- freely available
Int. J. Mol. Sci. 2014, 15(1), 787-797; doi:10.3390/ijms15010787
Published: 8 January 2014
Abstract: An edible fungal polysaccharide termed as ABP was obtained by extraction with hot water, and followed successive chromatographic purification using DEAE-Sepharose Fast Flow column and Sephacryl S-300 High-Resolution column. A symmetrical peak was obtained on high-performance size-exclusion chromatography with an average molecular weight of 5.17 × 104 Da, which was named ABP, and its main components were d-glucose and d-mannose. Based on the study of methylation analysis, along with FT-IR, GC, GC-MS, 1D 1H and 13C NMR and 2D NMR (H-HCOSY, TOCSY, HMQC, and NOESY), its chemical structure was featured with a repeating unit (1→6) linking β-d-Glcp as the main backbone with (1→4)-linked α-d-Manp units. The structure of the mainly repeating units of ABP was established as:
For thousands of years, mushrooms have been known as a source of medicine , many studies showed that polysaccharides were the main occurring biological constituents in common mushrooms. Polysaccharides are highly appreciated for their multiple biological and pharmacological activities such as antitumor, immune-modulating, anti-inflammatory, anti-atherogenic and hypoglycemic actions [2,3]. The polysaccharides from several species, such as Ganoderma, Lentinus, Agaricus or Flammulina, have been widely studied [4–6]. Some structural patterns of polysaccharides have been found from various mushrooms. Many evidences have indicated that the biological activities of polysaccharides depended on their structural features such as the compositions of sugar, type of glycosyl linkage, branch structures, molecular weight and concentration [7–9]. In this field, the β-(1→3), (1→6) glycosidic linkages are supposed to play an important role in enhancing the antitumor and the immunomodulatory effects [10–14]. Furthermore, other structural features, such as the (1→4), (1→6) moiety found in several fungal species, have also been demonstrated to enhance the immune system .
Agaricus bisporus (A. bisporus) is one of the most favorable mushrooms in the world market, and has been well characterized by not only its delicious taste and high protein content, but also the high content of dietary fiber and functional compounds, and is also considered to have immense potential as a source of valuable medicinal compounds. We have previously reported the antioxidant property, monosaccharide composition and molecular weight distribution of a water soluble crude polysaccharide from A. bisporus . As part of a continuing investigation of the chemical structures and biological activities of the polysaccharides from this fungus, in this manuscript, we report the isolation and structural characterization of A. bisporus polysaccharide (ABP) from A. bisporus.
2. Results and Discussion
2.1. Isolation and Purification
The water-soluble polysaccharide from the fruiting bodies of A. bisporus was purified by DEAE-Sepharose Fast Flow column and gel-permeation chromatography on Sephacryl S-300 High-Resolution column (XK 2.6 × 100 cm). Figure 1 showed the elution pattern of ABP. High-performance size-exclusion chromatography (HPSEC) gave a single symmetrical peak (Figure 2) with exclusion from the TSK gel G4000PWXL column, indicating that ABP was a homogeneous polysaccharide. The UV scanning found no absorption at both 260 and 280 nm and thus suggested the polysaccharide contained no nucleic acids and protein. The total sugar content of ABP was estimated as 99.1% by phenol-sulfuric method , and sugar compositional analysis indicated that sugar residues were composed of d-glucose, d-mannose, d-galactose and d-xylose in the molar ratio of 2.25:2.00: 0.35:0.20.
The weight-average molar mass of ABP was estimated to be 5.17 × 104 Da by the following equation: lg Mw = 11.5 − 0.376 Vt (R2 = 0.972), which was from the calibration curve of molecular size distribution with automatically calculated by GPC software from HPLC, and where Mw was the molecular weight of polysaccharide and V was the retention volume of polysaccharide.
2.2. Structural Characterization of ABP
The inter-glycosidic linkages between monosaccharide residues of ABP were investigated by methylation analysis. The polysaccharide was methylated three times, followed by hydrolysis and alditol acetate preparation. The complete methylation was confirmed by the disappearance of the hydroxyl peak (3200–3700 cm−1) in IR spectrum. According to sugar analysis of acetylated methyl glycosides and the GC-MS analysis of the alditol acetates, hydrolysates of ABP showed following methylated sugar derivatives: (I) 2,3,4-tri-O-methylglucose; (II) 2,3,6-tri-O-methylmannose; (III) 2,3,4-tri-O-methylgalactose and (IV) 2,3,4-tri-O-methylxylose in a molar ratio of 2.25:2.00:0.35:0.20, respectively, as summarized in Table 1.
These results indicated that the backbone chains of (1→6) linked-d-glucopyranosyl unit and (1→4) linking non-reducing-end mannopyranosyl unit were mainly present in the polysaccharide, and the component (III) and (IV) contained a relatively low amount of (1→6) linking mannopyranosyl and galactopyrannosyl residues. However, methylation analysis was not sufficient to distinguish different surroundings of residues with α or β linkage pattern. Some linkage patterns of sugar residues and structural characterizations need to be further confirmed by 1H, 13C and 2D NMR experiments.
A series of 1H and 13C and 2D-(H-HCOSY, TOCSY, HMQC, NOESY) NMR experiments were employed to assign the proton and carbon signals of the main residues of ABP. The 1H NMR spectrum (Figure 3) of the polysaccharide clearly showed two resonances of equal intensity in anomeric regions at δ 5.29 and δ 4.83, respectively. The sugar residues were correspondingly designated as a and b with other sugar protons in the regions of δ 3.50–δ 4.52. These characteristic signals were corresponding to the main parts of two sugar residue structures from mannose and glucose (residues a and b). The NMR signals of galactose and xylose were no indication owing to their low relative area and poor nuclear magnetic resonance characterizations.
The 13C NMR spectrum (Figure 4) of the polysaccharide showed the presence of two main anomeric carbons at δ 100.6 and δ 105.7 (corresponding to residues a and b), respectively, with other sugar ring carbons linked to oxygen atoms in the region of δ 63.4–δ 78.3. Characteristic fatty acids signals were identified as CH2–CH2–COOR (35.01 ppm), and a CH2-group at 30.39 ppm. The HMQC spectrum (Figure 5) showed two dominant cross-peaks at δ 5.29/100.6 and δ 4.83/105.7 corresponding to hexopyranosyl residues in the region of anomeric resonances, indicating that there were two main sugar residues in the polysaccharide. The 13C NMR was in agreement with the above 1H NMR analysis.
Residue a had an anomeric signal at δ 5.29. Cross-peaks at δ 5.29/4.51 and δ 4.51/4.16 were detected in 1H–1H COSY spectrum, and since δ 5.29 corresponded to H-1, the δ 4.51 and δ 4.16 signals were assigned to H-2 and H-3, respectively. The 1H resonances for H-4 and H-5 in residue a were assigned from the cross-peaks in 1H–1H COSY, TOCSY, NOSEY and HMBC spectra. The H-6a and H-6b resonances were obtained from 1H–1H COSY and TOCSY spectra. The carbon signals from C-1 to C-6 of residue a were identified from the HMQC spectra (Figure 4). The manno-configuration for residue a was supported from relatively small coupling constant value of JH-1, H-2 < 3 Hz and large coupling constant values of JH-3, H-4 (7.5 Hz), JH-4, H-5 (10 Hz) and JC-1, H-1 value (166 Hz) [18–20]. Residue a showed the down-field anomeric H-1 signals (H > δ 5.0) and the anomeric C-1 signal at δ 100.6, but did not provide information about glycosidic type linkage. The anomeric chemical shifts of mannose did not allow unambiguous determination of mannose linking configuration . A NOESY experiment revealed inter-residue correlations between H-1 and H-2, indicating that residue a was α-configuration . Additionally, the chemical shifts of the corresponding carbons were revealed from the HMQC spectrum with 13C resonances assigned in Table 2. The carbon shifts of the residues a showed C-1 at δ 100.6; C-2, δ 71.4; C-3, δ 75.9; C-4, δ 77.4; C-5, δ 74.7; C-6, δ 63.4. The downfield carbon chemical shift C-4 at δ 77.4 was reasonably assigned to the substituted C-4 as a result of the O-replace effect, which indicated the substitution of residue a at the C-4 position and the existence of (1→4)-linkage. The signal at δ 63.4 was assigned to the unsubstituted C-6, indicating that residue a was →4)-linked-α-d-Manp-(1→. The result was inconsistent with the GC-MS data for this linkage.
The proton chemical shifts of H-1 to H-6 from residue b were readily assigned by the 1H–1H COSY spectrum and further confirmed by the TOCSY spectrum. Magnetization relayed well through the spin system, as expected for the glucose-configuration, and all cross-peaks were clearly visible. The high-field H-1 signals (H < δ 5.0), the deshielded anomeric signal C-1 at δ 105.7 and the distinct splitting peak on the residue b revealed that the units of sugar residue b had β-configuration linkage, which was confirmed by JH-1, H-2 values (7.5 Hz) . Large coupling constants of JH-2, H-3 and JH-3, H-4 (9–10 Hz) indicated that residue b was a glucose-configuration [24,25], and presented as β-d-glucose glycosidic linkage. The carbon signals from C-1 to C-6 for residue b were identified from the HMQC spectrum. The glycosidic linkages of the residue b showed C-1 at δ 105.7; C-2, δ 73.6; C-3, δ 75.3; C-4, δ 72.0; C-5, δ 78.2; C-6, δ 68.9, respectively (Table 2). As a result of the glycosylation effect, the signal for C-6 of residue b was shifted downfield to δ 68.9, which indicated that residue b was substituted at C-6 position. The result suggested the presence of a (1→6) linkage glucose residue in the polysaccharide, and was identified as (1→6)-substituted β-d-glucosepyranoside. The above results were in agreement with data obtained from the sugar and methylation analysis of ABP.
The glycosidic linkages between the two residues were determined by the observed inter-residue connectivities generated by NOESY and HMBC experiments. Inter-residue NOEs connectivities were observed between H-1 of residue a and H-6 of residue b, between H-1 of residue b and H-6 of residue b, HMBC spectrum showed clear correlations between H-1 of residue a and C-6 of residue b, between H-1 of residue b and C-4 of residue a, between H-1 of residue b and C-6 of residue b. Based on the data presented above, it demonstrated that the mainly repeating units for ABP with the following structure:
3. Experimental Section
3.1. Materials and Methods
Fruiting bodies of A. bisporus (Yingxiu 1#) were collected from Zhejiang Agriculture Research Institute in Zhejiang province, China. T-series dextrans were purchased from Wuhan Putus Macromolecular Sci. & Tech. Co. Ltd., (Wuhan, China). Monosaccharide standards (d-galactose, d-arabinose, l-fucose, l-rhamnose, d-manonose, d-xylose, d-glucose and erythrose), trifluoroacetic acid (TFA) and dimethyl sulfoxide (DMSO) were purchased from Sigma (St. Louis, MO, USA). All other chemical reagents were of grade AR from Shanghai Chemical Co. (Shanghai, China). DEAE-Sepharose Fast Flow and Sephacryl S-300 High Resolution were purchased from Amersham Pharmacia Biotech (Uppsala, Sweden). TSKgel G4000PWXL column was purchased from Shanghai Biological Technology Co., Ltd. (Shanghai, China). Ultrahydrogel TM 120 and 1000 (78 × 300 mm) columns were purchased from Waters Co., Milford, MA, USA. HPLC was carried out on a waters 1525 HPLC system (1525 HPLC pump, 2414 refractive index detector; Waters Co., Milford, MA, USA).
3.2. Extraction of Crude Polysaccharides
The fruiting bodies of A. bisporus were dried at 50 °C for 48 h, and ground to obtain fine powder (40 meshes). The powder of fruiting bodies was extracted with 25 times’ volume of boiling water for 2 h. After filtration, the residues were re-extracted twice in the same way. The liquid extracts were combined and concentrated into one-fifth of the original volume under vacuum, and 95% ethanol was added slowly to a final concentration of 80% and kept at room temperature overnight. The precipitate was obtained by centrifugation (6000 rpm, 15 min, 4 °C), then washed three times with anhydrous ethanol, acetone and ether, and finally was lyophilized to obtain water soluble crude polysaccharides of A. bisporus.
3.3. Purification of Crude Polysaccharides
The crude polysaccharide was redissolved in deionized water and using a DEAE-Sepharose Fast Flow column (XK 2.6 × 100 cm), eluted first with water, followed stepwise by 0–1.0 M NaCl. The fractions were collected by a fraction collector and compounds were detected by the phenol-sulfuric method, then the fraction corresponding to major sugar peak was further purified, using gel-permeation chromatography on Sephacryl S-300 High-Resolution column (XK 2.6 × 100 cm) with distilled water as eluent at 0.6 mL/min. The sample was collected by 6 mL/tube using an auto-collector, and the main sugar peaks were collected and lyophilised to get a white homogeneous A. bisporus polysaccharide (ABP).
3.4. Methylation Analysis and Monosaccharide Composition Analysis
The polysaccharide ABP was treated three times by NaOH-DMSO-MeI method . The reaction mixture was extracted with CHCl3, and the solvent was then removed by evaporation. Complete methylation was confirmed by the disappearance of the OH band (3200–3700 cm−1) in IR spectrum. The methylated polysaccharide sample (4.0 mg) was hydrolyzed in a long tube with 6 mL of 2 M trifluoroacetic acid (TFA) at 110 °C for 2 h, and the excess acid was removed by azeotropic distillation with methanol. The resulting hydrolysates were reduced by NaBH4 (25 mg) and acetylated with acetic anhydride, then distilled with methanol to remove excess boric acid, followed by drying over P2O5. Monosaccharide compositions were analyzed by an Agilent 7890 A gas chromatograph system was equipped with a flame ionization detector (FID) using a DB-1701 capillary column (30 m × 0.25 mm × 0.25 μm). The methylated alditol acetates were analyzed by chromatography-mass spectrometry (GC-MS) using a Finnigan Trace Ultra-DSQ II (Thermo Co., Austin, TX, USA) system equipped with a TG-5MS column (30 m × 0.25 mm × 0.5 mm; Thermo Co., Austin, TX, USA). The column temperature was initially set at 120 °C, then programmed from 120 to 240 °C at a rate of 5 °C/min and held at 240 °C for 30 min. The split ratio was 1:25 and the injection volume was 1.0 μL. The injector and the detector temperatures were both set at 250 °C.
3.5. Determination of Purity and Molecular Weight
Determinations of the homogeneity and the molecular weight of the samples were done by high-performance size-exclusion chromatography (HPSEC), using a Waters 1525 HPLC system fitted with TSKgel G4000PWXL column (Sigma-Aldrich Co., Japan) and two serially linking Ultrahydrogel TM 120 and 1000 (78 × 300 mm) columns (Waters Co., Milford, MA, USA), respectively, a Waters 2414 RI detector (Waters Co., Milford, MA, USA), eluting with 0.01 M NaNO3 at pH 7.0 with a flow rate of 0.8 mL/min. The column was kept at 30.0 ± 0.1 °C. The linear regression was calibrated by T-series dextrans known molecular mass (T-110, 80, 70, 40, 25, 10) as standard. A calibration curve was prepared by plotting Ve/V0 (elution volume/void volume, mL) versus log molecular weight and molecular weight of the unknown polysaccharide was determined.
3.6. Spectroscopic Methods
Fourier-transform infrared (FT-IR) spectra was recorded from 4000 to 400 cm−1 with a 6700 Nicolet Fourier transform-infrared spectrophotometer (Thermo Co., Madison, WI, USA), using films prepared by the dried polysaccharides and KBr pellets.
3.7. Nuclear Magnetic Resonance (NMR) Analysis
The purified polysaccharide sample (20 mg) was deuterium-exchanged three times by lyophilization with D2O and then dissolved in D2O (99.9%, 0.5 mL). 1H NMR (25, 60 °C) and 13C NMR (25 °C) spectra were determined in 5-mm tubes using a Broker ANANC III (500M) spectrometer (Bruker Co., Fallanden, Switzerland). 1H chemical shifts were referenced to the HDO resonance at δ 4.78 (25 °C) as internal standard. 13C chemical shifts were determined in relation to DSS (sodium 2,2-dimethyl-2-5-sulfonate, δ 0.00) as external calibration. 1H–1H correlated spectroscopy (COSY), total correlation spectroscopy (TOCSY) and heteronuclear multiple quantum coherence (HMQC) were used to assign signals. Two-dimensional heteronuclear multiple-bond correlation spectroscopy (HMBC) and two-dimensional nuclear overhauser enhancement spectroscopy (NOESY) were used to assign inter-residue linkages and sequences.
In this study, we obtained a homogeneous polysaccharide from the fruiting bodies of A. bisporus by DEAE-Sepharose Fast Flow column (XK 2.6 × 100 cm) and gel-permeation chromatography on Sephacryl S-300 High-Resolution column (XK 2.6 × 100 cm), and identified its structural characteristics by UV, FT-IR, GC-MS, methylation analysis, 1H and 13C NMR spectrum (including COSY, TOCSY, HMQC, HMBC and NOESY). The results indicated that ABP was mainly composed of glucose and mannose with the molecular weight 5.17 × 104 Da, and its structure was featured with a repeating unit (1→6) linking β- d-Glcp as main backbone with (1→4)-linked α- d-Manp units. In most fungi examined, polysaccharides consisting of β-(1→3), β-(1→6)-d-Glcp, and α-(1→3)-d-Manp have been found in many mushroom-derived polysaccharides cultivar, and reported to be the major components of the cell wall and the intercellular matrix [27–31]. However, the structural characterization containing (1→6) linking β-d-Glcp as main backbone with (1→4)-linked α-d-Manp units of ABP has not been previously reported, and ABP is therefore a novel fungal polysaccharide.
The study was supported by Chinese Key Technology Research & Develop Program of the twelfth Five-year Plan (No. 2013BAD16B07).
Conflicts of Interest
The authors declare no conflict of interest.
- Zhao, L.; Dong, Y.; Chen, G.; Hu, Q. Extraction, purification, characterization and antitumoractivity of polysaccharides from Ganoderma lucidum. Carbohydr. Polym 2010, 80, 783–789. [Google Scholar]
- Soares, A.A.; Sá-Nakanishi, A.B.; Bracht, A.; Costa, S.M.G.; Koehnlein, E.A.; Souza, C.G.M.; Peralta, R.M. Hepatoprotective effects of mushrooms. Molecules 2013, 18, 7609–7630. [Google Scholar]
- Luo, Q.; Sun, Q.; Wu, L.S.; Yang, Z.R. Structural characterization of an immunoregulatory polysaccharide from the fruiting bodies of Lepista sordida. Carbohydr. Polym 2012, 88, 820–824. [Google Scholar]
- Li, J.-W.; Ding, S.-D.; Ding, X.-L. Optimization of the ultrasonically assisted extraction of polysaccharides from Zizyphus jujuba cv. Jinsixiaozao. J. Food Eng 2007, 80, 176–183. [Google Scholar]
- Xie, J.; Zhao, J.; Hu, D.-J.; Duan, J.-A.; Tang, Y.-P.; Li, S.-P. Comparison of polysaccharides from two species of ganoderma. Molecules 2012, 17, 740–752. [Google Scholar]
- Smiderle, F.R.; Carbonero, E.R.; Mellinger, C.G.; Sassaki, G.L.; Gorin, P.A.; Iacomini, M. Structural characterization of a polysaccharide and a β-glucan isolated from the edible mushroom Flammulina velutipes. Phytochemistry 2006, 67, 2189–2196. [Google Scholar]
- Jeff, I.B.; Yuan, X.; Sun, L.; Kassim, R.M.; Foday, A.D.; Zhou, Y. Purification and in vitro anti-proliferative effect of novel neutral polysaccharides from Lentinus edodes. Int. J. Biol. Macromol 2012, 52, 99–106. [Google Scholar]
- Sun, L.; Wang, C.; Shi, Q.; Ma, C. Preparation of different molecular weight polysaccharides from Porphyridium cruentum and their antioxidant activities. Int. J. Biol. Macromol 2009, 45, 42–47. [Google Scholar]
- Vetvicka, V.; Yvin, J.-C. Effects of marine β-1,3 glucan on immune reactions. Int. Immunopharmacol 2004, 4, 721–730. [Google Scholar]
- Palacios, I.; García-Lafuente, A.; Guillamón, E.; Villares, A. Novel isolation of water-soluble polysaccharides from the fruiting bodies of Pleurotus ostreatus mushrooms. Carbohydr. Res 2012, 358, 72–77. [Google Scholar]
- Carbonero, E.R.; Ruthes, A.C.; Freitas, C.S.; Utrilla, P.; Gálvez, J.; de Silva, E.V.; Sassaki, G.L.; Gorin, P.A.J.; Iacomini, M. Chemical and biological properties of a highly branched β-glucan from edible mushroom Pleurotus sajor-caju. Carbohydr. Polym 2012, 90, 814–819. [Google Scholar]
- Ruthes, A.C.; Carbonero, E.R.; Córdova, M.M.; Baggio, C.H.; Santos, A.R.S.; Sassaki, G.L.; Cipriani, T.R.; Gorin, P.A.J.; Iacomini, M. Lactarius rufus (1→3), (1→6)-β-d-glucans: Structure, antinociceptive and anti-inflammatory effects. Carbohydr. Polym 2013, 94, 129–136. [Google Scholar]
- Ukawa, A.Y.; Ito, H.; Hisamatsu, M. Antitumor effects of (l→3)-β-d-glucan and (l→6)-β-d-glucan purified from newly cultivated mushroom, Hatakeshimeji (Lyophyllum decastes Sing.). J. Biosci. Bioeng 2000, 90, 98–104. [Google Scholar]
- Zhang, Y.; Gu, M.; Wang, K.P.; Chen, Z.X.; Dai, L.Q.; Liu, J.Y.; Zeng, F. Structure, chain conformation and antitumor activity of a novel polysaccharide from Lentinus edodes. Fitoterapia 2010, 81, 1163–1170. [Google Scholar]
- Mandal, E.K.; Maity, K.; Maity, S.; Gantait, S.K.; Behera, B.; Maiti, T.K.; Sikdar, S.R.; Islam, S.S. Chemical analysis of an immunostimulating (1→4)-(1→6)-branched glucan from an edible mushroom Calocybe indica. Carbohydr. Res 2012, 347, 172–177. [Google Scholar]
- He, J.-Z.; Ru, Q.-M.; Dong, D.-D.; Sun, P.-L. Chemical characteristics and antioxidant properties of crude water soluble polysaccharides from four common edible mushrooms. Molecules 2012, 17, 4373–4387. [Google Scholar]
- Zhang, W.J. Biochemical Techniques in Complex Carbohydrates, 2nd ed; Zhejiang University Press: Hangzhou, China, 1999; p. 11. [Google Scholar]
- Yang, Y.; Zhang, J.; Liu, Y.; Tang, Q.; Zhao, Z.; Xia, W. Structural elucidation of a 3-O-methyl-d-galactose-containing neutral polysaccharide from the fruiting bodies of Phellinus igniarius. Carbohydr. Res 2007, 342, 1063–1070. [Google Scholar]
- Zhang, A.-Q.; Xiao, N.-N.; Deng, Y.-L.; He, P.-F.; Sun, P.-L. Purification and structural investigation of a water-soluble polysaccharide from Flammulina velutipes. Carbohydr. Polym 2012, 87, 2279–2283. [Google Scholar]
- Du, X.; Zhang, J.; Yang, Y.; Ye, L.; Tang, Q.; Jia, W.; Liu, Y.; Zhou, S.; Hao, R.; Gong, C. Structural elucidation and immuno-stimulating activity of an acidic heteropolysaccharide (TAPA1) from Tremella aurantialba. Carbohydr. Res 2009, 344, 672–678. [Google Scholar]
- Garozzo, D.; Impallomeni, G.; Spina, E.; Sturiale, L. The structure of the exocellular polysaccharide from the cyanobacterium Cyanospira capsulata. Carbohydr. Res 1998, 307, 113–124. [Google Scholar]
- Senchenkova, S.; Shashkov, A.; Knirel, Y.A.; Ahmed, M.; Mavridis, A.; Rudolph, K. Structure of the O-polysaccharide of Erwinia carotovora ssp. atroseptica GSPB 9205 containing a new higher branched monosaccharide. Russ. Chem. Bull 2005, 54, 1276–1281. [Google Scholar]
- Ge, Q.; Zhang, A.-Q.; Sun, P.-L. Structural investigation of a novel water-soluble heteropolysaccharide from the fruiting bodies of Phellinus baumii Pilát. Food Chem 2009, 114, 391–395. [Google Scholar]
- Ge, Q.; Zhang, A.; Sun, P. Purification and structural elucidation of a novel fucoglucan from the fruiting bodies of Phellinus baumii Pilat. J. Sci. Food Agric 2009, 89, 343–348. [Google Scholar]
- Mondal, S.; Chakraborty, I.; Rout, D.; Islam, S.S. Isolation and structural elucidation of a water-soluble polysaccharide (PS-I) of a wild edible mushroom Termitomyces striatus. Carbohydr. Res 2006, 341, 878–886. [Google Scholar]
- Ciucanu, I.; Kerek, F. A simple and rapid method for the permethylation of carbohydrates. Carbohydr. Res 1984, 131, 209–217. [Google Scholar]
- Pramanik, M.; Mondal, S.; Chakraborty, I.; Rout, D.; Islam, S.S. Structural investigation of a polysaccharide (Fr. II) isolated from the aqueous extract of an edible mushroom Pleurotus sajor-caju. Carbohydr. Res 2005, 340, 629–636. [Google Scholar]
- Duda, K.A.; Fruth, A.; Holst, O. Structural studies of the O-antigenic polysaccharide of the bovine mastitis isolate Escherichia coli serotype O174. Carbohydr. Res 2013, 373, 18–21. [Google Scholar]
- Santos-Neves, J.C.; Pereira, M.I.; Carbonero, E.R.; Gracher, A.H.P.; Alquini, G.; Gorin, P.A.; Sassaki, G.L.; Iacomini, M. A novel branched αβ-glucan isolated from the basidiocarps of the edible mushroom Pleurotus florida. Carbohydr. Polym 2008, 73, 309–314. [Google Scholar]
- De Lourdes Corradi da Silva, M.; Izeli, N.L.; Martinez, P.F.; Silva, I.R.; Constantino, C.J.; Cardoso, M.S.; Barbosa, A.M.; Dekker, R.F.; da Silva, G.V. Purification and structural characterisation of (1→3;1→6)-β-d-glucans (botryosphaerans) from Botryosphaeria rhodina grown on sucrose and fructose as carbon sources: A comparative study. Carbohydr. Polym 2005, 61, 10–17. [Google Scholar]
- Guan, J.; Li, S.-P. Quality Control of Polysaccharides from Medicanal Plants and Fungi. In Chinese Herbal Drug Research Trends; Ching, F.M., Ed.; Nova Science Publishers Inc: New York, NY, USA, 2007; p. 31. [Google Scholar]
|Table 1. GC-MS data for methylation analysis of ABP isolated from the fruiting bodies of A. bisporus.|
|Methylated sugar||Linkage type||Molar ratio||Major mass fragment (m/z)|
|2,3,4-tri-O-methylglucose||→6)-d-Glcp-(1→||2.25||43, 87, 101, 117, 129, 161, 189, 233|
|2,3,6-tri-O-methylmannose||→4)-d-Manp-(1→||2.00||43, 87, 101, 117, 129, 161, 189, 261|
|2,3,4-tri-O-methylgalactose||→6)-d-Galp-(1→||0.35||43, 87, 101, 117, 129, 161, 173, 189, 233|
|2,3,4-tri-O-methylxylose||→6)-d-Xylp-(1→||0.20||87, 99, 117, 139, 161, 217, 233|
|Table 2. Chemical shift data for ABP isolated from the fruiting bodies of A. bisporus.|
|Residue||Proton or carbon (1H/13C)|
|→4)-α-d-Manp (1→ (a)||H||5.29||4.51||4.16||3.93||3.87||4.04 3.89|
|→6)-β-d-Glcp (1→ (b)||H||4.83||3.63||4.02||3.78||3.79||3.98|
The NMR signals of galactose and xylose were no indication owing to their poor nuclear magnetic resonance characterizations.
© 2014 by the authors; licensee MDPI, Basel, Switzerland This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).