean hull polysaccharide samples were dissolved in 0.1 mol/L NaNO 3 ultrapure water solution, and its mass concentration was 10mg/ml. After filtration by microporous membrane, gel permeation filtration chromatography was used to analyze the sample, and the injection volume was 20 μL. Chromatographic analysis conditions: column: Ultrahydrogel™ Linear 300 mm ×7.8 mmid×2; flow rate: 0.9 ml/min; and column temperature: 45℃. The standard used for molecular weight correction curve is Dextran T series.

| Monosaccharide composition determination
5.0 mg of the soybean hull polysaccharide sample was dissolved in 4 mol/L TFA; it was hydrolyzed in oven at 110℃ for 6hr; methanol was added repeatedly and blow it dry with nitrogen blower; deionized water was used to fix volume to 25 ml; and the monosaccharide composition of soybean seed coat polysaccharide was analyzed by ion chromatography. The monosaccharide composition of soybean seed coat polysaccharide was analyzed by chromatograph. Determination conditions of ion chromatography: column: CarboPac PA20 column (150 mm ×3 mm); detector: pulse amperometric detector, gold electrode; injection volume: 25 μl; flow rate: 0.5 ml/min; and mobile phase: sodium hydroxide solution and sodium acetate solution.

| FT-IR and SEM analysis
A Tracer-100 Fourier-transform infrared spectrometer (Shimadzu, Japan) was used to evaluate the FT-IR spectra of SSCPs. Briefly, 1 mg of the dry SSCP powder was mixed with 100 mg KBr powder and then pressed into tablet for FT-IR measurement in the frequency range of 4000-400 cm−1.
The freeze-dried SSCPs were fixed onto a copper stub. After sputtering with a layer of gold, the SEM images were observed and recorded using a S-4800 SEM (JEOL Ltd., Japan) under a high vacuum condition at an accelerating voltage of 5 kV and image magnification of 30-50k×.

| Antioxidant activity assays
2.6.1 | DPPH radical scavenging activity Various concentrations of SSCPs (2, 4, 6, 8, 10 mg/ml, previously dissolved in ethanol) were reacted with DPPH solution (0.004% w/v dehydrated ethanol) for 30 min at 25℃ in the dark followed by absorbance determination at 517 nm. Ascorbic acid was used as positive control. The DPPH radical scavenging rate was calculated by the following formula: where A 0 : the absorbance without sample, A 1 : the absorbance of the sample and DPPH solution, and A 2 : the absorbance without DPPH.
2.6.2 | ABTS + radical scavenging activity Eighty-eight μl (140 mmol/L) oxidant potassium persulfate solution was mixed with 5 ml (7 mmol/L) ABTS solution and stayed overnight under room temperature in dark conditions for ABTS raw liquor.
ABTS solution was diluted with distilled water to 0.700 ~ 0.720 absorbance value at 734 nm, counting as A 0 . 0.1 ml polysaccharide solution in different concentrations (2, 4, 6, 8, 10 mg/ml) was admixed with 1.4 ml ABTS working fluid by a whirlpool oscillator and reacted in dark for 6 min at room temperature.
The absorbance A i at 734 nm was then determined. ABTS+radical scavenging rate is gauged in the light of the following formula:

| Total reducing ability
In 25 ml plugged colorimetric tube, 2.5 ml of different concentrations (2-10 mg/ml) of polysaccharide solution, PBS buffer solution (0.2 mol/L, pH 6.6), and 1% potassium ferricyanide [K 3 Fe (CN) 6 ] solution were added, respectively, and the mixture was retained in water bath at 50℃ for 20 min, cooled rapidly after reaction, and added 2.5 ml 10% trichloroacetic acid (Metcalfe). After the reaction, the supernatant was centrifuged at 4,000 r/min for 10 min. 2.5 ml of distilled water and 0.5 ml 0.1% of ferric chloride solution were then added into the test tube and let standing for 10 min. The absorption value A i of mixing group at 700 nm wavelength was determined.
Distilled water was used to determine the absorbance value A 0 . The larger the absorbance value, the stronger the reduction ability.

| Animal and experimental design
The Kunming mice (8 weeks old) were purchased from Jinzhou Medical University Laboratory Animal Center (Jinzhou, China). The mice were kept under controlled conditions of 12-hr light/dark cycles at 22 ± 2℃ and 50%-55% relative humidity. All food, water, and experimental equipment used were sterilized. After a week acclimatization, mice were randomly divided into the following five groups From days 1-7, mice in treatment groups NC group and MC group received sterilized distilled water by gavage administration once a day around 10 a.m.; mice in treatment groups A-Pro, S-Pro, and H-Pro received 400 mg/kg bw body weight aqueous solution of A-SSCP, S-SSCP, and H-SSCP, respectively, again once a day by intragastric administration at the above-mentioned time. On the 8th day, mice in the NC group received a gavage injection of 1 ml/kg body weight olive oil; all other groups received an intragastric injection of 1 ml/kg body weight CCl 4 (1:4, v/v, in olive oil). After 24 hr (day 9), NC group and MC group continued to receive the sterilized distilled water; A-Pro, S-Pro, and H-Pro received polysaccharides for a further 7 days. The whole experiment was lasted for 16 consecutive days. At the end of the experiment, all mice were anesthetized with isoflurane gas, and under aseptic conditions, laparotomies were performed via a midline incision and livers harvested for enzyme activity evaluation. The blood samples were laid at 4℃ for 30 min and centrifuged at 2,000 × g and 4℃ for 20 min.

| Liver histopathology studies
Mice livers from all groups were removed and fixed immediately in 4% neutral buffered formalin, dehydrated in gradual ethanol (30%-100%), cleaned in xylene, and embedded in paraffin. Sections were prepared and stained with hematoxylin and eosin (H&E) for photomicroscopic observation.

| Statistical analysis
The data of all experiments were recorded as means ± standard deviations and were analyzed with SPSS (version 19.0, SPSS Inc.).
Differences were considered significant at p < .05.

| Effects of extraction methods on yield of SSCPs
SSCPs were extracted by three methods, viz. hot water extraction (H-SSCP), microwave-assisted ammonium oxalate extraction (A-SSCP), and microwave-assisted sodium citrate extraction (S-SSCP). The yields of SSCPs were as follows: H-SSCP dicating that microwave-assisted ammonium oxalate/citrate extraction is a promising alternative technique for the production of

| Effects of extraction methods on chemical composition of SSCPs
The main chemical components of SSCPs are summarized in Table 1.
A-SSCP and S-SSCP contained low levels of sugar and protein, while

| Molecular weight and monosaccharide composition of SSCP
Molecular weight reflects the molecular chain of polysaccharides and is closely related to biological activity. The molecular weight of the SSCPs is presented in Table 2 and Figure S1. The weight average molecular weight (Mw) and number average molecular weight (Mn) of H-SSCP were significantly higher than for A-SSCP and S-SSCP. The Mw and Mn of A-SSCP were 251 kDa and 41 kDa, respectively, which were higher than S-SSCP (149 kDa and 36 kDa).
The difference of molecular weight may be due to the different functional groups in the polysaccharide or the rearrangement or combination of polysaccharides in the extraction process. The molecular weights of these three SSCPs demonstrated considerable variation, suggesting that these differences caused by the extraction method might also affect their bioactivities (Liao et al., 2020). (Zeng et al., 2012) claimed that polysaccharides obtained from Auricularia auricular displayed significant antioxidant activity in a dose-dependent pattern and to a greater extent than described by (Fan et al., 2007). The discrepancy in these reports may be due to differences in extraction method (microwave-assisted versus.

| Fourier-transform infrared spectroscopic analysis
FT-IR spectra of A-SSCP, S-SSCP, and H-SSCP are illustrated in

| SEM of SSCPs
SEM is a useful tool for observing surface features in the micron to submicron range on polymeric materials. As shown in Figure 2, A-SSCP morphology was significantly different from the other polysaccharides. The surface of A-SSCP was smooth with a large sheet structure. In contrast, S-SSCP and H-SSCP were dispersed into relatively loose, irregular fibrous strips. This difference can be attributed to the differing monosaccharide compositions, particularly uronic acid, the protein content, and different glycosidic links within the three SSCPs Ji et al., 2020).

| In vitro antioxidant activity assays
3.6.1 | DPPH radical scavenging activity assay DPPH is a stable free radical molecule centered on a nitrogen atom with an unpaired electron. It absorbs strongly at 517 nm. The abundance of this free radical readily decreases following exposure to proton radical scavengers. A deep-purple solution of DPPH changes to yellow as it is quenched by antioxidants. DPPH is the most common free radical used to determine antiradical and antioxidant activities of natural polysaccharides. As shown in Figure 3a, all the SSCPs displayed a significant dose-dependent increase in radical scavenging activity at concentrations of 2-10 mg/ml. The DPPH radical scavenging effects of A-SSCP, S-SSCP, and H-SSCP at 10 mg/ml were 76.9 ± 1.9%, 63.6 ± 3.3%, and 63.1 ± 3.2%, respectively, and all were lower than Vc (97.0 ± 2.1%).
3.6.2 | ABTS + radical scavenging activity ABTS + radicals are widely used for the determination of total antioxidant capacity. The ABTS + radical scavenging capacity of SSCPs from different extraction methods is shown in Figure 3b. All three SSCPs exhibited significant concentration-dependent ABTS + scavenging ability. As SSCP concentration increased, the scavenging effect of A-SSCP increased from 14.0 ± 3.0% to 85.3 ± 3.8%. S-SSCP and H-SSCP at 10.0 mg/ml reached 68.7 ± 4.5% and 50.9 ± 4.0%, respectively, less than Vc (96.0 ± 3.3%), but similar to results reported by Zhang et al. In addition, SSCPs were more effective at scavenging ABTS + radicals than DPPH radicals. This may be because the DPPH scavenging assay is more applicable for evaluating hydrophobic antioxidants, while the ABTS + scavenging assay is more suitable for evaluating hydrophilic antioxidants (Liao et al., 2015).

| Total reducing ability
The reducing ability of a compound can serve as a significant indicator of its potential antioxidant activity. Figure 3c illustrates the reducing power of A-SSCP, S-SSCP, and H-SSCP. Higher absorbance is generally associated with greater reducing power. In the concentration range 1-5 mg/ml, all the SSCPs displayed significant reducing fractions have a greater chance to come in contact with free radicals due to their larger surface area (Mirzadeh et al., 2020). The presence of -OSO 3 H groups in the polysaccharide could also activate the hydrogen atom of an anomeric carbon, giving it a stronger donating capacity (Song et al., 2018). This may be one of the most important reasons that A-SSCP exhibited greater antioxidant activity than S-SSCP and H-SSCP.

| Correlation analysis
The relationships between the composition of the three polysaccharides and their antioxidant capacity were elucidated by correlation analysis as shown in Table 3. DPPH radical scavenging activity was significantly (p < .01) and positively correlated with arabinose and galacturonic acid content and negatively correlated with galactose and mannose content. It can be concluded that the antioxidant capacity of these polysaccharides may be closely related to their unique F I G U R E 3 In vitro antioxidant activity of SSCPs: (a) DPPH radical scavenging activity, (b) ABTS + radical scavenging activity, and (c) total reducing ability. Data are mean ± standard error of the mean (n = 3) structure and monosaccharide contents. ABTS + scavenging data were very similar to DPPH except for rhamnose content which had a weaker influence on DPPH radical scavenging activity. The contents of rhamnose and galacturonic acid were positively related to total antioxidant capacity (as indicated by total reducing ability), the increase in rhamnose and galacturonic acid contents enhancing total reducing ability. The differing physicochemical properties of the three polysaccharides produced different free radical scavenging profiles.

TA B L E 3 Correlation analysis (R values) of polysaccharide composition and antioxidant capacity
Molecular weight was significantly (p < .01) and negatively correlated with ABTS + scavenging activity and total reducing ability. It can be concluded that the antioxidant capacity of polysaccharides may be closely related to, and weakens with, an increase in molecular weight. Protein content was significantly (p < .01) and positively correlated with DPPH scavenging, ABTS + scavenging, and total antioxidant capacity. In addition, the sulfate content of the polysaccharides correlated positively with their DPPH and ABTS + radical scavenging activity.
In summary, the higher antioxidant capacity of A-SSCP compared with S-SSCP and H-SSCP may be attributed to the higher contents of arabinose, galacturonic acid, sulfate, the lower protein content, and low Mw. This is in accordance with the conclusions of (Mirzadeh et al., 2020).

| Effect of SSCPs on ALT and AST activity
Hepatoprotective activity of SSCPs against CCl 4 -induced liver damage in mice was also evaluated by analyzing serum ALT and AST activity ( Figure 4)

| Histopathological examination
The histopathological appearance of the livers of control and treated mice is shown in Figure 5. Liver sections from the NC group showed normal hepatocytes with preserved cytoplasm and nucleus. In con-

| CON CLUS ION
The influence of extraction methods of SSCPs from soybean hulls was studied. A-SSCP had the highest yield compared with S-SSCP and H-SSCP but all displayed typical polysaccharide characteristics.
All three exhibited similar monosaccharide profiles but significantly different concentrations. A-SSCP showed higher antioxidant activity than S-SSCP and H-SSCP, which was attributed to its higher content of arabinose, galacturonic acid, sulfate, lower protein content, and low Mw. A-SSCP also exhibited considerable protective effects against CCl 4 -induced liver damage in mice. This study indicates that polysaccharides extracted from soybean hulls via microwaveassisted ammonium oxalate extraction have the potential to be developed as a new functional food contributing to the alleviation of liver damage Guo et al., 2019;Yue et al., 2014;Zhang et al., 2018). for the expert linguistic services provided.

CO N FLI C T O F I NTE R E S T
The authors of this manuscript state that they do not have conflict of interest to declare. F I G U R E 5 Histopathological effects of SSCPs on mice liver hepatocytes stained with H&E (400×)